Greater expression of TLR2, TLR4, and IL6 due to negative energy balance is associated with lower expression of HLA-DRA and HLA-A in bovine blood neutrophils after intramammary mastitis challenge with Streptococcus uberis |
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Authors: | Kasey M. Moyes James K. Drackley Dawn E. Morin Juan J. Loor |
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Affiliation: | 1. Department of Animal Sciences, University of Illinois, Urbana, IL, 61801, USA 3. Mammalian NutriPhysioGenomics, University of Illinois, 1207 W. Gregory Dr., Urbana, IL, 61801, USA 5. Faculty of Agricultural Sciences, Aarhus University, Blichers Allé, P.O. Box?50, Tjele, 8830, Denmark 4. University of Illinois, 1207 W. Gregory Dr., Urbana, IL, 61801, USA 2. College of Veterinary Medicine, University of Illinois, Urbana, IL, 61801, USA
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Abstract: | Our objectives were to compare gene expression profiles in blood polymorphonuclear cells (PMN) during a Streptococcus uberis intramammary challenge between lactating cows subjected to feed restriction to induce negative energy balance (NEB; n = 5) and cows fed ad libitum to maintain positive energy balance (PEB; n = 5). After 5 days of feed restriction, one rear mammary quarter of each cow was inoculated with 5,000 cfu of S. uberis. Blood PMN were isolated at 24 h post-inoculation from all cows for mRNA expression via quantitative polymerase chain reaction for 20 genes associated with immune response and metabolism. A total of 12 genes were differentially expressed in blood PMN in NEB versus PEB cows. Upregulated genes by NEB were ALOX5AP, CPNE3, IL1R2, IL6, TLR2, TLR4, and THY1, and downregulated genes were HLA-DRA, HLA-A, IRAK1, SOD1, and TNF. Network analysis revealed that TNF was associated with several of the affected genes in NEB cows compared with PEB cows. Results showed that 24 h after intramammary challenge with S. uberis, cows in NEB had altered PMN expression of genes involved with immune response. Our data provide new information on transcriptomic mechanisms associated with NEB and the corresponding inhibition of immune response in lactating dairy cows. |
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