Occurrence of Antibiotic Resistance in Bacteria Isolated from Milk of Dairy Cows in Small-Holder Farms in Juja Sub-County, Kenya
Asian Journal of Research in Animal and Veterinary Sciences,
Page 36-45
Abstract
Sub-clinical mastitis (SCM) remains a serious hindrance to small-holder dairy farms in Kenya. A cross-sectional study was conducted to determine the risk factors associated with occurrence of SCM and antibiotic resistance in smallholder dairy farms in a peri-urban set-up area of Juja Sub-county, Kenya. Milk samples was obtained from 120 lactating dairy cows in 60 farms and screened for SCM using California mastitis test (CMT). Positive CMT samples were cultured and bacteria identification was done using standard methods. A questionnaire survey was administered at the household level to assess the risk factors associated with SCM. Sensitivity of the Staphylococcus aureus and Escherichia coli isolated from milk against commonly used antibiotics was determined using disc diffusion method. The prevalence of SCM at cow and udder level was found to be 66.7% and 61.3%, respectively. The highest prevalence of SCM was in Kalimoni (88.8%), Murera (82.7%) and Witeithe (71.4%) wards. The least affected area being Juja (60%) and Theta (44.4%) wards. Sub-clinical mastitis was significantly higher (p=0.007) in Friesian (74.1%) and Guernsey (66.7%) breeds as compared to the indigenous breed (53.8%). Cows with parity of four and above had higher (p=0.001) prevalence of SCM (73.7%) as compared to those of lower parity stage. Additionally, the prevalence (81%) of SCM in cows at late lactation was higher (P=0.002) compared to early (61.5%) and mid-lactation (56.4%), respectively. Higher prevalence (59%) of SCM was found in cows kept in less frequently cleaned housing compared to those more frequently cleaned (10%). The bacterial organisms isolated from the milk were Staphylococcus spp. (41.7%), Klebsiella spp. (24.5%), Pseudomonas spp. (22.1%), Escherichia coli (6.8%), Shigella spp. (1.8%) and Salmonella spp. (3.1%). The isolated Staphylococcus spp. and E. coli were most resistant to Oxytetracycline (79%, 100%, respectively) and Streptomycin (44%, 90%, respectively). Multidrug resistance (MDR) involving a combination of oxytetracycline, tetracycline, streptomycin and chloramphenicol and gentamycin was observed amongst Staphylococcus spp. (29.4%) and E. coli (45.5%) isolates. In conclusion, the study showed that large proportion of dairy cows was affected by SCM and the antibiotic resistance (AR) was high. This calls for animal health extension experts and other relevant stakeholders in the industry to train farmers on efficient control of SCM and emerging cases of AR.
Keywords:
- Sub-clinical mastitis
- milk
- risk factors
- peri-urban
- antibiotic resistance
- Kenya
How to Cite
References
Available:http://www.fao.org/3/a-i7348e.pdf.
Mugambi DK, Maina MW, Kairu S, Gitunu AMM. Assessment of performance of smallholder dairy farms in Kenya: An econometric approach. J. Appl. Biosci. 2015;85:7891– 7899.
Bedane A, Kasim G, Yohannis T, Habtamu T, Asseged B, Demelash B. Study on prevalence and risk factors of bovine mastitis in Borana pastoral and agro-pastoral settings of Yabello District, Borana zone, Southern Ethiopia. Am. Eurasian J. Agric. Environ. Sci. 2012;12:1274-1281.
Bereda A, Yilma Z, Eshetu M, Yousuf M, Assefa G. Socioeconomic characteristics of dairy production in the selected areas of Ethiopian central highlands. J. Vet. Med. Anim. Health. 2017;9:193-203.
Bekele T, Lakew M, Terefe G, Koran T, Olani A, Yimesgen L, Demissie T. Study on bovine mastitis with isolation of bacterial and fungal causal agents and assessing antimicrobial resistance patterns of isolated Staphylococcus species in and around Sebeta town, Ethiopia. J. Vet. Med. Anim. Health. 2019;9:196-213.
Motaung TE, Petrovski KR, Petzer IM, Thekisoe O, Tsilo TJ. Importance of bovine mastitis in Africa. Anim. Health Res. Rev. 2017;18:58-69.
Ibrahim N. Review on mastitis and its economic effect. Can. J. Sci. Res. 2017;6:13-22.
KNBS. Kenya National Bureau of Statistics. 2019 Kenya Population and Housing Census. Government Printers, Nairobi; 2019.
Thrushfield M. Veterinary epidemiology (3rd ed.). Oxford: Black Well Science. 2005;233.
Orwa JD, Matofari JW, Muliro PS, Lamuka P. Assessment of sulphonamides and tetracyclines antibiotic residue contaminants in rural and peri urban dairy value chains in Kenya. Int. J. Food Contam. 2017;4:5.
Mahlangu P, Maina N, Kagira JM. Prevalence, risk factors, and antibiogram of bacteria isolated from milk of goats with subclinical mastitis in Thika East Subcounty, Kenya. J. Vet. Med: vol. 2018;Article ID 3801479:8. Available: https://doi.org/10.1155/2018/3801479
Ferronatto JA, Ferronatto TC, Schneider M, Pessoa LF, Blagitz MG, Heinemann MB, Souza FN. Diagnosing mastitis in early lactation: Use of Somaticell®, California mastitis test and somatic cell count. Ital. J. Anim. Sci. 2018;17:723-729.
Ganda EK, Bisinotto RS, Decter DH, Bicalho RC. Evaluation of an on-farm culture system (Accumast) for fast identification of milk pathogens associated with clinical mastitis in dairy cows. PloS one. 2016;11:e0155314.
Available:https://doi.org/10.1371/journal.pone.0155314
CLSI: Performance Standards for Antimicrobial Susceptibility Testing, Twenty Fifth Information Supplement, Clinical and Laboratory Standards Institute, Wayne, PA, USA; 2015.
Abunna F, Fufa G, Megersa B, Regassa A. Bovine mastitis: Prevalence, risk factors and bacterial isolation in small-holder dairy farms in Addis Ababa City, Ethiopia. Glob. Vet. 2013;10:647-652.
Biffa D, Debela E, Beyene F. Prevalence and risk factors of mastitis in lactating dairy cows in Southern Ethiopia. Int. J. Appl. Res. Vet. Med. 2005;3:189-198.
Gitau GK, Bundi RM, Vanleeuwen J, Mulei CM. Mastitogenic bacteria isolated from dairy cows in Kenya and their antimicrobial sensitivity. J. S. Afr. Vet. 2014;85:01-08.
Abo-shama UH. Prevalence and antimicrobial susceptibility of Staphylococcus aureus isolated from cattle, buffalo, sheep and goat`s raws milk in Sohag governorate, Egypt. Assiut Vet. Med. J. 2014;60:141.
Byarugaba DK, Nakavuma JL, Vaarst M, Laker C. Mastitis occurrence and constraints to mastitis control in smallholder dairy farming systems in Uganda. Livestock Research for Rural Development; 2008.
Available:https://www.lrrd.cipav.org.co/lrrd20/1/byar20005.htm
Mdegela RH, Nonga HE, Karimuribo ED, Mwesongo J, Kimera ZI, Mabiki F, Mhaiki CJ. Determination of oxytetracycline residues in cattle meat marketed in the Kilosa district, Tanzania: Research communication. Onderstepoort J. Vet. Res. 2015;82:1-5.
Almaw G, Molla W, Melaku A. Prevalence of bovine subclinical mastitis in Gondar town and surrounding areas, Ethiopia. Livestock Research and Rural Development; 2009.
Available:http://lrrd.cipav.org.co/lrrd21/7/alma21106.htm
Shittu M, Abdullahi J, Jibril A, Mohamed AA, Fasina FO. Subclinical mastitis and associated risk factors on lactating cows on Savannah Region of Nigeria. BMC Vet Res. 2012;8:134.
Pal M, Lemu D, Bilata T. Isolation, identification and antibiogram of bacterial pathogens from bovine subclinical mastitis in Asella, Ethiopia. Int. J. Livest. Res. 2017;7: 62-70.
Suleiman TS, Karimuribo ED, Mdegela RH. Prevalence of bovine subclinical mastitis and antibiotic susceptibility patterns of major mastitis pathogens isolated in Unguja island of Zanzibar, Tanzania. Trop. Anim. Health Pro. 2018; 50:259-266.
Tesfaye B, Abera A. Prevalence of mastitis and associated risk factors in Jimma Town Dairy Farms, Western Ethiopia. J. Vet. Sci. Anim. Husband. 2018;6:1-8.
Hagnestam-Nielsen C, Emanuelson U, Berglund B, Strandberg E. Relationship between somatic cell count and milk yield in different stages of lactation. Int. J. Dairy Sci. 2009;92:3124-3133.
Niozas G, Tsousis G, Malesios C, Steinhöfel I, Boscos C, Bollwein H, Kaske M. Extended lactation in high-yielding dairy cows. II. Effects on milk production, udder health, and body measurements. J. Dairy Sci. 2019;102:811-823.
Mureithi DK, Njuguna MN. Prevalence of subclinical mastitis and associated risk factors in dairy farms in urban and peri-urban areas of Thika Sub County, Kenya. J. Dairy Sci. 2016;50:259-266.
Manyi-Loh CE, Mamphweli SN, Meyer EL, Makaka G, Simon M, Okoh AI. An overview of the control of bacterial pathogens in cattle manure. Int. J. Environ. Res. Public Health. 2016;13: 843.
Abebe R, Hatiya H, Abera M, Megersa B, Asmare K. Bovine mastitis: prevalence, risk factors and isolation of Staphylococcus aureus in dairy herds at Hawassa milk shed, South Ethiopia. BMC Vet. Res. 2016;12:270.
Mulugeta Y, Wassie, M. Prevalence, risk factors and major bacterial causes of bovine mastitis in and around Wolaita Sodo, Southern Ethiopia. Glob. J. Microbiol. Res; 2013.
Available:http: //globalscienceresear chjournals.org/gjmr/645722013621.
Zaatout N, Ayachi A, Kecha M, Kadlec K. Identification of staphylococci causing mastitis in dairy cattle from Algeria and characterization of Staphylococcus aureus. J. Appl. Microbiol. 2019;127:1305-1314.
Tadesse HA, Gidey NB, Workelule K, Hailu H, Gidey S, Bsrat A, Taddele H. Antimicrobial resistance profile of e. coli isolated from raw cow milk and fresh fruit juice in Mekelle, Tigray, Ethiopia. Vet. Med. Int. 2018;6:1-9.
Abraha H, Hadish G, Aligaz B, Eyas G, Workelule K. Antimicrobial resistance profile of Staphylococcus aureus isolated from raw cow milk and fresh fruit juice in Mekelle, Tigray, Ethiopia. J. Vet. Med. Anim. Hlth. 2018;10:106-113.
Gunga PMA. Antibiotic resistance phenotypes and genotypes of Staphylococcus aureus isolated from milk submitted to the central veterinary laboratories. Doctoral dissertation, University of Nairobil; 2018.
Seyoum B, Kefyalew H, Abera B, Abdela N. Prevalence, risk factors and antimicrobial susceptibility test of Staphylococcus aureus in bovine cross breed mastitic milk in and around Asella town, Oromia regional state, southern Ethiopia. Acta Trop. 2018;177:32-36.
Chehabi CN, Nonnemann B, Astrup LB, Farre M, Pedersen K. In vitro antimicrobial resistance of causative agents to clinical mastitis in Danish dairy cows. Foodborne Pathog. Dis. 2019;16:562-572.
Roulette CJ, Caudell MA, Roulette JW, Quinlan RJ, Quinlan MB, Subbiah M, Call DR. A two-month follow-up evaluation testing interventions to limit the emergence and spread of antimicrobial resistant bacteria among Maasai of northern Tanzania. BMC Infect. Dis. 2017;17:770.
Okubo T, Yossapol M, Maruyama F, Wampande EM, Kakooza S, Ohya K, Ushida K. Phenotypic and genotypic analyses of antimicrobial resistant bacteria in livestock in Uganda. Transbound Emerg. Dis. 2019;66:317-326.
Elemo KK, Sisay T, Shiferaw A, Fato MA. Prevalence, risk factors and multidrug resistance profile of Staphylococcus aureus isolated from bovine mastitis in selected dairy farms in and around Asella town, Arsi Zone, South Eastern Ethiopia. Afr J Microbiol. Res. 2017;11:1632-42.
Sharma L, Verma AK, Kumar A, Rahat A, Neha, Nigam R. Incidence and pattern of antibiotic resistance of Staphylococcus aureus isolated from clinical and subclinical mastitis in cattle and buffaloes. Asian J. Anim. Sci. 2015;9:100-109.
Wang S, Wu C, Shen J, Wu Y, Wang Y. Hypermutable Staphylococcus aureus strains present at high frequency in subclinical bovine mastitis isolates are associated with the development of antibiotic resistance. Vet. Microbiol. 2013;165:410-415.
Kivaria FM, Noordhuizen JPTM, Nielen M. Interpretation of California mastitis test scores using Staphylococcus aureus culture results for screening of subclinical mastitis in low yielding smallholder dairy cows in the Dar es Salaam region of Tanzania. Prev Vet Med. 2007;17:274-85.
DOI: 10.1016/j.prevetmed.2006.10.011
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