Asian Journal of Dairy and Food Research

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Prevalence and Risk Factors for Bovine Mastitis: A Review based on Selected Sub-saharan African Countries

Mpho Ramuada1, Thobela Louis Tyasi1, Lungile Gumede1, Teedzai Chitura2,*
  • 0000-0001-9676-7166, 0000-0002-3519-7806, 0000-0002-4510-5733, 0000-0002-6048-6917
1Department of Agricultural Economics and Animal Production, University of Limpopo, Private Bag X1106, Sovenga 0727, South Africa.
2Department of Animal Science, University of Venda, Private Bag X5050, Thohoyandou 0950, South Africa.

Mastitis is one of the major diseases affecting dairy farmers since it is associated with direct and indirect losses and expenditures due to low milk yield and poor milk quality in Sub Saharan countries (South Africa, Ethiopia, Nigeria and Kenya) as well as other parts of the world. Prevalence of mastitis in dairy herds has gained increasing attention in recent years. This narrative review article provides a comprehensive backup of literature on the prevalence, its causal agents, environmental and management-related risk factors for bovine mastitis according to studies conducted in the selected countries. The literature review indicated that from South African-based studies, average prevalence of subclinical mastitis (SCM) is 17.8% and 18.5% Clinical mastitis (CM). The average prevalence of mastitis based on studies from Ethiopia is 39.8% (SCM) and 22.1% (CM). Nigerian-based studies reported an average prevalence of 33.8% (SCM) and 4.1% (CM). Studies carried out in Kenya reported a prevalence rate of 69.6% (SCM) and 27.2% (CM). Antibiotic resistance, lack of implementation of adequate management practices for mastitis control such as teat disinfection, provision of clean bedding and clean housing were identified as the most common risk factors. Findings of this study revealed a high prevalence of mastitis in the selected countries and presence of risk factors for bovine mastitis. Therefore, addressing the identified risk factors could help to reduce direct and indirect losses in dairy enterprises because of subclinical and clinical mastitis.

Mastitis is an inflammation of the parenchyma of the mammary gland produced by infectious agents that infiltrate the udder, multiply and produce toxins.  Mastitis is a multifactorial disease involving microbes, the host and the environment and is classified as either sub-clinical or clinical mastitis. Clinical mastitis is characterized by visible abnormalities in the milk or the udder tissue while subclinical mastitis is inflammation of the mammary gland that does not create visible changes in the milk or the udder tissue. Although the milk appears normal, sub-clinically infected cows will produce less milk and the quality of the milk will be reduced (Hadef et al., 2022). Clinical mastitis can occur in one or more quarters of the udder and can range from mild to severe. Acute clinical mastitis is the severe form of the disease and is characterized by a sudden onset of symptoms and visible abnormalities such as udder swelling, hardness of the affected quarter, pain, watery milk and reduced milk yield (Kidanu, 2022) In some cases, the cow may display symptoms of infection, such as loss of appetite, fatigue and a decline in milk supply (Kumar et al., 2020). The California Mastitis Test (CMT) and Bacteriological Culturing (BC) of milk are the most employed diagnostic methods. However, conducting epidemiological investigations of bovine mastitis, including infection status and treatment patterns, would offer valuable management insights for producers, veterinarians and other members of the mastitis control team (Sharun et al., 2021).
       
Mastitis contributes significantly to revenue losses in the dairy farming industry worldwide (Singh, 2022). Furthermore, the condition may pose a serious public health threat in cases where zoonotic pathogens such as Staphylococcus aureus, Streptococcus agalactiae, Mycoplasma spp, Escherichia coli and Enterococcus spp are implicated (Ngu Ngwa et al., 2020). Mastitis causes economic losses to dairy farms as well as public health concerns (Paramasivam et al., 2023). The profitability of dairy operations is significantly affected by the reproductive efficiency of their dairy herds, which is highly correlated with the health of the cows (Dalanezi et al., 2020). Mastitis causes a decline in milk production as well as loss of quality of milk (Harjanti and Sambodho, 2020; Lahiri, 2023). The costs that are involved in the management of cases of mastitis such as attending to milking hygiene practices, udder health monitoring, individual cow treatment and other veterinary services related costs further add to the economic burdens of mastitis (Aghamohammadi et al., 2018). Kumar et al., (2017) reported a relationship between mastitis and decreased fertility in dairy cows because of reduced conception rates and longer intervals between conception and calving among other disturbances (Ibrahim et al., 2023). Furthermore, cows with chronic or recurring mastitis may need to undergo early culling bringing in extra costs of buying new cows or rearing more replacement heifers (Diniso and Jaja, 2021; Rodríguez, 2024).
       
Subclinical mastitis is asymptomatic and characterised by the absence of visible changes to the udder. However, the physical and chemical composition of the milk is altered (Yehia et al., 2024).  Subclinical mastitis can lead to a decrease in milk production (Antanaitis et al., 2021). Cows with infections might experience a decrease in milk production, along with a decline in milk quality due to elevated somatic cell counts (SCC) and potential issues like off-flavors and irregularities in composition. Reduced milk quality can lead to the milk being downgraded or declined by dairy processors, resulting in financial setbacks (Alhussien et al., 2021). Clinical mastitis is characterised by the presence of indicators of inflammation in the mammary gland such as swelling, heat, pain, as well as changes in the milk such as flakes and clots (Negash, 2023). Krueger (2019) and Ginger et al., (2023) pointed out that the pain associated with clinical mastitis severely affects animal welfare. Sadiq et al., (2020) and Eryýlmaz (2022) identified early detection, prompt treatment and the implementation of preventative measures such as maintaining excellent milking hygiene, ensuring clean and dry bedding and conducting routine udder health assessments as key measures towards reducing the occurrences of clinical mastitis in dairy herds.
       
This review paper was consolidated from studies published between 2003 and 2024 in various scientific journals. Electronic databases, such as Google Scholar, Science Direct and Research Gate were searched to gather relevant information for this review. The search was conducted using keywords such as ‘mastitis’, ‘prevalence’, ‘risk factors’, ‘South Africa’, ‘Ethiopia’, ‘Kenya’, ‘Nigeria’ and ‘economic losses. The four Sub-Saharan African countries were selected for the study due to the abundance of scientific literature on dairy cattle mastitis from studies that were carried out in these countries. Articles were gathered from scientific databases such as Google Scholar, Sci Direct, Web of Science and PubMed. Inclusion criteria was studies published in English that described the prevalence of mastitis and associated risk factors in South Africa, Ethiopia, Kenya and Nigeria, for both clinical and subclinical mastitis.
 
Prevalence of mastitis
 
Mastitis is among the most prevalent diseases of dairy cattle worldwide. The prevalence of bovine mastitis varies across countries, regions and individual farms partly due to differences in climatic conditions, herd management practices and genetics (Fulasa and Deressa, 2021; Singha et al., 2021). According to the studies included in our review, the average prevalence of clinical mastitis ranges from 5%-20% while subclinical mastitis prevalence is higher and ranges between 15% to 50%. Several risk factors contribute to the occurrence and spread of mastitis in the study area (Table 1). Studies based on bovine mastitis in Kenya reported the highest prevalence of subclinical mastitis while studies based on bovine mastitis in South Africa reported the lowest prevalence rate (Fig 1). Studies conducted on bovine mastitis in Kenya reported the highest prevalence of clinical mastitis standing on (27, 2%) while studies on bovine mastitis in Nigeria reported the lowest prevalence rate (4.1 %) (Fig 2).

Table 1: Prevalence and risk factors for bovine mastitis in selected Sub-Saharan African countries (South Africa, Ethiopia, Nigeria, Kenya).



Fig 1: Average prevalences of subclinical mastitis as reported by studies based on bovine mastitis in the selected Sub-Saharan countries (South Africa, Ethiopia, Nigeria and Kenya).



Fig 2: Average prevalence of clinical mastitis as reported by studies on South Africa, Ethiopia, Nigeria and Kenya.


 
Prevalence of bovine mastitis and associated risk factors
 
Several studies investigated the prevalence of bovine mastitis. Kumari et al., (2018) reported a range of 5 to 20 % for clinical mastitis and 15 to 50% for subclinical mastitis. Findings of the present study revealed that generally, there were more studies conducted on bovine subclinical mastitis (40 articles) as compared to studies conducted on bovine clinical mastitis (18 articles). These articles were published during the period 2005 to 2023. This observation underscores the significance of subclinical mastitis that necessitates its early detection in dairy cattle farming. From the selected Sub-Saharan African countries, majority of the studies were on bovine mastitis in Ethiopia. This observation could indicate that bovine mastitis is a major challenge in Ethiopia probably since majority of the producers are smallholder farmers who are resource limited.  South Africa had the lowest number of studies on bovine mastitis. This could highlight the need for more studies to provide key information on the disease situation in South Africa. From the 58 articles reviewed in this study, it is evident that studies on bovine mastitis in Kenya reported the highest pooled prevalence of both subclinical and clinical mastitis with averages of 69.6% and 27.2% respectively while studies on Ethiopia reported the second highest prevalence rates with 39.8% and 22.1% for subclinical and clinical mastitis respectively. This agrees with the findings by Ndirangu et al., (2022) and Michira et al., (2023). Mbindyo et al., (2020) and Duguma (2020) reported that high prevalences of bovine mastitis are largely due to traditional farming practices, lack of farmer awareness about the disease and limited access to veterinary services and modern dairy management techniques. Several risk factors can be attributed to high prevalences of bovine mastitis. Sombie et al., (2022) and Nyokabi et al., (2021) reported lack of cattle farmer knowledge on mastitis as a significant risk factor in Kenya. Studies on bovine subclinical mastitis in South Africa reported the lowest prevalence rate. This could be partly due to few studies published on bovine mastitis in South African as compared to the other countries that were selected for this study. However, when comparing the findings of Taoana (2005) and Khasapane et al., (2023), there is an indication of an increased prevalence of clinical mastitis in South Africa. Prevalence rates for bovine subclinical mastitis in Ethiopia that were reported in this study correspond with the observations of Umaru et al., (2017) and Gelgelu et al., (2023). High prevalence of bovine mastitis in the study area are associated production losses, risks of antibiotic residues in milk and the involuntary culling or death of affected animals. Hogeveen et al., (2011) stated that the effects of bovine mastitis on milk quality in addition to the cost of treating infected animals may have consequences that extend beyond the dairy farm.  Belay et al., (2022) indicated the high prevalence of bovine mastitis poses a zoonotic risk as mastitis-causing pathogens can be transferred to humans through contaminated milk. Makatu et al., (2021) highlighted the animal welfare concerns caused by bovine mastitis due to pain, stress and discomfort that affect the well-being of cows.
       
Elsewhere, studies were also conducted on bovine mastitis prevalence. In the South American region, studies carried out in Brazil and Argentina reported ranges between 20 to 50% for bovine subclinical mastitis prevalence and an average of 10% for bovine clinical mastitis. Freitas et al., (2018) and Schunig et al., (2024) indicated that factors such as intensive dairy farming practices and environmental conditions such as high humidity and high temperatures contribute to the spread of the disease. Dego (2020) indicated that the widespread use of antibiotics and the resulting antimicrobial resistance further complicate mastitis management in these regions. In South Asia, Ali et al., (2021) stated that Pakistan exhibits one of the highest mastitis prevalence rates, with clinical and subclinical mastitis affecting between 20% and 53% of cattle. Poor management practices and inadequate sanitary conditions on farms were cited as the key reasons for the high prevalence of bovine mastitis in Pakistan. In China, Liang et al., (2023) reported prevalences of around 10% for clinical mastitis while Wang et al., (2022) reported a decline in mastitis prevalence in China during the period 2011–2020 as compared to the period of 2000–2010. The authors suggested the rapid developments in technology targeted against major pathogens such as S. aureus, advanced milking techniques and strict biosecurity measures undertaken by the farms as some of the reasons for the observed decline (Mooventhan et al., 2016).
       
Regarding risk factors for bovine mastitis, Singha et al., (2021) identified some of the major factors that are responsible for the variations in the prevalence of the disease across countries, regions and individual farms. These include differences in climate, herd management practices and genetics. Fulasa and Deressa (2021) classified risk factors into management-related and cow-specific factors. The authors further indicated that effective management practices to prevent mastitis at the farm level include regular floor cleaning, proper milking techniques, udder washing before milking and pre- and post-milking teat dipping in antiseptic solutions while cow-specific factors include the stage of lactation, breed, history of mastitis and parity (Ulla et al., 2021). In addition to similar observations on risk factors as indicated above, our study identified microbiological resistance as a common risk while advanced age, higher parity and an advanced stage of lactation (third stage and beyond) poor hygiene management, such as lack of sanitation, hand milking, provision of improper bedding material and poor sanitary measures on the udder and milking equipment were identified as the common risk factors for clinical mastitis.  These findings indicate that there are major concerns regarding practices for reducing bovine mastitis prevalence by the farmers in the study area. Petzer et al., (2018) and Diniso and Jaja (2021) indicated that the type of production system, such as pasture-based farming, is a risk factor in South Africa.
 
Prevention and control measures for bovine mastitis
 
Zigo et al., (2019) emphasized prevention of bovine mastitis to safeguard animal health, ensure high milk quality and to optimize cow productivity.  El-Sayed and Kamel (2021) pointed out that strategies for mastitis prevention and control vary based on factors like farm size, management practices and the prevalence of specific pathogens in the area. Breen (2019) highlighted a five-point core plan for mastitis prevention and control that includes disinfecting teats, adhering to hygienic milking procedures, removing cows with chronic mastitis, administering dry cow therapy with antibiotics and treatment of cows with clinical mastitis. Patel et al., (2021) identified bedding materials provided to dairy cows as the primary sources of environmental mastitis and indicated that measures to reduce bacterial counts in bedding generally lower the risk. Vargova et al., (2023) indicated that cleaning teats and pre-milking teat dipping in antiseptic solution can help to reduce bacterial counts on the skin of the udder. Tiwari et al., (2020) mentioned post-milk teat dipping as a significant measure to reduce the rate of new infections, particularly from contagious mastitis pathogens. Tegegne et al., (2020). stated that dry cow therapy is the most effective method for curing chronic and subclinical mastitis and that timely and effective treatment of active cases also helps prevent new infections (Sinha et al., 2018).
Bovine mastitis is highly prevalent in selected countries. Understanding the risk factors for bovine mastitis is essential for controlling the disease at the farm level and as a result reduce both direct and indirect losses in dairy enterprises due to subclinical and clinical mastitis.
The present study was supported by Department of Agricultural Economics and Animal Production, University of Limpopo and the University of Venda’s Department of Animal Science.
 
Disclaimers
 
The views and conclusions expressed in this article are solely those of the authors and do not necessarily represent the views of their affiliated institutions. The authors are responsible for the accuracy and completeness of the information provided, but do not accept any liability for any direct or indirect losses resulting from the use of this content.
 
Informed consent
 
This review complies with rigorous ethical standards in scientific research and reporting. All referenced information has been properly cited to ensure due credit is given to previous work. The is no conflicts of interest regarding the publication of this article. No funding or sponsorship influenced the design of the study, data collection, analysis, decision to publish, or preparation of the manuscript.
The authors declare that there are no conflicts of interest regarding the publication of this article. No funding or sponsorship influenced the design of the study, data collection, analysis, decision to publish, or preparation of the manuscript.

  1. Abebe, R., Markos, A., Abera, M. and Mekbib, B. (2023). Incidence rate, risk factors and bacterial causes of clinical mastitis on dairy farms in Hawassa City, Southern Ethiopia. Scientific Reports. 13(1): 10945. https://doi.org/10.1038/ s41598-023-37328-1.

  2. Aghamohammadi, M., Haine, D., Kelton, D.F., Barkema, H.W., Hogeveen, H., Keefe, G.P. and Dufour, S. (2018). Herd-level mastitis- associated costs on Canadian dairy farms. Frontiers in Veterinary Science. 5: 355975. https://doi.org/10.3389/ fvets.2018.00100.

  3. Alhussien, M.N., Panda, B.S. and Dang, A.K. (2021). A comparative study on changes in total and differential milk cell counts, activity and expression of milk phagocytes of healthy and mastitis indigenous Sahiwal cows. Frontiers in Veterinary Science. 8: 670811. https://doi.org/10.3389/fvets.2021. 670811.

  4. Ali, T., Kamran, N., Raziq, A., Wazir, I., Ullah, R., Shah, P., Ali, M.I., Han, B. and Liu, G.(2021). Prevalence of mastitis pathogens and antimicrobial susceptibility of isolates from cattle and buffaloes in Northwest of Pakistan. Frontiers in Veterinary Science. 8: 746755. https://doi.org/10.3389/fvets.2021. 746755.

  5. Amuta, P.O., Okolocha, E.C., Kudi, C.A. and Gates, M.C. (2021). Assessing the perceptions and practices of peri-urban dairy farmers regarding bovine mastitis management in North-Western Nigeria. Preventive Veterinary Medicine. 194: 105442. https://doi.org/10.1016/j.prevetmed.2021.105442

  6. Antanaitis, R., Juozaitienë, V., Jonike, V., Baumgartner, W. and Paulauskas, A. (2021). Milk lactose as a biomarker of subclinical mastitis in dairy cows. Animals. 11(6): 1736. https://doi.org/ 10.3390/ani11061736.

  7. Anueyiagu, K.N., Benson, N.P., Daniel, J., Nze, C. and Esilonu, J.T. (2022). Prevalence of methicillin-resistant Staphylococcus aureus in Bovine Subclinical Mastitis in Jos South Local Government Area of Plateau State, Nigeria. European Journal of Veterinary Medicine. 2(6): 7-11. https://doi.org/10.24018/ejvetmed. 2022.

  8. Balemi, A., Gumi, B., Amenu, K., Girma, S., Gebru, M.U., Tekle, M., Rius, A.A., D’Souza, D.H., Agga, G.E. and Kerro Dego, O. (2021). Prevalence of mastitis and antibiotic resistance of bacterial isolates from CMT positive milk samples obtained from dairy cows, camels and goats in two pastoral districts in Southern Ethiopia. Animals. 11(6): 1530. https://doi.org/ 10.3390/ani11061530

  9. Banza, J.L. (2020). Milk quality and prevalence of mastitis pathogens in infected bovine mammary glands and their sensitivity to local plant extracts (Doctoral dissertation, University of South Africa).

  10. Belay, N., Mohammed, N. and Seyoum, W.(2022). Bovine mastitis: Prevalence, risk factors and bacterial pathogens isolated in lactating cows in Gamo zone, southern Ethiopia. Veterinary Medicine: Research and Reports. 9-19. https:// doi.org/10.2147/vmrr.s344024.

  11. Breen, J.  (2019). The importance of teat disinfection in mastitis control. Livestock. 24(3): 122-128. https://doi.org/10. 12968/live.2019.24.3.122.

  12. Dabele, D.T., Borena, B.M., Admasu, P., Gebremedhin, E.Z. and Marami, L.M. (2021). Prevalence and risk factors of mastitis and isolation, identification and antibiogram of staphylococcus species from mastitis positive zebu cows in toke kutaye, cheliya and dendi districts, west shewa zone, Oromia, Ethiopia. Infection and Drug Resistance. 987-998. https:// doi.org/10.2147/idr.s295257.

  13. Dalanezi, F.M., Joaquim, S.F., Guimarães, F.F., Guerra, S.T., Lopes, B.C., Schmidt, E.M.S., Cerri, R.L.A. and Langoni, H. (2020). Influence of pathogens causing clinical mastitis on reprod- uctive variables of dairy cows. Journal of dairy science. 103(4): 3648-3655. https://doi.org/10.3168/jds.2019-16841.

  14. Dego, O.K. (2020). Current status of antimicrobial resistance and prospect for new vaccines against major bacterial bovine mastitis pathogens. Animal Reproduction in Veterinary Medicine. 78921. https://doi.org/10.5772/intechopen.94227.

  15. Demil, E., Teshome, L., Kerie, Y., Habtamu, A., Kumilachew, W. andualem, T. and Mekonnen, S.A. (2022). Prevalence of subclinical mastitis associated risk factors and antimicrobial susceptibility of the pathogens isolated from milk samples of dairy cows in Northwest Ethiopia. Preventive Veterinary Medicine. 205: 105680.https://doi.org/10.1016/j.prevetmed.2022. 105680.

  16. Diniso, Y.S. and Jaja, I.F. (2021). Dairy farmworkers knowledge of factors responsible for culling and mortality in the Eastern Cape Province, South Africa. Tropical Animal Health and Production. 53(3): 398. https://doi.org/10.1007/s11250- 021-02845-6.

  17. Duguma, B. (2020). A survey of management practices and major diseases of dairy cattle in smallholdings in selected towns of Jimma zone, south-western Ethiopia. Animal Production Science. 60(15): 1838-1849. https://doi.org/10.1071/AN19079.

  18. El-Sayed, A. and Kamel, M. (2021). Bovine mastitis prevention and control in the post-antibiotic era. Tropical Animal Health and Production. 53: 1-16. https://doi.org/10.1007/s11250- 021-02680-9.

  19. Eryýlmaz, G. A., Garipoðlu, A. and Kýlýç, O. (2022). Animal health and welfare, milk safety and hygiene practices in dairy cattle farms: Türkiye sample. Türkiye Tarýmsal Araþtýrmalar Dergisi.  9(3):  395-401. https://doi.org/10.19159/tutad.1173509.

  20. Fesseha, H., Mathewos, M., Aliye, S. and Wolde, A. (2021). Study on prevalence of bovine mastitis and associated risk factors in dairy farms of Modjo town and suburbs, central Oromia, Ethiopia. Veterinary Medicine: Research and Reports. 271-283. https://doi.org/10.2147/vmrr.s323460.

  21. Freitas, C.H., Mendes, J.F., Villarreal, P.V., Santos, P.R., Gonçalves, C.L., Gonzales, H.L. and  Nascente, P.S. (2018). Identification and antimicrobial suceptibility profile of bacteria causing bovine mastitis from dairy farms in Pelotas, Rio Grande do Sul. Brazilian Journal of Biology. 78: 661-666.  https:// doi.org/10.1590/1519-6984.170727.

  22. Fulasa, T.T. and Deressa, F.B. (2021). Bovine mastitis in Ethiopia.

  23. Geleta, B., Beyene, D., Wubete, A. and Abunna, F. (2019). Sub clinical mastitis in dairy farms of Addis Ababa and Sebeta Towns, Ethiopia. Biomedical Journal of Scientific and Technical Research. 12(5): 9566-9571. 

  24. Gelgelu, M.G., Abebe, T.K. and Mulugeta, W. (2023). Prevalence of bovine mastitis, Associated risk factors and major bacterial causes in and around Sagure town, arsi zone, Oromia, Ethiopia. Journal of Reproduction and Infertility. 14(1): 01-09. https://doi.org/10.5829/idosi.jri.2023.01.09.

  25. Ginger, L., Ledoux, D., Bouchon, M., Rautenbach, I., Bagnard, C., Lurier, T., Foucras, G., Germon, P., Durand, D. and Des Roches, A.D.B. (2023). Using behavioral observations in freestalls and at milking to improve pain detection in dairy cows after lipopolysaccharide-induced clinical mastitis. Journal of Dairy Science. 106(8): 5606-5625. https://doi.org/ 10.3168/jds.2022-22533.

  26. Girma, A. and Tamir, D. (2022). Prevalence of bovine mastitis and its associated risk factors among dairy cows in Ethiopia during 2005-2022: A systematic review and meta analysis. Veterinary Medicine International. 2022(1): 7775197. https://doi.org/10.1155/2022/7775197.

  27. Hadef, L., Hamad, B. and Aggad, H. (2022). Risk factors associated with subclinical mastitis and its effect on physico-mineral features of camel milk. Tropical Animal Health and Production. 54(4): 224. https://doi.org/10.1007/s11250-022-03220-9.

  28. Harjanti, D.W. and Sambodho, P. (2020). Effects of mastitis on milk production and composition in dairy cows. Earth and Environmental Science. 518(1): 012032. https://doi.org/ 10.1088/1755-1315/518/1/012032.

  29. Hogeveen, H., Huijps, K. and Lam, T.J.G.M. (2011). Economic aspects of mastitis: New developments. New Zealand Veterinary Journal. 59(1): 16-23.https://doi.org/10.1080/00480169. 2011.547165.

  30. Ibrahim, N., Regassa, F., Yilma, T. and Tolosa, T. (2023). Impact of subclinical mastitis on uterine health, reproductive perfor- mances and hormonal profile of Zebu ´ Friesian crossbred dairy cows in and around Jimma town dairy farms, Ethiopia. Heliyon. 9(6). https://doi.org/10.1002/vms3.1420.

  31. Kabui, S., Kimani, J., Ngugi, C. and Kagira, J. (2024). Prevalence and antimicrobial resistance profiles of mastitis causing bacteria isolated from dairy goats in Mukurweini Sub County, Nyeri County Kenya. Veterinary Medicine and Science.  10(3): 1420. https://doi.org/10.1002/vms3.1420.

  32. Kagira, J.M., Ngotho, M., Mugo, E., Kiplimo, M. and Maina, N. (2022). 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. 9(3): 36-45.

  33. Karzis, J., Petzer, I.M., Donkin, E.F., Naidoo, V. and Etter, E.M. (2020). Surveillance of antibiotic resistance of maltose-negative Staphylococcus aureus in South African dairy herds.  Antibiotics. 9(9): 616. https://doi.org/10.3390/antibiotics 9090616.

  34. Khasapane, N.G., Khumalo, Z.T.H., Kwenda, S., Nkhebenyane, S.J. and Thekisoe, O. (2023). Characterisation of milk microbiota from subclinical mastitis of apparent healthy dairy cattle in Free State Province, South Africa. Veterinary Sciences. 10(10): 616. https://doi.org/10.3390/vetsci10100616.

  35. Kidanu, S. (2022). Prevalence of Mastitis and its Associated Risk Factors Local and Crossbred Dairy Cows of Small Holder Farmers in Machakel District, Northwest Ethiopia (Doctoral dissertation).

  36. Kitila, G., Kebede, B. and Wakgari, M. (2021). Prevalence, aetiology and risk factors of mastitis of dairy cows kept under extensive management system in west Wollega, western Oromia, Ethiopia. Veterinary Medicine and Science. 7(5): 1593-1599. https://doi.org/10.1002/vms3.503.

  37. Krueger, A.K. (2019). Reconstruction and validation of the integrated diagnostic system for dairy cow welfare (IDEAL) to assess real-time animal well-being on confined and grazing dairy farms.

  38. Kumar, N., Manimaran, A., Kumaresan, A., Jeyakumar, S., Sreela, L., Mooventhan, P. and Sivaram, M. (2017). Mastitis effects on reproductive performance in dairy cattle: A review. Tropical Animal Health and Production. 49: 663-673. https://doi.org/10.1007/s11250-017-1253-4.

  39. Kumar, P., Deora, A., Himanshu, S., Sharma, S., Mittal, D., Bhanot, V., Prakash, A., Yadav, R. and Diwaka, R.P. (2020). Bovine mastitis: A review. Middle-East Journal of Scientific Research. 28: 497-507. https://doi.org/10.5829/idosi.mejsr. 2020.497.507.

  40. Kumari, T., Bhakat, C. and Choudhary, R.K. (2018). A review on subclinical mastitis in dairy cattle. International Indian Journal of Pure and Applied Biosciences. 6(2): 1291-1299. http://dx.doi. org/10.18782/2320-7051.6173.

  41. Kwaga, J.K.P., Bello, M., Raji, M.A., Maitala, Y.S. and Junaidu, K. (2019). Prevalence and antibiotic susceptibility of methicillin resistant Staphylococcus aureus (MRSA) isolated from bovine mastitis in settled Fulani herds in Kaduna State. Nigerian Veterinary Journal. 40(3): 190-200. https:// doi.org/10.4314/nvj.v40i3.3.

  42. Lahiri, P. (2023). Understanding the pathophysiology of bovine digital dermatitis (Doctoral dissertation, University of Calgary).

  43. Lakew, B.T., Fayera, T. and Ali, Y.M. (2019). Risk factors for bovine mastitis with the isolation and identification of Streptococcus agalactiae from farms in and around Haramaya district, eastern Ethiopia. Tropical Animal Health and Production. 51: 1507-1513. https://doi.org/10.1007/s11250-019- 01838-w.

  44. Liang, Z., Shen, J., Liu, J., Sun, X., Yang, Y., Lv, Y., Zheng, J., Mou, X., Li, H., Ding, X. and Yang, F. (2023). Prevalence and characteri- zation of Serratia marcescens isolated from clinical bovine mastitis cases in Ningxia Hui Autonomous Region of China.  Infection and Drug Resistance. 2727-2735. https://doi.org/ 10.2147/idr.s408632.

  45. Makatu, M.Y., Alcindo, J.F., Ramos, G.C.F., Bresciani, K.D.S. and Marinho, M. (2021). Sanitary practices associated with animal welfare in the control of mastitis in the dairy herd. Research, Society and Development. 10(17): 102101724467- 102101724467.https://doi.org/10.33448/rsd-v10i17. 24467.

  46. Makolo, D., Suleiman, A.B., Olonitola, O.S., Bello, M. and Ahmadu, I. (2020). Genotypic identification of coliforms isolated from cases of subclinical mastitis among pastoral herds in parts of Kaduna State, Nigeria. African Journal of Clinical and Experimental Microbiology. 21(2): 114-122. https:// doi.org/10.4314/ajcem.v21i2.5.

  47. Makolo, D., Suleiman, A.B., Olonitola, O.S., Bello, M., Alfa, M.I., Ahmadu, I. and Awulu, F.O. (2019). Antimicrobial susceptibility profile of coliforms from bovine mastitis cases among pastoral herds in parts of Kaduna State, Nigeria: Curbing the environmental health risk. Asian Journal of Advanced Research and Reports. 3(2): 1-12.

  48. Mbindyo, C.M., Gitao, G.C. and Mulei, C.M. (2020). Prevalence, aetiology and risk factors of mastitis in dairy cattle in Embu and Kajiado Counties, Kenya. Veterinary Medicine International.  2020(1): 8831172. https://doi.org/10.1155/2020/ 8831172.

  49. Michira, L., Kagira, J., Maina, N., Waititu, K., Kiboi, D., Ongera, E. and Ngotho, M. (2023). Prevalence of subclinical mastitis associated risk factors and antimicrobial susceptibility pattern of bacteria isolated from milk of dairy cattle in Kajiado Central sub county, Kenya. Veterinary Medicine and Science.  9(6): 2885-2892. https://doi.org/10.1002/vms3.1291.

  50. Mooventhan, P., Manimaran, A., Kumar, R.S., Selvan, A.S. and Prakash, M.A. (2016). Indigenous ethnoveterinary medicinal practices for management of mastitis in dairy cattle. Indian Journal of Animal  Research. 50(1): 137-139. https://doi.org/10. 18805/ijar.8568.

  51. Motaung, T.E., Petrovski, K.R., Petzer, I.M., Thekisoe, O. and Tsilo, T.J. (2017). Importance of bovine mastitis in Africa. Animal Health Research Reviews. 18(1): 58-69. https://doi.org/ 10.1017/S1466252317000032.

  52. Mphahlele, M.P., Oguttu, J.W., Petzer, I.M. and Qekwana, D.N. (2020). Prevalence and antimicrobial drug resistance of Staphylococcus aureus isolated from cow milk samples. Veterinary World. 13(12): 2736.  https://doi.org/10.14202/vetworld.2020. 2736-2742.

  53. Muturi, E.W. (2020). Effect of mastitis on milk production in dairy cows in Kenya. Journal of Animal Health. 2(1): 85-91.

  54. Ndirangu, P.N., Kipronoh, A.K., Mungube, E.O., Ogali, I.N., Omwenga, S.G., Ndung’u, D.N. and Maichomo, M.W. (2022). Prevalence of bovine mastitis and antimicrobial sensitivities of the bacterial causes in smallholder farms of Kisumu County, Kenya. Journal of Agriculture and Rural Development in the Tropics and Subtropics (JARTS). 123(2): 247-255. https://doi.org/10.17170/kobra-202212057194.

  55. Negash, S. (2023). Review on bovine mastitis and assessments of its associated risk factors in lactating dairy cows. International Journal of Advanced Research in Biological Sciences. 10(3): 59-65. http://dx.doi.org/10.22192/ijarbs. 2023.10.03.006.

  56. Ngu Ngwa, V., Cuteri, V., Awah-Ndukum, J., Viban Tangwa, B., Tanyi Manchang, K. and Attili, A. (2020). Bacterial pathogens involved in bovine mastitis and their antibiotic resistance patterns in the Adamawa region of Cameroon. Journal of Dairy Research and Technology. 3(1): 1-8. https:// hdl.handle.net/11581/434797.

  57. Nyakiti, A.A.O., Oliech, G.W.O. and Osano, O. (2022). Mastitis incidences and antibiotic resistance in bovines in uasin gishu county, Kenya. Africa Environmental Review Journal. 5(2): 128-143.

  58. Nyokabi, S., Luning, P.A., de Boer, I.J., Korir, L., Muunda, E., Bebe, B.O., Lindahl, J., Bett, B. and Oosting, S.J. (2021). Milk quality and hygiene: Knowledge, attitudes and practices of smallholder dairy farmers in central Kenya. Food Control. 130: 108303. https://doi.org/10.1016/j.foodcont. 2021.108303.

  59. Olatoye, O., Amosun, A., Ogbu, U. and Okunlade, Y. (2018). Bulk tank somatic cell counts and associated microbial quality of milk from selected dairy cattle herds in Oyo State, Nigeria. Italian Journal of Food Safety. 7(2).

  60. Otenga, F.O. (2023). Risk factors of sub-clinical mastitis, antibiogram and genotypic analysis of Staphylococcus spp. and enterobacteria-resistant bacteria isolated from humans and lactating dairy cows from smallholder farms in Gatundu sub-County, Kenya (Doctoral dissertation, JKUAT-COPAS).

  61. Paramasivam, R., Gopal, D.R., Dhandapani, R., Subbarayalu, R., Elangovan, M.P., Prabhu, B., Veerappan, V., Nandheeswaran, A., Paramasivam, S. and Muthupandian, S. (2023). Is AMR in dairy products a threat to human health? An updated review on the origin, prevention, treatment and economic impacts of subclinical mastitis. Infection and Drug Resistance. 155-178.  https://doi.org/10.2147/idr.s384776.

  62. Patel, K., Godden, S.M., Royster, E.E., Crooker, B.A., Johnson, T.J., Smith, E.A. and Sreevatsan, S. (2021). Prevalence, antibiotic resistance, virulence and genetic diversity of Staphy- lococcus aureus isolated from bulk tank milk samples of US dairy herds. Biomechanical Genomics. 22(1): 367. https://doi.org/10.1186/s12864-021-07603-4.

  63. Petzer, I.M., Blignaut, D. and Thompson, P. (2018). Prevalence of mastitis pathogens in South African pasture-based and total mixed ration-based dairies during 2008 and 2013.  Onderstepoort Journal of Veterinary Research. 85(1): 1-7. https://hdl. handle.net/10520/EJC-ed5590817.

  64. Phophi, L., Petzer, I.M. and Qekwana, D.N. (2019). Antimicrobial resistance patterns and biofilm formation of coagulase- negative Staphylococcus species isolated from subclinical  mastitis cow milk samples submitted to the Onderstepoort Milk Laboratory. Biomechanical Veterinary Research. 15: 1-9. https://doi.org/10.1186/s12917-019-2175-3.

  65. Rodríguez, Z., Cabrera, V.E., Hogeveen, H. and Ruegg, P.L. (2024). Economic impact of subclinical mastitis treatment in early lactation using intramammary nisin. Journal of Dairy Science. 107(7): 4634-4645. https://doi.org/10.3168/jds.2023- 24311.

  66. Singh, A.K. (2022). A comprehensive review on subclinical mastitis in dairy animals: Pathogenesis, factors associated, prevalence, economic losses and management strategies. Cabi Reviews. 3. http://dx.doi.org/10.1079/cabireviews 202217057.

  67. Sadiq, M.B., Ramanoon, S.Z., Shaik Mossadeq, W.M., Mansor, R. and Syed-Hussain, S.S. (2020). Cow- and herd-level factors associated with lameness in dairy farms in Peninsular Malaysia. Preventive Veterinary Medicine. 105163. https:// doi.org/10.1016/j.prevetmed.2020.105163.

  68. Schmidt, A.P., Vieira, L.V., Barbosa, A.A., Marins, L., Corrêa, M.N., Del Pino, F.A.B., Brauner, C.C., Rabassa, V.R., de Oliveira Feijó, J. and Schmitt, E. (2021). Use of the rumination profile through collar sensors for mastitis diagnosis in dairy cows. Acta Scientiae Veterinariae. 49. https://doi.org/ 10.22456/1679-9216.108269.

  69. Schunig, R., Busanello, M., Nogara, K.F. and Zopollatto, M. (2024). Cow-level risk factors associated with the increase in somatic cell count and the occurrence of subclinical mastitis in Brazilian Holstein and Jersey dairy cows.  Preventive Veterinary Medicine. 227: 106208. https:// doi.org/10.3390/ani11082255.

  70. Sharun, K., Dhama, K., Tiwari, R., Gugjoo, M.B., Iqbal Yatoo, M., Patel, S.K., Pathak, M., Karthik, K., Khurana, S.K., Singh, R., Puvvala, B., Amarpal, Singh, R., Singh, K.P. and Chaicumpa, W. (2021). Advances in therapeutic and managemental approaches of bovine mastitis: A comprehensive review.  The Veterinary Quarterly. 41(1): 107-136. https://doi.org/ 10.1080/01652176.2021.1882713.

  71. Singha, S., Koop, G., Persson, Y., Hossain, D., Scanlon, L., Derks, M., Hoque, M.A. and Rahman, M.M. (2021). Incidence, etiology and risk factors of clinical mastitis in dairy cows under semi-tropical circumstances in Chattogram, Bangladesh. Animals. 11(8): 2255. https://doi.org/10.3390/ani1108 2255.

  72. Sinha, R., Bhakat M., Mohanty K.T., Ranjan A., Kumar R., Lone A.S., Rahim A., Paray R.A., Khosla K., Danish Z. (2018). Infrared thermography as non-invasive technique for early detection  of mastitis in dairy animals-A review. Asian Journal of Dairy and Food Research. 37(1): 1-6. https://doi.org/ 10.18805/ajdfr.R-1746.

  73. Sombie, J.I.N., Kagira, J. and Maina, N. (2022). Prevalence and Antibiogram of Escherichia coli  and  Staphylococcus  spp.      Isolated from cattle milk products sold in Juja sub-county, Kenya. Journal of Tropical Medicine. 2022: 5251197. https://doi.org/10.1155/2022/5251197.

  74. Taoana, L.K. (2005). The effect of management on mastitis incidence in dairy cows in Qwaqwa (Doctoral dissertation, Bloemfontein: Central University of Technology, Free State).

  75. Tegegne, D.T., Yalew, S.T., Emeru, B.A., Messele, Y.E., Werid, G.M., Bora, S.K. and Bobura, M.D. 2020. Study of prevalence associated risk factors and causative bacteria of bovine mastitis in Ethiopia. International Journal of Veterinary Science and Technology. 4(1): 001-006.

  76. Tezera, M. and Aman A.E. (2021). Prevalence and associated risk factors of Bovine mastitis in dairy cows in and around Assosa town, Benishangul Gumuz Regional State,Western Ethiopia. Veterinary Medicine and Science. 7(4):1280- 1286. https://doi.org/10.1002/vms3.454.

  77. Thomas, A., Chothe, S., Byukusenge, M., Mathews, T., Pierre, T., Kariyawasam, S., Luley, E., Kuchipudi, S. and Jayarao, B. (2021). Prevalence and distribution of multilocus sequence types of Staphylococcus aureus isolated from bulk tank milk and cows with mastitis in Pennsylvania. 16(3): 0248528. https://doi.org/10.1371/journal.pone. 0248528.

  78. Thomas, F.C., Alarape, O.O., Oliwo, O.M., Omoshaba, E., Ojo, O.E.,    Oyewusi, J.A., Ajibola, E.S., (2021). Somatic cell counts and bacteria in milk from two nomadic herds in Abeokuta, Nigeria. Sokoto Journal of Veterinary Sciences. 2: 112- 120.  https://doi.org/10.4314/sokjvs.v19i2.6.

  79. Tiwari, R.K., Ranjan Kumar, R.K.., Kumar, A.S., Kumar, S., Ghosh, S. and Upadhaya, B. (2020). Use of dry cow therapy for control of mastitis in dairy animals. Journal of Krishi Vigyan.  8: 303-307. https://doi.org/10.5958/2349-4433. 2020.00061.6.

  80. Ulla, M.K., Kotresh, A.M., Krishna, L.R., Madhavaprasad, C.B., Shridhar, N.B., Shambulingappa, B.E. and Rudresh, B.H. (2021). Effect of extra-mammary diseases on udder health and biochemical changes in crossbred cows with subclinical mastitis. Asian Journal of Dairy and Food Research. 40(2):172-176. https://doi.org/10.18805/ ajdfr.DR-1622.

  81. Umar, A., Whong, C.M.Z., Abdullahi, I.O., Usman, M. (2023). Bacteriolo- gical quality of fresh cow milk from dairy farms in parts of Kaduna State, Nigeria. Internal  Medicine Journal. 1(5): 214-223. https://doi.org/10.21203/rs.3.rs-3385467/v1.

  82. Umaru, G.A., Kwaga, J.K.P., Bello, M., Raji, M.A., Maitala, Y.S. (2017). Occurrence of bovine mastitis and isolation of Staphyloccocus species from fresh cow milk in settled Fulani herds in Kaduna State, Nigeria. Bayero Journal of Pure and Applied Sciences. 10: 259-263. https:// doi.org/10.4314/bajopas.v10i1.38.

  83. Van der Westhuizen, C.G. (2021). Zoonotic diseases in high-risk populations in the Free State province, South Africa.

  84. Vargova, M., Vyrostkova, J., Lakticova, K.V. and Zigo, F. (2023). Effectiveness of sanitation regime in a milking parlour to control microbial contamination of teats and surfaces teat cups. Annals of Agricultural and Environmental Medicine. 30(1): 55-60. https://doi.org/10.26444/aaem/ 161037.

  85. Wang, K., Cha, J., Liu, K., Deng, J., Yang, B., Xu, H., Wang, J., Zhang, L., Gu, X., Huang, C. and Qu, W. (2022). The prevalence of bovine mastitis-associated Staphylococcus aureus in China and its antimicrobial resistance rate: A meta-analysis. Frontiers in Veterinary Science. 9: 1006676. https:// doi.org/10.3389/fvets.2022.1006676.

  86. Yehia, S.G., Saad, M.F., Mosallam, T.E., Abdel-Mobdy, A.E., Megahed, E.A., Aly, H.H., Salem, N.Y., Ramadan, E.S. (2024). Evaluation of oxidative stress, compositional and biochemical changes in milk and serum of cows with subclinical mastitis. Comparative Clinical Pathology. 1-10.  https:// doi.org/10.1007/s00580-024-03582-6.

  87. Zigo, F., Eleèko, J., Farkašová, Z., Zigová, M., Vasi¾, M., Ondrašovièová,  S., Kudìlková, L. (2019). Preventive methods in reduction of mastitis pathogens in dairy cows. Occurrence and Prevention of Mastitis in Dairy Farms Situated in Marginal Regions.

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