Abstract
Buffaloes play a vital role in Bangladesh's livestock sector, contributing significantly to the nation’s milk and meat production. However, their productivity remains below potential due to limited genetic capacity, poor reproductive performance, and inadequate health and management practices. This review critically synthesizes findings from scientific literature, field studies, and national reports to assess the status of buffalo production, reproductive efficiency, genetic improvement efforts, and disease management strategies in Bangladesh. Major challenges include low milk yield (average 2.50-4.00 liters/day), imbalanced nutrition, reliance on traditional feeding systems, and minimal mechanization. Reproductive inefficiencies are characterized by low conception rates (below 40%), prolonged calving intervals (local:19.36 ± 2.39 months; crossbred: 19.37 ± 2.63 months), delayed onset of puberty (30 to 36 months), and ineffective estrus detection. Although crossbreeding programs with high-yielding breeds such as Murrah and Nili-Ravi have been introduced, progress has been limited due to inadequate record-keeping, lack of performance monitoring, and continued dependence on conventional breeding methods. Disease prevention and control are further impeded by insufficient veterinary infrastructure, low vaccination coverage, and limited farmer awareness. Structural barriers such as the absence of integrated development frameworks, restricted access to artificial insemination (AI), and a shortage of superior germplasm also hinder sectoral advancement. To address these multifaceted issues, the review advocates for enhanced farmer education, expansion of AI services, development of region-specific disease control strategies, and the implementation of systematic genetic improvement programs incorporating molecular technologies. Strengthened collaboration among government agencies, research institutions, and farming communities is essential to foster a resilient, productive, and sustainable buffalo industry in Bangladesh.
Keywords: Buffalo, Breeding strategies, Genetic improvement, Reproductive efficiency, Health management, Bangladesh
1. Introduction
Buffalo (Bubalus bubalis) is an important domesticated livestock species in Bangladesh, playing a significant role in rural livelihoods and contributing to the national economy (Habib et al., 2017). The current buffalo population is approximately 1.508 million, predominantly of indigenous origin (DLS, 2024). Two subspecies are found in the country: The Riverine type (Bubalus bubalis bubalis) and the Swamp type (Bubalus bubalis carabanensis), which differ in morphology and chromosome number. Riverine buffaloes possess 50 chromosomes, while Swamp buffaloes have 48 (Hamid et al., 2017). Among the Riverine breeds, Murrah, Nili-Ravi, Surti, and Jaffarabadi are famous for their superior milk production. Crossbreeding between indigenous and neighboring Indian breeds occurs along the border areas due to transboundary animal movement (Hamid et al., 2016a). Approximately 40.00% of the buffalo population resides in coastal regions, with the rest distributed across the Meghna-Ganga and Jamuna-Brahmaputra floodplains. Buffaloes in Bangladesh are raised under various management systems: extensive (56.00%), semi-intensive (42.00%), and intensive (2.00%) (Sultana et al., 2024). Despite their adaptability and production potential, buffaloes contribute only 1.40% to the national milk output and 0.95% to meat production, far below the levels observed in neighboring countries such as India (51.20%), Pakistan (59.50%), Nepal (66.60%), and Sri Lanka (18.00%) (Hamid et al., 2016b; Siddiky & Faruque, 2017). According to global estimates, buffaloes contribute significantly to milk and meat production, particularly in India, while Bangladesh lags behind (Fig. 1).
Fig. 1.
Sankey diagram showing the global distribution of buffalo population, milk, and meat production, highlighting Asia, especially India, dominates globally, while Bangladesh contributes modestly (FAO, 2021 and other regional statistics).
Additionally, buffalo is the second most important livestock species in Bangladesh after cattle, with significant contributions to rural livelihoods and the national economy (Hamid et al., 2016b). Their ability to utilize poor-quality roughage, withstand harsh environmental conditions, and yield relatively high economic returns makes them ideal for sustainable livestock development. However, they have historically been neglected in terms of policy, research, and development support. In contrast, buffaloes have played a central role in the dairy industry in countries like India. According to FAO (2021), global trends in buffalo production are on the rise, particularly in Asia and South Asia, including Bangladesh. Several challenges hinder buffalo productivity in Bangladesh. These include inadequate feed and fodder availability, declining grazing land, insufficient access to clean water and veterinary services, low genetic merit, and limited application of reproductive technologies such as artificial insemination (AI) (Islam et al., 2017; Pehan et al., 2022). Addressing these issues necessitates a thorough understanding of both genetic and non-genetic factors that influence key economic traits. Partitioning phenotypic variation into genetic and environmental components is essential for effective breeding program design (Abou-Bakr, 2009). Performance traits like milk yield and fertility are also influenced by environmental factors such as season of calving and parity (Aziz et al., 2001; El-Arian et al., 2012; Hassan et al., 2017). Given that reproductive efficiency and milk production are major determinants of dairy profitability, improving these parameters is imperative (LeBlanc, 2010). Conserving and improving indigenous buffalo germplasm is vital for long-term productivity enhancement (Aminafshar et al., 2008). Crossbreeding with high-performing exotic breeds holds great potential, but breeding strategies need to be adapted to the country’s diverse agro-ecological zones. Assisted reproductive technologies (ARTs) like embryo transfer, multiple ovulation and embryo transfer (MOET), ovum pick-up (OPU), and in vitro fertilization (IVF), estrous synchronization, AI, can accelerate genetic improvement (Kumar et al., 2024; Muner et al., 2025). However, adoption remains limited due to seasonal breeding tendencies and low conception rates. Furthermore, buffaloes, especially the Riverine type, are known for their adaptability to varied topographies and climates but remain vulnerable to several diseases and health disorders that can negatively impact production and lead to mortality (Villanueva et al., 2018). Therefore, any genetic improvement strategy must be integrated with robust health management systems. Effective health interventions, including vaccination, regular health screenings, biosecurity measures, and parasite control, are crucial to improving reproductive performance and reducing economic losses (Jadav et al., 2022; Dodiya et al., 2024). Proper health management not only ensures feed efficiency and production sustainability but also prolongs the productive lifespan of breeding stock.
Although buffaloes are increasingly important in Bangladesh's livestock sector, no comprehensive review currently synthesizes the interconnected domains of productivity, reproduction, genetics, and health management. Existing literature often addresses these areas in isolation and lacks contextual integration. Considering rising demand for milk and meat, environmental constraints, and the growing accessibility of advanced technologies, a holistic and evidence-based evaluation is urgently required. Therefore, this review aims to provide a comprehensive assessment of buffalo productivity, reproductive efficiency, genetic improvement, and disease management in Bangladesh. It identifies current limitations, explores technological advancements, and offers strategic recommendations for developing a sustainable and health-resilient buffalo production system suited to the specific context of Bangladesh. Additionally, this manuscript takes a structured narrative approach, combining research findings, national statistics, and expert perspectives to provide a holistic and integrated view of advanced buffalo production, reproduction, genetics, and buffalo health management in Bangladesh.
2. Methodology
2.1. Data collection
Though not a systematic review, this narrative review used a structured and transparent literature search and inclusion process to ensure replicability. A systematic approach was adopted to collect relevant literature on buffalo genetics, breeding strategies, and health management practices in Bangladesh. Sources included peer-reviewed scientific articles, government reports, and publications from recognized national and international organizations, such as the Department of Livestock Services (DLS), the Food and Agriculture Organization of the United Nations (FAO), and the International Buffalo Federation. To ensure the inclusion of up-to-date and high-quality literature, extensive literature searches were conducted using electronic databases, including PubMed, Scopus, Web of Science, and Google Scholar. Search terms were applied using specific keywords and Boolean operators, such as: “Buffalo breeding in Bangladesh,” “Genetic improvement in buffalo,” “Crossbreeding with riverine breeds,” “Reproductive technologies in buffalo,” “Buffalo milk and meat production,” “Prevalent diseases in buffalo,” “Buffalo Health Management,” and “Buffalo Health and Productivity”. The inclusion criteria focused on publications from 2000 to 2025, with emphasis on studies relevant to the agro-ecological conditions and socio-economic context of Bangladesh.
2.2. Literature review
A structured review was conducted to assess current literature on buffalo breeding, genetic improvement, and health management in Bangladesh. The analysis incorporated peer-reviewed journal articles, national reports, and case studies, focusing on core areas such as crossbreeding strategies, genetic evaluation techniques, reproductive biotechnology, and enhancements in milk and meat production.
Emphasis was placed on evaluating studies involving crossbreeding with high-yielding Riverine breeds (e.g., Murrah, Nili-Ravi) to determine their impact on the genetic performance and productivity of indigenous buffalo populations. Research on reproductive biotechnologies-including artificial insemination (AI), estrus synchronization (ES), and in vitro fertilization (IVF) was reviewed to assess their adaptability and effectiveness under local production systems.
Health management practices were analyzed for their influence on reproductive efficiency, feed conversion, disease control, and herd productivity. Particular attention was given to the relationship between infectious disease prevalence, mortality rates, and the implementation of preventive veterinary interventions. The integration of genetic improvement programs with comprehensive health management was recognized as a critical component of sustainable buffalo production systems. This review identifies recent innovations, persistent constraints, and emerging trends relevant to improving buffalo productivity, particularly in terms of milk and meat yield, providing evidence-based insights for strategic development in the Bangladeshi context.
2.3. Inclusion and exclusion criteria
To maintain the relevance, scientific rigor, and focus of this review, clearly defined inclusion and exclusion criteria were applied during the selection of literature. Studies were included if they addressed key aspects of buffalo genetics, breeding strategies, and reproductive technologies, or with particular emphasis on research involving Bangladeshi buffalo populations or closely related riverine breeds like Murrah and Nili-Ravi. Priority was given to peer-reviewed publications in English, published between 2000 and 2025, to ensure the incorporation of current and credible information. Conversely, studies were if they focused on livestock species other than buffalo, lacked peer review or a clearly defined methodology, did not present substantial or relevant data, were published in languages other than English, or were identified as duplicate records across different databases (Fig. 2).
Fig. 2.
Flow diagram illustrating the systematic process used for data collection, literature screening, and application of inclusion and exclusion criteria in the preparation of this review.
3. Buffalo genetic resources in Bangladesh and their population
Bangladesh harbors several indigenous buffalo populations that play a vital role in milk production, meat supply, and draught power. The buffalo population in Bangladesh has shown a gradual increase in the last two decades (Fig. 3). These buffaloes are primarily classified into two types: riverine and swamp. Riverine buffaloes are mostly distributed in the southern coastal regions, including Khulna, Barisal, Bhola, and Patuakhali, while swamp buffaloes are predominant in hilly and floodplain areas, such as Sylhet and Sunamganj in the northeast, and in the northern river basin districts like Sirajganj, Jamalpur, and Kurigram (Fig. 4) (Hamid et al., 2016b; Sarker et al., 2024). In addition to indigenous types, purebred buffaloes such as Murrah and Nili-Ravi have been introduced in border regions through transboundary movement from neighboring India (Habib et al., 2023). Although indigenous buffaloes generally produce lower milk yields than exotic breeds, they are known for high milk fat content (6–8%) and are highly valued for their adaptability, disease resistance, and performance under semi-intensive production systems (Habib et al., 2017). An overview of the key characteristics of buffalo genotypes in Bangladesh is summarized in Table 1, while representative images of these genotypes are illustrated in Fig. 5.
Fig. 3.
Buffalo population growth trend in Bangladesh from 2001 to 2024 (Source: DLS, 2024).
Fig. 4.
Map showing buffalo-concentrated areas in Bangladesh is highlighted in green, with a scale bar and north arrow for orientation.
Table 1.
Overview of buffalo genotypes in Bangladesh (Rashid et al., 2019).
| Type / Breed | Region | Genotypic and Phenotypic Characteristics |
|---|---|---|
| Indigenous (River type) | Central & Western parts | Medium-sized; jet black to black coat; 50 chromosomes |
| Indigenous (Swamp type) | Eastern part | Small-sized; grey coat with chevron and white markings; crescent-shaped horns; 48 chromosomes |
| Bangladeshi (Local Mixed Type) | Southwest & Central | Medium-sized; light black coat with chevron and white stockings; 50 chromosomes |
| Indigenous (River), Murrah × Indigenous Crossbred, Nili-Ravi × Indigenous Crossbred | Bangladesh Livestock Research Institute (BLRI) | Medium-sized; jet black to black coat; medium to small horns (either back coiled or medium long); brownish-black variation with white markings on forehead and limbs; 50 chromosomes |
| Crossbred (Murrah, Nili-Ravi types) | Southern parts, Indian border regions | Medium-sized; phenotypic traits vary depending on parent breeds (e.g., coat color, horn shape, body size); 50 chromosomes |
| Nili-Ravi, Murrah, Indigenous (crossbred) | Bagerhat (Buffalo Breeding Farm) | Nili-Ravi characteristics: large body 0’osize, curved horns, white markings, high milk yield potential; 50 chromosomes |
Fig. 5.
Representative images of buffalo genotypes found in Bangladesh. (A, B) Indigenous riverine-type buffaloes (C, D), indigenous Murrah-type buffaloes (E, F), swamp-type buffaloes, and (G, H) crossbred buffaloes (Hamid et al., 2017).
4. Production performance of buffaloes in Bangladesh
Buffalo farming is an important component of Bangladesh’s livestock sector, particularly in rural floodplains, haor ecosystems, and coastal zones, where buffaloes exhibit strong adaptability to environmental stressors (Samad, 2020). While indigenous buffalo genotypes are still predominant, there is a growing trend toward crossbreeding with genetically superior breeds such as Murrah and Nili-Ravi to improve productive performance traits, especially milk and meat yield (Gowane & Vohra, 2022). However, challenges such as endemic diseases, feed shortages, and genetic limitations hinder optimal productivity (Habib et al., 2023).
4.1. Milk production performance
In Bangladesh, buffaloes are a valuable source of high-fat milk, containing 6.50–8.00% fat, significantly higher than the 3.50–4.00% found in cow milk (Habib et al., 2017). The average daily milk yield of indigenous buffalo ranges from 2.50 to 4.00 liters but can be increased to 6.00 to 10.00 liters through crossbreeding with superior breeds like Murrah and Nili-Ravi (Hamid et al., 2016b; Islam et al., 2017; Samad, 2020). Lactation length in indigenous buffalo spans 270–300 days, whereas crossbred buffaloes exhibit extended lactation periods of 300–330 days (Kabir et al., 2017; Omar et al., 2024). Prominent buffalo milk-producing areas include Noakhali, Bhola, and Patuakhali (Habib et al., 2023). A recent study recorded an average daily milk yield of 3.00 liters and a lactation period of 179.90 ± 3.84 days (Habib et al., 2023). Despite genetic and management improvements, milk production remains suboptimal due to nutritional deficiencies, limited veterinary services, and insufficient adoption of modern husbandry practices (Hamid et al., 2016a).
4.2. Meat production performance
Buffalo meat, known locally as buff, is becoming increasingly popular in Bangladesh due to its leanness (fat 1.15%) and lower cholesterol (46 mg/100 g) compared to beef (fat 4.33%; cholesterol 70 mg/100 gm) (Naveena et al., 2014). Indigenous buffaloes generally reach a mature live weight of 300–400 kg by 3–4 years of age, while crossbred buffaloes, including Murrah and Nili-Ravi types, can attain 500–600 kg under improved feeding and management systems (Islam et al., 2017; Saha et al., 2018). The carcass dressing percentage typically ranges from 50% to 55%, reflecting their potential for meat production (Maheswarappa et al., 2022). However, the slow growth rate (250–350 g/day) of indigenous genotypes remains a significant constraint to enhancing buffalo meat productivity (Karim et al., 2023).
5. Reproductive efficiency of buffaloes in Bangladesh
Buffaloes are valuable livestock in Bangladesh, yet their reproductive performance remains markedly lower than that of cattle. Key limitations include delayed onset of puberty (Buffaloes is around 36-42 months compared to 18-24 months in cattle), prolonged calving intervals (buffaloes 18-24 months versus cattle 12-14 months), low conception rates (buffaloes are typically 30–45% compared to 50–60% in cattle), postpartum anestrus, and distinct seasonal breeding patterns (Rahman et al., 2019; Mohammed et al., 2018). These reproductive inefficiencies are attributed to a combination of genetic, nutritional, environmental, and managerial factors.
5.1. Puberty and sexual maturation
The onset of puberty in buffalo heifers in Bangladesh is considerably delayed, typically occurring between 30 to 36 months (Jahan et al., 2024), which is later than buffaloes managed under improved farming systems (18 to 24 months). This delay is primarily attributed to poor nutrition, environmental stress, and inadequate management (Rahman et al., 2019; Rahman et al., 2020). Puberty is influenced by several factors, including genotype, climate, nutrition, and husbandry practices. In comparison, under improved conditions, breeds such as Murrah and Nili-Ravi reach puberty earlier, typically between 24 and 30 months (Perera, 2011). According to Jainudeen & Hafez (2000), buffaloes typically attain puberty at 60% of their adult body weight (250 - 400 kg), with age at puberty ranging from 18 to 46 months.
5.2. Silent estrus, estrous behavior, and detection
Buffaloes often display weak or silent estrus signs, making visual detection difficult and contributing to missed breeding opportunities and longer calving intervals (Ahmed et al., 2012a). Estrus in buffaloes typically lasts 12–24 h and is more visible during cooler months (Jainudeen & Hafez, 2000; Barile, 2005), contributing to seasonal breeding patterns. The hot and humid climate of Bangladesh further reduces the visibility of estrous signs, complicating timely detection by farmers (Sarder et al., 2007). Estrus synchronization using hormonal treatments such as prostaglandins and GnRH has shown effectiveness (Akhter et al., 2013), yet adoption remains limited due to high costs and inadequate technical knowledge among rural farmers (Rashid et al., 2019).
5.3. Age at first calving
The average age at first calving for indigenous buffaloes under traditional management is 42–48 months (Rashid et al., 2019), while crossbred buffaloes may calve slightly earlier, around 36–40 months (Rahman et al., 2020). Additionally, Rashid et al. (2019) reported first calving ages for local, crossbred, Nilli, and Murrah buffaloes in Bangladesh as 46.12 ± 1.66, 46.56 ± 1.64, 46.18 ± 0.88, and 46.25 ± 1.81 months, respectively. Delayed attainment of puberty and first calving significantly reduces the reproductive lifespan and productivity of female buffaloes.
5.4. Postpartum anestrus
Postpartum anestrus, defined as the absence of estrous cycles following parturition, presents a major barrier to reproductive efficiency in buffaloes. This anestrous interval often exceeds 120 days and is commonly associated with poor body condition, hormonal imbalance, and physiological stress (Barile, 2005; Qureshi et al., 2007). Paul and Prakash (2005) reported postpartum estrus intervals of approximately 153 days in buffaloes from Pirojpur and Barguna districts. Similarly, El-Wishy (2007) recorded an average interval of 146.2 days, while Rashid et al. (2019) observed postpartum estrus resumption ranging from 30 to 171 days across different genotypes. Habib et al. (2023) recorded the postpartum heat period as 90 days in the Lalmonirhat district. Hormonal interventions, including GnRH and progesterone-based protocols, have shown potential in reducing the anestrous period (Haque et al., 2020); however, limited accessibility and infrastructure in rural regions constrain their widespread application.
5.5. Calving interval
In traditional buffalo production systems in Bangladesh, calving intervals commonly range from 16 to 18 months, which exceeds the optimal 12 to 14 months necessary for maximum reproductive efficiency (Islam et al., 2017; Rashid et al., 2019). Extended calving intervals reduce both the number of calves produced and the total milk yield over the productive lifespan of the animal. Rashid et al. (2019) reported mean calving intervals of 19.36 ± 2.39 months in local buffaloes, 19.37 ± 2.63 months in crossbred buffaloes, 19.41 ± 1.66 months in Nilli Ravi, and 18.31 ± 1.97 months in Murrah buffaloes. Similarly, Habib et al. (2023) recorded an average calving interval of 478 days in buffaloes from northern Bangladesh.
5.6. Conception rates and pregnancy maintenance
Conception rates in buffaloes vary from 45% to 55% under natural mating but decline to 30% to 40% when artificial insemination (AI) is employed (Mohammed et al., 2018). Low AI success is attributed to poor estrus detection, improper timing, poor semen quality, and inadequate insemination techniques. Additionally, embryonic mortality is relatively high during early gestation, ranging from 15% to 20%, often resulting from nutritional deficiencies, infectious diseases, and endocrine imbalances (Khan et al., 2009). To improve reproductive outcomes, it is critical to enhance nutritional management, reproductive health protocols, and access to veterinary reproductive services. A summary of reproductive performance indicators is illustrated in Fig. 6.
Fig. 6.
Average values on reproductive performances of buffaloes in Bangladesh.
5.7. Fertility management and nutritional factors
Nutrition is a key determinant of reproductive function in buffaloes, with ovarian inactivity commonly resulting from nutritional deficiencies (Qureshi, 2007; Vale et al., 2019). In Bangladesh, buffaloes predominantly graze on low-quality communal pastures, particularly in bathan systems, which limits their nutrient intake (Uddin et al., 2016). Nutritional supplementation during the transition period has been shown to enhance reproductive efficiency; Habib et al. (2020) reported that concentrate feeding reduced postpartum anestrus (90 days) duration and open days (90 to 120 days). Singh et al. (2022) demonstrated that molasses supplementation in Murrah calves accelerated puberty onset (24–30 months) and improved semen quality (volume: 2.35±0.10 ml; concentration: 985.30±52.42; individual motility: 65.67±2.01). While Afroz et al. (2020) observed no significant effect of varying concentrate levels on age at puberty, other studies highlight the reproductive benefits of supplementing diets with α-tocopherol, vitamin E, selenium, niacin, and bypass fats (Sarwar et al., 2009; Ganie et al., 2014).
5.8. Seasonality and environmental factors
The tropical climate of Bangladesh, characterized by temperatures between 32 and 40°C and high humidity, imposes significant heat stress on buffaloes, suppressing secretion of luteinizing hormone (LH), follicle-stimulating hormone (FSH), progesterone, and estradiol (Table 2). This hormonal disruption adversely affects estrus expression and embryonic development (Alam et al., 2010; Habib et al., 2017; Krishnan et al., 2017). Buffaloes exhibit greater reproductive activity during cooler seasons, whereas prolonged heat reduces estrus frequency and conception rates (Chawicha & Mummed, 2022; Omar et al., 2024). Cooling interventions such as showering buffalo bulls have been shown to improve semen quality by enhancing sperm motility and volume (Hoque et al., 2011). Management practices such as cooling systems, fixed-time AI, additional water, and nutritional supplementation during hot periods can mitigate the negative impacts of heat stress (Balhara et al., 2017; Fournel & Charbonneau, 2017).
Table 2.
Impact of heat stress on reproductive performance in buffaloes.
| Physiological Aspect | Effect of Heat Stress | Reproductive Consequences | Researchers |
|---|---|---|---|
| Feed intake | Reduced voluntary feed intake up to 10-30% when THI >75 | Sperm production declined by 13.16% (from 3.95 ± 0.33 ml in neutral conditions to 3.43 ± 0.21 ml under heat stress), with prolonged reaction time and disrupted cycles. | Roth (2017); Bhakat et al. (2009) |
| Endocrine function | Induce hormonal disruptions | Conception rate decreased by 15-25%, calving interval extended by 30-50 days | Khan et al. (2023) |
| Gonadotropin secretion | Suppressed release of FSH and LH | Impaired spermatogenesis and ovarian inactivity | Habib et al. (2017) |
| Estradiol synthesis | Inhibited estradiol production | Reduced intensity and frequency of estrus expression | Pasha et al. (2024) |
| Prolactin concentration | Elevated circulating prolactin levels | Irregular estrous cycles and impaired reproductive rhythms | Dash et al. (2016) |
| Core body temperature | Increased due to environmental heat load | Cellular dysfunction in the female reproductive tract | Ahmad et al. (2020) |
Given the detrimental effects of heat stress on reproductive physiology in buffaloes, various nutritional interventions have been explored to mitigate these impacts. These strategies aim to enhance thermotolerance, support hormonal regulation, and improve reproductive outcomes. Given the significant impact of heat stress on the reproductive efficiency of buffaloes, several feed supplementation strategies have been proposed to alleviate its negative effects. These dietary interventions aim to improve the animal's physiological resilience to heat, support endocrine balance, and enhance reproductive functions. Vitamins, minerals, antioxidants, and natural additives have shown promising results in minimizing the impact of high temperatures on reproductive parameters such as hormone levels, estrus expression, and conception rates. Table 3 summarizes the commonly recommended feed supplements for reducing heat stress and improving the reproductive performance of buffaloes.
Table 3.
Nutritional interventions to mitigate heat stress in buffaloes.
| Feed Additive | Physiological Function | Investigators |
|---|---|---|
| Vitamins A, C, E; Zn, Cu, Se, Na, NaHCO₃ | Enhance antioxidant defense and maintain electrolyte homeostasis | Dash et al. (2016) |
| Bypass fat | Improves energy balance and supports reproductive efficiency | Ahmad et al. (2020) |
| Moringa oleifera leaves | Provide phytogenic antioxidants and modulate endocrine responses | Wafa et al. (2017) |
| Vitamins E, A, and Selenium | Reduce oxidative stress and support reproductive function | Das (2018) |
| Beta-carotene | Stimulates ovarian activity and enhances conception rates | Mitsuishi & Yayota (2024) |
| Sodium bicarbonate | Buffers ruminal pH and promotes dry matter intake | Sarwar et al. (2007) |
| Melatonin | Regulates circadian rhythms and reproductive hormone secretion | Domple et al. (2021) |
| Yeast, Niacin, Zn, and Chromium | Enhance metabolic adaptation and immune function under heat stress | Purwar & Dang (2017) |
6. Breeding and selection of buffaloes in Bangladesh
Selective breeding of dairy buffaloes is fundamental for increasing milk yield and enhancing the livelihoods of rural communities in Bangladesh. Despite their significant economic and cultural values, buffaloes have historically received limited attention due to the absence of systematic breeding programs and genetic improvement initiatives. This has resulted in lower productivity compared to neighboring countries such as India and Pakistan (Uddin et al., 2016; Hamid et al., 2017). To enhance buffalo production, a breeding program focused on milk yield, adaptability, body conformation, and reproductive traits, including age at first calving and calving intervals, is essential (Rashid et al., 2019). Indigenous buffaloes are relatively low milk producers, but their productivity can be enhanced through selective breeding with exotic breeds such as Murrah and Nili-Ravi, which are globally recognized for their high milk production and strong pedigree records (Dhanda, 2013; Hamid et al., 2016a; Samad, 2020). A well-structured breeding program integrating indigenous conservation with selective crossbreeding, AI and performance recording can significantly improve indigenous buffalo productivity.
6.1. Crossbreeding for genetic improvement
The DLS of Bangladesh initiated a crossbreeding program for indigenous buffaloes by introducing Murrah and Nili-Ravi bulls from Pakistan in the mid-19th century. Subsequently, the Buffalo Breeding Farm (BBF) in Bagerhat was established to support this effort (Hamid et al., 2017). While indigenous buffaloes are highly adaptable, they produce less milk and have shorter lactation periods compared to exotic breeds. To combine local adaptability with enhanced productivity, crossbreeding with Murrah and Nili-Ravi is considered effective due to their higher milk yields and longer lactation lengths (Rashid et al., 2019; Samad, 2020). This approach has been a key strategy in improving the productive and reproductive performance of indigenous buffaloes (Omar et al., 2024). Studies indicate that crossbred buffaloes outperform local breeds in milk production and reproductive traits under improved management (Rashid et al., 2019; Shahjahan, 2021). Since 2011, Lal Teer (LTL), a private organization, has also introduced Italian Mediterranean bull semen in its research and development farm to further support genetic improvement (Hamid et al., 2017). Thus, upgrading indigenous buffaloes using elite local females and semen from proven imported bulls presents a promising pathway for breed development in Bangladesh (Habib et al., 2017). However, appropriate planning and monitoring are vital to preserve genetic diversity and prevent increased disease susceptibility as native traits risk erosion (Hamid et al., 2017).
6.2. Artificial insemination (AI) in buffaloes
AI is an important tool for genetic improvement in livestock, but its use in buffalo production in Bangladesh remains very limited. Most buffaloes are still bred naturally, and AI is practiced only in selected coastal and central areas (Uddin et al., 2016; Habib et al., 2017). Several factors contribute to this low adoption, such as difficulties in detecting estrus, the seasonal breeding pattern of buffaloes, and a shortage of trained AI technicians (Hamid, 2018).
Buffaloes often exhibit silent or weak estrus signs, making it difficult for farmers to identify the optimal time for insemination. The commonly used "am-pm rule" from cattle does not always apply to buffaloes because of their different reproductive physiology (Sarker et al., 2024). Research suggests that in intensive farming conditions, insemination should preferably occur 12-18 h after the onset of estrus to achieve better conception rates (Hamid, 2018). However, in extensive or semi-intensive systems where estrus detection is often delayed, then inseminating 25-36 h after the first signs of estrus may yield better results (Rahman et al., 2020). Another major challenge is the availability and storage of semen. Although Murrah and Nili-Ravi semen are imported for crossbreeding, the scale of AI services is restricted because of inadequate semen production, limited semen bank facilities, and poor cold chain management (Rashid et al., 2019). The use of high-quality semen from improved riverine Murrah and Nili-Ravi bulls can further enhance the milk and meat production of indigenous buffaloes. A big problem is the lack of buffalo-specific AI protocols and limited extension services to support farmers (Rashid et al., 2019). To promote wider use of AI, Bangladesh needs to improve farmer training in estrus detection, enhance the semen supply chain, and develop breeding management programs specifically designed for buffalo.
6.3. Assisted reproductive technologies (ARTs) in Bangladeshi buffaloes
In Bangladesh, the application of ARTs in buffalo production is still at a very early stage, constraining opportunities to enhance reproductive efficiency and productivity. Conception rates often remain below 40%, primarily due to inadequate estrus detection, seasonal anestrus, and insufficient technical expertise (Hamid, 2018; Rashid et al., 2019). Hormonal protocols like Ovsynch and CIDR-based synchronization have shown good potential to improve conception rates, but their use at the field level is still very limited (Habib et al., 2023). Advanced biotechnologies such as embryo transfer, MOET, OPU, and IVF are commonly practiced in many South Asian countries like India and Pakistan (Srirattana et al., 2022; Kumar et al., 2024; Muner et al., 2025), but these technologies are almost non-existent in Bangladesh. The reasons include inadequate infrastructure, lack of skilled manpower, and limited institutional capacity. Although crossbreeding with Murrah and Nili-Ravi buffaloes has started to improve milk production, the progress is slow because of poor genetic recording and evaluation systems (Charlini & Sinniah, 2015; Habib et al., 2023). However, recent genomic studies on buffalo diversity in the region provide a solid base for future precision breeding programs (Rehman et al., 2021; Ahlawat et al., 2024). To overcome these limitations, a well-defined coordinated national approach is needed that integrates, estrus synchronization, embryo transfer, OPU-IVF, MOET, and genomics, combined with proper training (Kumar et al., 2024). This would help improve reproductive efficiency and ensure sustainable development of the buffalo sector.
6.4. Selection and genetic evaluation
The rich genetic diversity of buffaloes in Bangladesh is under threat due to disorganized and uncontrolled breeding practices (Hamid et al., 2017). To improve productivity, proper selection and genetic evaluation, focusing on productive, reproductive, adaptive, and disease-resistant traits, are essential. Phenotypic traits with economic significance should be prioritized, and the genetic uniqueness of indigenous buffaloes should be preserved. In a notable effort, Lal Teer Livestock Limited (LTL), in collaboration with the Beijing Genomics Institute (BGI), successfully sequenced the buffalo genome in 2011, offering new prospects for enhancing the productivity of indigenous buffaloes (Hamid et al., 2017). Despite relatively low average milk production (600–1000 L per lactation, 250–270 days), structured selection and breeding strategies hold promise for significant improvement (Habib et al., 2023). Moreover, ongoing initiatives aimed at buffalo development further underscore the commitment to boosting the productivity and sustainability of the indigenous buffalo population (Omar et al., 2024).
7. Major diseases of buffalo and their management
Health management is an essential component of buffalo husbandry, as disease constraints significantly reduce productivity and profitability (Jadav et al., 2022). The hot and humid climate of Bangladesh further predisposes a variety of infectious and non-infectious diseases, thereby increasing veterinary costs (Rahman et al., 2022; Rahman et al., 2024). Buffaloes are susceptible to numerous diseases, in which bacterial and viral infections are major contributors to health losses, with individual diseases often showing morbidity exceeding 70% and mortality up to 25% (Samad, 2020; Ali et al., 2025). Limited awareness among farmers and insufficient diagnostic facilities hinder timely and proper treatment of diseases (Ahmed et al., 2025). Key viral, bacterial, and metabolic diseases that impair buffalo growth and reproductive performance are detailed in Tables 4, 5, and 6, along with their management strategies. Parasitic diseases also present a major challenge to buffalo production worldwide, including in Bangladesh (Biswas et al., 2021). The prevalence of parasitic infections is influenced by a combination of environmental factors such as ecological conditions, geographic location, and farm management practices, including housing, grazing, and deworming schedules. Other factors such as age, sex, body condition, parasite species, and parasite load also affect infection rates (Rizwan et al., 2024). The agroecological and geo-climatic characteristics of Bangladesh are highly conducive to the proliferation of parasites (Ali et al., 2020a; Biswas et al., 2021). The principal parasitic diseases affecting buffalo productivity are summarized in Table 7.
Table 4.
Important viral diseases of buffalo.
| Disease | Causative Agent | Transmission | External Factors | Clinical Signs | Morbidity and Mortality | Control & Prevention | References |
|---|---|---|---|---|---|---|---|
| Foot and Mouth Disease (FMD) | FMD virus (Picornaviridae) | Aerosol, ingestion, direct contact with infected animals/products | Temperature (20–34°C), humidity (50–60%), poor biosecurity | High fever, salivation, blisters on tongue, gums, teats, feet | Morbidity: ∼100%; Mortality: 20–25% | Vaccination, isolation, antimicrobials, and antiseptics (e.g., KMnO₄, glycerin) | Ali et al. (2020b); Paton et al. (2021) |
| Bovine Ephemeral Fever (BEF) | BEF virus (Rhabdoviridae) | Biting insects (mosquitoes), especially Culex annulirostris | Wet or dry seasons, hot and humid conditions, rainfall, and groundwater sources | Sudden fever (41°C), sharp milk drop, arthritis with a serofibrinous exudate, muscle swelling, mastitis | Morbidity: ∼100%; Mortality: 1–20% |
Vaccination, vector control, NSAIDs, calcium borogluconate, antibiotics | Lee (2019); Martínez-Burnes et al. (2024) |
| Buffalopox | Buffalopox virus (Poxviridae) | Direct contact, biting insects as vectors (ticks, mosquitoes) | High humidity, poor hygiene, stress (transport, weather change) | Fever, pustular skin lesions on teats, udder, muzzle, ears, eyes | Morbidity: ∼70%; Mortality: 1–2% | Vaccination, strict biosecurity, vector control, topical antibiotics, NSAIDs | Lima et al. (2019); Kabir et al. (2023) |
| Bovine Viral Diarrhea (BVD) | BVD virus (Flaviviridae) | Vertical transmission, horizontal transmission via direct contact | Poor biosecurity, dirty pens and inadequate manure management | Mild diarrhea, reproductive loss, congenital defects (e.g., cerebellar hypoplasia), ataxia | Morbidity: 70–100%; Mortality: 1–50% (phase dependent) | Partial protection via vaccination; prevent carrier contact, supportive care | Primawidyawan et al. (2016); Martínez-Burnes et al. (2024) |
Table 5.
Important bacterial diseases of buffalo.
| Disease | Causative Agent | Transmission | External Factors | Clinical Signs | Morbidity & Mortality | Control & Prevention | References |
|---|---|---|---|---|---|---|---|
| Haemorrhagic Septicemia (HS) | Pasteurella multocida (Gram-negative) | Ingestion/inhalation of contaminated feed, water, secretions or excretions | Stress, high humidity, and rainy weather | Fever, nasal discharge, hypersalivation, respiratory distress, Pharyngeal edema, sudden death | Morbidity: 60–80%, Mortality: 10–25% |
Vaccination, early antibiotics (tetracycline, enrofloxacin), adjust based on AST | Moustafa et al. (2017); Abbas et al. (2018) |
| Anthrax | Bacillus anthracis (Gram-positive) | Ingestion of contaminated feed/water, entry via mucosal lesions | Climate shifts, alkaline calcium-rich soil, temp >15.5°C | High fever, hemorrhagic mucosa, dyspnea, bleeding from orifices, rapid death | Morbidity: 25–80%; Mortality: 2–20% | Vaccination, carcass disposal, disinfection, antibiotics with supportive care | Hassan et al. (2015); Alam et al. (2022) |
| Brucellosis | Brucella abortus (Gram-negative) | Contact/ingestion of infected fetal material, milk, aerosol, venereal | High-density herds, communal water sources | Abortions, retained placenta, infertility, mastitis in females; orchitis, epididymitis in males | Morbidity: 10–40%; Mortality: 2–5% | Vaccination, test and cull, biosecurity, tetracycline or streptomycin | Ghanbari et al. (2020); Khurana et al. (2021) |
| Mastitis | Staphylococcus aureus, Streptococci, E. coli, Klebsiella, Bacillus spp. | Contaminated milking equipment, direct contact | Poor housing, cylindrical teats, seasonal stress, dirty bedding | Fever, reduced milk, udder inflammation, altered milk, high SCC | Morbidity: 20–60%; Mortality: 1–3% | Hygiene, post-milking disinfection, antibiotics (ampicillin, sulfonamides), supportive care | Hoque et al. (2022); Chowdhury et al. (2024) |
Table 6.
Major metabolic disorders in buffalo.
| Disease | Etiology | Predisposing Factors | Clinical Manifestations | Mortality | Control and Prevention | References |
|---|---|---|---|---|---|---|
| Milk Fever (Parturient Paresis) | Hypocalcemia at parturition. | High-calcium diets in prepartum period impair calcium mobilization | Anorexia, muscle tremors, incoordination, hypothermia (36.5–38°C), sternal or lateral recumbency, head turned toward the flank, flaccid paralysis | <10% | Prepartum low-calcium diet; oral calcium and vitamin D supplementation; intravenous calcium-magnesium therapy postpartum. | Kumari et al. (2022); Tufarelli et al. (2024) |
| Ketosis | Negative energy balance in early lactation, excessive fat mobilization | Energy-deficient or imbalanced diet, concurrent diseases, environmental or physiological stress | Reduced dry matter intake, decreased milk yield, ketone odor in breath, urine, and milk; elevated ketones; mucus-coated feces. | 5–10% | Maintain energy-rich, balanced ration during transition; intravenous glucose administration; corticosteroid therapy (e.g., dexamethasone). | Bradford and Swartz (2020); Cascone et al. (2022) |
| Subacute Ruminal Acidosis (SARA) | Accumulation of volatile fatty acids due to excessive fermentable carbohydrates and inadequate fiber intake. | Rapid dietary transition to high-concentrate, low-forage diets, insufficient rumen buffering | Low appetite, decreased milk production, ruminal hypomotility, laminitis, soft feces with gas | <5% | Gradual adaptation to high-concentrate diets postpartum; adequate physically effective fiber; proper ration formulation. | Kitkas et al. (2019); Elmhadi et al. (2022) |
| Grass Tetany (Hypomagnesemia) | Hypomagnesemia due to low magnesium intake and absorption | Grazing on rapidly growing fertilized pastures, high lactational demand, stress | Hyperexcitability, muscle spasms, stiff gait, ataxia, tachypnea, convulsions, sudden death | Up to 40% if untreated | Oral or injectable magnesium supplementation; mineral-balanced rations; proper pasture management and stress reduction. | McCann et al. (2016); Tufarelli et al. (2024) |
Table 7.
Important parasitic diseases of buffalo.
| Disease | Etiology | Transmission | External Factors | Clinical Signs | Mortality | Control and Prevention | References |
|---|---|---|---|---|---|---|---|
| Fasciolosis | Fasciola gigantica, Fasciola hepatica | Ingestion of metacercariae on plants or water via snail hosts (Lymnaea, Galba) | Presence of snail, marshy or waterlogged grazing areas, irregular deworming | Anemia, weight loss, submandibular edema, decreased milk, liver damage | <5%, increasing to 10–15% in severe cases | Routine deworming (Triclabendazole, Nitroxynil, Albendazole), drainage improvement, snail control | Hassan et al. (2020); Lalor et al. (2021) |
| Paramphistomosis | Paramphistomum cervi, Paramphistomum microbothrium | Ingestion of metacercariae from plants contaminated by cercaria from freshwater snails (Planorbis, Lymnaea, Bulinus) | High rainfall, dense snail populations, grazing behavior, irregular deworming | Anemia, hypoproteinemia, edema, diarrhea, anorexia, weight loss, rectal hemorrhage, decreased production | 20–50% if untreated | Routine deworming (Oxyclozanide, Niclosamide), fluid/electrolyte therapy, avoid snail-infested grazing areas | Mohanta et al. (2017); Rafiq et al. (2020) |
| Ascariasis | Toxocara vitulorum | Transmammary, ingestion of infective eggs from contaminated feed, soil, or water | Poor sanitation, climatic factors, host age, and nutritional status | Swollen face, anorexia, colic, constipation, dehydration, weight loss, foul feces | 35–50% in untreated calves | Routine deworming protocols (Ivermectin, Levamisole), good hygiene, and management | Biswas et al. (2021); Gholve et al. (2024) |
8. Constraints and challenges in Buffalo production
Buffalo production in Bangladesh faces several constraints, including poor nutrition, reproductive inefficiency, low genetic merit, and health challenges, all of which adversely affect productivity and disease resistance. Dependence on low-quality natural pastures, particularly during the dry season, results in micronutrient deficiencies that reduce milk yield and prolong the calving interval (Habib et al., 2023). The absence of structured breeding programs, ineffective estrus detection, and limited use of artificial insemination (AI) further impair reproductive success by delaying puberty and reducing the rate of conception (Srirattana et al., 2022). Limited AI usage also restricts the introduction of superior germplasm from elite breeds such as Murrah and Nili-Ravi.
Another important issue is the management of disease. The prevalence of parasitic illnesses and endemic diseases like foot-and-mouth disease has increased due to inadequate veterinary infrastructure, low vaccination coverage, and a lack of awareness among farmers (Samad, 2020; Ali et al., 2020b). In addition, inadequate disease diagnosis and insufficient expert manpower negatively affect buffalo health (Ahmed et al., 2025). The severity of these problems is increased in remote and low-resource rural areas.
Genetic improvement is hindered by the lack of pedigree records, genomic tools, estimated breeding value (EBV) systems, and systematic performance recording (Rahman et al., 2020; Sarker et al., 2024). Reproductive challenges such as extended postpartum anestrus, subtle estrus expression, and seasonal breeding behavior further complicate breeding management (Jainudeen & Hafez, 2000; Perera, 2011). The lack of adequate infrastructure for AI and genomic selection continues to limit productivity gains in the absence of comprehensive national policies and integrated breeding programs (Bhuiyan et al., 2017).
8.1. Potential for improvement and future prospects
Despite these challenges, buffalo production in Bangladesh has great prospects for improvement and expansion. Ongoing government and non-governmental programs focusing on genetic enhancement, feed resource development, and farmer capacity building show promising results (El Debaky et al., 2019). Improved nutritional management, including the use of high-yielding fodder species, urea-molasses mineral blocks, and mineral supplementation, can substantially increase productivity (Hazra et al., 2014). High-yielding riverine breeds can be used in crossbreeding programs to improve feed conversion efficiency, growth performance, and milk yield (Islam et al., 2017; Karim et al., 2023). Sustainable genetic progress will require systematic genetic evaluation utilizing EBVs, genomic selection, and consistent performance recording (Sarker et al., 2024). Reproductive constraints such as seasonal breeding and poor estrus synchronization can be mitigated through hormonal protocols. Fixed-time artificial insemination (FTAI) protocols have demonstrated effectiveness in improving conception rates and reproductive efficiency (Table 8).
Table 8.
Synchronization protocols and pregnancy rates in buffaloes.
| Synchronization Protocol | Pregnancy Rate (%) | References |
|---|---|---|
| PGF2α | 41 | Jisna et al. (2024) |
| GnRH + PGF2α + GnRH | 60 | Gallab et al. (2022) |
| OVS + Resynch | 84 | Otava et al. (2021) |
| PGF2α | 21 | Atabay et al. (2020) |
| PGF2α + GnRH | 37 | Atabay et al. (2020) |
| PGF2α + GnRH | 36 | Atabay et al. (2024) |
| PGF2α + GnRH + HGG | 39 | Atabay et al. (2024) |
| CIDR + PGF2α | 60 | Amin et al. (2015) |
| CIDR + PGF2α | 50 | Samir et al. (2019) |
| CIDR + OVS | 67 | Samir et al. (2019) |
| PGF2α + GnRH + GnRH + PGF2α + GnRH | 56 | Waqas et al. (2016) |
| GnRH + PGF2α | 100 | Yendraliza et al. (2011) |
| CIDR | 37 | Naseer et al. (2011) |
| GnRH + PGF2α + GnRH | 36 | Warriach et al. (2008) |
Protocols integrating Controlled Internal Drug Release (CIDR) devices with Gonadotropin-Releasing Hormone (GnRH)-based treatments consistently show improved pregnancy rates in buffaloes, including heat-stressed and anestrous animals. Such synchronization techniques can significantly enhance reproductive efficiency. With strategic implementation of these protocols and broader systemic reforms, Bangladesh’s buffalo industry has the potential to become a highly productive and sustainable sector, thereby supporting rural livelihoods and contributing to national economic development (Barile, 2005; Rahman et al., 2020).
8.2. Integration for sustainable buffalo development
A comprehensive strategy that connects productivity, reproduction, genetics, and health is necessary for the sustainable development of buffalo. According to De Rosa et al. (2009) and Borghese (2013), increasing animal health and well-being must coexist with improving genetic potential and reproductive efficiency to increase productivity. Selective breeding, improved nutrition, and disease prevention are all essential components of integrated management techniques. In addition, policy assistance is essential for giving farmers incentives, infrastructure, and training. According to Nanda & Nakao (2003), providing farmers with resources and information guarantees sustained growth and fortifies rural economies that rely on buffalo farming. A comprehensive strategy that integrates productivity, reproduction, genetics, and health is required for the sustainable development of buffalo. To increase resilience and lower costs in buffalo farming, recent methods have a strong emphasis on implementing sustainable practices such as rotational grazing, integrated pest management, and organic farming (EssFeed, 2024). The use of Integrated Farming Systems (IFS), which combine crops, livestock, aquaculture, and agroforestry, has been shown by Researchers to empower farmers and promote sustainable wealth. The International Buffalo Workshop 2024 in Bangladesh emphasized the significance of effective production, practical training for farmers and field veterinarians, and ways to mitigate climate change to create a sustainable buffalo milk value chain (UHB, 2024). Additionally, developing skills and guaranteeing the prosperity of buffalo farming communities depend on empowering buffalo farmers through focused training programs in animal health, reproductive technologies, and farm management (El Debaky et al., 2019; Jacobs, 2024a). Further enhancing the sustainability and effectiveness of buffalo agricultural operations are innovations like genetic breakthroughs and precision farming (Jacobs, 2024b; Chiariotti et al., 2025).
8.3. Nutritional and sanitary management of buffaloes in Bangladesh
Buffalo productivity in Bangladesh remains below potential, largely due to chronic nutritional deficiencies and poor hygienic conditions. Most smallholder farmers still depend heavily on low-quality roughages and crop residues, while seasonal shortages of green fodder further reduce nutrient availability. These feeding practices limit energy intake and restrict growth, milk yield, and reproductive efficiency (Chanda et al., 2021). Recently, field-level efforts have introduced more targeted feeding strategies. Precision supplementation using energy-protein concentrates and mineral mixtures formulated based on physiological requirements has led to visible improvements in body condition, metabolic status, and overall productivity (Faruque & Hossain, 2007; Mohd Azmi et al., 2021; Sultana et al., 2024). Alongside nutritional gains, improvements in sanitation and hygiene, including access to clean drinking water, improved waste drainage, and low-cost biosecure housing designs, have helped reduce disease burden and improve health outcomes (Jimenez et al., 2023).
However, the broader application of these strategies is limited by fragmented extension services, low farmer awareness, and poor adoption at the field level. To maximize the benefits of these interventions, a coordinated national approach linking evidence-based nutritional strategies with sanitary best practices and supported by farmer training and input access is essential to improve the sustainability and efficiency of buffalo production in Bangladesh.
8.4. Strategic interventions for improvement
To overcome the various challenges facing buffalo production in Bangladesh, it's essential to implement targeted, evidence-based strategies. These should be designed to address specific issues related to nutrition, reproduction, genetics, health, and policy support. Table 9 presents practical measures that can help improve productivity, boost reproductive performance, and strengthen herd health, which ultimately support the sustainable growth of the buffalo sector.
Table 9.
Strategic interventions for improvement.
| Area of Focus | Strategic Interventions | References |
|---|---|---|
| Nutrition | Distribution of urea-molasses mineral blocks; cultivation of high-yielding fodder (Napier, Berseem); use of balanced concentrate rations; routine mineral and vitamin supplementation. | Habib et al., 2020; Chaudhary et al., 2024 |
| Reproduction | Adoption of estrus synchronization protocols (PGF2α, CIDR, GnRH-based); expansion of AI and FTAI programs; improved estrus detection methods; reproductive management training for farmers. | Choudhary et al., 2022; Hufana-Duran et al., 2025 |
| Genetic Improvement | Structured crossbreeding using Murrah/Nili-Ravi semen; introduction of performance recording systems; use of genomic tools and estimated breeding values (EBV) for sire selection. | Rashid et al., 2019; Kumar et al., 2024 |
| Health Management | Routine vaccination against endemic diseases (FMD, HS); targeted deworming protocols; mobile veterinary services; health education programs for smallholder farmers. | Samad, 2020; Ahmed et al., 2025 |
| Infrastructure & Policy Support | Buffalo-specific extension services; farmer training in feeding, health, and reproductive management; support for buffalo milk marketing and value chain development; national buffalo breeding policy. | El Debaky et al., 2019; Jacobs, 2024a |
9. Conclusions
The buffalo sector in Bangladesh holds considerable potential to boost milk and meat production through targeted genetic improvement and crossbreeding with high-yielding riverine breeds such as Murrah and Nili-Ravi. These interventions have shown promising results in enhancing milk yield and growth rates. However, the lack of structured breeding programs, systematic genetic evaluation, performance recording, and reproductive biotechnologies continues to hinder sustainable progress. To fully harness the genetic potential of the national buffalo herd, it is essential to implement comprehensive breeding strategies that incorporate tools such as estimated breeding values and genomic selection. Equally important is the integration of strong animal health management through regular vaccinations, health monitoring, biosecurity measures, and parasite control to reduce mortality, improve feed efficiency, and extend the productive lifespan of buffalo. This review provides strategic insights for stakeholders, policymakers, researchers, extension agents, and farmers, both nationally and globally, offering a foundation for evidence-based interventions and policies aimed at building a productive, resilient, and health-optimized buffalo sector in Bangladesh. Collaborative efforts among government agencies, research institutions, NGOs, and farming communities will be crucial for achieving sustainable genetic and productivity gains.
10. Recommendations
To achieve sustainable buffalo production in Bangladesh, the following measures are recommended:
-
I.
Develop and enforce a national buffalo breeding strategy incorporating systematic performance recording and genomic selection methodologies.
-
II.
Expand artificial insemination and estrus synchronization programs through effective public-private partnerships and comprehensive farmer capacity-building.
-
III.
Strengthen animal health and extension services to improve disease prevention, reproductive efficiency, and herd productivity.
-
IV.
Promote climate-smart, community-based farming systems to enhance production efficiency and environmental resilience.
-
V.
Facilitate collaboration among government bodies, non-governmental organizations, research institutions, and farmers to ensure broad adoption of advanced reproductive technologies and best management practices.
Funding statement
No funding was received for this research.
Consent for publication
Not applicable.
Declaration of generative AI and AI-assisted technologies in the writing process
During the preparation of this manuscript, the authors used ChatGPT (free version) to improve language clarity and readability. All use was conducted under human oversight, and the outputs were critically reviewed and edited by the authors to ensure the accuracy and integrity of the scientific content
Ethical statement
This review article is based solely on previously published data and does not involve any original research involving animals or human subjects. Therefore, ethical approval was not necessary.
CRediT authorship contribution statement
Eshtiak Ahamed Pehan: Writing – review & editing, Writing – original draft, Visualization, Methodology, Conceptualization. Manik Miah: Writing – review & editing, Writing – original draft, Visualization, Resources. Md Habibur Rahman: Writing – review & editing, Writing – original draft, Visualization, Supervision, Methodology, Conceptualization. Shahanaj Ferdousi Shejuty: Writing – original draft, Visualization, Resources. Md Nurul Haque: Writing – original draft, Resources. Md Nazmul Huda: Writing – original draft, Resources. Md Rezwanul Habib: Writing – review & editing, Writing – original draft, Supervision. Md Younus Ali: Writing – review & editing, Writing – original draft, Visualization, Supervision, Conceptualization.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Contributor Information
Md Habibur Rahman, Email: habibratan@blri.gov.bd.
Md Younus Ali, Email: younus_abg@bau.edu.bd.
Data availability
Data sharing is not applicable to this article.
References
- Abbas A.M., Abd El-Moaty D.A., Zaki E.S., El-Sergany E.F., El-Sebay N.A., Fadl H.A., Samy A.A. Use of molecular biology tools for rapid identification and characterization of Pasteurella spp. Veterinary World. 2018;11(7):1006–1014. doi: 10.14202/vetworld.2018.1006-1014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Abou-Bakr S. Genetic and phenotypic trends of 305-day milk yield of Holstein cows raised at commercial farm in Egypt. Egyptian Journal of Animal Production. 2009;46(2):85–92. https://journals.ekb.eg/article_94031_0.html [Google Scholar]
- Afroz M.F., Hossain S.M., Deb G.K., Amanullah S.M., Habib M.A. Effect of feed supplementation on age at puberty in growing buffalo heifers. GJABG. 2020;8(3):495–498. https://scholar.google.com/scholar?cluster=6146251036673342581&hl=en&as_sdt=2005&sciodt=0,5 Retrieved from. [Google Scholar]
- Ahlawat S., Sharma U., Chhabra P., Arora R., Sharma R., Singh K.V., Vijh R.K. Maternal genetic diversity and phylogenetic analysis of Indian riverine and swamp buffaloes: Insights from complete mitochondrial genomes. Mammalian Genome. 2024;35(3):390–398. doi: 10.1007/s00335-024-10048-1. [DOI] [PubMed] [Google Scholar]
- Ahmad Para I., Ahmad Dar P., Ahmad Malla B., Punetha M., Rautela A., Maqbool I., Mohd A., Ahmad Shah M., Ahmad War Z., Ishaaq R., Akram Malla W. Impact of heat stress on the reproduction of farm animals and strategies to ameliorate it. Biological Rhythm Research. 2020;51(4):616–632. doi: 10.1080/09291016.2018.1548870. [DOI] [Google Scholar]
- Ahmed E., Yousuf M.A., Rahman H., Ahmed S., Ahmed S., Khatun R., Rahman M.H. Health challenges in cattle farming: A study on common cattle diseases and disorders in a selective cattle farm of Bangladesh. Egyptian Journal of Veterinary Sciences. 2025:1–9. doi: 10.21608/EJVS.2025.337400.2505. [DOI] [Google Scholar]
- Ahmed F., Mahabubul G., Al-Amin A.Q., Hassan C.B. The impact of climate changes on livestock sector: Challenging experience from Bangladesh. Asian Journal of Animal and Veterinary Advances. 2012;8(1):29–40. doi: 10.3923/ajava.2013.29.40. [DOI] [Google Scholar]
- Akhtar M.S., Ullah S., Farooq A.A., Mazhar M., Murtaza S. Pregnancy rate in lactating buffaloes treated with or without estradiol after estrus synchronization protocols at timed AI. Buffalo Bulletin. 2013;32:366–369. https://www.cabidigitallibrary.org/doi/full/10.5555/20143083943 [Google Scholar]
- Alam M.E., Kamal M.M., Rahman M., Kabir A., Islam M.S., Hassan J. Review of anthrax: A disease of farm animals. Journal of Advanced Veterinary and Animal Research. 2022;9(2):323. doi: 10.5455/javar.2022.i599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Alam M., Gregory N., Uddin M., Jabbar M., Silva-Fletcher A., Kempson A.G., Saifuddin A.K. Frequency of heat stress in cattle and water buffalo at livestock markets in Bangladesh. Journal of the Commonwealth Veterinary Association. 2010;26(1):13–17. doi: 10.3390/ani13193103. [DOI] [Google Scholar]
- Ali M.Z., Giasuddin M. Detection of an emerging novel sublineage Ind2001BD1 and lineage PanAsia of foot-and-mouth disease virus serotype O in cattle in Manikgonj district of Bangladesh, 2018. Open Veterinary Journal. 2020;10(3):347–353. doi: 10.4314/ovj.v10i3.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ali M.Z., Carlile G., Giasuddin M. Impact of global climate change on livestock health: Bangladesh perspective. Open Veterinary Journal. 2020;10(2):178–188. doi: 10.4314/ovj.v10i2.7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ali M.Z., Khan M.M., Sami M.D., Rahman M.H., Islam S., Rahman M.A., Karim M.R., Manu M.R., Islam M.S. Bovine mastitis: Epidemiology, diagnosis, and control strategies in dairy sectors of Bangladesh. Egyptian Journal of Veterinary Sciences. 2025:1–8. doi: 10.21608/ejvs.2025.341835.2539. [DOI] [Google Scholar]
- Amin M.R., Siddiki M.A., Kabir A., Faruque M.O., Khandaker Z.H. Status of buffalo farmers and buffaloes at Subornochar upozila of Noakhali district in Bangladesh. Progressive Agriculture. 2015;26:71–78. doi: 10.3329/pa.v26i1.24519. [DOI] [Google Scholar]
- Aminafshar M., Amirinia C., Torshizi R.V. Genetic diversity in buffalo population of Guilan using microsatellite markers. Journal of Animal and Veterinary Advances. 2008;7:1499–1502. https://scholar.google.com/scholar?cluster=17066303030437085829 [Google Scholar]
- Atabay E.C., Maylem E.R., Salazar R.L. Enhancing prostaglandin-based estrus synchronization protocol for artificial insemination in water buffaloes. Buffalo Bulletin. 2020;39(1):53–60. http://kuojs.lib.ku.ac.th/index.php/BufBu/article/view/1572 [Google Scholar]
- Atabay E., Atabay E., Cruz C.D., Ferrer A. Pregnancy outcomes following GnRH- or prostaglandin-based timed artificial insemination protocols in water buffaloes (Bubalus bubalis) Journal of Buffalo Science. 2024;13:90–97. doi: 10.6000/1927-520X.2024.13.10. [DOI] [Google Scholar]
- Aziz M.A., Schoeman S.J., Jordaan G.F., El-Chafie O.M., Mahdy A.T. Genetic and phenotypic variation of some reproductive traits in Egyptian buffalo. South African Journal of Animal Science. 2001;31(3):195–199. doi: 10.4314/sajas.v31i3.3802. [DOI] [Google Scholar]
- Balhara A., Nayan V., Dey A., Singh K.P., Dahiya S.S., Singh I. Climate change and buffalo farming in major milk producing states of India—Present status and need for addressing concerns. Indian Journal of Animal Sciences. 2017;87(4):403–411. doi: 10.56093/ijans.v87i4.69476. [DOI] [Google Scholar]
- Barile V.L. Improving reproductive efficiency in female buffaloes. Livestock Production Science. 2005;92(3):183–194. doi: 10.1016/j.livprodsci.2004.06.014. [DOI] [Google Scholar]
- Bhakat M., Mohanty T.K., Gupta A.K., Raina V.S. Effect of season and management on semen quality of breeding bulls—A review. Agricultural Reviews. 2009;30(2):79–93. https://www.cabidigitallibrary.org/doi/full/10.5555/20093205531 [Google Scholar]
- Bhuiyan M.S., Bhuiyan A.F., Lee J.H., Lee S.H. Community based livestock breeding programs in Bangladesh: Present status and challenges. Journal of Animal Breeding and Genomics. 2017;1(2) doi: 10.12972/jabng.20170009. [DOI] [Google Scholar]
- Biswas H., Roy B.C., Dutta P.K., Hasan M.M., Parvin S., Choudhury D.K., Begum N., Talukder M.H. Prevalence and risk factors of Toxocara vitulorum infection in buffalo calves in coastal, northeastern and northwestern regions of Bangladesh. Veterinary Parasitology: Regional Studies and Reports. 2021;26 doi: 10.1016/j.vprsr.2021.100656. [DOI] [PubMed] [Google Scholar]
- Borghese A. Buffalo livestock and products in Europe. Scientific Bulletin of ESCORENA. 2013;7:47–73. https://www.cabidigitallibrary.org/doi/full/10.5555/20133419029 [Google Scholar]
- Bradford B.J., Swartz T.H. Following the smoke signals: Inflammatory signaling in metabolic homeostasis and homeorhesis in dairy cattle. Animal. 2020;14(S1):S144–S154. doi: 10.1017/S1751731119003203. [DOI] [PubMed] [Google Scholar]
- Cascone G., Licitra F., Stamilla A., Amore S., Dipasquale M., Salonia R., Antoci F., Zecconi A. Subclinical ketosis in dairy herds: Impact of early diagnosis and treatment. Frontiers in Veterinary Science. 2022;9 doi: 10.3389/fvets.2022.895468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chanda R.C., Moniruzzaman M., Alam M.H., Khatun A., Islam M.N., Kabir M.E., Islam M.A., Amin M.R. Buffalo production in small scale and commercial farms in Bangladesh. Asian Journal of Medical and Biological Research. 2021;7(4):323–331. doi: 10.3329/ajmbr.v7i4.57612. [DOI] [Google Scholar]
- Charlini B.C., Sinniah J. Performance of Murrah, Surti, Nili-Ravi buffaloes and their crosses in the intermediate zone of Sri Lanka. Livestock Research for Rural Development. 2015;27(3):47. http://www.lrrd.cipav.org.co/lrrd27/3/char27047.html [Google Scholar]
- Chaudhary S.K., Dutta N., Jadhav S.E., Singh G., Singh S.K., Tewari D. Effect of strategic supplementation of a novel feed supplement on zoo-technical attributes, metabolic profile, production and reproduction performance of buffaloes. Buffalo Bulletin. 2024;43(2):209–225. doi: 10.56825/bufbu.2024.4325485. [DOI] [Google Scholar]
- Chawicha T.G., Mummed Y.Y. An overview of how heat stress impacts dairy cattle fertility. Multidisciplinary Reviews. 2022;5(3) doi: 10.31893/multirev.2022014. Article. [DOI] [Google Scholar]
- Chiariotti A., Borghese A., Boselli C., Barile V.L. Water buffalo’s adaptability to different environments and farming systems: A review. Animals. 2025;15(11):1538. doi: 10.3390/ani15111538. Article. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Choudhary S., Kamboj M.L., Ungerfeld R., Singh P. Calf-cow and bull-cow management in buffaloes: Effects on growth, productive and reproductive performance of mothers and their calves. Reproduction in Domestic Animals. 2022;57(11):1428–1439. doi: 10.1111/rda.14219. [DOI] [PubMed] [Google Scholar]
- Chowdhury M.S., Rahman M.M., Hossain H., Ghosh P., Islam M.R., Lamichhane B., Gomaa F.A., Selim H., Hossain M.M., Helmy Y., El Zowalaty M. Subclinical mastitis of buffaloes in Asia: Prevalence, pathogenesis, risk factors, antimicrobial resistance, and current treatment strategies. Journal of Animal Science and Technology. 2024 doi: 10.5187/jast.2024.e66. [DOI] [Google Scholar]
- Das S.K. Impact of climate change (heat stress) on livestock: Adaptation and mitigation strategies for sustainable production. Agricultural Reviews. 2018;39(2):130–136. doi: 10.18805/ag.R-1777. [DOI] [Google Scholar]
- Dash S., Chakravarty A.K., Singh A., Upadhyay A., Singh M., Yousuf S. Effect of heat stress on reproductive performances of dairy cattle and buffaloes: A review. Veterinary World. 2016;9(3):235. doi: 10.14202/vetworld.2016.235-244. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Rosa G., Grasso F., Pacelli C., Napolitano F., Winckler C. The welfare of dairy buffalo. Italian Journal of Animal Science. 2009;8(sup1):103–116. doi: 10.4081/ijas.2009.s1.103. [DOI] [Google Scholar]
- Department of Livestock Service (DLS) DLS; Dhaka, Bangladesh: 2024. Livestock economy at a glance 2023–24.https://dls.gov.bd/site/page/22b1143b-9323-44f8-bfd8-647087828c9b/Livestock-Economy (Accessed December 15, 2024) [Google Scholar]
- Dhanda O.P. Proceedings. 2013. Changing dynamics in buffalo production systems in South Asian region; pp. 311–317.https://www.cabidigitallibrary.org/doi/full/10.5555/20133419051 [Google Scholar]
- Dodiya V.A., Sabapara G.P., Garg D.D., Odedra M.D., Ahlawat A.R., Kasondra S.M. Health care practices of Jaffarabadi buffalo farmers in rural areas of Junagadh district of Gujarat, India. Indian Journal of Animal Production and Management. 2024;40(2):128–133. doi: 10.48165/ijapm.2024.40.2.11. [DOI] [Google Scholar]
- Domple V.D., Padol A.R., Malapure C.D., Kamdi B.P., Sarode R.M. Effect of melatonin supplementation on heat shock proteins expression profile in buffalo calves under summer stress. International Journal of Chemical Studies. 2021;9(1):1197–1203. doi: 10.22271/chemi.2021.v9.i1q.11388. [DOI] [Google Scholar]
- El Debaky H.A., Kutchy N.A., Ul-Husna A., Indriastuti R., Akhter S., Purwantara B., Memili E. Potential of water buffalo in world agriculture: Challenges and opportunities. Applied Animal Science. 2019;35(2):255–268. doi: 10.15232/aas.2018-01810. [DOI] [Google Scholar]
- El-Arian M.N., Shalaby N.A., Khattab A.S., Darwish S.A., Abou-Gamous R.H. Phenotypic and genetic trends for some milk yield traits of Egyptian buffaloes. Journal of Animal and Poultry Production. 2012;3(7):353–364. doi: 10.21608/jappmu.2012.82938. [DOI] [Google Scholar]
- Elmhadi M.E., Ali D.K., Khogali M.K., Wang H. Subacute ruminal acidosis in dairy herds: Microbiological and nutritional causes, consequences, and prevention strategies. Animal Nutrition. 2022;10:148–155. doi: 10.1016/j.aninu.2021.12.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- El-Wishy A.B. The postpartum buffalo. II. Acyclicity and anestrus. Animal Reproduction Science. 2007;97(3–4):216–236. doi: 10.1016/j.anireprosci.2006.03.003. [DOI] [PubMed] [Google Scholar]
- EssFeed. (2024). Climate change and buffalo farming: Challenges and adaptation strategies [Website]. Retrieved May 20, 2025, from https://essfeed.com/climate-change-and-buffalo-farming-challenges-and-adaptation-strategies/.
- Faruque M.O., Hossain M.I. The effect of feed supplement on the yield and composition of buffalo milk. Italian Journal of Animal Science. 2007;6(sup2):488–490. doi: 10.4081/ijas.2007.s2.488. [DOI] [Google Scholar]
- Food and Agriculture Organization (FAO) Rome; 2021. World food and agriculture – Statistical yearbook 2021. [DOI] [Google Scholar]
- Fournel S., Ouellet V., Charbonneau É. Practices for alleviating heat stress of dairy cows in humid continental climates: A literature review. Animals. 2017;7(5):37. doi: 10.3390/ani7050037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gallab R.S., Hassanein E.M., Rashad A.M., El-Shereif A.A. Maximizing the reproductive performances of anestrus dairy buffalo cows using GnRH analogue-loaded chitosan nanoparticles during the low breeding season. Animal Reproduction Science. 2022;244 doi: 10.1016/j.anireprosci.2022.107044. [DOI] [PubMed] [Google Scholar]
- Ganie M.A., Prabhakar S., Singh A.K., Brar P.S. Effect of supplementary feeding of glucogenic and lipogenic diet on body parameters and onset of ovarian cyclicity in postpartum dairy buffaloes. The Indian Journal of Animal Sciences. 2014;84(4):422–423. https://www.cabidigitallibrary.org/doi/full/10.5555/20143185834 [Google Scholar]
- Ghanbari M.K., Gorji H.A., Behzadifar M., Sanee N., Mehedi N., Bragazzi N.L. One health approach to tackle brucellosis: A systematic review. Tropical Medicine and Health. 2020;48:1–10. doi: 10.1186/s41182-020-00272-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gholve M.S., Kalwaghe S.T., Palampalle H.Y., Chigure G.M., Ingle S.A., Bhangale G.N. Age but not sex is a primary predisposing factor for Ascariosis in buffalo calves: An evidence from Mumbai, India. Buffalo Bulletin. 2024;43(1):95–103. doi: 10.56825/bufbu.2024.4314850. [DOI] [Google Scholar]
- Gowane G.R., Vohra V. Biotechnological Applications in Buffalo Research. Springer; Singapore: 2022. Advances in buffalo breeding: A journey from classical breeding to genomic selection; pp. 57–77. [DOI] [Google Scholar]
- Habib M.A., Rahman M.S., Khatun A., Ali M.Y. The scenario of buffalo production and research in Bangladesh. Journal of Buffalo Science. 2023;12:28–37. doi: 10.6000/1927-520X.2023.12.04. [DOI] [Google Scholar]
- Habib M.R., Haque M.N., Rahman A., Aftabuzzaman M., Ali M.M., Shahjahan M. Dairy buffalo production scenario in Bangladesh: A review. Asian Journal of Medical and Biological Research. 2017;3(3):305–316. doi: 10.3329/ajmbr.v3i3.34518. [DOI] [Google Scholar]
- Habib M.R., Islam M.Z., Bari M.S., Sarker M.A., Rashid M.H., Islam M.A. Effect of concentrate supplementation during transition period on production and reproduction of indigenous buffalo. Bangladesh Journal of Animal Science. 2020;49(1):83–90. doi: 10.3329/bjas.v49i1.4938. [DOI] [Google Scholar]
- Hamid M.A. Study on the effect of insemination time on pregnancy rate of Bangladeshi buffalo in intensive farming. SAARC Journal of Agriculture. 2018;16(2):143–152. doi: 10.3329/sja.v16i2.40266. [DOI] [Google Scholar]
- Hamid M.A., Ahmed S., Rahman M.A., Hossain K.M. Status of buffalo production in Bangladesh compared to SAARC countries. Asian Journal of Animal Sciences. 2016;10(6):313–329. https://www.researchgate.net/publication/310431796 [Google Scholar]
- Hamid M.A., Siddiky M.N., Rahman M.A., Hossain K.M. Scopes and opportunities of buffalo farming in Bangladesh: A review. SAARC Journal of Agriculture. 2016;14(2):63–77. doi: 10.3329/sja.v14i2.31246. [DOI] [Google Scholar]
- Hamid M.A., Zaman M.A., Rahman A., Hossain K.M. Buffalo genetic resources and their conservation in Bangladesh. Research Journal of Veterinary Sciences. 2017;10(1):1–3. doi: 10.3923/rjvs.2017.1.13. [DOI] [Google Scholar]
- Haque M.S., Alam M.J., Asad L.Y., Kabir M.E., Sikder T. Socio-economic status of buffalo farmers and management practices of buffaloes in selected areas of Jamalpur district in Bangladesh. Asian-Australasian Journal of Food Safety and Security. 2020;4(2):49–57. doi: 10.3329/aajfss.v4i2.53880. [DOI] [Google Scholar]
- Hassan F.A., Ali M.A., El-Tarabany M.S. Economic impacts of calving season and parity on reproduction and production traits of buffaloes in the sub-tropics. Environmental Science and Pollution Research. 2017;24:10258–10266. doi: 10.1007/s11356-017-8686-1. [DOI] [PubMed] [Google Scholar]
- Hassan J., Murshidul Ahsan M., Bahanur Rahman M., Md Ziqrul Haq Chowdhury S., Shafiullah Parvej M., et al. Factors associated with repeated outbreak of anthrax in Bangladesh: Qualitative and quantitative study. Journal of Advanced Veterinary and Animal Research. 2015;2(2):158–164. https://banglajol.info/index.php/JAVAR/article/view/23210 [Google Scholar]
- Hassan M.Z., Rahman M.M., Ali M.Z., Yousuf M.A., Hasan M., Akther S., Rahman H.H., Islam M.A., Hossen A., Mondal M.F. A study on prevalence of ecto-and endo-parasitic infection of cattle at Savar, Dhaka. Bangladesh Journal of Livestock Research. 2020:29–35. doi: 10.3329/bjlr.v0i0.45444. [DOI] [Google Scholar]
- Hazra C.R. Feed and forage resources for sustainable livestock development. Range Management and Agroforestry. 2014;35(1):1–4. https://www.cabidigitallibrary.org/doi/full/10.5555/20143381722 [Google Scholar]
- Hoque M.N., Talukder A.K., Kamal M.M., Jha A.K., Bari F.Y., Shamsuddin M. Ovulation synchronization in water buffaloes guided by milk progesterone Elisa. Journal of Embryo Transfer. 2011;26(2):105–109. https://koreascience.kr/article/JAKO201124359110389.page [Google Scholar]
- Hoque M.N., Talukder A.K., Saha O., Hasan M.M., Sultana M., Rahman A.A., Das Z.C. Antibiogram and virulence profiling reveals multidrug resistant Staphylococcus aureus as the predominant aetiology of subclinical mastitis in riverine buffaloes. Veterinary Medicine and Science. 2022;8(6):2631–2645. doi: 10.1002/vms3.942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hufana-Duran D., Chaikhun-Marcou T., Duran P.G., Atabay E.P., Nguyen H.T., Atabay E.C., Nguyen U.T., Nguyen H.T., Hiew M.W., Punyawai K., Ginting N. Future of reproductive biotechnologies in water buffalo in Southeast Asian countries. Theriogenology. 2025;233:123–130. doi: 10.1016/j.theriogenology.2024.11.016. [DOI] [PubMed] [Google Scholar]
- Islam S., Nahar T.N., Begum J., Deb G.K., Khatun M., Mustafa A. Economic evaluation of buffalo production in selected regions of Bangladesh. Journal of Stock & Forex Trading. 2017;5(3):1–27. https://www.researchgate.net/publication/325544072 [Google Scholar]
- Jacobs, A. K. (2024a). Empowering buffalo farmers: Training and development for building skills and success [Website]. Retrieved May 20, 2025, from https://ajaykuriakosejacobs.com/empowering-buffalo-farmers/.
- Jacobs, A. K. (2024b). Innovations in buffalo farming: Harnessing new technologies for efficiency and sustainability [Website]. Retrieved May 20, 2025, from https://ajaykuriakosejacobs.com/innovations-in-buffalo-farming/.
- Jadav S.J., Patel Y.G. Prevailing buffalo calf rearing practices and mortality patterns in the operational area of Dairy Vigyan Kendra, Gujarat. Asian Journal of Dairy and Food Research. 2022;1756:1–6. doi: 10.18805/ajdfr.DR-1756. Article. [DOI] [Google Scholar]
- Jahan I., Sarker N., Alam S., Rahman M.K., Alam M.K., Khandakar M.M., Bari M.S., Habib M.R., Islam M.A. Productive and reproductive performances of buffaloes in Bhola district of Bangladesh. Bangladesh Journal of Animal Science. 2024;53(3):111–120. doi: 10.3329/bjas.v53i3.76546. [DOI] [Google Scholar]
- Jainudeen M.R., Hafez E.S.E. Cattle and buffalo. Hafez E.S.E., editor. Cattle and buffaloReproduction in farm animals (7th ed., pp. [specific pages if known]) 2000 doi: 10.1002/9781119265306.ch11. [DOI] [Google Scholar]
- Jimenez C.E., Keestra S., Tandon P., Cumming O., Pickering A.J., Moodley A., Chandler C.I. Biosecurity and water, sanitation, and hygiene (WASH) interventions in animal agricultural settings for reducing infection burden, antibiotic use, and antibiotic resistance: A One Health systematic review. The Lancet Planetary Health. 2023;7(5):e418–e434. doi: 10.1016/S2542-5196(23)00049-9. [DOI] [PubMed] [Google Scholar]
- Jisna K.S., Rajput A.S., Nivetha P., Jinagal S., Rafiq M.M., Pandey A.K.…Patra M.K. Seasonal Variations in Luteal Dynamics and Serum Progesterone Levels in Murrah Buffaloes. The Indian Veterinary Journal. 2024;101(07):22–26. doi: 10.62757/IVA.2024.101.7.22-26. [DOI] [Google Scholar]
- Kabir A., Rahman A., Shah I.A., Rahman I. Buffalo pox transmission dynamics: Understanding the interplay between buffaloes, humans, and vectors. Research Journal of Veterinary Practice. 2023;11(3):34–41. doi: 10.17582/journal.rjvp/2023/11.3.34.41. [DOI] [Google Scholar]
- Kabir M.E., Sultana M.A. Assessment of performance and profitability of buffalo rearing in selected coastal areas of Bangladesh. International Journal of Veterinary Sciences and Animal Husbandry. 2017;2(5):43–47. https://www.veterinarypaper.com/pdf/2017/vol2issue5/PartA/6-5-1-827.pdf [Google Scholar]
- Karim M.R., Habib R., Hossain M.I., Wadud A. Productive and reproductive performance of indigenous buffaloes in four selected upazillas under Mymensingh district of Bangladesh. Asian Journal of Medical and Biological Research. 2023;9(2):30–37. doi: 10.3329/ajmbr.v9i2.65519. [DOI] [Google Scholar]
- Khan H.M., Mohanty T.K., Raina V.S., Gupta A.K., Bhaka M. Effect of peripartum disorders on reproduction performance traits in Murrah buffaloes at an organized farm. Buffalo Bulletin. 2009;28:176–183. https://www.cabidigitallibrary.org/doi/full/10.5555/20103310667 [Google Scholar]
- Khan I., Mesalam A., Heo Y.S., Lee S.H., Nabi G., Kong I.K. Heat stress as a barrier to successful reproduction and potential alleviation strategies in cattle. Animals. 2023;13(14):2359. doi: 10.3390/ani13142359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Khurana S.K., Sehrawat A., Tiwari R., Prasad M., Gulati B., Shabbir M.Z., Chhabra R., Karthik K., Patel S.K., Pathak M., Iqbal Yatoo M. Bovine brucellosis–A comprehensive review. Veterinary Quarterly. 2021;41(1):61–88. doi: 10.1080/01652176.2020.1868616. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kitkas G.C., Valergakis G.E., Kritsepi-Konstantinou M., Gelasakis A.I., Arsenos G., Kalaitzakis E., Panousis N. Effects of ruminal pH and subacute ruminal acidosis on milk yield and composition of Holstein cows in different stages of lactation. Journal of the Hellenic Veterinary Medical Society. 2019;70(2):1551–1560. doi: 10.12681/jhvms.20861. [DOI] [Google Scholar]
- Krishnan G., Bagath M., Pragna P., Vidya M.K., Aleena J., Archana P.R., Sejian V., Bhatta R. Theriogenology. IntechOpen; 2017. Mitigation of the heat stress impact in livestock reproduction. [DOI] [Google Scholar]
- Kumar D., Tiwari M., Goel P., Singh M.K., Selokar N.L., Palta P. Comparative transcriptome profile of embryos at different developmental stages derived from somatic cell nuclear transfer (SCNT) and in-vitro fertilization (IVF) in riverine buffalo (Bubalus bubalis) Veterinary Research Communications. 2024;48(4):2457–2475. doi: 10.1007/s11259-024-10419-8. [DOI] [PubMed] [Google Scholar]
- Kumari A., Kumar Jain V., Kumar Nehra A., Kumar M., Sharma M., Kumar A., Gupta S., Singh Y. Assessment of haematological and biochemical alterations in recumbent buffaloes. Biological Rhythm Research. 2022;53(11):1670–1691. doi: 10.1080/09291016.2021.2007330. [DOI] [Google Scholar]
- Lalor R., Cwiklinski K., Calvani N.E., Dorey A., Hamon S., Corrales J.L., Dalton J.P., De Marco Verissimo C. Pathogenicity and virulence of the liver flukes Fasciola hepatica and Fasciola gigantica that cause the zoonosis Fasciolosis. Virulence. 2021;12(1):2839–2867. doi: 10.1080/21505594.2021.1996520. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leblanc S. Assessing the association of the level of milk production with reproductive performance in dairy cattle. Journal of Reproduction and Development. 2010;56(S):S1–S7. doi: 10.1262/jrd.1056S01. [DOI] [PubMed] [Google Scholar]
- Lee F. Bovine ephemeral fever in Asia: Recent status and research gaps. Viruses. 2019;11(5):412. doi: 10.3390/v11050412. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lima M.T., Oliveira G.P., Afonso J.A., Souto R.J., de Mendonça C.L., Dantas A.F., Abrahao J.S., Kroon E.G. An update on the known host range of the Brazilian vaccinia virus: An outbreak in buffalo calves. Frontiers in Microbiology. 2019;9:3327. doi: 10.3389/fmicb.2018.03327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maheswarappa N.B., Muthupalani M., Mohan K., Banerjee R., Sen A.R., Barbuddhe S.B. Asiatic water buffalo: A sustainable and healthy red meat source. Springer Nature Singapore; 2022. Buffalo slaughtering, dressing, and carcass fabrication; pp. 35–48. [DOI] [Google Scholar]
- Martínez-Burnes J., Barrios-García H., Carvajal-de la Fuente V., Corona-González B., Obregón Alvarez D., Romero-Salas D. Viral diseases in water buffalo (Bubalus bubalis): New insights and perspectives. Animals. 2024;14(6):845. doi: 10.3390/ani14060845. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCann J.C., Luan S., Cardoso F.C., Derakhshani H., Khafipour E., Loor J.J. Induction of subacute ruminal acidosis affects the ruminal microbiome and epithelium. Frontiers in Microbiology. 2016;7:701. doi: 10.3389/fmicb.2016.00701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mitsuishi H., Yayota M. The efficacy of β-carotene in cow reproduction: A review. Animals. 2024;14(14):2133. doi: 10.3390/ani14142133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohammed K.M. Application of advanced reproductive biotechnologies for buffalo improvement with focusing on Egyptian buffaloes. Asian Pacific Journal of Reproduction. 2018;7(5):193–205. doi: 10.4103/2305-0500.241177. [DOI] [Google Scholar]
- Mohanta U.K., Rana H.B., Devkota B., Itagaki T. Molecular and phylogenetic analyses of the liver amphistome Explanatum explanatum (Creplin, 1847) Fukui, 1929 in ruminants from Bangladesh and Nepal based on nuclear ribosomal ITS2 and mitochondrial nad1 sequences. Journal of Helminthology. 2017;91(4):497–503. doi: 10.1017/S0022149×16000420. [DOI] [PubMed] [Google Scholar]
- Mohd Azmi A.F., Ahmad H., Mohd Nor N., Goh Y.M., Zamri-Saad M., Abu Bakar M.Z., Salleh A., Abdullah P., Jayanegara A., Abu Hassim H. The impact of feed supplementations on Asian buffaloes: A review. Animals. 2021;11(7):2033. doi: 10.3390/ani11072033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moustafa A.M., Ali S.N., Bennett M.D., Hyndman T.H., Robertson I.D., Edwards J. A case–control study of Haemorrhagic septicaemia in buffaloes and cattle in Karachi, Pakistan, in 2012. Transboundary and Emerging Diseases. 2017;64(2):520–527. doi: 10.1111/tbed.12393. [DOI] [PubMed] [Google Scholar]
- Muner R.D., Moaeen-ud-Din M., Saleem A.H., Ullah Q., Abbas G., Maqbool B., Babar M.E., Bi Y., Farooq F. Genomic selection, gene editing, and reproductive biotechnology: A triad for the improvement of native buffalo breeds in a developing country perspective like Pakistan. Tropical Animal Health and Production. 2025;57(2):1–6. doi: 10.1007/s11250-025-04352-4. [DOI] [PubMed] [Google Scholar]
- Nanda A.S., Nakao T. Role of buffalo in the socioeconomic development of rural Asia: Current status and future prospectus. Animal Science Journal. 2003;74(6):443–455. doi: 10.1046/j.1344-3941.2003.00138.x. [DOI] [Google Scholar]
- Naseer Z., Ahmad E., Singh J., Ahmad N. Fertility following CIDR based synchronization regimens in anoestrous Nili-Ravi buffaloes. Reproduction in Domestic Animals. 2011;46:814–817. doi: 10.1111/j.1439-0531.2010.01746.x. [DOI] [PubMed] [Google Scholar]
- Naveena B.M., Kiran M. Buffalo meat quality, composition, and processing characteristics: Contribution to the global economy and nutritional security. Animal Frontiers. 2014;4(4):18–24. doi: 10.2527/af.2014-0029. [DOI] [Google Scholar]
- Omar A.I., Khan M.Y., Su X., Dhakal A., Hossain S., Razu M.T., Si J., Pauciullo A., Faruque M.O., Zhang Y. Factors affecting the milk production traits and lactation curve of the indigenous river buffalo populations in Bangladesh. Animals. 2024;14(8):1248. doi: 10.3390/ani14081248. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Otava G., Squicciarini S., Marc S., Suici T., William Onan G., Hutu I., Torda I., Mircu C. Effects of age and season on conception rate of Mediterranean Italian Dairy Buffalo (Bubalus bubalis) following oestrus synchronization and fixed-time artificial insemination. Reproduction in Domestic Animals. 2021;56(12):1511–1518. doi: 10.1111/rda.14013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pasha M.M., Rahman M.Z., Sultana N., Moniruzzaman M. Impact of heat stress on female reproduction in farm animals: Challenges and possible remedies. Bangladesh Journal of Animal Science. 2024;53(3):77–100. doi: 10.3329/bjas.v53i3.76533. [DOI] [Google Scholar]
- Paton D.J., Di Nardo A., Knowles N.J., Wadsworth J., Pituco E.M., Cosivi O., Rivera A.M., Kassimi L.B., Brocchi E., de Clercq K., Carrillo C. The history of foot-and-mouth disease virus serotype C: The first known extinct serotype? Virus Evolution. 2021;7(1):veab009. doi: 10.1093/ve/veab009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paul V., Prakash B.S. Efficacy of the Ovsynch protocol for synchronization of ovulation and fixed-time artificial insemination in Murrah buffaloes (Bubalus bubalis) Theriogenology. 2005;64(5):1049–1060. doi: 10.1016/j.theriogenology.2005.02.004. [DOI] [PubMed] [Google Scholar]
- Pehan E.A., Shejuty S.F., Islam M.R., Husain S.S., Khandoker M.Y. Current scenario of cattle breeding practices in Netrokona district. Bangladesh Journal of Livestock Research. 2022:53–61. doi: 10.3329/bjlr.v29i1.72076. [DOI] [Google Scholar]
- Perera B.M. Reproductive cycles of buffalo. Animal Reproduction Science. 2011;124(3–4):194–199. doi: 10.1016/j.anireprosci.2010.08.022. [DOI] [PubMed] [Google Scholar]
- Primawidyawan A., Indrawati A., Lukman D.W. Deteksi penyakit bovine viral diarrhea pada sapi potong impor melalui pelabuhan tanjung priok [Detection of bovine viral diarrhea disease in imported beef cattle through Tanjung Priok port] Acta Veterinaria Indonesiana. 2016;4(1):7–13. doi: 10.29244/avi.4.1.7-13. [DOI] [Google Scholar]
- Purwar V., Oberoi P.S., Dang A.K. Effect of feed supplement and additives on stress mitigation in Karan Fries heifers. Veterinary World. 2017;10(12):1407–1412. doi: 10.14202/vetworld.2017.1407-1412. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qureshi M.S., Khan S., Ahmad N. Pregnancy depresses milk yield in dairy buffaloes. Italian Journal of Animal Science. 2007;6(Suppl 2):1290–1293. doi: 10.4081/ijas.2007.s2.1290. [DOI] [Google Scholar]
- Rafiq N., Niaz S., Zeb I., Ayaz S., da Silva Vaz I., Jr., Ali A. Molecular characterization of Paramphistomum cervi in buffaloes. Acta Scientiae Veterinariae. 2020:48. doi: 10.22456/1679-9216.107107. [DOI] [Google Scholar]
- Rahman M.H., Ahmed E., Haque M.N., Hassan M.Z., Ali M.Z. Major respiratory diseases of goat and their epidemiology, prevention and control. Bangladesh Journal of Livestock Research. 2022:1–20. doi: 10.3329/bjlr.v29i1.72031. [DOI] [Google Scholar]
- Rahman M.H., Alam M.S., Ali M.Z., Haque M.N., Akther S., Ahmed S. First report of contagious caprine pleuropneumonia (CCPP) in Bangladeshi goats: Seroprevalence, risk factors and molecular detection from lung samples. Heliyon. 2024;10 doi: 10.1016/j.heliyon.2024.e40507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rahman M.K., Sarkar M., Rahim A., Nandi R., Hasan M.M., Debnath R.C. Effectiveness of artificial insemination in buffalo at coastal region of Bangladesh. International Journal of Current Research in Life Sciences. 2020;9(12):3385–3388. https://scholar.google.com/scholar?cluster=6277730958681198087 [Google Scholar]
- Rahman S.R., Islam M.N., Harun-ur-Rashid M.D., Siddiki M.S., Islam M.A. Dairy buffalo production under intensive system in semi-arid area of Bangladesh. Buffalo Bulletin. 2019;38(1):83–98. http://kuojs.lib.ku.ac.th/index.php/BufBu/article/view/1108 [Google Scholar]
- Rehman S.U., Hassan F.U., Luo X., Li Z., Liu Q. Whole-genome sequencing and characterization of buffalo genetic resources: Recent advances and future challenges. Animals. 2021;11(3):904. doi: 10.3390/ani11030904. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rashid M.H., Sarkar A.K., Hasan M.M., Hasan M., Juyena N.S. Productive, reproductive, and estrus characteristics of different breeds of buffalo cows in Bangladesh. Journal of Advanced Veterinary and Animal Research. 2019;6(4):553–560. doi: 10.5455/javar.2019.f382. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rizwan H.M., Zohaib H.M., Sajid M.S., Tahir U.B., Kausar R., Nazish N., Ben Said M., Anwar N., Maqbool M., Fouad D., Ataya F.S. Unveiling the hidden threat: Investigating gastrointestinal parasites and their costly impact on slaughtered livestock. Revista Brasileira de Parasitologia Veterinária. 2024;33(3) doi: 10.1590/S1984-29612024061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roth Z. Effect of heat stress on reproduction in dairy cows: Insights into the cellular and molecular responses of the oocyte. Annual Review of Animal Biosciences. 2017;5(1):151–170. doi: 10.1146/annurev-animal-022516-022849. [DOI] [PubMed] [Google Scholar]
- Saha N.G., Hasan M.S., Gazi M.R., Riad M.M. Morphological identification of buffaloes in the coastal region of Bangladesh. Bangladesh Livestock Journal. 2018;1:22–29. https://www.researchgate.net/publication/342888123 [Google Scholar]
- Samad M. A systematic review of research findings on buffalo health and production published during the last six decades in Bangladesh. Journal of Veterinary Medical and One Health Research. 2020;2(1):1–62. doi: 10.36111/jvmohr.2020.2(1).0016. [DOI] [Google Scholar]
- Samir H., Kandiel M.M., El-Maaty A.M., Sediqyar M., Sasaki K., Watanabe G. Ovarian follicular changes and hemodynamics in Egyptian buffaloes under CIDR-PGF2α and Ovsynch-CIDR estrus synchronization treatments. Journal of Reproduction and Development. 2019;65(5):451–457. doi: 10.1262/jrd.2019-035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sarder M.J., Rahman M.M., Ahmed S., Sultana M.R., Alam M.M., Rashid M.M. Consequence of dam genotypes on productive and reproductive performance of dairy cows under the rural condition in Bangladesh. Pakistan Journal of Biological Sciences. 2007;10(19):3341–3349. doi: 10.3923/pjbs.2007.3341.3349. [DOI] [PubMed] [Google Scholar]
- Sarker A., Biswas D., Fakruzzaman M., Deb G.K., Hossain S.M.J., Alam M.A., Paul A.K. Enhancement of the pregnancy rate of buffalo cows through intra-vaginal bio-stimulation with penis-like device in the coastal area of Bangladesh. Advances in Animal and Veterinary Sciences. 2024;12(7):1301–1308. doi: 10.17582/journal.aavs/2024/12.7.1301.13. [DOI] [Google Scholar]
- Sarwar M., Khan M.A., Nisa M., Bhatti S.A., Shahzad M.A. Nutritional management for buffalo production. Asian-Australasian Journal of Animal Sciences. 2009;22(7):1060–1068. doi: 10.5713/ajas.2009.r.09. [DOI] [Google Scholar]
- Sarwar M., Shahzad M.A., Nisa M.U. Influence of varying level of sodium bicarbonate on milk yield and its composition in early lactating Nili Ravi buffaloes. Asian-Australasian Journal of Animal Sciences. 2007;20(12):1858–1864. https://www.animbiosci.org/journal/view.php?doi=10.5713/ajas.2007.1858 [Google Scholar]
- Shahjahan M. Assessment of growth potentials between indigenous and crossbred buffaloes. Journal of Agriculture, Food and Environment (JAFE) 2021;2(1):77–80. doi: 10.47440/JAFE.2021.2113. [DOI] [Google Scholar]
- Siddiky M.N., Faruque M.O. Buffaloes for dairying in South Asia: Potential, challenges and way forward. SAARC Journal of Agriculture. 2017;15(2):227–239. doi: 10.3329/sja.v15i2.35167. [DOI] [Google Scholar]
- Singh P., Panchbhai G., Bhatt N., Barman D., Lathwal S.S., Mukesh M., Tyagi A.K., Singh S.V., Uddin J. Effect of management practices on the age of puberty in Murrah buffalo male calves. Preprint. 2022 doi: 10.21203/rs.3.rs-2170042/v1. [DOI] [Google Scholar]
- Srirattana K., Hufana-Duran D., Atabay E.P., Duran P.G., Atabay E.C., Lu K., Liang Y., Chaikhun-Marcou T., Theerakittayakorn K., Parnpai R. Current status of assisted reproductive technologies in buffaloes. Animal Science Journal. 2022;93(1) doi: 10.1111/asj.13767. Article. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sultana N., Miah M., Alam M.A., Islam M.T., Amin M.R., Majumdar M.K., Deb G.K. Rearing and feeding strategies of indigenous buffalo in selected area of Bangladesh. African Journal of Agriculture and Food Science. 2024;7(3):126–136. doi: 10.52589/AJAFS-UMKVIIUB. [DOI] [Google Scholar]
- Tufarelli V., Puvača N., Glamočić D., Pugliese G., Colonna M.A. The most important metabolic diseases in dairy cattle during the transition period. Animals. 2024;14(5):816. doi: 10.3390/ani14050816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Uddin M.K., Mintoo A.A., Awal T.M., Kondo M., Kabir A.K. Characterization of buffalo milk production system in Bangladesh. Bangladesh Journal of Animal Science. 2016;45(1):69–77. doi: 10.3329/bjas.v45i1.27492. [DOI] [Google Scholar]
- United Humanitarian Bangladesh (UHB). (2024). Recommendations from International Buffalo Workshop 2024 [Website]. Retrieved May 20, 2025, from https://uhb.org.bd/2024/09/25/recommendations-from-international-buffalo-workshop-2024/.
- Vale P., Gibbs H., Vale R., Christie M., Florence E., Munger J., Sabaini D. The expansion of intensive beef farming to the Brazilian Amazon. Global Environmental Change. 2019;57 doi: 10.1016/j.gloenvcha.2019.05.006. [DOI] [Google Scholar]
- Villanueva M.A., Mingala C.N., Tubalinal G.A., Gaban P.B., Nakajima C., Suzuki Y. Emerging infectious diseases in water buffalo: An economic and public health concern. 2018 doi: 10.5772/intechopen.73395. [DOI] [Google Scholar]
- Wafa W.M., El-Nagar H.A., Gabr A.A., Rezk M.M. Impact of dietary Moringa oleifera leaves supplementation on semen characteristics, oxidative stress, physiological response and blood parameters of heat stressed buffalo bulls. Journal of Animal and Poultry Production. 2017;8(9):367–379. doi: 10.21608/jappmu.2017.46008. [DOI] [Google Scholar]
- Waqas A., Afzal M., Zaman F., Sabir M. The impact of social networking sites’ usage on the academic performance of university students of Lahore, Pakistan. International Journal of Social Sciences and Management. 2016;3(4):267–276. doi: 10.3126/ijssm.v3i4.15962. [DOI] [Google Scholar]
- Warriach H.M., Ahmad N. Follicular waves during the oestrous cycle in Nili-Ravi buffaloes undergoing spontaneous and PGF2α-induced luteolysis. Animal Reproduction Science. 2008;101:332–337. doi: 10.1016/j.anireprosci.2007.01.01. [DOI] [PubMed] [Google Scholar]
- Yendraliza Y., Zesfin B., Udin Z., Jaswandi J., Arman C. Effect of combination of GnRH and PGF2α for estrus synchronization on onset of estrus and pregnancy rate in different postpartum in swamp buffalo in Kampar regency. Journal of the Indonesian Tropical Animal Agriculture. 2011;36(1):9–13. doi: 10.14710/jitaa.36.1.9-13. [DOI] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data sharing is not applicable to this article.






