Skip to main content
Science in One Health logoLink to Science in One Health
. 2025 Jun 28;4:100116. doi: 10.1016/j.soh.2025.100116

Milk and meat safety in Nepal: addressing challenges and exploring solutions

Deepak Subedi a,⁎,1, Sameer Thakur b,1, Anil Gautam c, Madhav Poudel d, Sumit Jyoti e, Abhinandan Devkota f, Milan Kandel g,h, Ananda Tiwari i,⁎⁎
PMCID: PMC12308024  PMID: 40740965

Abstract

The transmission of zoonotic diseases through animal-derived food products poses a significant global public health challenge, with contaminated milk and meat serving as major transmission pathways. In Nepal, the growing consumption of these products has amplified the risk of foodborne illnesses, largely due to widespread bacterial contamination. This review systematically explores the prevalence, distribution, and public health significance of key bacterial pathogens, including Salmonella, Escherichia coli, Shigella, Staphylococcus aureus, Brucella, Bacillus cereus, Mycobacterium tuberculosis, and Campylobacter in Nepalese milk and meat products. The analysis identifies major contributing factors: inadequate hygiene and sanitation practices, weak regulatory frameworks, insufficient infrastructure, improper antibiotic usage, and limited public awareness. The high levels of bacterial contamination, coupled with the emergence of antibiotic-resistant strains, underscore the urgency for strategic interventions. Recommended measures include strict enforcement of hygiene and sanitation standards, strengthening regulatory policies, enhancing infrastructure, comprehensive public education campaigns, and prudent antibiotic stewardship. Implementation of these strategies is imperative to improve food safety, protect public health, and mitigate the risks posed by bacterial zoonotic diseases in Nepal.

Keywords: Bacteria, Developing country, Escherichia coli, Food safety, Nepal, Public health, Salmonella

1. Introduction

Zoonotic diseases, which are naturally transmitted between vertebrate animals and humans, represent a significant public health concern worldwide. Alarmingly, more than 60 % of all infectious diseases and 75 % of emerging infectious diseases are estimated to be of zoonotic origin [1]. These diseases are typically transmitted through direct contact with infected animals [2] or humans [3], consumption of contaminated food or water [4], and contact with contaminated environments, fomites, or vectors [5]. Foodborne zoonoses are acquired through the consumption of animal-derived products like unpasteurized milk, raw or undercooked meat, and contaminated eggs [6,7]. These diseases pose a significant risk to public health and disrupt the production and trade of animal products for food and other purposes [8]. According to the World Health Organization (WHO), unsafe food causes 600 million illnesses and 420,000 deaths annually, with children under five accounting for 30 % of these fatalities [9]. Around 10 % of the global population falls ill each year due to the consumption of contaminated food, with milk and meat accounting for the largest share of these cases [10].

In Nepal, the rising consumption of milk and meat, currently averaging 79 L and 18 kg per capita per year, respectively, reflects the rapid growth of the billion-rupee livestock industry [11]. However, this increase in demand has not been matched by commensurate improvements in hygiene practices, regulatory oversight, or food safety infrastructure [12]. The lack of modern slaughterhouses and cold chain infrastructure, poor milk and meat handling practices, environmental contamination, and the widespread use of antibiotics have all contributed to significant bacterial contamination in the milk and meat supply [13,14]. Numerous studies from Nepal have reported alarming levels of bacterial contamination in milk and meat products, including the presence of foodborne pathogens like Salmonella, Escherichia coli, Shigella, Staphylococcus aureus, Campylobacter, Brucella, Bacillus cereus, and Mycobacterium tuberculosis [[13], [14], [15], [16], [17]]. These bacteria are responsible for significant public health burdens, especially among vulnerable populations. The situation is further compounded by the misuse of antibiotics in food animals, which has contributed to the emergence and spread of antimicrobial-resistant pathogens, posing additional threats to both human and animal health [18]. Despite the presence of food safety standards, including the Food Act (1967), the Animal Slaughterhouse and Meat Inspection Act (1999), and the Food Safety Policy (2019), enforcement remains weak due to limited infrastructure, technical capacity, and public awareness [14,17]. Traditional practices, including the consumption of raw milk and undercooked meat, further increase the population's exposure to foodborne pathogens.

Given these multifaceted challenges and public health implications, a comprehensive understanding of the extent and nature of bacterial contamination in milk and meat is essential. Although numerous studies have reported the presence of bacterial pathogens in milk and meat, the data remain scattered, often lacking integration across microbial, regulatory, and socio-cultural domains. This review critically examines the prevalence, types, and public health significance of bacterial pathogens in milk and meat supply chains in Nepal. It also assesses the risk factors and challenges associated with food safety and outlines targeted strategies for improving hygiene practices, regulatory compliance, antibiotic stewardship, and public education. The outcomes are intended to inform science-driven policy formulation, enhance national food safety strategies, and support the development of a resilient, health-conscious livestock production system in Nepal.

2. Milk and meat production in Nepal

Over the decade from 2013/2014 to 2022/2023, national milk production experienced a notable upward trajectory, with total output rising by 53.8 %, from 1.70 million t to 2.61 million t (Fig. 1) [19]. This represents an average annual growth rate of 5.4 %. Cattle milk production accounted for the most significant increase, more than doubling from 532,300 t to 1,214,046 t—an overall rise of 128.1 % and an average annual growth rate of 12.8 %. In contrast, buffalo milk production demonstrated a relatively modest growth of 19.9 %, increasing from 1,167,773 t to 1,399,797 t over the same period, with an average annual increase of 2 %. While buffalo milk still represents a larger share of national milk output, the proportion of cattle milk has risen considerably. This shift highlights evolving trends in dairy production systems, driven primarily by breed improvement, changes in feed and management practices, market preferences, and policy support favoring higher-yielding cattle breeds [20].

Fig. 1.

Fig. 1

Milk production in Nepal over the past decade from the fiscal year 2013/2014 to 2022/2023.

Between 2013/14 and 2022/23, total meat production (buffalo, mutton, chevon, pork, chicken and duck) in Nepal increased by 44.20 %, from 298,244 t to 430,085 t, with an average annual growth rate of 4.40 % (Fig. 2) [19]. However, trends varied by meat types. Poultry showed the most substantial growth: chicken surged by 365.30 % (from 43,133 t to 200,658 t), with an average annual increase of 36.52 %, while duck meat surged by 496.50 % (from 227 t to 1355 t), growing 49.65 % annually. In contrast, red meats such as buffalo and mutton production declined. Buffalo meat dropped by 33.01 % (from 173,906 t to 116,503 t), and mutton by 29.40 % (from 2656 t to 1874 t), with negative annual growth rates of −3.30 % and −2.90 %, respectively. Goat meat (chevon) increased moderately by 30.67 % (from 59,053 t to 77,162 t), averaging 3.10 % growth, while pork rose by 68.80 % (from 19,269 t to 32,533 t), averaging 6.90 % annual growth. These shifts reflect changing consumer preferences and production practices, with poultry gaining dominance, likely due to its shorter production cycle, lower input costs, and broader market appeal, while the large ruminant meat production is declining, possibly due to higher production costs, land constraints, and changing dietary trends. With increasing milk and meat consumption, this paper explores the associated food safety risks and challenges in Nepal.

Fig. 2.

Fig. 2

Meat production in Nepal over the past decade from the fiscal year 2013/2014 to 2022/2023.

3. Challenges of milk and meat safety in Nepal

3.1. Bacterial contamination of milk

3.1.1. Salmonella

Salmonellosis is one of the most prevalent foodborne bacterial diseases globally [21]. In many developed nations, Salmonella ranks as the second most leading cause of foodborne illnesses, causing symptoms like diarrhea, abdominal cramps, vomiting, and fever [22]. In Nepal and other developing countries, however, it remains a neglected zoonotic disease [23]. A study by Parajuli et al. [24] found Salmonella in 7.5 % of 60 raw milk samples collected from local dairies (45 samples) and cow farms (15 samples) across the Kathmandu Valley. Another study examining 14 milk brands from valley outlets reported a 3 % contamination rate in raw milk samples [25]. The 2017 Salmonella agona contamination of Lactalis baby formula, linked to infant deaths across Europe, also raised global food safety concerns, including in Nepal [26]. Contributing factors to Salmonella contamination in milk likely include poor hygiene, use of contaminated utensils, and adulteration with unsafe water [27].

3.1.2. Escherichia coli

Shiga toxin-producing E. coli (STEC), also known as verotoxin-producing E. coli (VTEC), is characterized by the presence of stx1 and stx2 genes [28]. This pathogen poses serious global public health and economic risks, primarily transmitted through contaminated milk, meat, and dairy products [29]. Symptoms of STEC infections range from mild diarrhea to severe illnesses like hemorrhagic colitis (HC) and hemolytic uremic syndrome (HUS), which occurs in 5 %–15 % of cases [30].

Numerous studies have reported E. coli contamination in milk across Nepal. One study found 92 % of raw milk samples from 14 brands in the Kathmandu Valley were contaminated [25]. Another reported contamination in 27.3 % of samples—18.8 % in pasteurized, 40 % in unpasteurized, and 20 % in raw milk (Table 1) [[30], [34]]. In Kathmandu district, 45.7 % of 70 milk samples (52.5 % raw, 36.7 % pasteurized) tested positive [33], while Parajuli et al. [24] found E. coli in 32 % of samples from local dairies and 24 % from cow farms in Kathmandu Valley. In Dharan, E. coli was detected in 55 % of raw and 30 % of pasteurized milk samples from five dairy industries [34]. Shrestha et al. [35] found 33.3 % of raw and 6.7 % of pasteurized samples contaminated in Kathmandu, Bhaktapur, Lalitpur, and Kavrepalanchok. Bohara et al. [36] reported a 43.3 % overall prevalence in Kathmandu, with 60 % of raw and 26.6 % of pasteurized samples testing positive. Gautam et al. [37] found E. coli in 29.4 % of 102 raw buffalo milk samples in Rupandehi. A recent study by Shrestha et al. [38] found E. coli in 29.6 % of 267 raw cattle milk samples, with STEC identified in 11.6 %. Among these, 1.1 % were O157 STEC and 10.5 % non-O157 STEC. The z3276 gene, specific to O157, was found in only three isolates, all of which carried stx genes. These findings highlight the widespread contamination of milk with E. coli, including pathogenic STEC strains, across Nepal, underscoring urgent food safety challenges and the pressing need for stronger regulatory and hygiene measures.

Table 1.

Prevalence of Escherichia coli in milk samples from various regions of Nepal.

Study location Year Milk type Sample size Microbiological test Escherichia coli prevalence (%) Reference
Kathmandu Valley and Kavrepalanchok districts 2023 Pasteurized and raw milk 30 (15 each) Total viable count (TVC) by pour plate method, E. coli isolation and identification by inoculation on MacConkey agar 6.67 % for pasteurized and 33.33 % for raw milk [35]
Kathmandu district 2021 Pasteurized and raw milk 30 (15 each) Total coliform count by violet red bile agar (VRBA), E. coli isolation and identification by inoculation on MacConkey agar Overall 43.3 %, 26.6 % for pasteurized, and 60 % for raw milk [36]
Rupandehi district 2021 Raw buffalo milk 102 E. coli isolation and identification by inoculation on eosin methylene blue (EMB) agar, isolated colonies of E. coli were confirmed by Gram staining and biochemical tests 29.4 % [37]
Chitwan district 2020 Raw cattle and buffalo milk 972 quarters from 243 animals (193 cows and 50 buffalo) E. coli isolation and identification by inoculation on EMB agar, isolated colonies of E. coli were confirmed by Gram staining and biochemical tests 5 % (49/972) [32]
Kathmandu district 2020 Pasteurized and raw milk 70 (30 pasteurized and 40 raw milk) Total coliform count by pour plate method, E. coli isolation by enrichment in buffered peptone water and culture on EMB agar Overall 45.71 %, 36.7 % for pasteurized, and 52.5 % for raw milk [33]
Dharan district 2019–2020 Pasteurized and raw milk 40 (20 pasteurized and 20 raw milk) Total plate count (TPC) by plate count agar, total coliform count (TCC) by VRBA, and thermoduric bacterial count (TBC), E. coli isolation and identification by inoculation on MacConkey agar 30 % for pasteurized and 55 % for raw milk [34]
Kathmandu Valley 2019 Raw milk 60 (40 local dairies and 15 cow farms) TPC by plate count agar, TCC by VRBA 32 % [24]
Chitwan district 2018–2019 Raw cattle milk 267 E. coli isolation and identification by inoculation on MacConkey agar for non-O157 and sorbitol MacConkey (SMAC) agar for O157, confirmation with biochemical tests Overall 29.6 % and 11.6 % for Shiga toxin-producing E. coli (STEC) (1.1 % for O157 STEC and 10.5 % for non-O157 STEC) [38]
Kathmandu Valley 2017 Pasteurized, unpasteurized, and raw milk 66 (16 pasteurized, 25 unpasteurized, and 25 raw milk) TPC, total coliform count by pour plate method, biochemical tests 18.8 % for pasteurized, 40 % for unpasteurized, and 20 % for raw milk [31]
Kathmandu Valley 2004 Raw milk (14 different milk brands) 140 (10 samples of each brand) Methylene blue reduction time test (MBRT), direct microscopic count (DMC), TPC 92 % [25]

3.1.3. Shigella

Shigella, commonly found in water and feces, can contaminate milk, causing bacillary dysentery, especially in developing countries [39]. Although a significant global health threat, Shigella is often overlooked in animals such as cows, chickens, pigs, and monkeys [40]. In countries like Nepal, shigellosis remains a major foodborne illness, particularly affecting children and immunocompromised individuals [41]. A study by Arjyal et al. [25] found Shigella in 3 % of raw milk samples from 14 milk brands in the Kathmandu Valley. Another study detected Shigella species, including S. boydii, S. flexneri, S. sonnei, and S. dysenteriae—in ice cream samples from Kathmandu, indicating poor hygiene and careless manufacturing practices [42]. However, a more recent study by Parajuli et al. [24] found no Shigella contamination in 60 raw milk samples from local dairies and cow farms in the Kathmandu Valley.

3.1.4. Staphylococcus aureus

Staphylococcal food poisoning is a major global foodborne illness, second only to salmonellosis. S. aureus, a key pathogen in fresh and ready-to-eat foods, contaminates products through poor storage, handling, unsanitary utensils, and milking conditions, producing harmful enterotoxins that reduce food quality and safety [[43], [44]]. Studies from Nepal, especially in the Kathmandu Valley, report notable S. aureus contamination in milk. Arjyal et al. [25] found 15 % contamination in raw milk from 14 milk brands. Acharya et al. [31] reported 16 % contamination in unpasteurized, 12.5 % in pasteurized milk, and 24% in raw milk samples. Rai et al. [33] found S. aureus in 67.5 % of raw and 10 % of pasteurized milk samples (42.9 % overall). Another study reported contamination in 40 % of farm milk, 30 % of dairy milk, and 10 % of packaged milk (26.7 % overall) [18]. Bohora et al. [36] found 50 % contamination, mostly in raw milk (86.7 %). In Pokhara, Joshi et al. [45] found S. aureus in 29.7 % and methicillin-resistant Staphylococcus aureus (MRSA) in 11.25 % of 400 milk samples from 10 farms. In Dharan, prevalence was 45 % in raw and 20 % in pasteurized milk [34]. Tiwari et al. [46] reported an exceptionally high prevalence (93.3 %) in California mastitis test-positive raw buffalo and cattle milk in Chitwan. The prevalence of S. aureus and MRSA in milk samples from different regions of Nepal is summarized in Table 2.

Table 2.

Prevalence of Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) in milk samples from different regions of Nepal.

Study location Year Milk type Sample size Prevalence (%) Reference
Kathmandu district 2023 Farm milk 30 40 % [18]
Dairy milk 30 30 %
Pasteurized packaged milk 30 10 %
Kathmandu Valley 2023 Raw milk 15 86.7 % [36]
Pasteurized milk 15 13.3 %
Chitwan district 2022 Raw buffalo and cattle milk 104 93.3 % [46]
Kathmandu district 2020 Raw milk 40 67.5 % [33]
Pasteurized milk 30 10 %
Dharan district 2020 Raw milk 20 45 % [34]
Pasteurized milk 20 20 %
Kathmandu Valley 2017 Pasteurized milk 12.5 % [31]
Unpasteurized milk 16 %
Pokhara Valley 2014 Raw milk 400 29.7 % for S. aureus and 11.3 % for MRSA [45]
Kathmandu Valley 2004 Raw milk 14 brands 15 % [25]

3.1.5. Brucella

Brucellosis is a major public health and livestock concern in developing countries, affecting both humans and animals [47]. Human infections are primarily caused by Brucella abortus, Brucella melitensis, Brucella suis, and Brucella canis, with B. melitensis being the most virulent, followed by B. suis [48]. As few as 10–100 organisms can cause infection. Transmission occurs mainly through unpasteurized milk, dairy products, or undercooked meat [49]. Symptoms are often non-specific—fatigue, malaise, arthritis, and fever—and while rarely fatal, the illness can be long-lasting and debilitating [50]. In animals, brucellosis impairs reproduction, reduces milk yield, and affects offspring survival [47]. National surveys by Nepal's Department of Health Services indicate a 2 %–3 % seroprevalence in cattle [17]. Although no studies have confirmed Brucella in raw milk or meat in Nepal, the high seroprevalence in livestock and human cases indicate a probable association.

3.1.6. Bacillus cereus

B.cereus has emerged as a significant foodborne pathogen, frequently found in meat, milk, and dairy products [51]. Commonly found in soil, B. cereus likely enters the food chain through soil or water contamination [52]. It often causes outbreaks linked to heat-treated foods, where spore germination occurs. Without competing microbes, B. cereus proliferates post-cooking, producing enterotoxins that lead to illness [53]. Understanding its toxin profiles has clarified its role in foodborne disease [54]. Arjyal et al. [25] found Bacillus in 18 % of milk samples from 14 milk brands in Kathmandu Valley. Another study of 240 ready-to-eat foods in Kathmandu reported B. cereus in 40 % of the samples, with 28 % contamination in dairy products. Among 80 dairy samples, bacterial growth was found in 50 % of butter (3/6) and 37 % of cheese (19/52), while cream, ghee, and yogurt showed no growth [55].

3.1.7. Mycobacterium tuberculosis and Mycobacterium bovis

Tuberculosis (TB) in humans is caused by M. tuberculosis, results in millions of infections and hundreds of thousands of deaths worldwide [56]. M. bovis, in contrast, causes bovine TB in cattle, also known as zoonotic TB, which humans can contract through unpasteurized dairy products, handling sick animals, or occupational exposure. The connection between zoonotic TB in humans and cattle in Nepal remains unclear [16]. Bovine TB is globally widespread, causing substantial economic losses in animal production. It is a major infectious disease in cattle, other domestic animals, and some wildlife, posing a public health risk through the consumption of raw milk, close proximity of cattle to human dwellings, and in individuals with immunosuppressive conditions [57]. Due to its severe impact on animal and human health, rigorous control measures are essential to mitigate the risk of M. bovis infection [50].

In Mahendranagar, Kanchanpur, researchers tested 70 symptomatic individuals (40 males and 30 females) from 125 households, analyzing a total of 200 samples. They found 10 cases positive for tuberculosis, indicating a 9 % prevalence rate (Table 3). To explore the potential for animal-to-human transmission, livestock from these households were also examined. Among the 70 livestock tested, 8 were positive, indicating an 11 % prevalence rate [58]. Additionally, a retrospective matched case–control study conducted at the National Tuberculosis Center (NTC) in Bhaktapur, Nepal, further explored the link between cattle exposure and human TB. The study found that cattle exposure was a significant risk factor for human TB, with 9.76 % of cattle testing positive by tuberculin, 37.4 % by the rapid test, and 5.7 % by ELISA, showing strong agreement between the tuberculin and ELISA results [16]. Similarly, a study conducted by Jha et al. [59] on milk and fecal samples from 36 buffaloes and 32 cattle in Kathmandu, all of which tested positive for the single intradermal cervical tuberculin (SICT) test, identified 36 mycobacterial strains. Of these, 13 strains were classified as M. bovis, affecting 17 % of buffaloes and 16 % of cattle. M. bovis was detected in both the milk and feces of one buffalo and one cattle, in the milk of three buffaloes and three cattle, and in the feces of two buffaloes and one cattle. The remaining 23 strains were found to be atypical mycobacteria [59]. In a study conducted by Pandey et al. [60] in Chitwan, 100 bovines (22 cattle and 78 buffalo) from 60 farms with tuberculosis-positive patients were tested for bovine tuberculosis. The overall prevalence was 15 % with 13.6 % of cattle and 15.4 % of buffaloes testing positive. Furthermore, 24 % of the tuberculosis patients reported consuming raw milk, suggesting that milk could be a potential channel for M. bovis transmission to humans [60]. More recently, a surveillance study by Upadhyaya et al. [61] involving 400 blood samples from cattle and buffalo found that 74 animals (18.75 %) tested positive for M. bovis, with the majority being cattle (71 samples, 17.75 %) and only three cases in buffalo (<1 %). This high prevalence of M. bovis in dairy animals poses a significant public health threat, especially to those consuming milk. These findings underscore the urgent need for improved hygiene, regulatory enforcement, pasteurization, and public education to mitigate the risk of milk-borne diseases.

Table 3.

Prevalence of tuberculosis (TB) in livestock from various regions of Nepal.

Location Year Sample size Test used TB prevalence Reference
Eastern Nepal 2023 400 (cattle and buffalo) Rapid bovine TB test kit 18.75 % (17.75 % in cattle and 0.75 % in buffalo) [61]
Kathmandu, Bhaktapur, Lalitpur and Kavrepalanchok districts 2020 123 cattle Tuberculin, rapid test, ELISA 9.76 % of the cattle were positive by tuberculin, 37.4 % by the rapid test, and 5.7 % by ELISA [16]
Chitwan district 2013 100 bovines (22 cattle and 78 buffalo) Intradermal tuberculin test 15 % (13.6 % in cattle and 15.4 % in buffaloes) [60]
Kathmandu district 2007 36 buffaloes, 32 cattle Single intradermal cervical tuberculin (SICT) 17 % in buffaloes and 16 % in cattle [59]
Mahendranagar and Kanchanpur districts 2003 70 humans, 70 livestock Direct sputum examination in humans and intradermal tuberculin test in livestock 9 % in humans and 11 % in livestock [58]

3.2. Bacterial contamination of meat

3.2.1. Salmonella

Salmonella is a widespread pathogen affecting both humans and animals. In humans, salmonellosis often presents as a self-limiting form of food poisoning (gastroenteritis), but it can occasionally develop into a severe systemic infection (enteric fever) that necessitates immediate antibiotic treatment [62]. The zoonotic potential of Salmonella and the growing antimicrobial resistance (AMR) in its strains are important topics in scientific discussions. In Nepal, contaminated meat is a primary source of Salmonella infections in humans [63]. Major routes of contamination include fecal contamination from the gut and the use of substandard water during meat preparation and for cleaning chopping materials.

Research conducted in Nepal consistently shows that Salmonella is more prevalent in chicken meat compared to other types of meat, such as pork, buffalo meat, and chevon. For example, a study analyzing 123 raw meat samples from local markets in Kathmandu reported an overall prevalence of Salmonella in 11.4 % of the samples, with the highest detection rates in chicken meat (14.5 %), followed by buffalo meat (13.5 %), and chevon (3.3 %) (Table 4) [64]. Similarly, another study in Dharan found that 34 % of the 50 meat samples collected from local markets were tested positive for Salmonella, with chicken meat showing the highest prevalence at 60 %, followed by chevon (33.3 %), buffalo meat (20 %), and pork (10 %) [12]. Additionally, in another study involving 320 samples of chicken meat, chevon, buffalo meat, and pork (80 samples each), 26 samples were tested positive for Salmonella, resulting in an overall prevalence of 8.13 %. The specific prevalence rates were 10 % in both buffalo and chicken meat, 7.5 % in chevon, and 5 % in pork [65]. Moreover, in a study conducted in Bhaktapur Metropolitan City, 140 raw meat samples—70 each of buffalo and chicken—were tested, revealing a Salmonella prevalence of 8.6 % (6 out of 70) in both meat types [66]. Unhygienic slaughtering methods and environments significantly contribute to Salmonella contamination.

Table 4.

Prevalence of Salmonella in meat samples from various regions of Nepal.

Study location Year Sample type Sample size Salmonella prevalence % Reference
Chitwan district 2020 Chicken meat (fresh and frozen) 100 10 % [68]
Bhaktapur district 2019 Raw meat (buffalo, chicken) 140 (70 each) 8.6 % (8.6 % in buffalo meat and 8.6 % in chicken meat) [66]
Dharan city 2019 Chicken meat 35 % [72]
Kathmandu Valley 2019 Chicken meat 81 16 % [73]
Dharan city 2018 Raw meat (various types) 50 34 % (60 % in chicken meat, 33.3 % in chevon, 20 % in buffalo meat, and 10 % in pork) [12]
Chitwan district 2017 Chicken meat 26.2 % [71]
Kanchanpur district 2017 Fresh chicken meat 45 38 % [74]
Pokhara Valley 2016 Raw meat (chicken, chevon, buffalo, and pork) 320 (80 each) 8.13 % (10 % in chicken meat, 10 % in buffalo meat, 7.5 % in chevon, and 5 % in pork) [65]
Chitwan district 2013 Chicken meat 46.2 % [69]
Chitwan district 2013 Chicken meat 18.8 % [70]
Kathmandu district 2012 Environmental swabs (chopping boards, knives, and tables) 492 swabs 40.2 % (36 % in chopping boards, 32.9 % in knives, and 25 % in tables) [67]
Kathmandu district 2006 Raw meat (various types) 123 11.4 % (14.5 % in chicken meat, 13.5 % in buffalo meat, and 3.3 % in chevon) [64]

A study analyzing 492 environmental swab samples from 82 retail meat shops in Kathmandu found that 40.2 % of the shops were Salmonella-positive. The contamination rates were particularly high on chopping boards (36.0 %), knives (32.9 %), and tables (25.0 %) [67]. Another study conducted in Bharatpur, Chitwan, analyzed 100 chicken meat samples (70 fresh and 30 frozen) from wholesale and retail shops, revealing a 10 % prevalence of Salmonella. The consistent isolation rate across both fresh and frozen samples indicates that freezing does not eliminate contamination. This finding underscores the need for stricter hygiene practices and enhanced regulatory oversight to ensure food safety [68]. The prevalence of Salmonella in chicken meat varies across different regions of Nepal, with reported rates of 46.2 % and 18.88 % in the Chitwan district [[69], [70]], 26.2 % in Bharatpur Metropolitan [71], 38 % in Kanchanpur [53], 35 % in Dharan [72], and 16 % in the Kathmandu Valley [73].

3.2.2. E. coli

E. coli are generally harmless bacteria that reside in the intestines of humans and animals, playing a role in maintaining intestinal health [75]. However, consuming food or water contaminated with certain strains of E. coli can lead to mild to severe gastrointestinal issues [76]. Some pathogenic strains, such as STECs, can cause life-threatening conditions [77]. Different E. coli strains are associated with various types of food and water contamination. E. coli O157 is commonly transmitted to humans through the consumption of contaminated food, particularly undercooked ground meat and raw milk [76]. Members of the Enterobacteriaceae family, such as E. coli, account for up to 40 % of foodborne illnesses caused by bacteria [78].

In Nepal, E. coli contamination in meat continues to pose a serious food safety concern, as consistently emphasized in scientific discussions. Among the published data from various regions of Nepal, the highest prevalence of E. coli contamination (100 %) was reported by Gautam et al. [73], who found all 81 raw chicken meat samples from retail shops in the Kathmandu, Lalitpur, and Bhaktapur districts to be positive. In the Kathmandu Valley, several studies have reported varying levels of E. coli contamination in raw meat. One study found a 10 % (4/40) prevalence in buffalo meat samples from local markets [79], while a similar study reported a 22.5 % (9/40) prevalence in chicken meat [80]. Additionally, research conducted in Bhaktapur Metropolitan City on 140 raw meat samples, comprising 70 buffalo and 70 chicken meat samples, revealed 34.3 % (24/70) E. coli prevalence in buffalo meat and 47.14 % (33/70) prevalence in chicken meat [66].

Studies conducted in the eastern region of Nepal also indicate a concerning level of E. coli contamination in meat samples. Research from a butcher's shop in Dharan involving 24 samples (6 chicken meat, 6 buffalo meat, 6 pork, and 6 chevon) found a 41.66 % incidence of non-sorbitol fermenting E. coli O157, with prevalence rates of 50 % in both chicken and buffalo meat, and 33.33 % in pork and chevon (Table 5) [81]. Another study in Dharan reported 54 % of the 50 meat samples (15 chicken meat, 15 pork, 10 buffalo meat, and 10 chevon) from local markets were contaminated with E. coli, with contamination levels of 66.6 % in chicken meat, 60 % in pork, 40 % in buffalo meat, and 46.7 % in chevon [12]. Similarly, Bantawa et al. (2019) found that 53 % of 83 meat samples (33 chicken meat, 27 pork, 13 buffalo meat, and 10 chevon) collected from various meat shops in Dharan were positive for E. coli [72]. In Biratnagar, Morang, a study involving 80 meat samples from 40 outlets (40 chicken and 40 mutton) revealed an overall E. coli prevalence of 61.3 %, with 62.5 % in chicken and 60 % in mutton [82].

Table 5.

Prevalence of Escherichia coli in meat samples from various regions of Nepal.

Study location Year Meat type Sample size E coli prevalence % Reference
Chitwan district 2024 Chicken meat 105 58.1 % [83]
Kathmandu Valley 2023 Chicken meat 40 22.5 % [80]
Dharan city 2022 Mixed meat (chicken, buffalo, pork, and chevon) 24 (6 each) 41.66 % (E. coli O157), 50 % in both chicken and buffalo, and 33.33 % in pork and chevon [81]
Chitwan district 2022 Chopping board meat samples 33 % [84]
Kathmandu Valley 2021 Buffalo meat 40 10 % [79]
Chitwan district 2020 Chicken (fresh and frozen) 100 56 % [68]
Kathmandu Valley 2019 Raw chicken meat 81 100 % [73]
Bhaktapur district 2019 Raw meat (buffalo and chicken) 140 (70 each) 34.3 % [66]
Dharan city 2019 Mixed meat (chicken, buffalo, pork, and chevon 83 (33 chicken, 27 pork, 13 buffalo, and 10 chevon) 53 % [72]
Biratnagar district 2019 Chicken and mutton 80 (40 each) 61.3 % overall (62.5 % in chicken and 60 % in mutton) [82]
Dharan city 2018 Mixed meat (chicken, buffalo, pork, and chevon 50 (15 chicken, 15 pork, 10 buffalo, and 10 chevon) 54 % overall (66.6 % in chicken, 60 % in pork, 40 % in buffalo, and 46.7 % in chevon) [12]
Chitwan district 2017 Chicken meat 38 4.8 % [84]
Kanchanpur district 2017 Fresh chicken meat 45 40 % [74]
Nepal (various regions) 2019 Chicken meat (skin, flesh, and liver) 180 (60 each) 33.3 % overall and 26.7 % of isolates resistant to colistin (mcr-1 gene detected) [85]

Several studies from the Chitwan district also highlight E. coli contamination in meat. In Bharatpur, 56 % of 100 chicken samples from wholesale and retail shops were contaminated, with a higher rate in fresh samples (72.8 %) [68]. Ranabhat et al. [83] reported a 58.1 % prevalence in 105 broiler meat samples, while Regmi et al. [84] found 33 % contamination in meat samples from chopping boards, though non-ESBL-producing strains. A study by Shrestha et al. [71] detected E. coli in 4.8 % of 38 chicken meat samples. Similarly, in a single study from western Nepal, 45 fresh chicken meat samples from Kanchanpur were analyzed, where 40 % (18/45) were contaminated with E. coli [74]. In addition to the high prevalence of E. coli across various regions of Nepal, the detection of antibiotic-resistant genes is particularly alarming. A study by Joshi et al. [85] examined 180 chicken meat samples (60 each of skin, flesh, and liver), isolating E. coli in 33.3 % (60/180) of the samples. Notably, 26.66 % (16/60) of these isolates were resistant to colistin and carried the mcr-1 gene, highlighting a serious public health concern.

3.2.3. Campylobacter

Campylobacter species are major causes of human gastrointestinal infections globally, with Campylobacter jejuni and Campylobacter coli frequently causing gastroenteritis [86]. These bacteria are common in infants with diarrhea in developing countries like Nepal due to contaminated food or water [87]. Poultry, along with other domestic animals, are a major source and reservoir of these zoonotic pathogens, facilitating the transmission of campylobacteriosis to humans [88]. In Nepal, Campylobacter is one of the leading causes of foodborne infections, and antibiotic-resistant strains of this bacterium have been reported in poultry and pig carcasses [87,89,90]. Research on campylobacteriosis in Nepal is limited, largely because many cases go undiagnosed due to the lack of hospitalization requirements and the need for advanced laboratory procedures, which are not widely accessible. Ghimire et al. [90] analyzed 139 pork samples from the neck, ham, shoulder, and skin, finding a Campylobacter prevalence of 38.85 % (54/139). Of the isolates, 77.8 % were C. coli and 22.2 % were C. jejuni. Similarly, Bhattarai et al. [91] collected 400 retail broiler meat samples from Chitwan, with 44.8 % testing positive for Campylobacter. Among these, C. jejuni was the most prevalent at 80.4 %, followed by C. coli at 14.5 % and C. lari at 4.9 %. Additionally, 7.3 % of the samples were infected with multiple Campylobacter species. Moreover, Bhattarai et al. [89] sampled water from 200 slaughterhouse sites in Kathmandu and Rupandehi districts, finding a Campylobacter prevalence of 12 % in Rupandehi and 0 % in Kathmandu.

3.2.4. Shigella

Shigella is a major cause of diarrhea, particularly dysentery, often referred to as bacillary dysentery. Among the four species of Shigella, serotype A (Shigella dysenteriae) and serotype B (Shigella flexneri) are the most commonly associated with shigellosis in Nepal [92]. Globally, changes in prevalent serogroups have been observed, and Nepal is no exception. While S. dysenteriae was the predominant species in Nepal during 2003 and 2004, S. flexneri has been the most prevalent since 2005 [[92], [93], [94]]. This global trend is mirrored in local studies. A study conducted in 45 samples of fresh chicken meat from Kanchanpur found that 17 samples (38 %) were contaminated with Shigella [74]. Similarly, in Dharan, 6 % of 50 meat samples (15 chicken, 15 pork, 10 buffalo, and 10 chevon) collected from local markets were tested positive for Shigella, with specific prevalence rates of 4 % in chicken, 0 % in pork, 2 % in buffalo, and 0 % in chevon [12]. Bantawa et al. [72] reported a 6 % positive rate for Shigella in 83 meat samples (33 chicken, 27 pork, 13 buffalo, and 10 chevon) from various meat shops in Dharan. Additionally, a study in the Kathmandu Valley revealed a 2.5 % prevalence of Shigella in 40 raw chicken meat samples from local markets [80].

3.2.5. S. aureus

S. aureus is a significant foodborne pathogen found in both fresh and ready-to-eat foods, and it is associated with a range of infections globally [95]. Due to its strong adaptability, S. aureus can adjust to diverse environmental conditions and quickly develop resistance to nearly all antibiotics [96]. Recently, MRSA has gained significant attention due to its AMR to multiple antibiotics. In 2017, the WHO identified it as one of the 12 bacterial families representing the greatest threat to human health [97]. In a study, 57 % of 45 fresh chicken meat samples from Kanchanpur were tested positive for S. aureus [74]. Bantawa et al. [12] found that 68 % of the 50 meat samples from Dharan were positive, with prevalence rates of 53.33 % in chicken meat, 73.33 % in pork, 80 % in buffalo meat, and 70 % in chevon. A subsequent study reported a 68 % positive rate for S. aureus in 83 meat samples from Dharan [72]. In Bhaktapur, 8.6 % of 70 buffalo meat and 12.9 % of 70 chicken meat samples were positive for S. aureus [66]. In Biratnagar, 48.8 % of 80 meat samples (40 chicken and 40 mutton) were tested positive, with 52.5 % in chicken meat and 45 % in mutton [82]. Additionally, a study conducted by Devkota et al. [98], isolated 139 S. aureus strains (67.8 %) from 205 samples, including 71.2 % from eggs and 62.5 % from chicken meat, with an overall MRSA prevalence of 12.94 %. These findings underscore the urgent need for enhanced monitoring and control measures.

3.2.6. Listeria monocytogenes

L. monocytogenes, the primary cause of listeriosis, is a significant emerging foodborne bacterial zoonotic pathogen of global importance. This bacterium has been found in meat, poultry, milk, cheese, other dairy products, and vegetables [99]. L. monocytogenes is a major food safety concern as it can cause disease in humans and can be transmitted through animal-derived food products [100]. Refrigeration doesn't inactivate or kill bacteria, so adequate cooking is of great importance [101]. Due to its high mortality rate, listeriosis and outbreaks caused by L. monocytogenes have a significant economic impact on public health and the food industry. This disease particularly affects young children (neonates) and the immunocompromised elderly population [102]. There are no published data on the direct presence of Listeria in milk and meat in Nepal. A study conducted at the College of Medical Sciences, Bharatpur, screened 234 antenatal mothers aged 17–39 years, who were between 7 and 36 weeks of gestation and exhibited flu-like symptoms, for L. monocytogenes. The study found a 16.7 % prevalence of L. monocytogenes (39/234), with the highest infection rate (53.1 %) observed among women aged 25 to 32, predominantly from urban areas. The study identified that the highest rates of listeriosis were associated with the consumption of meat (97.4 %, 38/39), fish (100 %, 39/39), non-pasteurized boiled milk (100 %, 39/39), and vegetables such as salad (82.1 %, 32/39) [103]. These findings highlight an urgent need for surveillance and control measures for L. monocytogenes in Nepal, particularly in high-risk food items and vulnerable populations.

3.3. Raw milk and meat consumption in Nepal

Nepal is a multi-cultural nation with diverse ethnic and cultural practices, many of which lack scientific validation. One such practice is the consumption of raw milk and meat. Every day, a significant quantity of inadequately pasteurized milk and dairy products is consumed in Nepal, and several reports have documented contamination of these products with harmful microorganisms [60]. A recent survey revealed that many individuals regularly consume raw milk [[60], [104]], increasing the risk of acquiring zoonotic foodborne illnesses. Additionally, in various regions, raw milk serves as the base for traditional products such as dahi (yogurt), gheu (dried butter), and mohi (buttermilk) [105], further elevating the risk of zoonotic disease transmission. While these dairy products are consumed across Nepal, they are particularly common in rural areas and among subsistence farmers [105].

Knowledge of zoonotic risks among livestock farmers in Nepal remains alarmingly low. A recent study of 380 livestock farmers found that only 1.6 % were aware of zoonotic brucellosis, and just 3.1 % knew about bovine TB [106]. These findings highlight a significant gap in awareness regarding zoonotic diseases. More than 80 % of Nepal's population adheres to Hinduism, with approximately 16 % identifying as Chhetri and 12 % as Brahmin [107]. Within Hindu religious practices, especially among Chhetri and Brahmin communities, consuming Panchamrit—a sacred mixture of five ingredients, including raw cow milk—is customary during almost all religious ceremonies (puja) [108]. Although typically only 1–2 spoonfuls of Panchamrit are consumed on these occasions, the risk of zoonotic transmission cannot be overlooked, particularly since around 28 % of Nepalese people consume Panchamrit at least once annually.

Although properly cooked meat is commonly consumed in Nepal, a significant portion of the population also consumes raw or undercooked meat products, contributing to zoonotic disease risks. Various ethnic communities maintain unique traditions involving raw meat consumption. For example, the Newar community prepares indigenous dishes such as Kachela (minced raw buffalo meat) and Chhoyla (smoked buffalo meat). Similarly, Sekuwa—roasted pork, chicken, or chevon cooked over a natural wood fire—is often consumed semi-cooked. The Dum communities in southeastern Nepal traditionally consume raw or undercooked meat and viscera from scavenging pigs during religious and social festivals. In the hilly and Himalayan regions of far-western Nepal, people consume Kachmali, which includes raw chevon with body parts such as ears, tail, liver, kidney, tongue, skin, brain, sternum, and testicles. Additionally, the Indo-Aryan ethnic group in the far-western region frequently consumes raw wild boar meat, known as Bade. Cultural practices such as drinking fresh raw yak blood, believed to have medicinal benefits, are also observed among the Sherpa community in Solukhumbu and the Thakali people in Mustang [109].

Although several foodborne diseases in livestock capable of transmitting to humans through the consumption of raw or undercooked meat have been documented in Nepal, limited research has assessed the actual burden of these infections within the population.

Few studies are conducted for helminths and protozoa, and among the few studies available, serological research conducted in the western regions (Dang and Accham) reported a high prevalence of Toxoplasma gondii infection among the Indo-Aryan group, particularly those with raw meat-eating habits [110]. Furthermore, the frequent diagnosis of neurocysticercosis, primarily linked to consuming undercooked pork, underscores the urgent need for additional research and public health interventions [109].

Further studies are essential to identify the risk factors and prevalence of foodborne bacterial pathogens across various types of milk and meat in Nepal, especially among communities and ethnic groups that consume raw milk, meat, and blood.

3.4. Lack of regulatory framework and enforcement

In Nepal, the Department of Food Technology and Quality Control has set legal standards for milk and dairy products, including microbiological, chemical, and physical criteria to ensure their safety for consumption. The National Dairy Development Board introduced the Code of Practice for the Dairy Industry 2061 (2004), outlining six criteria for standardizing milk and dairy products: organoleptic, clot on boiling (COB), alcohol, milk fat (FAT) and solids not fat (SNF), adulteration, phosphate, and microbial and coliform testing [111]. Similarly, the Food Act (1967) and the Animal Slaughterhouse and Meat Inspection Act (1999) are the primary legal frameworks for meat safety in Nepal [14]. However, these laws fail to address modern food safety challenges due to factors such as lack of risk assessment principles, insufficient resources and infrastructure, inadequate facilities for food contamination analysis, and limited stakeholder awareness [112]. The Food Safety Policy 2076 was approved by the government on 23 June 2019, marking an initial step toward improving food safety [113]. In May 2021, Kathmandu Metropolitan City established eight slaughterhouses and cold storage facilities to handle large quantities of meat. In 2019, Heifer International Nepal partnered with five local governments—Pokhara, Biratnagar, Bharatpur, Butwal, and Kolhapur to develop modern abattoirs [114]. Dairy development is overseen by the Ministry of Agriculture and Livestock Development (MoALD) and implemented through the National Dairy Development Board (NDDB), the country's leading autonomous body for dairy development.

In Nepal, meat for consumption is sourced differently in urban and rural areas. In urban centers, meat is typically purchased from local butchers (Fig. 3), while in villages, communal animal slaughtering is common, and the meat is shared among several families on a cost-sharing basis. Lack of enforcement of meat inspection regulations and the absence of proper slaughterhouse facilities lead to unsanitary practices. Animals are slaughtered in unregulated spaces, including the premises of meat shops, streets, riversides, backyards, and open pasturelands, often lacking sanitation facilities and formal antemortem or postmortem examinations, increasing the potential risk of zoonotic and foodborne disease transmission. Additionally, inadequate sanitary and hygiene practices in butcheries during bleeding, handling, processing, retailing, and storage contribute to the microbial contamination of raw meat.

Fig. 3.

Fig. 3

A local poultry meat shop (butcher shop) in Bharatpur, Chitwan, Nepal, preparing chicken for sale. While this setup reflects the accessibility and community-based nature of meat distribution in the country, it also highlights opportunities for improvement in hygiene practices and infrastructure. Enhancing cold storage, introducing protective equipment, and providing training on sanitary meat handling can significantly uplift food safety standards and support the livelihoods of small-scale meat retailers.

The formal or organized sector accounts for only about 20 % of the total annual milk production in Nepal, while the remaining 80 % is handled by the informal sector, where milk is collected, processed, and distributed through traditional channels with minimal regulation and oversight [115]. This widespread reliance on informal markets presents significant challenges for ensuring milk safety, quality control, and public health protection.

Milk handling and distribution in Nepal present numerous challenges that significantly threaten public health. Collection, transportation, and sale of raw milk frequently occur without proper refrigeration or adherence to hygiene standards, leading to a high risk of microbial contamination. In rural areas, farmers often collect milk from multiple households and pool it together, increasing the likelihood of contamination. If even a small portion of the pooled milk contains pathogens, the entire batch becomes unsafe for consumption. This risk is further amplified by the lack of adequate screening and testing facilities to ensure milk safety before pooling and distribution [115].

Transporting raw milk over long distances without refrigeration remains a critical issue. In Nepal, milk is commonly transported in non-refrigerated vehicles, exposing it to fluctuating temperatures and environmental conditions. Warm climate in the Terai region accelerates bacterial growth in unrefrigerated milk, making it unsafe by the time it reaches consumers. Furthermore, transporting milk in open containers, often on the backs of motorbikes or bicycles, exposes it to dust, dirt, and other contaminants, compounding the risk of microbial contamination.

One of the most significant shortcomings in Nepal's milk distribution system is the limited use of pasteurization, a crucial process that eliminates harmful bacteria and pathogens. In many rural areas, farmers sell milk directly to consumers without pasteurization, substantially increasing the risk of zoonotic diseases such as brucellosis and tuberculosis [16].

Infrastructural deficiencies further hinder milk safety. The absence of cold storage facilities at collection points and during transportation means that milk is often stored at ambient temperatures, which are unsuitable for preserving its safety and quality. Addressing these gaps requires investment in cold chain infrastructure, including refrigerated collection centers and transport vehicles, to reduce contamination risks [116].

Moreover, Nepal's regulatory framework for milk safety requires strengthening. There remains a significant disconnection between policies as written and their implementation in practice [117]. Implementing clear guidelines and standards for milk collection, transportation, and processing, alongside rigorous enforcement through regular inspections and quality control, is essential to safeguarding public health. However, small-scale farmers and local vendors often lack the financial resources to invest in proper storage and transportation equipment, forcing them to rely on traditional practices that fall short of modern hygiene standards.

3.5. Antibiotic residues in milk and meat

Antibiotics, whether naturally derived or synthetically produced, play a vital role in treating and preventing diseases in both humans and animals. However, their misuse, particularly as growth promoters in food animals and their indiscriminate administration without veterinary oversight, has led to two major concerns: the persistence of antibiotic residues in food products and the rise of AMR, both of which pose significant risks to food safety and human health [118].

In Nepal, several studies have reported the presence of antibiotic residues in milk and meat. Commonly used antibiotics in the livestock sector include cephalosporins, aminoglycosides, fluoroquinolones, macrolides, penicillin, sulfonamides, nitrofurans, tiamulin, and tetracyclines [118]. In 2019, the animal industry in Nepal consumed approximately 48 t of antibiotics. This included 9.1 t of third- and fourth-generation cephalosporins, 9.7 t of tetracyclines, 6.5 t of fluoroquinolones, and various quantities of other antibiotic classes [119].

The presence of antibiotic residues in milk has been well documented. Fresh milk samples collected from different areas of the Kathmandu Valley and tested by the Veterinary Standards and Drug Regulatory Laboratory reported that 5 % were positive for antibiotic residues, with sulfonamides being the most common [120]. Similarly, milk samples from five provinces of Nepal, including Bagmati, Gandaki, Koshi, Lumbini, and Madesh, tested in 2021 and 2022, showed a prevalence of 1.6 % for antibiotic residues [121]. Higher levels were reported in districts such as Kailali, Kaski, and Nuwakot, where residues of tetracyclines, streptomycin, and sulfonamides ranged from 44 % to 75 %, with sulfonamides frequently exceeding the national maximum residue limits [122]. Additionally, milk from individual farmers, cottage dairies, and organized dairies in the Kathmandu Valley contained sulfonamide and penicillin residues above the national limits [123].

Meat products have also shown significant contamination. In Kavrepalanchok and Kailali districts, over 20 % of tested meat samples from poultry, goats, buffaloes, and pigs contained residues of penicillin, tetracycline, aminoglycosides, macrolides, and sulfonamides [124]. Broiler meat samples from Kathmandu Metropolitan City showed an even higher prevalence of antibiotic residues at 28.25 % [125]. Quinolone residues, which belong to a critically important class of antibiotics, were detected in poultry meat and eggs from the Kathmandu Valley [126]. Furthermore, chicken meat from Kailali, Kaski, and Nuwakot districts contained residues of tetracyclines, sulfonamides, penicillin, gentamycin, and streptomycin, with contamination rates ranging from 50 % to 83 % [122].

These findings emphasize the widespread presence of antibiotic residues in milk and meat across Nepal. This contamination presents a serious threat to public health and food safety, highlighting the urgent need for stronger regulatory enforcement and responsible use of antibiotics in livestock production systems.

3.6. Limited public awareness and education

Ensuring the safety of animal-sourced foods such as meat and milk presents an important opportunity for improving public health in Nepal. However, challenges persist due to limited awareness and education among producers, traders, and consumers. For instance, dairy farmers are often unaware of proper barn hygiene, sanitation of milking equipment, and the importance of producing milk under hygienic conditions [127]. In many cases, milk becomes contaminated at the farm level, largely due to exposure to manure and poor hygiene practices within barns and among farmers. Essential practices such as handwashing, cleaning of teats and udders before milking, and proper sanitization of milking vessels and transport containers are frequently neglected due to a lack of training. As a result, milk can become contaminated with vegetation, soil, bedding materials, and microorganisms originating from these sources [128]. Transportation of milk also poses significant risks. Milk is commonly carried to collection centers in plastic containers, and many farmers are unaware that improper cleaning and sanitization of these containers can harbor harmful pathogens, increasing the risk of milk-borne diseases [129].

Similarly, meat safety is compromised by inadequate education and training among butchers and meat handlers regarding proper sanitation practices. Many meat sellers lack knowledge about the importance of disinfecting hands, tools, clothing, and using protective gear during meat handling and selling [130]. Furthermore, common practices such as displaying meat without refrigeration, maintaining poor cleanliness of premises, and using unclean water contribute to widespread contamination. These conditions attract flies, insects, and dirt, exacerbating the risk of meat contamination. A study conducted in retail meat shops within Butwal Municipality found that 70.0 % of meat handlers had no formal education, while 82.5 % had never received any training in meat handling or hygiene practices [131].

In addition to these food safety concerns, there is limited awareness of livestock-associated zoonoses among smallholder farmers in Nepal [132]. Women, who comprise most of the agricultural workforce and manage most livestock husbandry tasks, are often excluded from formal livestock education and training programs. This lack of access to education limits their understanding of zoonotic diseases originating from livestock [[133], [134]].

3.7. Inadequate infrastructure

Nepal holds significant potential to enhance food safety by improving infrastructure for hygienic meat and milk production. However, the country continues to face major challenges in this regard. There is a shortage of modern slaughterhouses, and many existing facilities are either non-operational or lack the basic infrastructure needed to ensure hygienic meat production [112]. In most cases, slaughtering takes place in environments with poor hygiene and safety standards, resulting in a high risk of contamination [135].

To address these concerns and safeguard consumer health, the Government of Nepal introduced the Slaughterhouse and Meat Inspection Act 1999. Despite this policy framework, the act has yet to be fully implemented [131]. Key provisions, such as ante- and post-mortem examinations of animals and regular inspections of meat facilities by government-appointed inspectors, are rarely enforced [136]. Several factors hinder effective implementation, including inadequate infrastructure, a shortage of trained personnel, weak regulatory enforcement, and limited financial resources. Butcheries remain the primary outlets for meat sales in Nepal, yet many lack even the most basic facilities for hygienic meat handling [131]. Essential infrastructure, such as tiled or marble surfaces for walls and floors, proper ventilation, air conditioning, reliable refrigeration, stainless steel equipment, effective waste disposal systems, and an uninterrupted power supply, is often missing. These deficiencies highlight an urgent need to upgrade infrastructure and enforce food safety standards to promote hygienic meat production.

The dairy sector faces similar constraints. Milk production in Nepal is primarily carried out by small-scale, scattered, and unorganized farmers, who often operate without the necessary infrastructure for proper collection, transportation, processing, and marketing [115]. The absence of specialized aseptic utensils for milk collection and transportation, combined with a lack of cold chain infrastructure from farms to collection centers and local retail outlets (Fig. 4), facilitates the growth of spoilage organisms and deteriorates milk quality. Furthermore, unpaved and rough roads in rural areas cause turbulence and delays during milk transportation, contributing to fat breakdown and the development of off-flavors [127].

Fig. 4.

Fig. 4

A local dairy (together with a grocery) shop in Bharatpur, Chitwan, Nepal, where raw milk is being poured into a plastic bag from the large metal container for direct sale to consumers. This setup demonstrates the community-based milk supply system that plays a vital role in meeting local dairy needs. While traditional methods remain prevalent, the scene also underscores the opportunity to strengthen milk hygiene and safety through the adoption of improved handling practices, cold chain infrastructure, and training for milk handlers.

Post-collection storage is another challenge. Many areas lack sufficient cold storage facilities, and limited access to processing plants further exacerbates the issue. Additionally, restricted access to veterinary services in rural areas, where most milk is produced, affects both milk quality and production. Together, these factors compromise the safety and hygiene of milk in Nepal's supply chain, underscoring the need for infrastructure development and improved veterinary support to ensure the production of safe, and high-quality milk [115].

4. Strategies to prevent milk-borne and meat-borne illnesses in Nepal

4.1. Upholding stringent hygiene practices in the meat and milk supply chain

It is essential to maintain rigorous hygiene protocols at all stages of the meat supply chain, including slaughtering, processing, storage, distribution, and retail [131]. Measures should include maintaining regular cleaning and disinfection of tools and facilities, proper disposal of animal waste, and the use of cold storage to prevent microbial growth. Enforcing strict personal hygiene practices for workers, such as mandatory handwashing after handling dirty objects like money, using the toilet, or touching the face, along with requiring them to wear clean work clothes and protective gear such as hair coverings, beard nets, and gloves, can significantly reduce the risk of contamination. Ensuring safe handling and protective measures during slaughtering, processing, transportation and sales will minimize contamination risks.

Similarly, strict food safety standards and regulations should be enforced for quality milk production and distribution in Nepal (Fig. 5) [116]. This includes the adoption of clean milking practices by farmers, such as washing hands, maintaining udder hygiene, and using clean milking equipment to prevent microbial contamination [137]. Provision of refrigeration facilities, especially in rural areas, and the establishment of a cold chain system, such as insulated containers during transportation, should be implemented. Containers for milk storage and transportation should be clean, regularly sanitized, and the use of food-grade containers should be made mandatory [138]. Facilities for regular microbial and quality testing at collection centers and dairy processing plants should be established.

Fig. 5.

Fig. 5

Strategies to improve milk and meat safety in Nepal.

4.2. Enforcement of the Animal Slaughter and Meat Inspection Act

The Animal Slaughter and Meat Inspection Act in Nepal serves as a crucial regulatory framework to ensure the safety and hygiene of meat products. The act mandates compulsory ante-mortem and post-mortem inspection of animals, proper slaughtering facilities, and hygienic handling of meat products [112]. Although the act was passed in 1999 and regulated in 2001, it has yet to be successfully enforced. Strict implementation of this act is crucial to ensuring the production of safe, high-quality meat for public consumption. The government and private sector should invest in establishing certified slaughterhouses equipped with modern facilities and ensure regular inspections of these meat enterprises by government-appointed meat inspectors to enforce compliance with regulations [136]. Provision of strict penalties should be enforced for non-compliance and unsafe practices, along with the introduction of traceability systems to enhance accountability throughout the supply chain [139]. Collaboration between government agencies, local authorities, and private stakeholders can further enhance the implementation of the act, ensuring safer meat production and distribution across Nepal.

4.3. Education and training for meat and milk handlers

Proper education and training for meat and milk handlers are essential to ensure food safety, hygiene, and quality throughout the supply chain. Lack of awareness and improper handling practices can lead to microbial contamination of meat and milk, posing serious health risks to consumers [140].

Butchers and meat handlers in Nepal should receive training on best practices for hygiene and food safety. These programs should cover topics such as safe handling, proper storage, thorough cleaning of tools and surfaces, and the use of personal protective equipment (PPE) [141]. Similarly, milk handlers should be trained in clean milking techniques, proper pasteurization, and safe storage to prevent microbial contamination [127]. Government agencies, along with food safety authorities should implement mandatory training and certification programs. Certification programs can validate their skills and incentivize adherence to hygiene standards [142]. Regular workshops and awareness campaigns can further reinforce safe handling and sanitation practices among food industry personnel. Ensuring all individuals involved in meat and milk processing receive proper training and education will contribute to improved public health and food safety standards in Nepal. A significant association was observed between maintaining sanitation and hygiene practices among meat sellers in Nepal compared to those who had not received any kind of training [[141], [143]]. Training food handlers on the importance of personal hygiene and educating them on better food safety practices play an important role in reducing the risk of foodborne illnesses and ensuring safe food products for consumers [144].

4.4. Public awareness campaigns

Public awareness campaigns should be launched to educate communities about the risks of consuming raw or undercooked meat and milk in Nepal. These campaigns should emphasize safe consumption practices, such as thorough cooking of meat and pasteurization of milk. In a recent study [140] conducted in various districts of Nepal among 280 livestock farmers, 11 % of farmers reported consuming undercooked or raw meat, while 19 % reported consuming raw or boiled milk. Most farmers and consumers in Nepal are unaware of the potential risks of zoonotic diseases transmitted through the consumption of raw or contaminated meat, and the practice of consuming sick or recently dead animals further exacerbates the situation [145]. A study conducted among 380 respondents in the Manang, Tanahun, and Nawalpur districts of Gandaki Province reported 17 % of participants were practicing the consumption of sick or dead animals, highlighting the need for increased awareness and food safety measures [106]. Messages tailored for both urban and rural populations can help address cultural traditions and practices while promoting safer food consumption and hygiene habits to reduce health risks [146]. For example, an educational workshop conducted in the United States effectively reduced the incidence of Salmonella Typhimurium, which was associated with consuming fresh cheese [147]. Similarly, a study conducted in Tanzania found that narrative messages can effectively promote healthy hygiene practices and improve milk quality in a pastoral community, even when cultural norms conflict with best health practices [148].

In Nepal, similar approaches should be implemented to enhance public awareness and encourage behavior change. Schools need to incorporate food safety education into their curriculum. Similarly, local leaders can play a key role in advocating for safe consumption practices within their communities, and media platforms can be utilized to disseminate informative campaigns on the risks of consuming raw or contaminated meat and milk. Besides these, information can be shared through mass media such as social media, radio, and television, along with printed materials like posters and brochures [111]. By leveraging these channels, awareness initiatives can effectively reach a wider audience, fostering long-term improvements in food safety and public health. Educational initiatives should be customized to meet the specific needs of urban and rural populations. For rural areas, focus on safe livestock handling, traditional slaughter practices, and proper meat storage. For urban populations, emphasize the importance of purchasing meat from certified vendors and safe preparation methods at home. These programs should respect cultural practices while promoting food safety. Consumers should be informed about the importance of boiling or pasteurizing milk, maintaining proper refrigeration for milk and meat, practicing hygienic handling of raw foods, thoroughly cooking meat, avoiding unpasteurized dairy products, choosing trusted sources, and adopting safe food practices to reduce the risk of foodborne illnesses (Fig. 6).

Fig. 6.

Fig. 6

Foodborne pathogens in milk and meat and strategies to prevent foodborne illnesses from these pathogens.

4.5. Regular monitoring and evaluation

Regular monitoring and evaluation by health authorities and local governments are crucial to preventing meat-borne and milk-borne illnesses in Nepal. Regular inspections of slaughterhouses, meat and dairy shops, milk parlors, and the entire meat and milk supply chain are essential to ensure compliance with hygiene standards. For hygienic meat production, authorities should proactively carry out regular monitoring of abattoirs and butcheries to enforce sanitary practices, including cleanliness of facilities, proper handling and storage of meat, waste disposal practices, and adherence to personal hygiene protocols among workers [149]. Similarly, for milk production, regular inspections should focus on ensuring that dairy farms, milk parlors, and milk collection centers maintain proper milking hygiene, safe storage temperatures, and sanitation of milking equipment to prevent contamination [150]. A license should be mandatory for all meat and dairy producers, sellers, and processors, with strict penalties enforced for those selling products without a valid license or violating food safety regulations [112]. Samples of meat and milk products should be collected for laboratory testing to detect adulterants and contaminants, and it should be prohibited to produce, sell, distribute, export, or import any adulterated or sub-standard food, or hold such food for any of these purposes [151]. Furthermore, proper labelling should be mandatory for all milk and meat products, including clear information on the name of the food, ingredients, the manufacturer's name and address, net quantity, production and expiration dates, nutritional content, and storage instructions to ensure consumer safety and transparency [152]. Authorities should establish a feedback system for consumers to report food safety concerns, allowing prompt action against violations. They should also publicly share periodic reports on inspection results and corrective measures to ensure transparency and enhance public awareness of food safety.

4.6. Investment in infrastructure for meat and milk processing and storage

Developing robust infrastructure for meat and milk processing and storage is essential to ensuring food safety, quality, and sustainability in Nepal's livestock sector. Large-scale meat and dairy industries are lacking in Nepal, with the sector primarily consisting of small-scale suppliers, local butcheries, and dairy farmers. In Nepal, only eight slaughterhouses have been registered to date; however, almost all of them are either non-operational or in poor condition [153]. Similarly, the dairy sector faces challenges such as inadequate milk collection centers, limited cold chain facilities, and poor processing infrastructure, leading to significant post-harvest losses and compromised milk quality [127].

The negligence from the government authorities, including a lack of funding, inadequate policies, and poor enforcement of regulations, has further hindered the development of a structured and hygienic meat [112,135] and dairy industry [116]. Investments should focus on upgrading and ensuring the functionality of already established slaughterhouses and dairy processing facilities, as well as constructing additional ones in different districts of Nepal based on need and demand. All three tiers of government in Nepal should allocate sufficient budget and also engage relevant stakeholders to invest in the development, maintenance, and modernization of the meat and milk processing infrastructure. For sustainability, these facilities should be established away from densely populated areas and natural environmental resources, in both rural and urban centers, to minimize the risk of contamination and pollution in residential environments and prevent contamination of water supplies [149]. The slaughterhouse facilities must be equipped with proper sewage and waste disposal systems, a clean water supply, cold storage, effective vector control measures, and must maintain strict hygiene protocols to ensure food safety and prevent contamination of meat, the environment, and the related food products [154]. Similarly, investments should be made in expanding cold chain infrastructure, including refrigerated transportation and storage facilities, to maintain milk quality, prevent spoilage, and reduce losses in the dairy sector [150]. The government should implement a public-private partnership model to invest in milk and meat infrastructure. Additionally, it should provide grants and subsidies to private organizations and cooperatives to support their establishment and ensure long-term, sustainable operations.

Besides this, the government should invest in improving road networks connecting slaughterhouses and milk collection/processing centers to facilitate the transportation of live animals and the distribution of processed meat [140]. Furthermore, resources should be allocated to establishing and upgrading laboratories with modern diagnostic equipment and skilled personnel for routine meat and milk testing.

4.7. Implementation of Hazard Analysis and Critical Control Points (HACCP) protocol

The implementation of HACCP protocols is crucial for systematically identifying and mitigating risks at critical points, ensuring the production of safe meat, milk, and their products. This approach integrates good hygienic practices and standard sanitation operating procedures across all stages of production, processing, distribution, and storage in the meat [155] and dairy [156] supply chain.

In the meat industry, contamination primarily occurs during processing when meat comes into contact with equipment, food handlers, and environmental factors [157]. The risk of contamination is particularly high through meat handlers’ hands and clothing, utensils (such as knives, saws, and mincers), cutting boards, and the transfer of bacteria from the meat surface to its internal parts during cutting and deboning [158,159]. To mitigate these risks, implementing a HACCP plan requires adhering to key prerequisites, including sanitary facility design, water quality management, proper sanitation of food contact surfaces, strict personal hygiene for food handlers, regular disinfection of utensils and equipment, effective pest control, proper waste disposal, and ensuring animal cleanliness [160]. Additionally, monitoring temperature controls during storage and distribution is crucial to preventing microbial growth and protecting meat from spoilage organisms throughout the supply chain [161].

Similar to the meat industry, the dairy sector requires HACCP implementation at various stages, including milk production on farms, processing in dairy facilities, and the storage and transportation of milk and its products to ensure safety, quality, and contamination control. The application of HACCP on dairy farms ensures safe and hygienic milk production, while also improving animal welfare and protecting the environment [162]. This can be done by monitoring major contamination routes, including infected animals, the hygiene and sanitation of farm workers, cleanliness of milking equipment, and water supplies for cleaning, and overall farm sanitation practices [163]. During dairy processing, HACCP should be implemented by identifying critical control points and control points at key stages, including milk reception, pasteurization, cooling, clean-in-place systems, drains inside the plant, dairy processing lines, packaging materials, and storage temperature, ensuring proper hygiene and product safety [164]. Furthermore, during transportation, HACCP should be implemented to ensure that raw milk is moved to processing plants in clean and disinfected tankers as quickly as possible. The tankers must be cleaned and disinfected immediately after unloading, and precautions should be taken to ensure that the driver is free from infectious diseases and follows strict hygiene practices throughout the process [156].

Besides this, comprehensive training on HACCP principles is essential for HACCP teams, managers, and food handlers, with the training being adjusted according to their technical expertise and the specific responsibilities they carry within the HACCP system [165]. Similarly, resources such as an adequate budget, manpower, monitoring equipment, and training facilities should be provided to the person in charge (supervisor) to ensure that an effective HACCP plan can be developed and implemented successfully. However, HACCP has not yet been made mandatory and is seldom applied by food producers, processors, and handlers in Nepal, and the government has yet to enforce regulations that would promote its widespread implementation by the industry [112].

4.8. Adopting a One Health approach

A One Health approach, integrating human, animal, and environmental health, is essential for managing meat- and milk-borne illnesses in Nepal. As human-animal interdependence intensifies within the global food system, associated health and environmental risks also increase [166]. Tackling foodborne diseases requires proactive, multi-disciplinary strategies under the One Health framework to develop effective and sustainable solutions (Fig. 7) [167]. Globally, approximately 12 % of diseases are linked to animal-source foods, with 4 % attributed to unsafe milk and milk products [168]. Key contributors to milk-borne illnesses include contamination during production, processing, transportation, and storage; zoonotic diseases in dairy herds; and consumption of unpasteurized milk [22].

Fig. 7.

Fig. 7

Model framework for action on milk and meat safety in developing countries like Nepal. This framework is modified from the framework provided by the World Health Organization for action on food safety in the Southeast Asia.

To improve milk and meat safety, One Health strategies should include livestock vaccination, improved farm sanitation, hygienic dairy and meat handling practices, strict quality control, and widespread public health education [169]. Antibiotics overuse in the livestock and dairy sectors also fuels AMR, posing a growing global health threat. Regulatory frameworks must promote the prudent use of antibiotics to protect animal welfare, food safety, and human health [170]. Meat-borne diseases, often resulting from contaminated meat, remain a major concern worldwide. Pathogens can originate from infected animals, unhygienic environments, or improper handling and cross-contamination during processing [171]. Applying One Health across the meat and milk supply chains from farm to table can significantly reduce these risks [7].

To implement One Health approaches effectively in Nepal, specific actions must be taken. Authorities should establish joint surveillance of zoonotic pathogens, enforce environmental health measures such as safe water use and waste management, and ensure farm-level biosecurity and hygiene. Antibiotic stewardship programs should be strengthened, and consumers must be educated on safe food practices. A coordinated, multi-sectoral effort involving the Government of Nepal, veterinary and public health agencies, international organizations, donors, researchers, and communities is crucial to translating the One Health concept into concrete improvements in food safety [[134], [172]].

5. Conclusion

Milk and meat safety remain crucial public health concerns in Nepal due to persistent challenges such as poor hygiene practices, inadequate infrastructure, and weak regulatory enforcement. Despite the existence of legal frameworks, gaps in implementation continue to undermine food safety efforts. The predominance of informal sectors in milk and meat production further exacerbates contamination risks, posing serious health threats to consumers. Addressing these issues requires coordinated actions, including investment in modern slaughterhouses, temperature-controlled transport, robust surveillance systems, and capacity-building initiatives. Public awareness and education on safe food handling, coupled with stronger regulatory oversight, are essential steps toward ensuring safer food supplies. A One Health approach, integrating animal, human, and environmental health sectors, is crucial for sustainable improvements in food safety. Strengthening these areas will help mitigate the risks associated with milk and meat consumption in Nepal and contribute to better public health outcomes.

CRediT authorship contribution statement

Deepak Subedi: Writing – review & editing, Writing – original draft, Supervision, Data curation, Visualization, Methodology, Conceptualization. Sameer Thakur: Writing – original draft, Data curation, Writing – review & editing, Visualization, Conceptualization. Anil Gautam: Writing – original draft, Data curation, Writing – review & editing, Investigation. Madhav Poudel: Writing – original draft, Data curation, Writing – review & editing, Investigation. Sumit Jyoti: Writing – original draft, Data curation, Writing – review & editing, Methodology. Abhinandan Devkota: Writing – original draft, Conceptualization, Writing – review & editing, Investigation. Milan Kandel: Writing – original draft, Data curation, Writing – review & editing, Investigation. Ananda Tiwari: Writing – review & editing, Methodology, Data curation, Writing – original draft, Investigation.

Informed consent statement

Verbal informed consent was obtained from the individuals for the inclusion of their images in this publication.

Ethics statement

The authors have nothing to report.

Funding

The authors did not receive specific funding for this work.

Declaration of competing interest

The authors declare no conflicts of interest.

Contributor Information

Deepak Subedi, Email: subedideepu26@gmail.com.

Sameer Thakur, Email: sameerthakurvet@gmail.com.

Anil Gautam, Email: anilg6623@gmail.com.

Madhav Poudel, Email: vet.madhav@gmail.com.

Sumit Jyoti, Email: sujy12@gmail.com.

Abhinandan Devkota, Email: abhinandandevkota800@gmail.com.

Milan Kandel, Email: milan.kandel@sydney.edu.au.

Ananda Tiwari, Email: ananda.tiwari@helsinki.fi.

References

  • 1.WHO . 2024. Zoonotic Disease: Emerging Public Health Threats in the Region.https://www.emro.who.int/fr/about-who/rc61/zoonotic-diseases.html [Google Scholar]
  • 2.Rahman M.T., Sobur M.A., Islam M.S., Ievy S., Hossain M.J., Zowalaty M.E.E., et al. Zoonotic diseases: etiology, impact, and control. Microorganisms. 2020;8:1405. doi: 10.3390/microorganisms8091405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Messenger A.M., Barnes A.N., Gray G.C. Reverse zoonotic disease transmission (zooanthroponosis): a systematic review of seldom-documented human biological threats to animals. PLoS One. 2014;9 doi: 10.1371/journal.pone.0089055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Loh E.H., Zambrana-Torrelio C., Olival K.J., Bogich T.L., Johnson C.K., Mazet J.A.K., et al. Targeting transmission pathways for emerging zoonotic disease surveillance and control. Vector Borne Zoonotic Dis. 2015;15:432–437. doi: 10.1089/vbz.2013.1563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Kilpatrick A.M., Randolph S.E. Drivers, dynamics, and control of emerging vector-borne zoonotic diseases. Lancet. 2012;380:1946–1955. doi: 10.1016/S0140-6736(12)61151-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Heredia N., García S. Animals as sources of food-borne pathogens: a review. Anim. Nutr. 2018;4:250–255. doi: 10.1016/J.ANINU.2018.04.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Ali S., Alsayeqh A.F. Review of major meat-borne zoonotic bacterial pathogens. Front. Public Health. 2022;10 doi: 10.3389/fpubh.2022.1045599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.WHO, Zoonosis . 2020. World Health Organization.https://www.who.int/news-room/fact-sheets/detail/zoonoses [Google Scholar]
  • 9.WHO . 2025. Estimating the Burden of Foodborne Diseases.https://www.who.int/activities/estimating-the-burden-of-foodborne-diseases [Google Scholar]
  • 10.Gao R., Liu X., Xiong Z., Wang G., Ai L. Research progress on detection of foodborne pathogens: the more rapid and accurate answer to Food Safety. Food Res. Int. 2024;193 doi: 10.1016/j.foodres.2024.114767. [DOI] [PubMed] [Google Scholar]
  • 11.Prasain S. 2021. Nepal Becomes Self-Sufficient in Egg and Meat Production, the Kathmandu Post.https://kathmandupost.com/money/2021/03/25/nepal-becomes-self-sufficient-in-egg-and-meat-production [Google Scholar]
  • 12.Bantawa K., Rai K., Subba Limbu D., Khanal H. Food-borne bacterial pathogens in marketed raw meat of Dharan, eastern Nepal. BMC Res. Notes. 2018;11:1–5. doi: 10.1186/s13104-018-3722-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Pandey H.P. Milk production and value chain in rural area of Nepal: a case from Gandaki river basin. J. Dairy Res. Technol. 2020;3:1–6. doi: 10.24966/DRT-9315/100022. [DOI] [Google Scholar]
  • 14.Subedi D., Paudel M., Poudel S., Koirala N. Food Safety in developing countries: common foodborne and waterborne illnesses, regulations, organizational structure, and challenges of food safety in the context of Nepal. Food Front. 2025;6:86–123. doi: 10.1002/FFT2.517. [DOI] [Google Scholar]
  • 15.Banskota N. Department of Rural Development; 2015. Milk Value Chain in Rural Dairy Farming System in the Selected Districts of Gandaki River Basin, Nepal: A Case Study of Gorkha, Tanahun, Chitwan Districts.https://www.academia.edu/112405350/Milk_Value_Chain_in_Rural_Dairy_Farming_System_in_The_Selected_Districts_of_Gandaki_River_Basin_Nepal_A_Case_Study_of_Gorkha_Tanahun_Chitwan_Districts [Google Scholar]
  • 16.Gompo T.R., Shrestha A., Ranjit E., Gautam B., Ale K., Shrestha S., et al. Risk factors of tuberculosis in human and its association with cattle TB in Nepal: a One Health approach. One Health. 2020;10:100156. doi: 10.1016/j.onehlt.2020.100156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Gautam A., Upadhayay P., Ghimre D., Khanal A., Gaire A., Kaphle K. Prioritised zoonotic diseases of Nepal: a review. Int. J. Appl. Sci. Biotechnol. 2021;9:1–15. doi: 10.3126/IJASBT.V9I1.34967. [DOI] [Google Scholar]
  • 18.Rizal S., Amatya N., Dhungana G., Saud B., Chand K., Paudel G., et al. Prevalence of microbiological contaminants in milk samples in Kathmandu. Nepal, Arch. Clin. Med. Microbiol. 2023;2:7–10. doi: 10.33140/ACMMJ.02.01.02. [DOI] [Google Scholar]
  • 19.Agriculture Information and Training Center. 2025. https://aitc.gov.np/en/resources/t02u8l1dz23abqozzz3vlvntvbgta1reos0xbzy9 [Google Scholar]
  • 20.Lamsal S., Subedi D., Kaphle K. Buffaloes production and reproduction efficiencies as reviewed for parity in Nepal. Int. J. Appl. Sci. Biotechnol. 2020;8:1–6. doi: 10.3126/IJASBT.V8I1.27802. [DOI] [Google Scholar]
  • 21.Plym Forshell L., Wierup M. Salmonella contamination: a significant challenge to the global marketing of animal food products. Rev. Sci. Tech. 2006;25:541–554. doi: 10.20506/rst.25.2.1683. [DOI] [PubMed] [Google Scholar]
  • 22.Zeinhom M.M.A., Abdel-Latef G.K. Public health risk of some milk borne pathogens. Beni Suef Univ. J. Basic Appl. Sci. 2014;3:209–215. doi: 10.1016/J.BJBAS.2014.10.006. [DOI] [Google Scholar]
  • 23.Sharma S., Fowler P.D., Pant D.K., Singh S., Wilkins M.J. Prevalence of Non-typhoidal Salmonella and Risk Factors on Poultry Farms in Chitwan, Nepal. Vet. World. 2021;14(2):426–436. doi: 10.14202/vetworld.2021.426-436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Parajuli L., Paudel S., Khadka R., Maharjan R., Shrestha A. Analysis of microbiological quality and adulteration of raw milk samples from different areas of Kathmandu Valley. Nepal J. Biotechnol. 2023;11:37–42. doi: 10.54796/NJB.V11I2.296. [DOI] [Google Scholar]
  • 25.Arjyal C., Dahal B.N., Khadka B. Microbial quality of milk available in Kathmandu Valley. J. Nepal Med. Assoc. JNMA. 2004;43:137–140. doi: 10.31729/jnma.475. [DOI] [Google Scholar]
  • 26.European Centre for Disease Prevention and Control . 2018. Salmonella Agona Outbreak Associated with Infant Formula Milk.https://www.ecdc.europa.eu/en/news-events/salmonella-agona-outbreak-associated-infant-formula-milk [Google Scholar]
  • 27.Dhanashekar R., Akkinepalli S., Nellutla A. Milk-borne infections. An analysis of their potential effect on the milk industry. Germs. 2012;2:101. doi: 10.11599/GERMS.2012.1020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Kaindama L., Jenkins C., Aird H., Jorgensen F., Stoker K., Byrne L. A cluster of Shiga Toxin-producing Escherichia coli O157:H7 highlights raw pet food as an emerging potential source of infection in humans. Epidemiol. Infect. 2021;149 doi: 10.1017/S0950268821001072. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Ullah S., Khan S.U.H., Khan M.J., Khattak B., Fozia F., Ahmad I., et al. Multiple-drug resistant Shiga toxin-producing E. coli in raw milk of dairy bovine. Trop. Med. Infect. Dis. 2024;9:64. doi: 10.3390/TROPICALMED9030064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Launders N., Byrne L., Jenkins C., Harker K., Charlett A., Adak G.K. Disease severity of Shiga toxin-producing E. coli O157 and factors influencing the development of typical haemolytic uraemic syndrome: a retrospective cohort study, 2009–2012. BMJ Open. 2016;6 doi: 10.1136/BMJOPEN-2015-009933. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Acharya S., Bimali N., Shrestha S., Lekhak B. Bacterial analysis of different types of milk (pasteurized, unpasteurized and raw milk) consumed in Kathmandu Valley. Tribhuvan Univ. J. Microbiol. 2017;4:32–38. doi: 10.3126/tujm.v4i0.21674. [DOI] [Google Scholar]
  • 32.Bhandari S., Subedi D., Tiwari B.B., Shrestha P., Shah S., Al-Mustapha A.I. Prevalence and risk factors for multidrug-resistant Escherichia coli isolated from subclinical mastitis in the western Chitwan region of Nepal. J. Dairy Sci. 2021;104:12765–12772. doi: 10.3168/jds.2020-19480. [DOI] [PubMed] [Google Scholar]
  • 33.Rai S., Karki B., Humagain S., Rimal S., Adhikari S., Adhikari S., et al. Antibiogram of Escherichia coli and Staphylococcus aureus isolated from milk sold in Kathmandu district, Nepal. J. Biotechnol. 2020;8:82–86. doi: 10.3126/njb.v8i3.30080. [DOI] [Google Scholar]
  • 34.Limbu D.S., Bantawa K., Limbu D.K., Devkota M., Ghimire M. Microbiological quality and adulteration of pasteurized and raw milk marketed in Dharan, Nepal. Himal. J. Sci. Technol. 2020;3:37–44. doi: 10.3126/hijost.v4i0.33864. [DOI] [Google Scholar]
  • 35.Shrestha R., Singh S. Presence of E. coli in raw and pasteurized milk in Bagmati province, Nepal. Nepalese J. Agric. Sci. 2023;25:225–236. [Google Scholar]
  • 36.Bohora S., Chaulagai S., Thapa S. Assessment of antibiotic resistant profile of coliform and Staphylococcus spp. isolated from milk from Kathmandu valley. Nepal J. Biotechnol. 2023;11:50–56. doi: 10.54796/njb.v11i2.294. [DOI] [Google Scholar]
  • 37.Gautam A., Bastola S., Lamsal K., Kaphle K., Shrestha P., Shah S., et al. Prevalence and risk factors of multidrug resistant (MDR) Escherichia coli isolated from milk of small scale dairy buffaloes in Rupandehi, Nepal. Zoonotic Dis. 2024;4:174–186. doi: 10.3390/ZOONOTICDIS4030016. [DOI] [Google Scholar]
  • 38.Shrestha S., Bhattarai R.K., Basnet H.B., Luitel H., Bastola S. Identification, antimicrobial resistance and molecular detection of Shiga toxin-producing E. coli (STEC) isolated from raw milk of cattle in Chitwan, Nepal. bioRxiv. 2024 doi: 10.1101/2024.01.30.578021. 2024.01.30.578021. [DOI] [Google Scholar]
  • 39.Elkenany R., Eltaysh R., Elsayed M., Abdel-Daim M., Shata R. Characterization of multi-resistant Shigella species isolated from raw cow milk and milk products. J. Vet. Med. Sci. 2022;84:890. doi: 10.1292/JVMS.22-0018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Mohammed A.N., Abdel-Latef G.K., Abdel-Azeem N.M., El-Dakhly K.M. Ecological study on antimicrobial-resistant zoonotic bacteria transmitted by flies in cattle farms. Parasitol. Res. 2016;115:3889–3896. doi: 10.1007/S00436-016-5154-7/METRICS. [DOI] [PubMed] [Google Scholar]
  • 41.Thapa K., Bhattachan B., Gurung R.R., Katuwal A., Khadka J.B. Antibiotic resistance pattern of Shigella spp. among gastroenteritis patients at tertiary care hospital in Pokhara, Nepal. Nepal J. Biotechnol. 2017;5:14–20. doi: 10.3126/njb.v5i1.18865. [DOI] [Google Scholar]
  • 42.Thapa K., Shrestha S. Microbiological analysis of ice-cream sold in Kathmandu Valley. J. Food Sci. Technol. Nepal. 2012;7:90–92. doi: 10.3126/JFSTN.V7I0.10615. [DOI] [Google Scholar]
  • 43.Gebremedhin E.Z., Ararso A.B., Borana B.M., Kelbesa K.A., Tadese N.D., Marami L.M., et al. Isolation and identification of Staphylococcus aureus from milk and milk products, associated factors for contamination, and their antibiogram in Holeta. Central Ethiopia, Vet. Med. Int. 2022;2022:6544705. doi: 10.1155/2022/6544705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Dong Q., Antelmann H., Zhang J., Wu S., Huang J., Wu Q., et al. Staphylococcus aureus isolated from retail meat and meat products in China: Incidence, Antibiotic Resistance and Genetic Diversity. Front Microbiol. 2011;9:2767. doi: 10.3389/fmicb.2018.02767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Joshi L.R., Tiwari A., Devkota S.P., Khatiwada S., Paudyal S., Pande K.R. International journal of veterinary science prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in dairy farms of Pokhara, Nepal. Int. J. Vet. Sci. 2014;3:87–90. [Google Scholar]
  • 46.Tiwari B.B., Subedi D., Bhandari S., Shrestha P., Pathak C.R., Chandran D., et al. Prevalence and risk factors of staphylococcal subclinical mastitis in dairy animals of Chitwan, Nepal. J. Pure Appl. Microbiol. 2022;16:1392–1403. doi: 10.22207/JPAM.16.2.67. [DOI] [Google Scholar]
  • 47.Franc K.A., Krecek R.C., Häsler B.N., Arenas-Gamboa A.M. Brucellosis remains a neglected disease in the developing world: a call for interdisciplinary action. BMC Public Health. 2018;18:1–9. doi: 10.1186/s12889-017-5016-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Olsen S.C., Palmer M.V. Advancement of knowledge of Brucella over the past 50 years. Vet. Pathol. 2014;51:1076–1089. doi: 10.1177/0300985814540545. [DOI] [PubMed] [Google Scholar]
  • 49.Addis M. Public Health and Economic Importance of Brucellosis: A Review. Public Policy and Administration Research. 2015;5(7):68–83. [Google Scholar]
  • 50.Kumar S., Dahiya S.P., Yadav A.S., Kumar S. Milk borne zoonoses: public health concern: a review. Indian J. Health Well-Being. 2017;8:1079–1082. [Google Scholar]
  • 51.Tewari A., Singh S.P., Singh R. Prevalence of multidrug resistant Bacillus cereus in foods and human stool samples in and around Pantnagar, Uttrakhand. J. Adv. Vet. Res. 2012;2:252–255. [Google Scholar]
  • 52.Buckley K., Grotticelli J. In: Encyclopedia of Toxicology, fourth edition. Wexler P., editor. Elsevier; Amsterdam: 2023. Bacillus cereus; pp. V1-889–V1-892. [DOI] [Google Scholar]
  • 53.Rather M.A., Aulakh R.S., Gill J.P.S., Ghatak S. Enterotoxin gene profile and antibiogram of Bacillus cereus strains isolated from raw meats and meat products. J. Food Saf. 2012;32:22–28. doi: 10.1111/j.1745-4565.2011.00340.x. [DOI] [Google Scholar]
  • 54.Tewari A., Abdullah S. Bacillus cereus food poisoning: international and Indian perspective. J. Food Sci. Technol. 2015;52:2500–2511. doi: 10.1007/s13197-014-1344-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Arjyal C., Manandhar S. Bacillus cereus in ready-to-eat foods available in Kathmandu, Nepal. Tribhuvan Univ. J. Microbiol. 2022;9:43–52. doi: 10.3126/tujm.v9i1.50398. [DOI] [Google Scholar]
  • 56.Tadesse T., Lelo U., Markos T., Tadesse T., Birhan F., Tona T. Review on the Epidemiology, Public Health and Economic Importance of Bovine Tuberculosis. J. Biol. Agric. Healthc. 2017;7:16–23. [Google Scholar]
  • 57.Lombard J.E., Patton E.A., Gibbons-Burgener S.N., Klos R.F., Tans-Kersten J.L., Carlson B.W., et al. Human-to-Cattle Mycobacterium tuberculosis complex transmission in the United States. Front. Vet. Sci. 2021;8:691192. doi: 10.3389/fvets.2021.691192. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Joshi Y.P. 2003. Prevalence of Bovine Tuberculosis Among Livestock and its Relation with Human Tuberculosis in Kanchanpur District. [Google Scholar]
  • 59.Jha V.C., Morita Y., Dhakal M., Besnet B., Sato T., Nagai A., et al. Isolation of Mycobacterium spp. from milking buffaloes and cattle in Nepal. J. Vet. Med. Sci. 2007;69:819–825. doi: 10.1292/jvms.69.819. [DOI] [PubMed] [Google Scholar]
  • 60.Pandey G., Dhakal S., Sadaula A., KC G., Subedi S., Pandey K., et al. Status of tuberculosis in bovine animals raised by tuberculosis infected patients in Western Chitwan, Nepal. Int. J. Infect. Microbiol. 2013;1:49–53. doi: 10.3126/ijim.v1i2.7407. [DOI] [Google Scholar]
  • 61.Upadhyaya N., Shrestha N., Dahal R., Yadav S.K., Thakur R., Aryal D., et al. High prevalence of Bovine tuberculosis reported in cattle and Buffalo of eastern Nepal. bioRxiv. 2023;2023 [Google Scholar]
  • 62.Giannella R.A. 1996. Salmonella, Medical Microbiology Chapter 21.https://www.ncbi.nlm.nih.gov/books/NBK8435/ [Google Scholar]
  • 63.Rai S.K. Changing trend of infectious diseases in Nepal. Infect. Dis. Nanomed. III. 2018;1052:19. doi: 10.1007/978-981-10-7572-8_3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Maharjan M., Joshi V., Joshi D.D., Manandhar P. Prevalence of Salmonella species in various raw meat samples of a local market in Kathmandu. Ann. N. Y. Acad. Sci. 2006;1081:249–256. doi: 10.1196/ANNALS.1373.031. [DOI] [PubMed] [Google Scholar]
  • 65.Laxman Bahadur D., Ishwari Prasad D., Saroj Kumar Y., Md A., Zohorul I. Md. Prevalence and antibiotic resistance profile of Salmonella from livestock and poultry raw meat. Nepal, Int. J. Mol. Vet. Res. 2016;6(1):1–22. doi: 10.5376/ijmvr.2016.06.0001. [DOI] [Google Scholar]
  • 66.Saud B., Paudel G., Khichaju S., Bajracharya D., Dhungana G., Awasthi M.S., et al. Multidrug-resistant bacteria from raw meat of buffalo and chicken. Nepal, Vet. Med. Int. 2019;2019:7960268. doi: 10.1155/2019/7960268. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Upadhyaya M., Poosaran N., Fries R. Prevalence and predictors of Salmonella spp. in retail meat shops in Kathmandu. J. Agric. Sci. Technol. B. 2012;2:1094–1106. doi: 10.17169/REFUBIUM-18583. [DOI] [Google Scholar]
  • 68.Thapa R., Thapa D.B., Chapagain A. Prevalence of Escherichia coli and Salmonella spp from chicken meat samples of Bharatpur, Chitwan. J. Inst. Agric. Anim. Sci. 2020:257–267. doi: 10.3126/jiaas.v36i1.48428. [DOI] [Google Scholar]
  • 69.Bhandari N., Nepali D., Paudyal S. Assessment of bacterial load in broiler chicken meat from the retail meat shops in Chitwan, Nepal. Int. J. Infect. Microbiol. 2013;2:99–104. doi: 10.3126/ijim.v2i3.8671. [DOI] [Google Scholar]
  • 70.Shrestha, P N., Prajapati M., Poudel N. Bhattarai, prevalence and antibiotic sensitivity of Salmonella isolates in chicken meat of Chitwan. Livest. Fish. Res. 2013;30:261. doi: 10.13140/RG.2.1.2597.2642. [DOI] [Google Scholar]
  • 71.Shrestha A., Bajracharya A.M., Subedi H., Turha R.S., Kafle S., Sharma S., et al. Multi-drug resistance and extended spectrum beta lactamase producing Gram negative bacteria from chicken meat in Bharatpur Metropolitan, Nepal. BMC Res. Notes. 2017;10:1–5. doi: 10.1186/s13104-017-2917-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Bantawa K., Sah S.N., Subba Limbu D., Subba P., Ghimire A. Antibiotic resistance patterns of Staphylococcus aureus, Escherichia coli, Salmonella, Shigella and Vibrio isolated from chicken, pork, buffalo and goat meat in eastern Nepal. BMC Res. Notes. 2019;12:1–6. doi: 10.1186/s13104-019-4798-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Gautam, N M.K., Poudel R., Lekhak B., Upreti Antimicrobial susceptibility pattern of gram-negative bacterial isolates from raw chicken meat samples. Tribhuvan Univ. J. Microbiol. 2019;6:89–95. doi: 10.3126/tujm.v6i0.26590. [DOI] [Google Scholar]
  • 74.Bohara M.S. Bacteriological quality of broiler chicken meat sold at local market of Kanchanpur district Nepal. Int. J. Life Sci. Technol. 2017;10:79–85. [Google Scholar]
  • 75.CDC . 2024. About Escherichia coli Infection.https://www.cdc.gov/ecoli/about/index.html [Google Scholar]
  • 76.WHO . 2018. E. coli.https://www.who.int/news-room/fact-sheets/detail/e-coli [Google Scholar]
  • 77.Jnani D., Ray S.D. In: Encyclopedia of Toxicology, fourth edition. Wexler P., editor. Elsevier; Amsterdam: 2023. Escherichia coli Infection; pp. V4-357–V4-367. [DOI] [Google Scholar]
  • 78.Painter J.A., Hoekstra R.M., Ayers T., Tauxe R.V., Braden C.R., Angulo F.J., et al. Attribution of foodborne illnesses, hospitalizations, and deaths to food commodities by using outbreak data, United States, 1998–2008. Emerg. Infect. Dis. 2013;19:407–415. doi: 10.3201/EID1903.111866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Koirala B., Bhattarai R., Maharjan R., Maharjan S., Shrestha S. Bacterial assessment of Buffalo meat in Kathmandu Valley. Nepal J. Sci. Technol. 2021;19:90–96. doi: 10.3126/njst.v20i1.39438. [DOI] [Google Scholar]
  • 80.Koirala B., Bhattarai R., Maharjan R., Maharjan S., Shrestha S. Isolation and identification of gram negative bacteria from chicken meat collected from retail meat shops of Kathmandu Valley. Nepal. Vet. J. 2023:54–61. doi: 10.3126/nvj.v37i37.55516. [DOI] [Google Scholar]
  • 81.Ghimire S., Thapa D., Ghimire A., Subba P., Sah S.N. Occurrence and antibiogram of non-sorbitol fermenting Escherichia coli in marketed raw meat of Dharan, Eastern Nepal. Tribhuvan Univ. J. Food Sci. Technol. 2022;1:9–15. doi: 10.3126/tujfst.v1i1.49931. [DOI] [Google Scholar]
  • 82.Mahato S. Relationship of sanitation parameters with microbial diversity and load in raw meat from the outlets of the metropolitan city Biratnagar, Nepal. Int J Microbiol. 2019;2019 doi: 10.1155/2019/3547072. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Ranabhat G., Subedi D., Karki J., Paudel R., Luitel H., Bhattarai R.K. Molecular detection of avian pathogenic Escherichia coli (APEC) in broiler meat from retail meat shop. Heliyon. 2024 doi: 10.1016/j.heliyon.2024.e35661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Regmi S., Mahato P.L., Upadhayaya S., Marasini H., Neupane R.P., Shrestha J., et al. Screening for Escherichia coli in chopping board meat samples and survey for sanitary and hygienic practices in retail meat shops of Bharatpur metropolitan city, Nepal. Microbiol. Res. 2022;13:872–881. doi: 10.3390/microbiolres13040061. [DOI] [Google Scholar]
  • 85.Joshi P.R., Thummeepak R., Leungtongkam U., Pooarlai R., Paudel S., Acharya M., et al. The emergence of colistin-resistant Escherichia coli in chicken meats in Nepal. FEMS Microbiol. Lett. 2019;366:1–7. doi: 10.1093/femsle/fnz237. [DOI] [PubMed] [Google Scholar]
  • 86.Zenebe T., Zegeye N., Eguale T. Prevalence of Campylobacter species in human, animal and food of animal origin and their antimicrobial susceptibility in Ethiopia: a systematic review and meta-analysis. Ann. Clin. Microbiol. Antimicrob. 2020;19:1–11. doi: 10.1186/s12941-020-00405-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Gautam A., Neupane S., Kaphle K. Campylobacter infection and its sensitivity in retail pork. Int. J. Appl. Sci. Biotechnol. 2020;8:132–139. doi: 10.3126/ijasbt.v8i2.29587. [DOI] [Google Scholar]
  • 88.Facciolà A., Riso R., Avventuroso E., Visalli G., Delia S.A., Laganà P. Campylobacter: from microbiology to prevention. J. Prev. Med. Hyg. 2017;58:E79. [PMC free article] [PubMed] [Google Scholar]
  • 89.Bhattarai D., Bhattarai N., Osti R. Prevalence of thermophilic Campylobacter isolated from water used in slaughter house of Kathmandu and Ruphendehi district, Nepal. Int. J. Appl. Sci. Biotechnol. 2019;7:75–80. doi: 10.3126/ijasbt.v7i1.23306. [DOI] [Google Scholar]
  • 90.Ghimire L., Singh D., Basnet H., Bhattarai R., Dhakal S., Sharma B. Prevalence, antibiogram and risk factors of thermophilic campylobacter spp. in dressed porcine carcass of Chitwan, Nepal. BMC Microbiol. 2014;14:85. doi: 10.1186/1471-2180-14-85. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Bhattarai R., Basnet H., Dhakal I., Thapaliya S. Prevalence, characterization and antimicrobial resistance pattern of thermophilic Campylobacter in broiler meat of Chitwan, Nepal. Nepal. Vet. J. 2016;33:69–80. [Google Scholar]
  • 92.Shakya G., Acharya J., Adhikari S., Rijal N. Shigellosis in Nepal: 13 years review of nationwide surveillance. J. Health Popul. Nutr. 2016;35:36. doi: 10.1186/s41043-016-0073-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Kansakar P., Malla S., Ghimire G.R. Shigella isolates of Nepal: changes in the incidence of shigella subgroups and trends of antimicrobial susceptibility pattern. Kathmandu Univ. Med. J. 2007;5:32–37. [PubMed] [Google Scholar]
  • 94.Bhattacharya S., Khanal B., Bhattarai N.R., Das M.L. Prevalence of Shigella species and their antimicrobial resistance patterns in Eastern Nepal. J. Health Popul. Nutr. 2005;23:339–342. [PubMed] [Google Scholar]
  • 95.Diep B.A., Gill S.R., Chang R.F., Van Phan T.H., Chen J.H., Davidson M.G., et al. Complete genome sequence of USA300, an epidemic clone of community-acquired meticillin-resistant Staphylococcus aureus. Lancet. 2006;367:731–739. doi: 10.1016/S0140-6736(06)68231-7. [DOI] [PubMed] [Google Scholar]
  • 96.McCallum N., Berger-Bächi B., Senn M.M. Regulation of antibiotic resistance in Staphylococcus aureus. Int. J. Med. Microbiol. 2010;300:118–129. doi: 10.1016/J.IJMM.2009.08.015. [DOI] [PubMed] [Google Scholar]
  • 97.Govindaraj Vaithinathan A., Vanitha A. WHO global priority pathogens list on antibiotic resistance: an urgent need for action to integrate One Health data. Perspect Public Health. 2018;138:87–88. doi: 10.1177/1757913917743881. [DOI] [PubMed] [Google Scholar]
  • 98.Devkota S.P., Paudel A., Gurung K. Vancomycin intermediate MRSA isolates obtained from retail chicken meat and eggs collected at Pokhara, Nepal. Nepal J. Biotechnol. 2019;7:90–95. doi: 10.3126/njb.v7i1.26958. [DOI] [Google Scholar]
  • 99.Zahedi Bialvaei A., Sheikhalizadeh V., Mojtahedi A., Irajian G. Epidemiological burden of Listeria monocytogenes in Iran. Iran J. Basic Med. Sci. 2018;21:770–780. doi: 10.22038/ijbms.2018.28823.6969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Haj Hosseini A., Sharifan A., Tabatabaee A. Isolation of Listeria monocytogenes from meat and dairy products. J. Med. Microbiol. Infect. Dis. 2014;2:159–162. [Google Scholar]
  • 101.Osek J., Lachtara B., Wieczorek K. Listeria monocytogenes – how this pathogen survives in food-production environments? Front. Microbiol. 2022;13 doi: 10.3389/fmicb.2022.866462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Dhama K., Verma A.K., Rajagunalan S., Kumar A., Tiwari R., Chakraborty S., et al. Listeria monocytogenes infection in poultry and its public health importance with special reference to food borne zoonoses. Pakistan J. Biol. Sci. 2013;16:301–308. doi: 10.3923/PJBS.2013.301.308. [DOI] [PubMed] [Google Scholar]
  • 103.Jha B.K., Adhikari N., Rajkumari S. Isolation, identification and antibiotic susceptibility patterns of Listeria monocytogens from pregnant women. J. Coll. Med. Sci. - Nepal. 2021;17:227–233. doi: 10.3126/jcmsn.v17i3.37062. [DOI] [Google Scholar]
  • 104.Niraula A., Sharma A., Dahal U. Knowledge, attitude, and practices (KAP) regarding zoonotic diseases among smallholder livestock owners of Tulsipur sub-metropolitan city, Nepal. J. Healthc. Develop. Countries (JHCDC) 2021;1:41–46. doi: 10.26480/jhcdc.03.2021.41.46. [DOI] [Google Scholar]
  • 105.Rai R., Shangpliang H.N.J., Tamang J.P. Naturally fermented milk products of the Eastern Himalayas. J. Ethnic Foods. 2016;3:270–275. doi: 10.1016/J.JEF.2016.11.006. [DOI] [Google Scholar]
  • 106.Bagale K.B., Adhikari R., Acharya D. Regional variation in knowledge and practice regarding common zoonoses among livestock farmers of selective districts in Nepal. PLoS Neglected Trop. Dis. 2023;17 doi: 10.1371/JOURNAL.PNTD.0011082. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Caste/Ethnicity Report | National Population and and Housing Census 2021 Results, (n.d.). https://censusnepal.cbs.gov.np/results/downloads/caste-ethnicity (accessed June 18, 2023).
  • 108.Singh R.B., Takahashi T., Elkilany G.N., Hristova K., Saboo B., Mahashwari A., et al. The human microbiome and the heart. World Heart J. 2016;8:371–378. [Google Scholar]
  • 109.Acharya K.P., Phuyal S., Saied A.R.A. A One Health approach to improve the safety of traditional yak blood drinking in Nepal. Commun. Med. 2025;5(1):1–2. doi: 10.1038/s43856-025-00763-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Rai S.K., Matsumura T., Ono K., Abe A., Hirai K., Rai G., et al. High toxoplasma seroprevalence associated with meat eating habits of locals in Nepal. Asia Pac. J. Publ. Health. 1999;11:89–93. doi: 10.1177/101053959901100207. [DOI] [PubMed] [Google Scholar]
  • 111.Upadhyay N., Khanal B., Acharya Y., Timsina K.P. Nepalese legal standard of milk and common milk products and its implications. J. Agric. Natural Resour. 2021;4:284–294. doi: 10.3126/JANR.V4I2.33924. [DOI] [Google Scholar]
  • 112.Bajagai S.Y. National Conference on Food Science and Technology (Food Conference-2012) 2012. Food Safety regulation in Nepal and issues in the regulation of meat safety.https://www.researchgate.net/publication/301634962_Food_Safety_Regulation_in_Nepal_and_Issues_in_the_Regulation_of_Meat_Safety?channel=doi&linkId=574e2c1108ae82d2c6be2aba&showFulltext=true Kathmandu. [Google Scholar]
  • 113.Joshi P., Karn S.K., Koirala P. Strengthening food safety governance in Nepal through collaborative capacity development and private sector engagement. J. Agric. Environ. 2023;24:235–242. doi: 10.3126/aej.v24i01.58197. [DOI] [Google Scholar]
  • 114.Heifer International . 2019. MOU Signed with Banks for Capital Deployment Heifer Partners with Nepal Government for Abattoir Development Using 4P Model.https://heifernepal.org/wp-content/uploads/2021/05/Heifer-Newsletter-Final1.pdf [Google Scholar]
  • 115.Shingh S., Kalwar C.S., Poudel S., Tiwari P., Jha S. A study on growth and performance of dairy sector in Nepal. Int. J. Environ. Agric. Biotechnol. 2020;5:1154–1166. doi: 10.22161/IJEAB.54.36. [DOI] [Google Scholar]
  • 116.Dhungana J., Gauchan D., Timsina K.P., Panta H.K. Insight into policy provisions and their gaps for dairy sector development in Nepal. J. Agric. Food Res. 2024;16 doi: 10.1016/J.JAFR.2024.101134. [DOI] [Google Scholar]
  • 117.Joshi G.R., Joshi B. Agricultural and natural resources policies in Nepal: a review of formulation and implementation processes and issues. Nepal Public Pol. Rev. 2021:212–227. https://www.nepjol.info/index.php/nppr/article/view/43459 [Google Scholar]
  • 118.Pandey S., Thapaliya S., Khanal D.R. Antimicrobials drug residues in chicken meat: a potential human health concern. Nepalese J. Agric. Sci. 2022;22:220–233. [Google Scholar]
  • 119.VSDRL . 2020. Status of Antimicrobial Use in Livestock Sector in Nepal.https://vsdrl.gov.np/progressfiles/b1-1721378210.pdf Kathmandu. [Google Scholar]
  • 120.Bhusal D.R., Chhetri B., Subedi J.R. Determination of antibiotics residues in milk samples collected in the different sites of Kathmandu, Nepal. Asian J. Dairy Food Res. 2020;39:195–200. doi: 10.18805/AJDFR.DR-186. [DOI] [Google Scholar]
  • 121.Pokharel S., Sedhai S., Thakur R., Gautam M.N., Aryal D., Upadhyaya N. Antibiotic residue in raw milk collected from dairy farm and markets in Nepal. Nepalese Vet. J. 2023;38:32–40. [Google Scholar]
  • 122.Gompo T.R., Sapkota R., Subedi M., Koirala P., Bhatta D.D. Monitoring of antibiotic residues in chicken meat, cow and Buffalo milk samples in Nepal. Int. J. Appl. Sci. Biotechnol. 2020;8:355–362. [Google Scholar]
  • 123.Khanal B.K.S., Sadiq M.B., Singh M., Anal A.K. Screening of antibiotic residues in fresh milk of Kathmandu Valley, Nepal. J. Environ. Sci. Health B. 2018;53:57–86. doi: 10.1080/03601234.2017.1375832. [DOI] [PubMed] [Google Scholar]
  • 124.Raut R., Mandal R.K., Kaphle K., Pant D., Nepali S., Shrestha A. Assessment of antibiotic residues in the marketed meat of Kailali and Kavre of Nepal. Int. J. Appl. Sci. Biotechnol. 2017;5:386–389. doi: 10.3126/IJASBT.V5I3.18302. [DOI] [Google Scholar]
  • 125.Maharjan B., Neupane R., Bhatta D.D. Antibiotic residue in marketed broiler meat of Kathmandu metropolitan city. Arch. Vet. Sci. Med. 2020;3:1–10. doi: 10.26502/avsm.010. [DOI] [Google Scholar]
  • 126.Shrestha N., Layalu S., Amatya S., Shrestha S., Basnet S., Shrestha M., et al. Higher Level of Quinolones Residue in Poultry Meat and Eggs; an Alarming Public Health Issue in Nepal. MedRxiv. 2022 doi: 10.1101/2022.09.03.22279573. [DOI] [Google Scholar]
  • 127.De Vries A., Kaylegian K.E., Dahl G.E. MILK Symposium review: improving the productivity, quality, and safety of milk in Rwanda and Nepal. J. Dairy Sci. 2020;103:9758–9773. doi: 10.3168/jds.2020-18304. [DOI] [PubMed] [Google Scholar]
  • 128.Lemma D H., Mengistu A., Kuma T., Kuma B. Improving milk safety at farm-level in an intensive dairy production system: relevance to smallholder dairy producers. Food Qual. Safe. 2018;2:135–143. doi: 10.1093/fqsafe/fyy009. [DOI] [Google Scholar]
  • 129.Dhungel D., Maskey B., Bhattarai G., Shrestha N.K. Hygienic quality of raw cows' milk at farm level in Dharan, Nepal. J. Food Sci. Technol. Nepal. 2019;11:39–46. doi: 10.3126/jfstn.v11i0.29686. [DOI] [Google Scholar]
  • 130.Bhattarai J., Badhu A., Shah T., Niraula S.R. Meat hygiene practices among meat sellers in Dharan Municipality of Eastern Nepal. Birat J. Health Sci. 2017;2:184–190. doi: 10.3126/bjhs.v2i2.18524. [DOI] [Google Scholar]
  • 131.Upadhayaya M., Ghimire B. Survey on good hygiene practices in retail meat shops in Butwal municipality, Nepal. Nepal. Vet. J. 2018;35:110–121. doi: 10.3126/NVJ.V35I0.25248. [DOI] [Google Scholar]
  • 132.Kelly T.R., Bunn D.A., Joshi N.P., Grooms D., Devkota D., Devkota N.R., et al. Awareness and practices relating to zoonotic diseases among smallholder farmers in Nepal. EcoHealth. 2018;15:656–669. doi: 10.1007/S10393-018-1343-4. [DOI] [PubMed] [Google Scholar]
  • 133.Thakur S. An overview of fasciolosis in Nepal: epidemiology, diagnosis, and control strategies. J. Parasit. Dis. 2024:1–13. doi: 10.1007/s12639-024-01700-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.Acharya K.P., Karki S., Shrestha K., Kaphle K. One Health approach in Nepal: scope, opportunities and challenges. One Health. 2019;8 doi: 10.1016/j.onehlt.2019.100101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Joshi D.D., Maharjan M., Johansen M.V., Willingham A.L., Sharma M. Improving meat inspection and control in resource-poor communities: the Nepal example. Acta Trop. 2003;87:119–127. doi: 10.1016/s0001-706x(03)00028-7. [DOI] [PubMed] [Google Scholar]
  • 136.Bhandari R., Singh A.K., Bhatt P.R., Timalsina A., Bhandari R., Thapa P., Baral J., Adhikari S., Poudel P., Chiluwal S. Factors associated with meat hygiene-practices among meat-handlers in Metropolitan City of Kathmandu, Nepal. PLOS Global Publ. Health. 2022;2 doi: 10.1371/journal.pgph.0001181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 137.Bekuma A., Galmessa U. Review on hygienic milk products practice and occurrence of mastitis in cow's milk. Agric. Res. Technol. 2018;18:1–11. doi: 10.19080/ARTOAJ.2018.18.556053. [DOI] [Google Scholar]
  • 138.Ndungu T.W., Omwamba M., Muliro P.S., Oosterwijk G. Hygienic practices and critical control points along the milk collection chains in smallholder collection and bulking enterprises in Nakuru and Nyandarua Counties, Kenya. Afr. J. Food Sci. 2016;10(11):327–339. doi: 10.5897/AJFS2016.1485. [DOI] [Google Scholar]
  • 139.Hobbs J.E. In: Advances in Food Traceability Techniques and Technologies. Espiñeira M., Santaclara F.J., editors. Elsevier; Amsterdam: 2016. Effective use of food traceability in meat supply chains; pp. 321–335. [DOI] [Google Scholar]
  • 140.Nyokabi N.S., Phelan L., Gemechu G., Berg S., Lindahl J.F., Mihret A., et al. From farm to table: exploring food handling and hygiene practices of meat and milk value chain actors in Ethiopia. BMC Public Health. 2023;23:899. doi: 10.1186/s12889-023-15824-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 141.Khanal G., Poudel S. Factors associated with meat safety knowledge and practices among butchers of Ratnanagar municipality, Chitwan, Nepal: a cross-sectional study. Asia Pac. J. Publ. Health. 2017;29:683–691. doi: 10.1177/1010539517743850. [DOI] [PubMed] [Google Scholar]
  • 142.Johnson N.L., Mayne J., Grace D., Wyatt A.J. How Will Training Traders Contribute to Improved Food Safety in Informal Markets for Meat and Milk? A Theory of Change Analysis, IFPRI Discussion Paper 1451. International Food Policy Research Institute; Washington, DC: 2015. [Google Scholar]
  • 143.Paudel M., Acharya B., Adhikari M. Social determinants that lead to poor knowledge about, and inappropriate precautionary practices towards, avian influenza among butchers in Kathmandu, Nepal. Infect. Dis. Poverty. 2013;2:1–10. doi: 10.1186/2049-9957-2-10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Subedi D., Bhattarai T., Acharya D.R. Meat handling practices among retail meat shops in Dharan sub-metropolitan city. Tribhuvan Univ. J. Food Sci. Technol. 2022;1:1–8. doi: 10.3126/tujfst.v1i1.49930. [DOI] [Google Scholar]
  • 145.Subedi D., Dhakal A., Jyoti S., Paudel S., Ranabhat G., Tiwari A., et al. Zoonotic diseases awareness and food safety practices among livestock farmers in Nepal. Front. Vet. Sci. 2025;11:1514953. doi: 10.3389/fvets.2024.1514953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146.Fagnani R., Nero L.A., Rosolem C.P. Why knowledge is the best way to reduce the risks associated with raw milk and raw milk products. J. Dairy Res. 2021;88:238–243. doi: 10.1017/s002202992100039x. [DOI] [PubMed] [Google Scholar]
  • 147.Bell R.A., Hillers V.N., Thomas T.A. The Abuela Project: safe cheese workshops to reduce the incidence of Salmonella typhimurium from consumption of raw-milk fresh cheese. Am. J. Publ. Health. 1999;89:1421–1424. doi: 10.2105/ajph.89.9.1421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 148.Caudell M.A., Charoonsophonsak P.V., Miller A., Lyimo B., Subbiah M., Buza J., et al. Narrative risk messages increase uptake and sharing of health interventions in a hard-to-reach population: a pilot study to promote milk safety among Maasai pastoralists in Tanzania. Pastoralism. 2019;9:1–12. doi: 10.1186/s13570-019-0142-z. [DOI] [Google Scholar]
  • 149.Ovuru K.F., Izah S.C., Ogidi O.I., Imarhiagbe O., Ogwu M.C. Slaughterhouse facilities in developing nations: sanitation and hygiene practices, microbial contaminants and sustainable management system. Food Sci. Biotechnol. 2024;33:519–537. doi: 10.1007/s10068-023-01406-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 150.Haldar L., V Raghu H., Ray P.R. Milk and milk product safety and quality assurance for achieving better public health outcomes. Agricult. Livest. Prod. Aquacult.: Adv. Smallhold. Farm. Syst. 2022;1:217–259. doi: 10.1007/978-3-030-93258-9_13. [DOI] [Google Scholar]
  • 151.Government of Nepal . Department of Food Technology and Quality Control; 2023. Food Act, 1967 (Revised 2023)www.dftqc.gov.np/downloadfile/foodact2023_1334043787_1382615399.pdf [Google Scholar]
  • 152.Kasapila W., Shaarani S.M.D. Harmonisation of food labelling regulations in Southeast Asia: benefits, challenges and implications. Asia Pac. J. Clin. Nutr. 2011;20:1–8. [PubMed] [Google Scholar]
  • 153.Animal Nepal . 2019. National Livestock Welfare Survey Report.www.AnimalNepal.Org.Np/Wp-Contents/Uploads//2019/06/National-Livestock-Welfare-Survey-Report-2-1.Pdf (accessed 2 April 2025) [Google Scholar]
  • 154.Adonu R.E., Dzokoto L., Salifu S.I. Sanitary and hygiene conditions of slaughterhouses and its effect on the health of residents: a case study of Amasaman slaughterhouse in the Ga west municipality, Ghana. Food Sci. Qual. Manag. 2017;65:11–15. [Google Scholar]
  • 155.Tomasevic I., Kuzmanović J., Anđelković A., Saračević M., Stojanović M.M., Djekic I. The effects of mandatory HACCP implementation on microbiological indicators of process hygiene in meat processing and retail establishments in Serbia. Meat Sci. 2016;114:54–57. doi: 10.1016/j.meatsci.2015.12.008. [DOI] [PubMed] [Google Scholar]
  • 156.Sandrou D.K., Arvanitoyannis I.S. Implementation of hazard analysis critical control point (HACCP) to the dairy industry: current status and perspectives. Food Rev. Int. 2000;16:77–111. doi: 10.1081/FRI-100100283. [DOI] [Google Scholar]
  • 157.Kim J.H., Hur S.J., Yim D.G. Monitoring of microbial contaminants of beef, pork, and chicken in HACCP implemented meat processing plants of Korea. Korean J. Food Sci. Anim. Resour. 2018;38:282. doi: 10.5851/kosfa.2018.38.2.282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 158.Nortjé G.L., Nel L., Jordaan E., Naudé R.T., Holzapfel W.H., Grimbeek R.J. A microbiological survey of fresh meat in the supermarket trade. Part 1: carcasses and contact surfaces. Meat Sci. 1989;25:81–97. doi: 10.1016/0309-1740(89)90024-7. [DOI] [PubMed] [Google Scholar]
  • 159.Nørrung B., Buncic S. Microbial safety of meat in the European Union. Meat Sci. 2008;78:14–24. doi: 10.1016/j.meatsci.2007.07.032. [DOI] [PubMed] [Google Scholar]
  • 160.Gebru G., Gebretinsae T. Evaluating the implementation of hazard analysis critical control point (HACCP) in small scale abattoirs of Tigray region, Ethiopia. Food Protect. Trends. 2018;38:250–257. [Google Scholar]
  • 161.Raab V., Petersen B., Kreyenschmidt J. Temperature monitoring in meat supply chains. Br. Food J. 2011;113:1267–1289. doi: 10.1108/00070701111177683. [DOI] [Google Scholar]
  • 162.Ntuli V., Sibanda T., Elegbeleye J.A., Mugadza D.T., Seifu E., Buys E.M. In: Present Knowledge in Food Safety. Knowles M.E., Anelich L.E., Boobis A.R., Popping B., editors. Elsevier; Amsterdam: 2023. Dairy production: microbial safety of raw milk and processed milk products; pp. 439–454. [DOI] [Google Scholar]
  • 163.Vilar M.J., Rodriguez-Otero J.L., Sanjuán M.L., Diéguez F.J., Varela M., Yus E. Implementation of HACCP to control the influence of milking equipment and cooling tank on the milk quality. Trends Food Sci. Technol. 2012;23:4–12. doi: 10.1016/j.tifs.2011.08.002. [DOI] [Google Scholar]
  • 164.Van Schothorst M., Kleiss T. HACCP in the dairy industry. Food Control. 1994;5:162–166. doi: 10.1016/0956-7135(94)90076-0. [DOI] [Google Scholar]
  • 165.Panisello P.J., Quantick P.C. Technical barriers to hazard analysis critical control point (HACCP) Food Control. 2001;12:165–173. doi: 10.1016/S0956-7135(00)00035-9. [DOI] [Google Scholar]
  • 166.Gizaw Z. Public health risks related to food safety issues in the food market: a systematic literature review. Environ. Health Prev. Med. 2019;24:1–21. doi: 10.1186/s12199-019-0825-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Pettengill J.B., Beal J., Balkey M., Allard M., Rand H., Timme R. Interpretative labor and the bane of nonstandardized metadata in public health surveillance and food safety. Clin. Infect. Dis. 2021;73:1537–1539. doi: 10.1093/cid/ciab615. [DOI] [PubMed] [Google Scholar]
  • 168.Grace D., Wu F., Havelaar A.H. MILK Symposium review: foodborne diseases from milk and milk products in developing countries—review of causes and health and economic implications. J. Dairy Sci. 2020;103:9715–9729. doi: 10.3168/jds.2020-18323. [DOI] [PubMed] [Google Scholar]
  • 169.Kapoor S., Goel A.D., Jain V. Milk-borne diseases through the lens of One Health. Front. Microbiol. 2023;14 doi: 10.3389/fmicb.2023.1041051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 170.Garcia S.N., Osburn B.I., Cullor J.S. A One Health perspective on dairy production and dairy Food Safety. One Health. 2019;7 doi: 10.1016/j.onehlt.2019.100086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 171.Lyu N., Feng Y., Pan Y., Huang H., Liu Y., Xue C., et al. Genomic characterization of Salmonella enterica isolates from retail meat in Beijing, China. Front. Microbiol. 2021;12:636332. doi: 10.3389/fmicb.2021.636332. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 172.Khatiwada A., Karna A., Bhat N., Deo S. One Health in Nepal-an overview. Nepal J. Health Sci. 2021;1:73–74. doi: 10.3126/njhs.v1i1.38738. [DOI] [Google Scholar]

Articles from Science in One Health are provided here courtesy of Elsevier

RESOURCES