Submit or Track your Manuscript LOG-IN

Bacteriology, Antimicrobials Resistance and Susceptibility Profiles of Bacteria from Mastitic Cattle and Buffaloes of Khyber Pakhtunkhwa

SJA_38_4_1240-1245

Research Article

Bacteriology, Antimicrobials Resistance and Susceptibility Profiles of Bacteria from Mastitic Cattle and Buffaloes of Khyber Pakhtunkhwa

Tariq Ali1,2*, Kamran1, Abdur Raziq1, Inam Ullah Wazir1, Anwar Ali1, Muhammad Ijaz Ali1, Muhammad Shuaib Khan2, Shakeeb Ullah2 and Sher Hayat Khan3

1Center of Microbiology and Biotechnology, Veterinary Research Institute Peshawar, Khyber Pakhtunkhwa, Pakistan; 2Faculty of Veterinary and Animal Sciences, Gomal University, D.I. Khan, Pakistan; 3Institute of Biotechnology and Genetic Engineering, University of Agriculture, Peshawar, Khyber Pakhtunkhwa, Pakistan.

Abstract | Mastitis is one of the major prevailing and costly diseases in dairy cattle and buffaloes. This study describes the current prevalence of mastitis in lactating cattle, and buffaloes in Khyber Pakhtunkhwa during 2019-2020, to identify bacterial pathogens of mastitis, and to determine the antimicrobial resistance. A total of 1013 milk samples belonging to 726 cattle and 287 buffaloes were examined to detect clinical mastitis (CM) and subclinical mastitis (SCM). Mastitic milk samples (n=541) were further used to investigate the prevalence of bacteria associated with mastitis and their antimicrobial susceptibilities by standard disc diffusion assay. The results showed that the prevalence of CM and SCM was 21.2% and 62.3% in cattle, while 17.8% and 68.9% in buffaloes, respectively. Additionally, it was noted that CM was higher in cattle, while SCM was higher in buffaloes. Amongst the bacterial isolates from mastitic milk the prevalence of Staphylococci spp. (24.6%) was at highest, which was followed by Escherichia coli (23.7%), then Streptococci spp. (8%) Salmonella spp. (5.9%), Klebsiella spp. (5.7%), Candida spp. (4.1%), and Proteus spp. (1.5%). The isolated bacteria were mostly resistant to ampicillin (96.5%), sulphamethoxazole (96.5%), streptomycin (95.1%), oxytetracycline (85%), and amoxicillin (78.1%). However, the isolates were highly susceptible to enrofloxacin (86.2%), gentamicin (83.5%), and florfenicol (82.6%). This study might be helpful to the clinicians and researchers associated with the dairy industry for designing prophylactic as well as therapeutic strategies for the control of bovine mastitis.


Received | March xx, 2021; Accepted | April 11, 2022; Published | September 21, 2022

*Correspondence | Tariq Ali, Center of Microbiology and Biotechnology, Veterinary Research Institute Peshawar, Khyber Pakhtunkhwa, Pakistan: Email: tariq.phd.18@gmail.com; tariq_ali@cau.edu.cn

Citation | Ali, T., Kamran, A. Raziq, I.U. Wazir, A. Ali, M.I. Ali, M.S. Khan, S. Ullah and S.H. Khan. 2022. Bacteriology, Antimicrobials resistance and susceptibility profiles of bacteria from mastitic cattle and buffaloes of Khyber Pakhtunkhwa. Sarhad Journal of Agriculture, 38(4): 1240-1245.

DOI | https://dx.doi.org/10.17582/journal.sja/2022/38.4.1240.1245

Keywords | Mastitis, Bacteriology, Antimicrobials susceptibility, Cattle, Buffaloes

Copyright: 2022 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



Introduction

Bovine mastitis (inflammation of mammary gland) is one of the most prevailing and economically destructive diseases affecting dairy animals across the globe (De Vliegher et al., 2012; Mbindyo et al., 2020), including Pakistan (Bachaya et al., 2011; Bhat et al., 2017; Ali et al., 2021). Bovine mastitis imparts huge financial losses, adversely affecting animal’s health and production, and welfare; besides, it deteriorates the milk quality and quantity capacities (De Vliegher et al., 2012). Bacterial pathogens are the major causing agents of mastitis. In addition, traumatic and mechanical injuries to the udder are also minor causes of mastitis (Bradley et al., 2002). Approximately 135 different bacterial species have been isolated from mastitic animals; however, about 20 types of bacterial pathogens are reported to be mostly associated with mastitis in dairy cattle (Bradley et al., 2002; Gao et al., 2017; Ali et al., 2021). Amongst the bacterial mastitis causing pathogens, coagulase-positive and –negative staphylococci, streptococci spp. Escherichia coli, Klebsiela spp. and Salmonella spp. are the main bacteria associated with mastitis (Ali et al., 2016; Yang et al., 2020; Aslam et al., 2021).

Different antimicrobials are commercially used to treat bacterial infections in livestock including intramammary bacterial infections. It has been reported that reproductive and mammary gland diseases are the main reasons to use antimicrobial agents in dairy animals for prolonged and frequent uses (Nobrega et al., 2017). These conditions paved the way to produce multi-drug resistant (MDR) bacterial pathogens (Ali et al., 2016; 2017). There is always a need of robust antimicrobial resistance surveillance systems of pathogenic bacteria from various sources (WHO, 2014). However, because of the economic constraints, national surveillance programs including monitoring systems of mastitis, the associated bacteria and their resistance profiles, are not present in Pakistan. Although, some regional studies were conducted on these aspects to fill the gaps (Mustafa et al., 2011; Ali et al., 2014; 2021). Thus, the current study was conducted with the aims to investigate the current prevalence of mastitis in lactating cattle, and buffaloes (Bubalus bubalis) in Khyber Pakhtunkhwa during 2019-2020, to detect bacterial pathogens associated with mastitis, and to evaluate their antimicrobial resistance.

Materials and Methods

Ethical statement

To conduct this study, ethical and technical guidance was obtained from the ethical and technical committee of the Veterinary Research Institute (VRI) Peshawar, Pakistan. Milk samples were obtained from cattle and buffaloes as per the guidelines of the National Mastitis Council (NMC) with the prior consent of the owners and without any harm to the animals.

Sampling and Processing

A total of 1013 milk samples were either collected directly from the animals or brought by the owners/farm managers to detect mastitis. Samples were processed at the Center of Microbiology and Biotechnology (CMB), VRI Peshawar, Pakistan during July, 2019 to June, 2020. Aseptic milk samples were collected from individual small farmers with 01 to 03 cattle or buffaloes. Dairy farmers were guided for the collection of aseptic samples from their animals as per NMC protocols. A total of 1013 milk samples from 726 cattle and 287 buffaloes of different areas of Khyber Pakhtunkhwa (KPK) were brought to our Mastitis Laboratory for detection of clinical mastitis (CM) and subclinical mastitis (SCM) as shown in Table 1 and Table 2. CM was detected with the help of visual observations as well as from the abnormal changes in milk (Ali et al., 2014). While, California mastitis test (CMT) kit (ImmuCell, Portland, ME) was used to diagnose SCM.

Bacteriology and antimicrobial resistance profiling of mastitic milk samples

A total of 541 samples from mastitic animals were further cultured to identify the bacterial pathogens. The identification of bacterial isolates was carried out up to the level of genus as described earlier (Ali et al., 2021). In addition, antimicrobial resistance and susceptibility profiling of the isolated bacteria from mastitic cattle and buffaloes was carried out on Muller-Hinton agar (OxoidTM, Thermo Scientific Inc. USA). Antimicrobial susceptibility testing of the bacterial isolates from mastitic milk samples was performed on Mueller-Hinton agar (OxoidTM) by the Kirby-Bauer disc diffusion assay according to the recommendations of the Clinical Laboratory Standard Institute (CLSI, 2014). Fourteen different antimicrobial agents were tested, including ampicillin, amoxicillin, augmentin, oxytetracycline, gentamicin, streptomycin, kanamycin, norfloxacin, enrofloxacin, sulphamethoxazole, doxycycline, erythromycin, florfenicol and flumequine.

Results and Discussion

Prevalence of bovine mastitis

The results of this study showed 21.2% and 62.3% of overall prevalence of CM and SCM in cattle and 17.8% and 68.9% in buffaloes, respectively (Table 1). Thus, CM was highest in cattle (21.2%) as compared to buffaloes (17.8%); however, prevalence of SCM

 

Table 1: Species-wise prevalence of mastitis in cattle and buffaloes of Khyber Pakhtunkhwa.

Species

Sample processed

Clinical mastitis

Subclinical mastitis

Negative sample

Blood in Milk

n

%

n

%

n

%

n

%

Cattle

726

156

21.2

452

62.3

118

16.3

92

12.7

Buffaloes

287

51

17.8

198

68.9

38

13.2

15

5.2

Total

1013

207

20.4

650

64.2

156

15.4

107

10.6

 

Table 2: Area-wise prevalence of subclinical mastitis (SCM) and clinical mastitis (CM).

Areas

Cow

Buffaloes

Total

SCM

CM

Neg.

Total

SCM

CM

Neg.

n

n

%

n

%

n

%

n

n

%

n

%

n

%

Peshawar

479

296

40.8

105

14.5

78

66.1

245

176

61.3

44

22.2

25

08.7

Charsada

93

60

08.3

18

11.5

15

12.7

21

11

03.8

05

02.2

05

02.2

Nowshera

26

21

02.9

03

01.9

02

01.7

09

06

03.0

00

00.0

03

01.1

Khyber

49

35

04.8

08

05.1

06

05.1

05

00

00.0

01

0.30

04

01.4

Sawbi

11

09

04.8

01

00.6

01

00.1

03

03

01.1

00

00.0

00

00.0

Mohmand

31

17

02.3

08

05.1

06

05.1

00

00

00.0

00

00.0

00

00.0

Mardan

23

06

00.8

08

05.1

09

07.6

02

01

0.30

00

00.0

01

0.30

Other*

14

08

01.1

05

03.2

00

00.0

02

00

00.0

01

0.30

00

00.0

Total

726

452

62.3

156

21.2

118

16.3

287

198

69.0

51

17.8

38

13.2

*other areas include Bajuar, Kohat and Karak

 

Table 3: Bacteriology of mastitic milk from cattle and buffaloes.

Bacteria isolated

Numbers (n)

Percentage (%)

Staphylococci spp

133

24.6

Escherichia coli

128

23.7

Streptococcus spp.

48

8.9

Klebsiella spp.

31

5.7

Salmonella spp.

32

5.9

Proteus spp.

08

1.5

Candida spp.

22

4.1

Culture Negative

161

29.8

Total samples

541

00

Note: High prevalence of Staphylococcus spp. (24.6%) was found which was followed by Escherichia coli (23.7%).

 

was highest in buffaloes (68.9%) in comparison to cattle (62.3%). Additionally, 12.7% of milk samples of cattle were mixed with blood, and 5.3% blood-mixed milk was observed in buffaloes. Table 2 shows the area-wise prevalence of CM and SCM in cattle and buffaloes of different areas of KPK. In districts Peshawar and Charsada, the topmost prevalence of CM and SCM was noted in cattle and buffaloes.

Bacteriology of mastitic milk samples

Isolation of different bacterial pathogens from mastitic dairy animals is presented in Table 3. Amongst the bacterial isolates from mastitic milk, Staphylococci spp. (24.6%) were the main prevailing bacteria. Besides, the other bacterial isolates included E. coli (23.7%), Streptococci spp. (8%), Klebsiella spp. (5.9%), Candida spp. (4.1%), and Proteus spp. (1.5%). Additionally, no bacterial growth was observed in 29.8% of samples from mastitic cattle and buffaloes.

Antimicrobial resistance and susceptibility of bacterial pathogens

Table 4 reveals the antimicrobial resistance and susceptibility profiles of different bacterial pathogens against fourteen antimicrobial agents. The isolated bacteria were highly resistant to ampicillin (96.5%), sulphamethoxazole (96.4%), streptomycin (95.1%), oxytetracycline (85%), and amoxicillin (78.1%). In addition, these isolates were mainly sensitive to enrofloxacin (86.2%), gentamicin (83.5%), and florfenicol (82.6%).

This study reported an overall prevalence of 21.2% and 62.3% of clinical mastitis (CM) and subclinical mastitis (SCM) in cattle; however, it was 17.8% and 68.9% in buffaloes of different areas of KPK. Thus, CM was highest in cows in comparison to buffaloes however SCM was highest in buffaloes. Mustafa et al. (2011) and our recent study (Ali et al., 2021) also reported higher prevalence of CM in cows than in buffaloes. It has been reported that buffaloes are generally more resilient to different diseases such as bovine mastitis due to their strong immune system (Pal and Chakravarty, 2020). Besides, the other contributing factors of high prevalence of mastitis in cattle might be the harsh environmental conditions of the province, and diminished immunity of exotic and crossbred cows. Also, this study reported higher prevalence of SCM in cows than reported by other studies such as Bachaya et al. (2011) reported 35% prevalence of SCM in cows of district Muzafar-Gharr, 30% in cattle belonging to Lahore (Mustafa et al., 2011), and 44% in Punjab province (Ali et al., 2011), and 42% in buffaloes belonging to district Dera Ismail Khan (Ali et al., 2014). This increase in the occurrence of bovine mastitis is worrying, which might be due to the reason that the dairy sector is swiftly growing in the KPK, and large numbers of commercial dairy farms are now developed in this area. Our previous study also reported that with the increase in herd size there is significant increase in the incidence of mastitis in buffaloes (Ali et al., 2014). This study is in line with other studies (Bhat et al., 2017; Ali et al., 2014) that reported a prevalence of 11.5% CM in cattle belonging to Azad Jamu Kashmir, and 11% in buffaloes of district Dera Ismail Khan. In contrast, the studies of Sharif et al. (2009) and Mustafa et al. (2011) observed the highest prevalence of CM in cows (61%) and buffaloes (61%). Additionally, this study was in line with some other studies (Mustafa et al., 2011: Sharif et al., 2009), we reported that 4.7% milk samples from cattle and 4.0% from buffaloes were mixed with blood. The findings of this study were partially according to other studies across the world, which reported the prevalence of bovine mastitis in India (Sinha et al., 2016), in China (Gao et al., 2017), in Ethiopia (Birhanu et al., 2017), in Poland (Sztachańska et al., 2016), and in Kenya (Mbindyo et al., 2020). Geo-climatic variations in different regions also affect the prevalence of bovine mastitis as investigated in this study and are also in line with other published work (Ali et al., 2011).

In the present study, contagious mastitis pathogens Staphylococci spp. (24.6%) were the most prevalent bacteria, followed by environmental mastitis pathogens E. coli (23.7%). The other bacterial isolates were Salmonella spp. (5.9%), Klebsiella spp. (5.7%), Candida spp. (4.1%) and Proteus spp. (1.5%). Several studies from Pakistan (Iqbal et al., 2004, Ali et al., 2011; Mustafa et al., 2011; Bhat et al., 2017; Aslam et al., 2021) and other countries (Ali et al., 2017; Birhanu et al., 2017) have also reported these bacterial pathogens from cases of bovine mastitis; although the bacterial prevalence was slightly different in different regions. The findings of Bhat et al. (2017) were in agreement with our findings. They also reported 61% prevalence of S. aureus, 13% E. coli, 13% coagulase-negative streptococci (CNS), 9% Streptococcus dysgalactiae, and 4% Streptococcus uberis in cattle of Jammu and Kashmir. Nevertheless, in contrast, researchers in China investigated 14% prevalence of E. coli, 10% CNS, 10% Staph. aureus, 11% Strep. dysgalactiae, 3% Strep. agalactiae, and 2% Strep. uberis (Gao et al., 2017). The reasons of this variation might be that the prevalence of bacterial pathogens associated with bovine mastitis is varying with topographical conditions and managemental practices.

 

Table 4: Antimicrobial susceptibility of bacterial isolates from mastitic cattle and buffaloes.

Antimicrobial agents

Concentrations

(μg)

Susceptible isolates

Resistant isolates

n

%

n

%

Ampicillin

10

08

03.5

220

96.5

Amoxicillin

20

52

21.9

185

78.1

Augmentin

20/10

74

58.7

52

41.3

Oxytetracycline

30

36

15.0

204

85.0

Gentamicin

10

101

83.5

20

16.5

Streptomycin

10

07

04.9

135

95.1

Kanamycin

30

48

35.3

88

64.7

Norfloxacin

10

152

65.2

81

34.8

Enrofloxacin

05

213

86.2

34

13.8

Sulphamethoxazole

300

06

03.6

163

96.5

Doxycycline

30

62

40.0

93

60.0

Erythromycin

15

20

15.8

107

84.3

Florfenicol

30

147

82.6

31

17.4

Flumequine

30

37

43.5

48

56.5

 

In our most recently published work (Ali et al., 2021), we isolated different bacteria from mastitic cattle and buffaloes, which were highly susceptible to enrofloxacin (86.2%), gentamicin (83.5%), and florfenicol (82.6%). These isolates were resistant to ampicillin (96.5%), sulphamethoxazole (96.4%), streptomycin (95.1%), oxytetracycline (85%), and amoxicillin (78.1%). Similarly, the findings of Iqbal et al. (2004) also suggested that several antimicrobial drugs such as aminoglycoside, enrofloxacin, and norfloxacin were highly effective drugs against bacterial isolates recovered from mastitic animals in Pakistan. Also, gentamicin, enrofloxacin, norfloxacin and ciprofloxacin were also found susceptible against bacterial pathogens in several studies (Sharif et al., 2009; Ali et al., 2011; Aslam et al., 2021). Strikingly, gentamicin and enrofloxacin are also in the approved and listed for veterinary usage by World Organization for Animal Health (OIE) and World Health Organization (WHO, 2016).

Conclusions and Recommendations

Our study revealed that contagious mastitis and environmental mastitis due to Staphylococcus spp. and E. coli were highly prevalent in cows and buffaloes of KPK and the recovered bacteria were mostly susceptible to enrofloxacin, gentamicin, and florfenicol. This study might be helpful to clinicians and researchers for designing and implementing prophylactic and therapeutic plans for bovine mastitis. In addition, this study recommends national level surveillance study on prevalence of bacterial pathogens associated with bovine mastitis and their resistance profiles across the country.

Acknowledgments

We highly appreciate the assistance of our para-Lab staff at the Center, especially, Mr. M. Rauf, Mr. Raham Dad, Mr. Haseeb Gul and Mr. Qaisar Khan.

Novelty Statement

This is an important surveillance study on bovine mastitis, the prevalence of different bacteria associated with mastitis and their antimicrobial resistance and susceptibility profiling. Such studies are always needed by the clinicians and researchers associated with dairy industry to design and implement strategies in order to control and prevent mastitis in cattle and buffaloes.

Author’s Contribution

Tariq Ali, Abdur Raziq and Muhammad Ijaz Ali: Designed and perceived this study.

Tariq Ali, Kamran, Anwar Ali and Inam Ullah Wazir: Performed the experimental work.

Muhammad Shuaib Khan, Shakeeb Ullah and Inam Ullah Wazir: Performed data analysis and wrote this article.

Abdur Raziq, Muhammad Ijaz Ali, Shakeeb Ullah and Sher Hayat Khan: Critically reviewed and revised the article.

All authors had read and approved the final draft for submission.

Conflict of Interest

No conflict of interest is declared by the authors.

References

Ali, M.A., Ahmad, M.D., Muhammad, K., Anjum, A.A. 2011. Prevalence of sub clinical mastitis in dairy buffaloes of Punjab, Pakistan. J. Anim. Plant Sci., 21: 477-480.

Ali, T., Kamran, Raziq, A., Wazir, I., Ullah, R., Shah, P., Ali, M.I., Han, B., Liu, G. 2021. Prevalence of mastitis pathogens and antimicrobial susceptibility of isolates from cattle and buffaloes in northwest of Pakistan. Front. Vet. Sci., 8:746755. https://doi.org/10.3389/fvets.2021.746755

Ali, T., Rahman, A., Qureshi, M.S., Hussain, M.T., Khan, M.S., Uddin, S. 2014. Effect of management practices and animal age on incidence of mastitis in Nili Ravi buffaloes. Trop. Anim. Health Prod., 46: 1279-1285. https://doi.org/10.1007/s11250-014-0641-2

Ali, T., ur Rahman, S., Zhang, L., Shahid, M., Zhang, S., Liu, G., Gao, J., Han, B. 2016. ESBL-producing Escherichia coli from cows suffering mastitis in china contain clinical class 1 integrons with CTX-M Linked to ISCR1. Front. Microbiol., 7: 1931. https://doi.org/10.3389/fmicb.2016.01931

Ali, T., Rahman, S.U., Zhang, L., Shahid, M., Han, D., Gao, J., Zhang, S., Ruegg, P.L., Saddique, U. and Han, B. 2017. Characteristics and genetic diversity of multi-drug resistant extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli isolated from bovine mastitis. Oncotarget, 8: 90144-90163. https://doi.org/10.18632/oncotarget.21496

Aslam, N., Khan, S.U., Usman, T. and Ali, T. 2021. Phylogenetic genotyping, virulence genes and antimicrobial susceptibility of Escherichia coli isolates from cases of bovine mastitis. J. Dairy Res. 24: 1-2. https://doi.org/10.1017/S002202992100011X

Bachaya, H.A., Raza, M.A., Murtaza, S. and Akbar. I.U.R. 2011. Subclinical bovine mastitis in Muzaffar Garh district of Punjab (Pakistan). J. Anim. Plant Sci., 21: 16-19. 

Bhat, A.M., Soodan, J.S., Singh, R., Dhobi, I.A., Hussain, T., Dar, M.Y. and Mir, M. 2017. Incidence of bovine clinical mastitis in Jammu region and antibiogram of isolated pathogens. Vet. World, 10: 984-989. https://doi.org/10.14202/vetworld.2017.984-989

Birhanu, M., Leta, S., Mamo G. and Tesfaye, S. 2017. Prevalence of bovine subclinical mastitis and isolation of its major causes in Bishoftu town, Ethiopia. BMC Res. Notes, 10: 767. https://doi.org/10.1186/s13104-017-3100-0

Bradley, A.J. and Green, M.J. 2002. Bovine mastitis: An evolving disease. Vet. J., 164: 116-128. https://doi.org/10.1053/tvjl.2002.0724

CLSI, 2014. Performance standards for antimicrobial susceptibility testing. Wayne, PA: Clinical and Laboratory Standard Institute. CLSI document M100–S124.

De Vliegher, S., Fox, L.K., Piepers, S., McDougall, S. and Barkema, H.W. 2012. Mastitis in dairy heifers: Nature of the disease, potential impact, prevention, and control. J. Dairy Sci., 95: 1025-1040. https://doi.org/10.3168/jds.2010-4074

Gao, J., Barkema, H.W., Zhang, L., Liu, G., Deng, Z., Cai, L., Shan, R., Zhang, S., Zou, J., Kastelic, J.P. and Han, B. 2017. incidence of clinical mastitis and distribution of pathogens on large Chinese dairy farms. J. Dairy Sci., 100: 4797-4806. https://doi.org/10.3168/jds.2016-12334

Iqbal, M., Khan, M.A., Daraz, B. and Saddique, U. 2004. bacteriology of mastitic milk and in vitro antibiogram of the isolates. Pak. Vet. J., 24: 161-164. https://doi.org/10.1080/01443610410001645479

Mbindyo, C.M., Gitao, G.C. and Mulei, C.M. 2020. Prevalence, etiology, and risk factors of mastitis in dairy cattle in Embu and Kajiado counties, Kenya. Vet. Med. Int., 2020: 8831172. https://doi.org/10.1155/2020/8831172

Mustafa, Y.S., Awan, F.N., Zaman, T., Chaudhry, S.R. and Zoyfro, V. 2011. Prevalence and antibacterial susceptibility in mastitis in buffalo and cow in and around the district Lahore-Pakistan. Pak. J. Pharmacol., 24: 29-33.

NMC, 2004. National Mastitis Council; Procedures for collecting milk samples in microbiological procedures for the diagnosis of bovine udder infection and determination of milk quality; Madison, USA.

Nobrega, D.B., De Buck, J., Naqvi, S.A., Liu, G., Naushad, S., Saini, V. and Barkema HW. 2017. Comparison of treatment records and inventory of empty drug containers to quantify antimicrobial usage in dairy herds. J. Dairy Sci., 100: 9736-9745. https://doi.org/10.3168/jds.2017-13116

Pal, A. and Chakravarty, A.K. 2020. Disease resistance for different livestock species. Genetics and Breeding for Disease Resistance of Livestock, 271–296. https://doi.org/10.1016/B978-0-12-816406-8.00019-X

Pumipuntu, N., Tunyong, W., Chantratita, N., Diraphat, P., Pumirat, P., Sookrung, N., Chaicumpa, W. and Indrawattana, N. 2019. Staphylococcus spp. associated with subclinical bovine mastitis in central and northeast provinces of Thailand. Peer J., 7: e6587. https://doi.org/10.7717/peerj.6587

Sharif, A., Muhammad, G. and Sharif, M.A. 2009. Mastitis in buffaloes. Pak. J. Zool., 9: 479-490.

Sinha, M.K., Thombare, N.N. and Mondal, B. 2014. Subclinical mastitis in dairy animals: Incidence, economics, and predisposing factors. Sci. World J., 2014: 1-4. https://doi.org/10.1155/2014/523984

Sztachańska, M., Barański, W., Janowski, T., Pogorzelska, J. and Zduńczyk, S. 2016. Prevalence and etiological agents of subclinical mastitis at the end of lactation in nine dairy herds in north-east Poland. Polish J. Vet. Sci., 19: 119-24. https://doi.org/10.1515/pjvs-2016-0015

Yang, X., Wang, D., Li, J., Meng, X,. Wei, Y., Tuerxun, G., Jin, Y., Xue, J., Ali, T., Han, B. and Jia, B. 2020. Molecular epidemiology and characteristics of Streptococcus agalactiae isolated from bovine mastitis in large dairy herds of China. Pak. Vet. J., 40: 301-306. https://doi.org/10.29261/pakvetj/2020.025

WHO, 2014. World Health Organization: Antimicrobial resistance: global report on surveillance. WHO, Geneva, Switzerland. (http://wwwwhoint/drugresistance/documents/surveillancereport/en/)

WHO, 2016. World Health Organization: Critically important antimicrobials for human medicince 5th revision, 2016. (http://who.int/foodsafety/publications/cia2017.pdf. 2016).

To share on other social networks, click on any share button. What are these?

Sarhad Journal of Agriculture

March

Sarhad Journal of Agriculture, Vol.40, Iss. 1, Pages 01-262

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe