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Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study

机译:人类对 S患者天然瓣膜金黄色葡萄球菌心内膜炎的遗传易感性。金黄色菌血症:全基因组关联研究

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Staphylococcus aureus infective endocarditis (SaIE) is a severe complication of S. aureus bacteremia (SAB) occurring in up to 22% of patients. Bacterial genetic factors and host conditions for SaIE have been intensely studied before; however, to date no study has focused on predisposing host genetic factors to SaIE. The present study aimed to identify genetic polymorphisms associated with SaIE by a Genome-Wide Association Study (GWAS) of 67 patients with definite native valve SaIE (cases) and 72 matched native valve patients with SAB but without IE (controls). All patients were enrolled in the VIRSTA cohort ( Le Moing et al., 2015 ) study. Four single nucleotide polymorphisms (SNPs) located on chromosome 3 were associated with SaIE ( P < 1 × 10~(-5)) without reaching conventional genome-wide significance. For all, the frequency of the minor allele was lower in cases than in controls, suggesting a protective effect of the minor allele against SaIE. The same association was observed using an independent Danish verification cohort of SAB with ( n = 57) and without ( n = 123) IE. Ex vivo analysis of aortic valve tissues revealed that SaIE associated SNPs mentioned above were associated with significantly higher mRNA expression levels of SLC7A14, a predicted cationic amino acid transporter protein. Taken together, our results suggest an IE-protective effect of SNPs on chromosome 3 during the course of SAB. The effects of protective minor alleles may be mediated by increasing expression levels of SLC7A14 in valve tissues. We conclude that occurrence of SaIE may be the combination of a well-adapted bacterial genotype to a susceptible host.
机译:金黄色葡萄球菌感染性心内膜炎(SaIE)是金黄色葡萄球菌菌血症(SAB)的严重并发症,其发生率高达22%。以前已经对SaIE的细菌遗传因素和宿主条件进行了深入研究。然而,迄今为止,尚无研究集中于将宿主遗传因素引入SaIE。本研究旨在通过基因组广泛关联研究(GWAS)来鉴定与SaIE相关的遗传多态性,该研究包括67例具有天然瓣膜SaIE的患者(病例)和72例具有SAB但无IE的匹配天然瓣膜患者(对照)。所有患者均参加了VIRSTA队列研究(Le Moing等,2015)。位于第3号染色体上的四个单核苷酸多态性(SNPs)与SaIE有关(P <1×10〜(-5)),而没有达到常规的全基因组意义。总体而言,病例中次要等位基因的频率低于对照组,这表明次要等位基因对SaIE的保护作用。使用具有(n = 57)和不具有(n = 123)IE的独立SAB丹麦验证队列观察到了相同的关联。对主动脉瓣组织的离体分析显示,上述与SaIE相关的SNP与预测的阳离子氨基酸转运蛋白SLC7A14的mRNA表达水平显着相关。两者合计,我们的结果表明在SAB过程中SNP对3号染色体的IE保护作用。保护性次要等位基因的作用可能通过增加瓣膜组织中SLC7A14的表达水平来介导。我们得出结论,SaIE的发生可能是对易感宿主具有良好适应性细菌基因型的组合。

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