Differential expression of genes during mastitis in Holstein-Zebu crossbreed dairy cows

Genetics and Molecular Research

Volumn 10, Issue 3, 2011, Pages 1295-1303

  Fonseca, I ^a   Antunes, G R ^b   Paiva, D S ^b   Lange, C C ^c   Guimaraes S E F ^a   Martins, M F ^c  

^a FEDERAL UNIVERSITY OF VIÇOSA   (Brazil)

^b FEDERAL UNIVERSITY OF JUIZ DE FORA   (Brazil)

^c EMBRAPA CERRADOS   (Brazil)

Author keywords

Immune response; Real time PCR; Resistance to mastitis; Toll like receptor 2 gene

Indexed keywords

RNA;

ANIMAL EXPERIMENT; ARTICLE; COAGULASE NEGATIVE STAPHYLOCOCCUS; CONTROLLED STUDY; CORYNEBACTERIUM; CROSS BREEDING; DAIRY CATTLE; FOREBRAIN EMBRYONIC ZINC FINGER LIKE GENE; GENE EXPRESSION; INTERFERON GAMMA GENE; INTERLEUKIN 12 GENE; INTERLEUKIN 2 GENE; INTERLEUKIN 6 GENE; INTERLEUKIN 8 GENE; MASTITIS; MICROBIOLOGICAL EXAMINATION; MILK; NONHUMAN; REAL TIME POLYMERASE CHAIN REACTION; RNA EXTRACTION; SEMAPHORIN 5A GENE; STREPTOCOCCUS; STREPTOCOCCUS AGALACTIAE; TOLL LIKE RECEPTOR 2 GENE; TUMOR NECROSIS FACTOR ALPHA GENE;

ANIMALS; CATTLE; FEMALE; GENE EXPRESSION REGULATION; HYBRIDIZATION, GENETIC; IMMUNITY, INNATE; MASTITIS, BOVINE; PHENOTYPE; TOLL-LIKE RECEPTOR 2;

ANIMALIA; BOS; BOS INDICUS;

EID: 79960405572     PISSN: None     EISSN: 16765680     Source Type: Journal    
DOI: 10.4238/vol10-3gmr1096     Document Type: Article

References (40)

1. Alluwaimi AM, Leutenegger CM, Farver TB, Rossitto PV, et al. (2003). The cytokine markers in Staphylococcus aureus mastitis of bovine mammary gland. J. Vet. Med. B. Infect. Dis. Vet. Public Health 50: 105-111.
2. Bannerman DD, Paape MJ, Lee JW, Zhao X, et al. (2004a). Escherichia coli and Staphylococcus aureus elicit differential innate immune responses following intramammary infection. Clin. Diagn. Lab. Immunol. 11: 463-472.
3. Bannerman DD, Paape MJ, Hare WR and Hope JC (2004b). Characterization of the bovine innate immune response to intramammary infection with Klebsiella pneumoniae. J. Dairy Sci. 87: 2420-2432.
4. Bannerman DD, Chockalingam A, Paape MJ and Hope JC (2005). The bovine innate immune response during experimentally-induced Pseudomonas aeruginosa mastitis. Vet. Immunol. Immunopathol. 107: 201-215.
5. Bannerman DD, Rinaldi M, Vinyard BT, Laihia J, et al. (2009). Effects of intramammary infusion of cis-urocanic acid on mastitis-associated infammation and tissue injury in dairy cows. Am. J. Vet. Res. 70: 373-382.
6. Bradley A (2002). Bovine mastitis: an evolving disease. Vet. J. 164: 116-128.
7. Burvenich C, Van M, V, Mehrzad J, Diez-Fraile A, et al. (2003). Severity of E. coli mastitis is mainly determined by cow factors. Vet. Res. 34: 521-564.
8. Cates EA, Connor EE, Mosser DM and Bannerman DD (2009). Functional characterization of bovine TIRAP and MyD88 in mediating bacterial lipopolysaccharide-induced endothelial NF-kappaB activation and apoptosis. Comp. Immunol. Microbiol. Infect. Dis. 32: 477-490.
9. Corl CM, Gandy JC and Sordillo LM (2008). Platelet activating factor production and proinfammatory gene expression in endotoxin-challenged bovine mammary endothelial cells. J. Dairy Sci. 91: 3067-3078.
10. Detilleux JC, Koehler KJ, Freeman AE, Kehrli ME Jr, et al. (1994). Immunological parameters of periparturient Holstein cattle: genetic variation. J. Dairy Sci. 77: 2640-2650.
11. Embrapa Gado de Leite (2003). Sistema de Produção de Leite (Zona da Mata Atlântica). Available at [http://sistemasdeproducao.cnptia.embrapa.br/FontesHTML/Leite/Leite ZonadaMataAtlantica/racas1.html]. Accessed October 5, 2009.
12. Embrapa Gado de Leite (2008). Estatística do Leite. Available at [http://www.cnpgl.embrapa.br/nova/informacoes/estatisticas/producao/tabela0230.php]. Accessed October 5, 2009.
13. Ferens WA, Goff WL, Davis WC, Fox LK, et al. (1998). Induction of type 2 cytokines by a staphylococcal enterotoxin superantigen. J. Nat. Toxins. 7: 193-213.
14. Fonseca I, Silva PV, Lange CC and Guimarães MFM (2009). Expression profile of genes associated with mastitis in dairy cattle. Genet. Mol. Biol. 32: 776-781.
15. Goldammer T, Zerbe H, Molenaar A, Schuberth HJ, et al. (2004). Mastitis increases mammary mRNA abundance of beta-defensin 5, toll-like-receptor 2 (TLR2), and TLR4 but not TLR9 in cattle. Clin. Diagn. Lab. Immunol. 11: 174-185.
16. Griesbeck-Zilch B, Meyer HH, Kuhn CH, Schwerin M, et al. (2008). Staphylococcus aureus and Escherichia coli cause deviating expression profiles of cytokines and lactoferrin messenger ribonucleic acid in mammary epithelial cells. J.Dairy Sci. 91: 2215-2224.
17. Hirschfeld M, Ma Y, Weis JH, Vogel SN, et al. (2000). Cutting edge: re-purification of lipopolysaccharide eliminates signaling through both human and murine toll-like receptor 2. J. Immunol. 165: 618-622.
18. Ibeagha-Awemu EM, Lee JW, Ibeagha AE, Bannerman DD, et al. (2008). Bacterial lipopolysaccharide induces increased expression of toll-like receptor (TLR) 4 and downstream TLR signaling molecules in bovine mammary epithelial cells. Vet. Res. 39: 11.
19. Janeway CA, Tavers P, Walport M and Sholmchik MJ (2002). Imunologia: o Sistema Imune na Saúde e na Doença. Artmed, Porto Alegre.
20. Lahouassa H, Moussay E, Rainard P and Riollet C (2007). Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 38: 12-21.
21. Leutenegger CM, Alluwaimi AM, Smith WL, Perani L, et al. (2000). Quantitation of bovine cytokine mRNA in milk cells of healthy cattle by real-time TaqMan polymerase chain reaction. Vet. Immunol. Immunopathol. 77: 275-287.
22. Mount JA, Karrow NA, Caswell JL, Boermans HJ, et al. (2009). Assessment of bovine mammary chemokine gene expression in response to lipopolysaccharide, lipotechoic acid + peptidoglycan, and CpG oligodeoxynucleotide 2135. Can. J. Vet. Res. 73: 49-57.
23. NMC (1987). Laboratory and Field Handbook on Bovine Mastitis. NMC (National Mastitis Council), Arlington.
24. Oviedo-Boyso J, Valdez-Alarcon JJ, Cajero-Juarez M, Ochoa-Zarzosa A, et al. (2007). Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis. J. Infect. 54: 399-409.
25. Petrovski KR, Trajcev M and Buneski G (2006). A review of the factors affecting the costs of bovine mastitis. J. S. Afr. Vet. Assoc. 77: 52-60.
26. Rainard P and Riollet C (2006). Innate immunity of the bovine mammary gland. Vet. Res. 37: 369-400.
27. Rambeaud M, Almeida RA, Pighetti GM and Oliver SP (2003). Dynamics of leukocytes and cytokines during experimentally induced Streptococcus uberis mastitis. Vet. Immunol. Immunopathol. 96: 193-205.
28. REST (Relative Expression Software Tool) (2009). Available at [http://www.gene-quantifcation.de/rest-2009.html].Accessed July 19, 2010.
29. Riollet C, Rainard P and Poutrel B (2000). Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with Escherichia coli and Staphylococcus aureus. Clin. Diagn. Lab. Immunol. 7: 161-167.
30. Shuster DE, Kehrli ME Jr and Stevens MG (1993). Cytokine production during endotoxin-induced mastitis in lactating dairy cows. Am. J. Vet. Res. 54: 80-85.
31. Shuster DE, Kehrli ME Jr, Rainard P and Paape M (1997). Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli. Infect. Immun. 65: 3286-3292.
32. Singh K, Davis SR, Dobson JM, Molenaar AJ, et al. (2008). cDNA microarray analysis reveals that antioxidant and immune genes are up regulated during involution of the bovine mammary gland. J. Dairy Sci. 91: 2236-2246.
33. Strandberg Y, Gray C, Vuocolo T, Donaldson L, et al. (2005). Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. Cytokine 31: 72-86.
34. Sugimoto M, Fujikawa A, Womack JE and Sugimoto Y (2006). Evidence that bovine forebrain embryonic zinc finger-like gene influences immune response associated with mastitis resistance. Proc. Natl. Acad. Sci. U. S. A. 103: 6454-6459.
35. Swanson KM, Stelwagen K, Dobson J, Henderson HV, et al. (2009). Transcriptome profling of Streptococcus uberis-induced mastitis reveals fundamental differences between immune gene expression in the mammary gland and in a primary cell culture model. J. Dairy Sci. 92: 117-129.
36. Takeuchi O, Hoshino K and Akira S (2000). Cutting edge: TLR2-defcient and MyD88-defcient mice are highly susceptible to Staphylococcus aureus infection. J. Immunol. 165: 5392-5396.
37. Tao W, Mallard B, Karrow N and Bridle B (2004). Construction and application of a bovine immune-endocrine cDNA microarray. Vet. Immunol. Immunopathol. 101: 1-17.
38. Vandesompele J, De Preter K, Pattyn F, Poppe B, et al. (2002). Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 3: RESEARCH0034.
39. Wang YH, Byrne KA, Reverter A, Harper GS, et al. (2005). Transcriptional profiling of skeletal muscle tissue from two breeds of cattle. Mamm. Genome 16: 201-210.
40. Yang W, Zerbe H, Petzl W, Brunner RM, et al. (2008). Bovine TLR2 and TLR4 properly transduce signals from Staphylococcus aureus and E. coli, but S. aureus fails to both activate NF-kappaB in mammary epithelial cells and to quickly induce TNFalpha and interleukin-8 (CXCL8) expression in the udder. Mol. Immunol. 45: 1385-1397.