High prevalence of antibiotic resistance in pathogenic foodborne bacteria isolated from bovine milk

Abstract

This study aimed to investigate the prevalence of foodborne pathogenic bacteria in bovine milk, their antibiogram phenotype, and the carriage of antibiotic resistance genes. Raw bovine milk samples (n = 100) were randomly collected from different suppliers in the northwest of Iran. Antibiotic-resistant patterns and the presence of antibiotic resistance genes were evaluated in the isolates. Escherichia coli, Listeria monocytogenes, Staphylococcus aureus, and Salmonella spp. were isolated from 78%, 47%, 25%, and 21% of samples, respectively. All isolates showed high rates of resistance to amoxicillin, penicillin, and cefalexin. The bla_TEM and bla_SHV genes were detected in 50.0% and 6.4% of E. coli isolates, respectively. Also, 28.5% and 19.0% of Salmonella isolates were positive for bla_TEM and bla_SHV. The frequency of mecA and bla_Z in S. aureus isolates was 20.0% and 12.0%, respectively. The high prevalence of bovine milk contamination with antimicrobial-resistant species in this study necessitates precise control on antibiotic prescription in veterinary medicine.

Introduction

The burden of foodborne diseases in humans remains largely unknown¹. During the past decade, the incidence of foodborne microbial diseases has considerably increased in most countries².

Milk and dairy products, as common food products in many countries, provide favorable environments for the growth of many microorganisms because of their nutrient composition³. Many studies have been performed to improve raw milk quality to reduce the risk of microbial contamination and to increase the chemical nutritional quality of dairy products^3,4. In recent years, the consumption of raw milk has been increasingly welcomed due to its potential benefits such as having high nutritional content and beneficial bacteria as well as the prevention of lactose intolerance. However, due to the potential presence of pathogens and their toxins, the consumption of raw milk can pose a serious risk of foodborne disease to public health^5–8. Staphylococcus aureus, Salmonella spp., Listeria monocytogenes, and Escherichia coli are the most common pathogens that can be found in raw milk and dairy products made from raw milk^4,7. Also, S. aureus, L. monocytogenes, and Salmonella spp. can contribute to bovine mastitis and be excreted directly into the milk^8–10.

Inappropriate use of antibiotics is a common problem in medical and veterinary medicine, which may result in the development of multidrug-resistant microorganisms¹¹. The antibiotic resistance in pathogenic bacteria is known as a big challenge for public health worldwide^12–14. One of the most important enzymes involved in antibiotic resistance of bacteria is beta-lactamase, especially extended-spectrum beta-lactamase (ESBL), which deactivate the beta-lactam antibiotics through hydrolysis of beta-lactam ring¹⁵. The most common ESBL-producing genes are SHV (bla_SHV), TEM (bla_TEM), and CTX-M genes (bla_CTX-M)¹⁶.

Over the last decades, mecA has been detected in S. aureusisolates¹⁷. The mecA gene is responsible for resistance to methicillin and other β-lactam antibiotics. This gene encodes a penicillin-binding protein (PBP2A) with a low affinity for β-lactam antibiotics^18,19. Also, bla_Z has been reported as the main gene in S. aureus responsible for resistance against several antibiotics²⁰. TEM and SHV-type β-lactamases are reported as the main causes of resistance in E. colistrains²¹. Also, numerous beta-lactamases such as TEM, SHV, PER, OXA, and CTX enzymes have been identified in different Salmonella species²². Therefore it seems important to investigate the antibiotic resistance patterns of pathogenic bacteria and the presence of associated encoding genes as the key elements of antibiotics resistance.

This study aimed to evaluate the prevalence of pathogenic foodborne bacteria in raw bovine milk through culture-based techniques, their antibiogram phenotype, and the presence of antibiotic resistance genes among the isolates using multiplex-PCR.

Material and methods

Sampling

Raw bovine milk samples (n = 100) were collected aseptically from different retail sellers in the northwest of Iran. At the seller level, all milk samples were stored in the refrigerator (≤ 4 °C). Samples were transported to the laboratory in an icebox at a temperature less than 4 °C. They were kept in a refrigerator at 4 ± 1 °C before analysis. The microbiological experiments were performed immediately. All microbiological culture mediums were provided by Merck Company (Darmstadt, Germany).

Total bacterial count

Serial tenfold dilutions of raw milk samples were prepared using the tubes containing 9 ml of sterile % 0.1 peptone water (up to 1:10,000 dilutions)²³. Then, 0.1 mL of each sample dilutions was cultured on Nutrient agar. The total mesophilic bacterial count was calculated after the plates were incubated aerobically at 37 °C for 48 h²⁴.

Isolation and detection of pathogenic bacteria

Eecherichia coli was isolated from samples according to the method of Feng et al.²⁵and Ombarak et al.²⁶ Three to five presumptive colonies (dark centered and flat colonies with metallic green sheen) from Levine’s Eosin Methylene Blue (L-EMB) agar plates were selected, transferred on tryptic soy agar (TSA), and incubated at 37 °C for 24 h. Biochemical confirmatory tests were performed according to the method of Feng et al.²⁵ and Quinn et al.²⁷.

Staphylococcus aureus was detected in the samples using Baird-parker agar. After incubation of plates at 37 °C for 48 h, typical black colonies with a clear zone were considered as presumptive S. aureus. The isolates were confirmed by biochemical tests such as coagulase, catalase, DNase, lecithinase, oxidase, Lysostaphin sensitivity, VP, urease, glucose, and mannitol fermentation²⁸.

For isolation and detection of L. monocytogenes, samples were enriched in Buffered Listeria enrichment broth (BLEB) at 30 °C for 48 h. The bacterial suspension was streaked onto PALCAM agar and incubated at 35 °C for 48 h. The isolates were confirmed by motility test, gram staining, and biochemical tests such as catalase, oxidase, hemolysis, nitrate reduction, carbohydrate fermentation, Christie-Atkins-Munch-Peterson test (CAMP), methyl red, and Voges-Proskauer (MR/VP)²⁹.

For isolation and detection of Salmonella spp., the raw milk samples were cultured on Bismuth Sulphite agar (BSA), Brilliant Green, and Phenol-Red agar (BGA) for 24 h (BGA)/48 h (BSA) at 37 °C. The suspected colonies were transferred to Samonella-Shigella agar plates and incubated at 37 °C for another 24 h. The presumptive colonies on the plates were subjected to biochemical tests using Lysine Iron agar, Triple Sugar Iron Agar, Sulfide-Indole-Motility medium, and Christensen’s Urea agar³⁰.

Antimicrobial susceptibility test

Antibiotic susceptibility tests of isolates were performed by the Kirby-Bauer disk diffusion method according to the guidelines of clinical laboratory standards³¹. Isolates were included in the study based on isolation rank (time criterion). Based on this criterion, the first isolate of a particular species isolated from a single sample was included in the analysis³². Briefly, bacterial suspensions were prepared in tubes containing 0.9% (w/v) phosphate-buffered saline with turbidity adjusted to 0.5 McFarland standard. Using a sterile cotton swab, bacterial suspension was streaked uniformly on the surface of Muller-Hinton agar. Antibiotic disks (Padtan Teb, Iran) including amoxicillin (25 μg/disk), azithromycin (15 μg), penicillin (10 IU), cephalexin (30 μg), ceftriaxone (30 μg), gentamicin(10 μg), chloramphenicol (30 μg), and tetracycline (30 μg) were placed on the surface of cultures. The selected antimicrobials were representative of the major classes of antibiotics commonly used in veterinary and human medicine in Iran. Finally, the diameter of the inhibition zone around the disks was measured after incubation of plates at 37 °C for 24 h.

Detection of bla_TEM, bla_SHV, mecA, and bla_Z genes using multiplex-PCR

The genomic DNA was extracted by boiling method³³. The primers used for the detection of target genes are listed in Table 1. The reaction contents for each 25 μL PCR consisted of 5.5 μL of deionized water, 12.5 μL RED-Extract-N-Amp master mix 2 × (containing buffer, salts, dNTPs, Taq polymerase, REDTaq dye, and JumpStart Taq antibody) (Sigma-Aldrich, USA), 1 μL of each primer and 3 μL of template DNA. The PCR program for bla_TEM and bla_SHV genes included initial denaturation for 5 min at 94 °C followed by 32 cycles of denaturation at 94 °C for 30 s, annealing step at 54 °C for 30 s, extension step at 72 °C for 60 s, and a final extension step at 72 °C for 10 min. The PCR condition for mecA and bla_Z were as follows: initial denaturation at 95 °C for 4 min, 30 cycles of denaturation at 95 °C for 60 s, annealing step at 58 °C for 60 s, extension step at 72 °C for 60 sand final extension step at 72 °C for 4 min. PCR products were subjected to electrophoresis using 1.5% (w/v) agarose gel. The gel was stained with ethidium bromide. Ultraviolet transillumination (Biorad, USA) was applied for the visualization of DNA.

Table 1.

PCR sets used for detection of target antibiotic-resistance genes in the selected foodborne bacterial isolated from bovine milk.

Genes	Primer sequence (5' → 3')	Accession number (GenBank)	Annealing (°C)	Amplicon size (bp)	References
blaTEM	F:ATC AGC AAT AAA CCA GC	NG_068216.1	54	516	Eid and Samir34
	R: CCC CGA AGA ACG TTT TC
blaSHV	F: AGG ATT GAC TGC CTT TTTG	NG_068212.1	54	392	Yukawa et al.35
	R: ATT TGC TGA TTT CGCTCG
mecA	F: AAA ATC GAT GGT AAA GGT TGG C	MK659556.1	58	532	Kim et al.36
	R: AGT TCT GCA GTA CCG GAT TTG C
blaZ	F: TGA CCA CTT TTA TCA GCA ACC	MN689952.1	58	700	Meroni et al.37
	R: GCC ATT TCA ACA CCT TCT TTC

Results and discussion

Several studies have revealed that food products such as raw milk and dairy products made from raw milk may be the main sources for the outbreak of antibiotic-resistance pathogens which are known as a challenge for the safety of food products³⁸. This problem is common in developing countries such as Iran, because of the poor food handling practices, inadequate food safety regulations, weak hygienic practices, insufficient financial resources to invest in food safety, weak regulatory systems, and inadequate education for food handlers. In the countries with outbreaks of foodborne diseases, the importance of pathogens like S. aureus, E. coli, L. monocytogenes, and Salmonella spp. has been reported as major causes³⁹.

Numerous researchers previously reported the antimicrobial resistance of E. coli and Salmonella isolates from raw milk to the most common antibiotics in their studies^39–42. Also, methicillin-resistant S. aureus as an emerging pathogen has become an important challenge for public health that has been isolated from raw milk^11,43. The multidrug-resistant of L. monocytogenes isolates from raw milk to some commonly used antibiotics is reported in various countries such as Ethiopia⁴⁴, Turkey⁴⁵, Egypt⁴⁶, and Pakistan⁴⁷. So, the present study was designed to study the occurrence of the most common antibiotic-resistant foodborne pathogens from raw milk in Iran.

Totalmesophilic bacterial count, isolation, and identification of bacterial species

The mean total mesophilic bacterial count of the examined raw milk samples in this study was 5.75 ± 0.85 log₁₀ cfu mL⁻¹ which was exceeded the permitted maximum value of raw milk contamination (5 log₁₀ cfu mL⁻¹)⁴⁸. Our findings of the high rate of contamination in raw milk are in agreement with that of the previous study conducted in Tabriz, indicating the poor microbial quality of raw milk delivered to pasteurized milk plants⁴. In another study which was conducted in Allahabad city (India), the total bacterial count of examined milk samples was reported between 4.79 log₁₀ cfu mL⁻¹ by Yadav et al.⁴⁸. Even, a higher level of contamination of about 6.32 ± 0.03 log₁₀ cfu mL⁻¹ was found for the raw milk samples from the collection centers of Guwahati city in India⁴⁹. In general, the total bacterial count of more than 6 log₁₀ cfu mL⁻¹ reported by many countries is not desirable for raw milk supplies and is not usable for human consumption⁵⁰.

The increased total bacterial count can be caused by the use of unsanitary equipment for milking, contamination of cow’s udders, inadequate cooling of milk, and occasionally by the milking of cows with mastitis⁵¹.

In the present study, 78% of samples were contaminated with E. coli with a mean count of 3.41 ± 0.41 log₁₀ cfu mL⁻¹. High rates of raw milk contamination with E. coli have been reported in many developing and developed countries. It has been reported that 90.67% of raw milk samples in Arusha, Tanzania were contaminated with E. coli⁵² as well as 76.4% of samples in Egypt²⁶.

In our study, 25% of the raw milk samples were contaminated with S. aureus at an average level of 2.91 ± 0.80 log₁₀ cfu mL⁻¹. In agreement with our study, a study in California showed that 25.3% of the raw milk samples were contaminated with S. aureus⁵. In another study in Mansoura City, Egypt, the mean S. aureus counts were found to be 3.49 log₁₀ cfu g⁻¹ in raw milk samples⁴³, and 70.4% of raw milk samples in Brazil were contaminated with S. aureus⁵³. These results indicate the different quality of milk samples in different regions of the world.

According to the results of the present study, L. monocytogenes was isolated from 47% of the raw milk samples. Over 70% of positive samples contained L. monocytogenes at a level of less than 10 cfu ml⁻¹. The mean count of this bacterium was detected at 0.60 ± 0.51 log₁₀ cfu mL⁻¹. Many studies in different countries reported the occurrence of L. monocytogenes by various rates of contamination in their raw milk supplies and related products. The occurrence of L. monocytogenes in raw milk has been reported in Kars city (Turkey)⁴⁵. However, in research in Antakya, Turkey, L. monocytogenes was not detected in any of the raw milk samples⁵⁴.

In the present study, Salmonella spp. was detected in 21% of the raw milk samples. After enrichment of samples followed by plating, the mean count of Salmonella spp. in the positive samples was detected at 0.26 ± 0.27 log₁₀ cfu mL⁻¹. Similar results have also been reported in different countries. The prevalence of Salmonella spp. in raw milk has also been reported in Arusha, Tanzania (37.33%)⁵², Egypt(44.44%)⁵⁵, and Dhaka Metropolis, Bangladesh (25.71%)⁵⁶.

Antimicrobial susceptibility of isolates to the used antibiotics and detection of bla_TEM,bla_SHV, mecA, and bla_Z genes in the isolates

In this study, it was shown that all strains of E. coli were highly resistant to penicillin (88.46%), cefalexin (82.05%), and amoxicillin (70.51%) (Table 2). Fifty percent (50%) of E. coli isolates had bla_TEM and 6.41%of them were positive for bla_SHV (Table 3). Consistent with our study, another study reported that 83.1% of isolates of highly antibiotic-resistant E. coli strains, with 100% resistance to acetyl spiramycin, 100% to penicillin, 98.8% to lincomycin, 98.8% to oxacillin, 32.5% to cephalosporin, and 30.1% to ampicillin. The bla_TEM was the most frequently detected resistance gene (83.1%)⁴².

Table 2.

Antibiotic resistance profile of Escherichia coli isolates (n = 78) from bovine milk samples.

Antimicrobial agent	Disk content	Interpretive categories and zone diameter breakpoints (nearest whole mm)*			No. of isolates (%)
		R**	I	S	R	I	S
Azithromycin	15 μg	≤ 12	–	≥ 13	53 (67.94)	–	25 (32.05)
Chloramphenicol	30 μg	≤ 12	13–17	≥ 18	15 (19.23)	2 (2.56)	61 (78.20)
Ceftriaxone	30 μg	≤ 19	20–22	≥ 23	17 (21.79)	14 (17.94)	47 (60.25)
Penicillin	10 IU	≤ 14	–	≥ 15	69 (88.46)	–	9 (11.53)
Gentamicin	10 μg	≤ 12	13–14	≥ 15	6 (7.69)	3 (3.84)	69 (88.46)
Amoxicillin	25 μg	≤ 13	14–16	≥ 17	55 (70.51)	3 (3.84)	20 (25.64)
Tetracycline	30 μg	≤ 11	12–14	≥ 15	20 (25.64)	9 (11.53)	49 (62.82)
Cephalexin	30 μg	≤ 14	–	≥ 15	64 (82.05)	–	14 (17.94)

*From CLSI³¹.

**S susceptible, I intermediate, R resistant.

Table 3.

Distribution of resistance genes in the selected foodborne bacterial isolated from bovine milk.

Target genes	No of isolates (%)
	E. coli	Salmonella spp.	L. monocytogenes	S. aureus
blaSHV	5 (6.41%)	4 (19.04)	–	–
blaZ	–	–	–	3 (12.00)
blaTEM	39 (50%)	6 (28.57)	–	–
mecA	–	–	–	5 (20.00)

In the present study, bla_TEM was the most common resistance gene in E. coli isolates. However, only 50% of the resistant isolates to both penicillin and amoxicillin harbored this gene. Also, bla_SHV was present in five isolates of E. coli. All isolates containing this gene showed resistance to cephalexin, penicillin, and amoxicillin in phenotypic experiments.

The isolated strains of L. monocytogenes in our study were highly resistant to penicillin, cefalexin, and amoxicillin (97.87%) (Table 4). Since ampicillin is an important first-choice antibiotic for the treatment of listeriosis⁵⁷, the isolates of L. monocytogenes were evaluated for the presence of known genes responsible for resistance to beta-lactam antibiotics (bla_TEM, bla_SHV, mecA, bla_Z) using the specific primers. However, none of the resistance genes were detected in L. monocytogenes (Table 3). Similar results were found by Marian et al.⁵⁸ that showed 100% of L. monocytogenes strains in their study were resistant to ampicillin and penicillin, with no involvement of bla_Z and mecA genes in their resistance. Also, Bertsch et al.⁵⁷ examined the antimicrobial susceptibility and antibiotic resistance genes in foodborne, clinical, and environmental isolates of L. monocytogenes that were negative for the presence of bla_Z and mecA genes.

Table 4.

Antibiotic resistance profile of Listeria monocytogenes isolates (n = 47) from bovine milk samples.

Antimicrobial agent	Disk content	Interpretive categories and zone diameter breakpoints (nearest whole mm)*			No. of isolates (%)
		R**	I	S	R	I	S
Azithromycin	15 μg	˂ 17	17–21	≥ 22	12 (25.53)	14 (29.78)	21 (44.68)
Chloramphenicol	30 μg	˂ 18	18–20	≥ 21	22 (46.80)	13 (27.65)	12 (25.53)
Ceftriaxone	30 μg	˂ 15	15–20	≥ 21	17 (36.17)	18 (38.29)	12 (25.53)
Penicillin	10 IU	< 8	8–28	≥ 29	46 (97.87)	0 (0)	1 (2.12)
Gentamicin	10 μg	< 18	18–20	≥ 21	24 (51.06)	21 (44.68)	2 (4.25)
Amoxicillin	25 μg	˂ 14	14–24	≥ 25	46 (97.87)	1 (2.12)	0 (0)
Tetracycline	30 μg	˂ 22	22–24	≥ 25	23 (48.93)	2 (4.25)	22 (46.80)
Cephalexin	30 μg	˂ 12	12–17	≥ 18	46 (97.87)	1 (2.12)	0 (0)

*From CA-SFM⁵⁹, CLSI³¹, Hansen et al.⁶⁰, and Soussy et al.⁶¹.

**S susceptible, I intermediate, R resistant.

The results of antimicrobial resistance tests showed that the isolated strains of Salmonella were highly resistant to penicillin (100%), cefalexin (100%), and amoxicillin (71.42%) (Table 5). High rates of antibiotic resistance for Salmonella spp. have been reported by many studies. In a study by Obaidat and Stringer (2019), more than 50% of S. enterica isolates in raw milk were resistant to kanamycin, streptomycin, amoxicillin, and tetracycline. In another study, the highest rate of antibiotic resistance for Salmonella was detected to ampicillin, chloramphenicol, streptomycin, sulfonamide, tetracycline, amoxicillin, ceftiofur, and ceftriaxone⁴¹. These results were consistent with the results obtained from the present study.

Table 5.

Antibiotic resistance profile of Salmonella spp. isolates (n = 21) from bovine milk samples.

Antimicrobial agent	Disk content	Interpretive categories and zone diameter breakpoints (nearest whole mm)*			No. of isolates (%)
		R**	I	S	R	I	S
Azithromycin	15 μg	≤ 12	–	≥ 13	8 (38.09)	–	13 (61.90)
Chloramphenicol	30 μg	≤ 12	13–17	≥ 18	6 (28.57)	1 (4.76)	14 (66.66)
Ceftriaxone	30 μg	≤ 19	20–22	≥ 23	5 (23.80)	3 (14.28)	13 (61.90)
Penicillin	10 IU	≤ 14	–	≥ 15	21 (100)	–	0 (0)
Gentamicin	10 μg	≤ 12	13–14	≥ 15	0 (0)	0 (0)	21 (100)
Amoxicillin	25 μg	≤ 13	14–16	≥ 17	15 (71.42)	3 (14.28)	3 (14.28)
Tetracycline	30 μg	≤ 11	12–14	≥ 15	5 (23.80)	7 (33.33)	9 (42.85)
Cephalexin	30 μg	≤ 14	–	≥ 15	21 (100)	–	0 (0)

*From CLSI³¹.

**S susceptible, I intermediate, R resistant.

In this study, six (28.57%) and 4 (19.04%) isolates of Salmonella spp. were positive for bla_TEM and bla_SHV, respectively (Table 3). Four isolates with multidrug resistance to penicillin, ceftriaxone, amoxicillin, and cephalexin, carried both bla_TEM and bla_SHV genes. In a study by Ranjbar et al.⁶² the frequency of Salmonella spp. with bla_TEM and bla_SHV genes was 29.9% and 2.89%, while the prevalence of these two genes in Salmonella in another study was reported 15.38% and 12.82%, respectively⁶³. The results of these studies were in agreement with the present study.

Staphylococcus aureus isolates were highly resistant to amoxicillin (100%), cephalexin (100%), and penicillin (84.00%), respectively (Table 6). Antimicrobial resistance in S. aureus species is very common in raw milk samples, as reported by many researchers. Li et al.⁶⁴ indicated that 80.5% of S. aureus isolates were resistant to penicillin and ampicillin. The resistance of S. aureus isolates to penicillin G (87.9%), cloxacillin (75.9%), and amoxicillin (55.6%) was also reported by Al-Ashmawyet al.⁴³ in Mansoura City, Egypt.

Table 6.

Antibiotic resistance profile of Staphylococcus aureus isolates (n = 25) from bovine milk samples.

Antimicrobial agent	Disk content	Interpretive categories and zone diameter breakpoints (nearest whole mm)*			No. of isolates (%)
		R**	I	S	R	I	S
Azithromycin	15 μg	≤ 13	14–17	≥ 18	8 (32.00)	8 (32.00)	9 (36.00)
Chloramphenicol	30 μg	≤ 12	13–17	≥ 18	6 (24.00)	13 (52.00)	6 (24.00)
Ceftriaxone	30 μg	≤ 13	14–20	≥ 21	6 (24.00)	12 (48.00)	7 (28.00)
Penicillin	10 IU	≤ 28	–	≥ 29	21 (84.00)	–	4 (16.00)
Gentamicin	10 μg	≤ 12	13–14	≥ 15	3 (12.00)	21 (84.00)	1 (4.00)
Amoxicillin	25 μg	≤ 28	–	≥ 29	25 (100)	–	0 (0)
Tetracycline	30 μg	≤ 14	15–18	≥ 19	7 (28.00)	11 (44.00)	7 (28.00)
Cephalexin	30 μg	≤ 21	–	≥ 22	25 (100)	–	0 (0)

*From CA-SFM⁵⁹, CLSI³¹.

**S susceptible, I intermediate, R resistant.

The presence of the mecA gene was found in five (20%) isolates of S. aureus and the bla_Z gene was positive in three (12.00%) isolates of S. aureus (Table 3). Notably, S. aureus isolates with phenotypic resistances to penicillin, amoxicillin, ceftriaxone, and cephalexin always harbored mecA and bla_Z either individually or concurrently. These two genes are common genes involved in the antibiotic resistance of S. aureus strains. The electrophoresis pattern of the PCR products of the resistance genes in the bacteria under this study is shown in Figs. 1, 2 and 3.

Figure 1.

Electrophoresis pattern obtained by multiplex PCR for detection of bla_TEM and bla_SHV genes in E. coli isolates. M: marker 100 bp; lane 1, 2, 3, 4, 5, 6, 7, 8, 9, 11: amplification of bla_TEM gene at 516 bp; lane 6, 10: amplification of bla_SHV gene at 392 bp.

Figure 2.

Electrophoresis pattern obtained by multiplex PCR for detection of bla_TEM and bla_SHV genes in Salmonella isolates. M: marker 100 bp; Lanes 2, 5, 6, 8, and 10: amplification of bla_TEM gene at 516 bp; lane 2, 3, 6: amplification of bla_SHV gene at 392 bp.

Figure 3.

Electrophoresis pattern obtained by multiplex PCR for detection of mecA and blaZ genes in S. aureus isolates. M: marker 100 bp; Lanes 5 and 9: amplification of mecA gene at 532 bp; lane 10: amplification of bla_Zgene at 700 bp.

The bla_Z and mecA were identified as resistance genes in S. aureus isolated from subclinical mastitis in Egypt⁶⁵. In another study that investigated the genomic profile of S. aureus isolates from bulk tank milk and dairy cows with clinical mastitis, the prevalence of bla_Z gene was detected in 17.2% of isolates⁶⁶.

Resistance to penicillin, amoxicillin, cephalexin, and ceftriaxone was more prevalent than the associated antibiotic resistance genes between isolates. The discrepancies between the phenotypic resistances and associated resistance genes in this study may be due to the fact that the entire suite of resistant genes, which could result in phenotypic resistance, was not evaluated in this study. Also, it is possible that the antibiotic-resistant genes detected may be mutated and/or non-functional, inducible or not expressed. Other mechanisms of resistance such as multidrug efflux pumps, mutations in outer membrane porins, or other unknown resistance genes may be involved in the phenotypic resistance^67,68.

In the present study, high resistance levels and multidrug resistances against up to 7 antibiotics were detected between the evaluated isolates, with a high proportion for beta-lactams. Since beta-lactams are the most commonly used antibiotics in veterinary medicine, the emergence of beta-lactam-resistant pathogenic bacteria can be a serious threat to the wide use of these drugs⁶⁹.

The occurrence of antibiotic-resistance pathogens in raw milk can be directly affected by farm management and practices. Regular cleaning of the farm can decrease the prevalence of antibiotic resistance pathogens⁷⁰. The types of animal breeding (intensive, semi-intensive, or free-ranging) can influence the occurrence of antibiotic resistance pathogens due to the inappropriate administration of antibiotics. Excessive use of antibiotics in therapeutic and sub-therapeutic levels in dairy cattle farms can result in the presence of antibiotic-resistant pathogens in raw milk. So, if raw milk is not heat-treated, the presence of antibiotic-resistant foodborne pathogens in raw milk may pose food safety hazards to humans^70,71.

Conclusion

Our results show that raw milk has a great potential for transmission of antibiotic-resistant pathogens such as E. coli, S. aureus, L. monocytogenes, and Salmonella spp. In the present study, high levels of resistance were observed among the screened isolates to the most common beta-lactams such as amoxicillin, penicillin, and cefalexin. Also, the prevalence of beta-lactamase genes in E. coli, S. aureus, and Salmonella spp. provided evidence on the high risk of resistant food-borne pathogens to humans through raw milk.

Since antibiotics have extensive applications in dairy cattle farms in developing countries such as Iran; the microbiota of raw milk may contain relatively high levels of antibiotic-resistance bacteria. Therefore, enhancing the safety of milk and implementing good manufacturing practices are extremely important for the health of consumers. Pasteurization of raw milk, prevention of cross-contamination, storage of raw milk in cold temperature, appropriate authority supervision, and regulatory monitoring on the use of antibiotics in dairy cattle farms are necessary to ensure the safety of milk and dairy products.

The main route for the contamination of raw milk with resistant bacteria can be the subject of future studies to determine whether these bacteria get into the milk via cow’s udder or mixed into the milk during or after milking. Since phylogenetic assays can be used to ensure the genetic variations of resistant bacteria; it is recommended that these assays be performed on foodborne pathogenic isolates in future studies.

Author contributions

S.H.: Data curation, funding, investigation, project administration, data analysis; M.-H.M.: Conceptualization, design of methodology, supervision for the research activities, verification of data; writing of the original draft, writing and editing of the manuscript; S.N.G.: Data curation, Design of methodology, supervision for the research activities, investigation, project administration, analysis and verification of data; S.A.K.: investigation, editing of the manuscript; A.H.: editing of the manuscript; Z.B.: editing of the manuscript. All authors have reviewed and approved the final manuscript.

Funding

This work was supported by the vice-chancellery for research and technology, University of Tabriz.

Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Competing interests

The authors declare no competing interests.