Verbeke Joren, Piccart Kristine, Piepers Sofie, Van Poucke Mario, Peelman Luc, De Visscher Anneleen, De Vliegher Sarne
M-team and Mastitis and Milk Quality Research Unit, Department of Reproduction, Obstetrics, and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke 9820, Belgium.
M-team and Mastitis and Milk Quality Research Unit, Department of Reproduction, Obstetrics, and Herd Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke 9820, Belgium.
Vet J. 2015 Jun;204(3):322-6. doi: 10.1016/j.tvjl.2015.04.010. Epub 2015 Apr 14.
Previous observational studies suggest an association between polymorphism c.980A>G in the CXCR1 gene, encoding the chemokine (C-X-C motif) receptor 1, and the innate immunity and infection status of the mammary gland. Mammary glands of eight Holstein heifers were experimentally infected with a Staphylococcus chromogenes isolate originating from a chronic intramammary infection (IMI) to study differences between CXCR1 genotypes c.980AG and c.980GG. Quarters from heifers with genotypes c.980AG and c.980GG developed subclinical mastitis but showed differences in the early response at 6-18 h post challenge. Bacterial count at 18 h post challenge tended to be higher in quarters from c.980AG heifers compared to c.980GG heifers. Somatic cell count (SCC) was higher at 6 h post challenge and tended to be higher at 9 h post challenge in c.980AG heifers compared to c.980GG heifers. Milk production decreased similarly. Milk neutrophils of c.980AG heifers showed more apoptosis at 9 h post challenge and tended to show more necrosis at 6, 9 and 12 h post challenge than c.980GG heifers. Differences were less pronounced in the later stage (>18 h) of infection. The results demonstrate that CXCR1 polymorphism can influence SCC and milk neutrophil viability following experimental IMI.
先前的观察性研究表明,编码趋化因子(C-X-C基序)受体1的CXCR1基因中的多态性c.980A>G与乳腺的先天免疫和感染状态之间存在关联。对8头荷斯坦小母牛的乳腺进行实验性感染,感染源是一株来自慢性乳房内感染(IMI)的产色葡萄球菌分离株,以研究CXCR1基因型c.980AG和c.980GG之间的差异。基因型为c.980AG和c.980GG的小母牛的乳腺区发生了亚临床乳腺炎,但在攻毒后6-18小时的早期反应中表现出差异。与c.980GG小母牛相比,c.980AG小母牛乳腺区在攻毒后18小时的细菌计数往往更高。与c.980GG小母牛相比,c.980AG小母牛在攻毒后6小时的体细胞计数(SCC)更高,在攻毒后9小时也往往更高。产奶量下降情况相似。与c.980GG小母牛相比,c.980AG小母牛的乳中性粒细胞在攻毒后9小时显示出更多的凋亡,在攻毒后6、9和12小时往往显示出更多的坏死。在感染后期(>18小时)差异不太明显。结果表明,CXCR1多态性可影响实验性IMI后的SCC和乳中性粒细胞活力。