DOI QR코드

DOI QR Code

Cytokine expression pattern in milk somatic cells of subclinical mastitis-affected cattle analyzed by real time PCR

  • Bhatt, Vaibhav D. (Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences) ;
  • Khade, Prasad S. (Department of Veterinary Medicine, College of Veterinary Science and Animal Husbandry, Anand Agricultural University) ;
  • Tarate, Sagar B. (Department of Animal Genetics and Breeding, College of Veterinary Science and Animal Husbandry, Anand Agricultural University) ;
  • Tripathi, Ajai K. (Department of Animal Biotechnology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University) ;
  • Nauriyal, Dev S. (Department of Veterinary Medicine, College of Veterinary Science and Animal Husbandry, Anand Agricultural University) ;
  • Rank, Dharamshi N. (Department of Animal Genetics and Breeding, College of Veterinary Science and Animal Husbandry, Anand Agricultural University) ;
  • Kunjadia, Anju P. (Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences) ;
  • Joshi, Chaitanya G. (Department of Animal Biotechnology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University)
  • Received : 2012.03.20
  • Accepted : 2012.10.25
  • Published : 2012.12.31

Abstract

The expression profiles of inflammatory cytokines viz. interleukins (IL)-6, IL-8, IL-12, granulocyte macrophage-colony stimulating factor, interferon-${\gamma}$ and tumor necrosis factor-${\alpha}$ in response to subclinical mastitis in indigenous cattle breed Kankrej (n = 6), Gir (Bos indicus) (n = 12) and crossbred (Bos taurus${\times}$Bos indicus) (n = 7) were investigated using quantitative real time PCR. Significant correlation (p < 0.05) was observed between total bacterial load and somatic cell count (SCC) in all three breeds of cattle. All the cytokines were observed to be up-regulated compared to cows with healthy quarters, however, level of their expression varied among three breeds of cattle. In Kankrej most cytokines were found to be transcribed to higher levels than in other two breeds; the milk had higher load of bacteria but not so high SCC, implying that Kankrej has a higher inherent resistance against mastitis. The results of present study indicated that mammary glands of crossbred cattle are more sensitive to bacterial infection than indigenous breed of cattle as they elicit immune response at lower bacterial load and result into higher SCC. Research on identification of factors responsible for differentially expressed cytokines profiles and use of cytokines as immunomodulatory tools can pave way for formulating control strategies against bovine mastitis.

Keywords

References

  1. Alluwaimi AM, Cullor JS. Cytokines gene expression patterns of bovine milk during middle and late stages of lactation. J Vet Med B Infect Dis Vet Publich Health 2002, 49, 105-110. https://doi.org/10.1046/j.1439-0450.2002.00515.x
  2. Alluwaimi AM, Leutenegger CM, Farver TB, Rossitto PV, Smith WL, Cullor JS. The cytokine markers in Staphylococcus aureus mastitis of bovine mammary gland. J Vet Med B Infect Dis Vet Public Health 2003, 50, 105-111. https://doi.org/10.1046/j.1439-0450.2003.00628.x
  3. Bannerman DD, Chockalingam A, Paape MJ, Hope JC. The bovine innate immune response during experimentallyinduced Pseudomonas aeruginosa mastitis. Vet Immunol Immunopathol 2005, 107, 201-215. https://doi.org/10.1016/j.vetimm.2005.04.012
  4. Blum JW, Dosogne H, Hoeben D, Vangroenweghe F, Hammond HM, Bruckmaier RM, Burvenich C. Tumor necrosis factor-alpha and nitrite/nitrate responses during acute mastitis induced by Escherichia coli infection and endotoxin in dairy cows. Domest Anim Endocrinol 2000, 19, 223-235. https://doi.org/10.1016/S0739-7240(00)00079-5
  5. Bradley A. Bovine mastitis: an evolving disease. Vet J 2002, 164, 116-128. https://doi.org/10.1053/tvjl.2002.0724
  6. Burvenich C, Van Merris V, Mehrzad J, Diez-Fraile A, Duchateau L. Severity of E. coli mastitis is mainly determined by cow factors. Vet Res 2003, 34, 521-564. https://doi.org/10.1051/vetres:2003023
  7. Campos M, Godson DL, Hughes HPA, Babiuk LA. Cytokine application in infectious diseases. In: Goddeeris BML, Morrison WI (eds.). Cell-mediated Immunity in Ruminants. 1st ed. pp. 229-37. CRC Press, Boca Raton, 1994.
  8. Caracciolo D, Clark SC, Rovera G. Human interleukin-6 supports granulocytic differentiation of hematopoietic progenitor cells and acts synergistically with GM-CSF. 1989, 73, 666-670.
  9. Chomczynski P, Sacchi N. The single-step method of RNA isolation by acid guanidinium thiocyanate-phenolchloroform extraction: twenty-something years on. Nat Protoc 2006, 1, 581-585. https://doi.org/10.1038/nprot.2006.83
  10. Cremonesi P, Castiglioni B, Malferrari G, Biunno I, Vimercati C, Moroni P, Morandi S, Luzzana M. Technical note: Improved method for rapid DNA extraction of mastitis pathogens directly from milk. J Dairy Sci 2006, 89, 163-169. https://doi.org/10.3168/jds.S0022-0302(06)72080-X
  11. DeGraves FJ, Fetrow J. Economics of mastitis and mastitis control. Vet Clin North Am Food Anim Pract 1993, 9, 421-434. https://doi.org/10.1016/S0749-0720(15)30611-3
  12. Devi BK, Shukla PC, Bagherwal RK. Incidence of subclinical mastitis in cows. Indian J Dairy Sci 1997, 50, 477-478.
  13. Dinarello CA. Molecular mechanisms in endotoxin fever. Agents Actions 1983, 13, 470-486. https://doi.org/10.1007/BF02176419
  14. Gaur GK, Kaushik SN, Garg RC. The Gir cattle breed of India - characteristics and present status. Anim Genet Resour Inf 2003, 33, 21-29. https://doi.org/10.1017/S1014233900001607
  15. Godson DL, Baca-Estrada ME, Babiuk LA. Application of bovine cytokines. In: Schijns VECJ, Horzinek MC (eds.). Cytokines in Vetetinary Medicine. 1 st ed. pp. 49, CAB International, New York, 1977.
  16. Hansen PJ, Soto P, Natzke RP. Mastitis and fertility in cattle - possible involvement of inflammation or immune activation in embryonic mortality. Am J Reprod Immunol 2004, 51, 294-301. https://doi.org/10.1111/j.1600-0897.2004.00160.x
  17. Hisaeda K, Hagiwara K, Eguchi J, Yamanaka H, Kirisawa R, Iwai H. Interferon-gamma and tumor necrosis factor-${\alpha}$ levels in sera and whey of cattle with naturally occurring coliform mastitis. J Vet Med Sci 2001, 63, 1009- 1011. https://doi.org/10.1292/jvms.63.1009
  18. Hoeben D, Burvenich C, Trevisi E, Bertoni G, Hamann J, Bruckmaier RM, Blum JW. Role of endotoxin and TNF-alpha in the pathogenesis of experimentally induced coliform mastitis in periparturient cows. J Dairy Res 2000, 67, 503-514. https://doi.org/10.1017/S0022029900004489
  19. Kaplanski G, Marin V, Montero-Julian F, Mantovani A, Farnarier C. IL-6: a regulator of the transition from neutrophil to monocyte recruitment during inflammation. Trends Immunol 2003, 24, 25-29. https://doi.org/10.1016/S1471-4906(02)00013-3
  20. Kauf AC, Rosenbusch RF, Paape MJ, Bannerman DD. Innate immune response to intramammary Mycoplasma bovis infection. J Dairy Sci 2007, 90, 3336-3348. https://doi.org/10.3168/jds.2007-0058
  21. Kehrli ME Jr, Harp JA. Immunity in the mammary gland. Vet Clin North Am Food Anim Pract 2001, 17, 495-516. https://doi.org/10.1016/S0749-0720(15)30003-7
  22. Lee JW, Bannerman DD, Paape MJ, Huang MK, Zhao X. Characterization of cytokine expression in milk somatic cells during intramammary infections with Escherichia coli or Staphylococcus aureus by real-time PCR. Vet Res 2006, 37, 219-229. https://doi.org/10.1051/vetres:2005051
  23. Lohuis JA, Verheijden JH, Burvenich C, van Miert AS. Pathophysiological effects of endotoxins in ruminants. 2. Metabolic aspects. Vet Q 1988, 10, 117-125. https://doi.org/10.1080/01652176.1988.9694158
  24. Mason IL. A World Dictionary of Livestock Breeds, Types and Varieties. 4th ed. pp. 273, CAB International, Wallingford, 1996.
  25. Matsukawa A, Hogaboam CM, Lukacs NW, Kunkel SL. Chemokines and innate immunity. Rev Immunogenet 2000, 2, 339-358.
  26. Mosmann TR, Sad S. The expanding universe of T-cell subsets: Th1, Th2 and more. Immunol Today 1996, 17, 138-146. https://doi.org/10.1016/0167-5699(96)80606-2
  27. Mukaida N. Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases. Am J Physiol Lung Cell Mol Physiol 2003, 284, L566-577. https://doi.org/10.1152/ajplung.00233.2002
  28. Muyzer G, De Waal EC, Uitterlinden AG. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA. Appl Environ Microbiol 1993, 59, 695-700.
  29. Nakajima Y, Mikami O, Yoshioka M, Motoi Y, Ito T, Ishikawa Y, Fuse M, Nakano K, Yasukawa K. Elevated levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) activities in the sera and milk of cows with naturally occurring coliform mastitis. Res Vet Sci 1997, 62, 297-298. https://doi.org/10.1016/S0034-5288(97)90209-5
  30. Petrovski KR, Trajcev M, Buneski G. A review of the factors affecting the costs of bovine mastitis. J S Afr Vet Assoc 2006, 77, 52-60.
  31. Riollet C, Rainard P, Poutrel B. Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with Escherichia coli and Staphylococcus aureus. Clin Diagn Lab Immunol 2000, 7, 161-167.
  32. Sakemi Y, Tamura Y, Hagiwara K. Interleukin-6 in quarter milk as a further prediction marker for bovine subclinical mastitis. J Dairy Res 2011, 78, 118-121. https://doi.org/10.1017/S0022029910000828
  33. Sordillo LM, Shafer-Weaver K, DeRosa D. Immunobiology of the mammary gland. J Dairy Sci 1997, 80, 1851-1865. https://doi.org/10.3168/jds.S0022-0302(97)76121-6
  34. Taylor BC, Keefe RG, Dellinger JD, Nakamura Y, Cullor JS, Stott JL. T cell populations and cytokine expression in milk derived from normal and bacteriainfected bovine mammary glands. Cell Immunol 1997, 182, 68-76. https://doi.org/10.1006/cimm.1997.1215
  35. Tiwari A, Sisodia RS, Sharma RK, Misraulia KS, Garg UK. Incidence of sub-clinical mastitis in cows of Malwa region of Madhya Pradesh. Indian J Dairy Sci 2000, 53, 328-331.
  36. Trinchieri G. Interleukin-12 and the regulation of innate resistance and adaptive immunity. Nat Rev immunol 2003, 3, 133-146. https://doi.org/10.1038/nri1001
  37. Verma Ak, Nauriyal DS. Prevalence of bovine sub-clinical mastitis in organized dairy farms in central Gujrat. Indian J Vet Med 2009, 29, 13-16.
  38. Viguier C, Arora S, Gilmartin N, Welbeck K, O'kennedy R. Mastitis detection: current trends and future perspectives. Trends Biotechnol 2009, 27, 486-493. https://doi.org/10.1016/j.tibtech.2009.05.004
  39. Xing Z, Gauldie J, Cox G, Baumann H, Jordana M, Lei XF, Achong MK. IL-6 is an antiinflammatory cytokine required for controlling local or systemic acute inflammatory responses. J Clin Invest 1998, 101, 311-320. https://doi.org/10.1172/JCI1368