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Relationship of bovine TNF-α gene polymorphisms with therisk of bovine tuberculosis in Holstein cattle

机译:牛TNF-α基因多态性与牛TNF-α关系的研究。荷斯坦牛的牛结核病风险

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摘要

Many studies suggest significant genetic variation in the resistance of cattle and humans to infection with Mycobacterium bovis (M. bovis), the causative agent of zoonotic tuberculosis. TNF-α promotes inflammation and induces apoptosis in response to mycobacterial infection. The aim of the present study was to investigate the influence of single nucleotide polymorphisms of the TNF-α gene on bovine tuberculosis (bTB) susceptibility. We genotyped the TNF-α gene in 74 bTB-infected Holstein cows and 90 healthy control animals. The influence in the exon 3 region of TNF-α polymorphisms on bTB susceptibility was subsequently investigated by association analysis. Our finding demonstrated that the g.27534932A>C polymorphism of the TNF-α is associated with bTB in Holstein cattle. The susceptibility of cattle with the g.27534932A>C genotype compared with the CC genotype was 4.11-fold (95% CI, 1.27–13.36; P=0.02) higher. The g.27534932A>C polymorphism located in exon 3 of the TNF-α gene, and the functional consequence was missense. The deduced amino acid sequence for the protein product revealed an arginine to serine conversion at position 159, which may affect initiation of protein synthesis and disrupt normal TNF-α function that protects animals against mycobacterial infection. A significant association wasobserved with the A allele as a risk factor for bTB susceptibility (OR, 3.84; 95% CI,1.21–12.17; P=0.02). In conclusion, this is the first report showing thatthe g.27534932A>C polymorphism may contribute to TNF-α-mediated bTBsusceptibility.
机译:许多研究表明,牛和人对人畜共患病结核病致病菌牛分枝杆菌(牛分枝杆菌)的抗药性存在显着的遗传变异。 TNF-α响应分枝杆菌感染而促进炎症并诱导凋亡。本研究的目的是研究TNF-α基因的单核苷酸多态性对牛结核病(bTB)敏感性的影响。我们对74例bTB感染的荷斯坦奶牛和90例健康对照动物的TNF-α基因进行了基因分型。随后通过关联分析研究了TNF-α多态性在外显子3区域对bTB敏感性的影响。我们的发现表明,TNF-α的g.27534932A> C多态性与荷斯坦牛的bTB有关。与CC基因型相比,具有g.27534932A> C基因型的牛的敏感性高4.11倍(95%CI,1.27-13.36; P = 0.02)。 g.27534932A> C多态性位于TNF-α基因的外显子3,其功能后果是错义。推导的蛋白质产物氨基酸序列揭示了在159位的精氨酸向丝氨酸的转化,这可能会影响蛋白质合成的启动并破坏正常的TNF-α功能,从而保护动物免受分枝杆菌感染。一个重要的关联是观察到A等位基因是bTB易感性的危险因素(OR为3.84; 95%CI,1.21–12.17; P = 0.02)。总之,这是第一份报告显示g.27534932A> C多态性可能有助于TNF-α介导的bTB易感性。

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