Seeta Dewali, Rimpy Sharma, Mokshi Sharma, Azra Naz, Vishakha Arya, Renu Gahtori, Kiran Arya, Jyoti Garjola, Anshika Tripathi, Palak Narang, Bhawana Fartyal, Kajal Bora, Deepak Kumar Arya, Satpal Singh Bisht and Netrapal Sharma*

Department of Zoology, D. S. B Campus, Kumaun University, Uttarakhand, India

*Corresponding Author:Netrapal Sharma, Department of Zoology, D. S. B Campus, Kumaun University, Uttarakhand, India.

Received: June 23, 2022; Published: July 04, 2022

Abstract

Domesticated cattle represent not only a large source of sustenance but also a source of income for billions of people. The dairy sector has a very significant role in the Indian economy, but many tasks need to be addressed in order to preserve governmental agencies, in order to maintain the competitiveness and long-term viability of the industry, we have been attempting to identify healthy dairy cows with enhanced or decreased potential. For many years, several diseases in cattle, including the development of mastitis, were reducing the milk industry. Furthermore, the disease has a significant detrimental influence on dairy industry production as a result of poor milk quality and decreased industrial yield. The present review aimed to provide complete information on mastitis in one place and to be helpful for researchers.

Keywords: Bacteria; Antibiotic; Mastitis; Dairy animals; Natural Products

References

1. Fagiolo and O Lai “Mastitis in buffalo”. Italian Journal of Animal Science2 (2007): 200-206.
2. Pamela L and Ruegg DVM MPVM. “Dip. ABVP (Dairy Practice) Department of Dairy Science, 1675 Observatory Dr., University of Wisconsin, Madison, WI53706 (2011).
3. Cheng WN and Han SG. “Bovine mastitis: risk factors, therapeutic strategies, and alternative treatments - A review”. Asian-Australasian Journal of Animal Sciences11 (2020): 1699-1713.
4. Vakkamäki J., et al. “Bacteriological etiology and treatment of mastitis in Finnish dairy herds”. Acta Veterinaria Scandinavica 59 (2017): 33.
5. Sharif A., et al. “Mastitis control in dairy production”. Journal of Agriculture and Social Sciences 5 (2009): 102-105.
6. Heikkilä AM., et al. “Pathogen-specific production losses in bovine mastitis”. Journal of Dairy Science 101 (2018): 9493-9504.
7. Saidani M., et al. “Epidemiology, antimicrobial resistance, and extended-spectrum Beta-lactamase-producing enterobacteriaceae in clinical bovine mastitis in Tunisia”. Microbial Drug Resistance 24 (2018): 1242-1248.
8. Jensen K., et al. “Escherichia coli- and Staphylococcus aureus-induced mastitis differentially modulate transcriptional responses in neighbouring uninfected bovine mammary gland quarters”. BMC Genomics 14 (2013): 36.
9. Davies PL., et al. “Molecular epidemiology of Streptococcus uberis clinical mastitis in daily herds: Strain heterogeneity and transmission”. Journal of Clinical Microbiology 54 (2016): 68-74.
10. Ogorevc J., et al. “Database of cattle candidate genes and genetic markers for milk production and mastitis”. Animal Genetics6 (2009): 832-851.
11. Halasa T., et al. “Economic effects of bovine mastitis and mastitis management”. Veterinary Quarterly 29 (2007): 18-31.
12. Ogorevc J., et al. “Database of cattle candidate genes and genetic markers for milk production and mastitis”. Animal Genetics6 (2009): 832-851.
13. Sharma BS., et al. “Detection and characterization of amplified fragment length “polymorphism markers for clinical mastitis in Canadian Holsteins”. Journal of Dairy Science 89 (2006): 3653-3663.
14. Ron M., et al. “Combining mouse mammary gland gene expression and comparative mapping for the identification of candidate genes for QTL of milk production traits in cattle”. BMC Genomics 8 (2007): 183.
15. Miroslav Benić., et al. “Bovine mastitis: a persistent and evolving problem requiring novel approaches for its control - a review”. VETERINARSKI ARHIV4 (2019): 535-557.
16. Takeuchi O and S Akira. “Pattern recognition receptors and inflammation”. Cell6 (2010): 805-812.
17. Zohaib A., et al. “The Role of Ubiquitination in Regulation of Innate Immune Signaling”. Current Issues in Molecular Biology 18 (2016): 1-10.
18. De Schepper S., et al. “Deciphering the palaeoecology of Late Pliocene and Early Pleistocene dinoflagellate cysts”. Palaeogeography, Palaeoclimatology, Palaeoecology1-2 (2011): 17-32.
19. Zhang LP., et al. “Toll-like receptor 2 gene polymorphism and its relationship with SCS in dairy cattle”. Animal Biotechnology (2009).
20. Kawai T and Akira S. “The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors”. Nature Immunology (2010).
21. Novak K. “Functional polymorphisms in Toll-like receptor genes for innate immunity in farm animals”. Veterinary Immunology and Immunopathology (2014).
22. Akira S., et al. “Pathogen recognition and innate immunity”. Cell4 (2006): 783-801.
23. Rehfeld IS., et al. “Clinical, hematological and biochemical parameters of dairy cows experimentally infected with Vaccinia virus”. Research in Veterinary Science 95-2 (2013): 752-757.
24. Yoneyama M., et al. “Viral RNA detection by RIG-I-like receptors”. Current Opinion in Immunology 32 (2015): 48-53.
25. Schlee M. “Master sensors of pathogenic RNA - RIG-I like receptors”. Immunobiology11 (2013): 1322- 1335.
26. Kowalinski E., et al. “Structural basis for the activation of innate immune pattern-recognition receptor RIG-I by viral RNA”. Cell2 (2011): 423-435.
27. Hou F., et al. “MAVS forms functional prion-like aggregates to activate and propagate antiviral innate immune response”. Cell3 (2011): 448-461.
28. Latz E., et al. “Activation and regulation of the inflammasomes”. Nature Reviews Immunology 6 (2013): 397-411.
29. Kanneganti TD., et al. “Intracellular NOD-like receptors in host defense and disease”. Immunity4 (2007): 549-559.
30. Cui J., et al. “NLRP4 negatively regulates type I interferon signaling by targeting the kinase TBK1 for degradation via the ubiquitin ligase DTX4”. Nature Immunology 4 (2012): 387-395.
31. Miao EA., et al. “Innate immune detection of the type III secretion apparatus through the NLRC4 inflammasome”. Proceedings of the National Academy of Sciences of the United States of America A7 (2010): 3076-3080.
32. Franchi L., et al. “Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1beta in salmonella-infected macrophages”. Nature Immunology 6 (2006): 576-582.
33. Pal A., et al. “Molecular Characterization of Bu-1 and TLR2 Gene in Haringhata Black Chicken”. Genomics1 (2019) :472-483.
34. Cheng Z., et al. “Combined effects of the plant growth-promoting bacterium Pseudomonas putidaUW4 and salinity stress on the Brassica napus proteome”. Applied Soil Ecology 61 (2012): 255-263.
35. Rosas-Taraco AG., et al. “CD14 C (-159) T polymorphism is a risk factor for development of pulmonary tuberculosis”. The Journal of Infectious Diseases 196 (2007): 1698-1706.
36. Pal A., et al. “Molecular characterization and SNP detection of CD14 gene of crossbred cattle”. Molecular Biology International (2011): 507346.
37. Crist WL., et al. “Mastitis and Its Control (2007).
38. Talbot BG and Lacasse P. “Progress in the development of mastitis vaccines”. Livestock Production Science 98 (2005): 101-113.
39. Zecconi A., et al. “Total and differential cell counts as a tool to identify intramammary infections in cows after calving”. Animals2 (2021): 727.
40. Baskaran AS., et al. “Antibacterial effect of plant-derived antimicrobials on major bacterial mastitis pathogens in vitro”. Journal of Dairy Science 4 (2009): 1423-1429.
41. Jeong CH., et al. “Bee venom decreases LPS-induced inflammatory responses in bovine mammary epithelial cells”. Journal of Microbiology and Biotechnology 27 (2017): 1827-1836.
42. Wang K., et al. “Effects of Chinese propolis in protecting bovine mammary epithelial cells against mastitis pathogens-induced cell damage”. Mediators of Inflammation2016 (2016).
43. El Hafez., et al. “Development of new strategy for non-antibiotic therapy: bovine lactoferrin has a potent antimicrobial and immunomodulator effects”. Advances in Infectious Diseases 3 (2013): 185-192.
44. Shaheen M., et al. “A treatise on bovine mastitis: disease and disease economics, etiological basis, risk factors, impact on human health, therapeutic management, prevention and control strategy”. Advances in Dairy Research 4 (2016): 1.
45. Pieterse R., et al. “Mode of action and In Vitro susceptibility of mastitis pathogens to macedocin ST91KM and preparation of a teat seal containing the bacteriocin”. Brazilian Journal of Microbiology 1 (2010): 133-145.
46. Rainard P. “Tackling mastitis in dairy cows”. Nature Biotechnology 23 (2005): 430-432.
47. Rasheed A., et al. “A review on bovinemastitis with special focus on CD4 as a potential candidate gene for mastitis resistance - a review”. Annals of Animal Science (2020).
48. Pamela L Ruegg “A 100-Year Review: Mastitis detection, management, and prevention”. Journal of Dairy Science 100 (2017): 10381-10397.
49. Ogorevc J., et al. “Database of cattle candidate genes and genetic markers for milk production and mastitis”. Animal Genetics 6 (2009): 832-851.
50. Sharma N., et al. “Impact of Mastitis on Reproductive Performance in Dairy Animals: A Review”. Theriogenology Insight1 (2017): 41-49.

Citation

Citation: Netrapal Sharma., et al. “Genetics and Therapies of Mastitis in Common Milch Animals: A Review". Acta Scientific Veterinary Sciences 4.8 (2022): 21-31.

Copyright

Copyright: © 2022 Netrapal Sharma., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.