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葡萄球菌凝固酶阳性现象的进化和功能分析。

Evolutionary and Functional Analysis of Coagulase Positivity among the Staphylococci.

机构信息

The Roslin Institute and Edinburgh Infectious Diseases, University of Edinburghgrid.4305.2, Easter Bush, Midlothian, Scotland, United Kingdom.

出版信息

mSphere. 2021 Aug 25;6(4):e0038121. doi: 10.1128/mSphere.00381-21. Epub 2021 Aug 4.

Abstract

The bacterial genus Staphylococcus comprises a large group of pathogenic and nonpathogenic species associated with an array of host species. Staphylococci are differentiated into coagulase-positive or coagulase-negative groups based on the capacity to promote clotting of plasma, a phenotype historically associated with the ability to cause disease. However, the genetic basis of this important diagnostic and pathogenic trait across the genus has not been examined to date. Here, we selected 54 representative staphylococcal species and subspecies to examine coagulation of plasma derived from six representative host species. In total, 13 staphylococcal species mediated coagulation of plasma from at least one host species including one previously identified as coagulase negative (Staphylococcus condimenti). Comparative genomic analysis revealed that coagulase activity correlated with the presence of a gene () encoding the von Willebrand binding protein (vWbp) whereas only the Staphylococcus aureus complex contained a gene encoding staphylocoagulase (Coa), the classical mediator of coagulation. Importantly, S. aureus retained -dependent coagulase activity in an S. aureus strain deleted for whereas deletion of in Staphylococcus pseudintermedius resulted in loss of coagulase activity. Whole-genome-based phylogenetic reconstruction of the Staphylococcus genus revealed that the gene has been acquired on at least four different occasions during the evolution of the Staphylococcus genus followed by allelic diversification via mutation and recombination. Allelic variants of vWbp from selected coagulase-positive staphylococci mediated coagulation in a host-dependent manner indicative of host-adaptive evolution. Taken together, we have determined the genetic and evolutionary basis of staphylococcal coagulation, revealing vWbp to be its archetypal determinant. The ability of some species of staphylococci to promote coagulation of plasma is a key pathogenic and diagnostic trait. Here, we provide a comprehensive analysis of the coagulase positivity of the staphylococci and its evolutionary genetic basis. We demonstrate that the von Willebrand binding protein rather than staphylocoagulase is the archetypal coagulation factor of the staphylococci and that the gene has been acquired several times independently during the evolution of the staphylococci. Subsequently, has undergone adaptive diversification to facilitate host-specific functionality. Our findings provide important insights into the evolution of pathogenicity among the staphylococci and the genetic basis for a defining diagnostic phenotype.

摘要

葡萄球菌属包含一大组与多种宿主物种相关的致病性和非致病性物种。根据促进血浆凝固的能力,葡萄球菌可分为凝固酶阳性或凝固酶阴性组,这种表型历史上与引起疾病的能力有关。然而,迄今为止,尚未对该属中这一重要的诊断和致病特征的遗传基础进行研究。在这里,我们选择了 54 种有代表性的葡萄球菌种和亚种,以检查来自 6 种有代表性的宿主物种的血浆的凝固。共有 13 种葡萄球菌种介导了至少一种宿主种的血浆凝固,包括一种先前被鉴定为凝固酶阴性的葡萄球菌种(葡萄球菌 condimenti)。比较基因组分析表明,凝固酶活性与编码血管性血友病结合蛋白(vWbp)的基因()的存在相关,而仅金黄色葡萄球菌复合体含有编码葡萄球菌凝固酶(Coa)的基因,Coa 是经典的凝血介质。重要的是,在金黄色葡萄球菌中,即使缺失了,也保留了依赖于的凝固酶活性,而在中间葡萄球菌中缺失了,则导致凝固酶活性丧失。葡萄球菌属的全基因组系统发育重建显示,在葡萄球菌属的进化过程中,基因已经至少被四次获得,随后通过突变和重组进行了等位基因多样化。从选定的凝固酶阳性葡萄球菌中选择的 vWbp 的等位基因变体以宿主依赖性方式介导凝固,表明其发生了宿主适应性进化。总之,我们确定了葡萄球菌凝固的遗传和进化基础,揭示 vWbp 是其原型决定因素。一些葡萄球菌种促进血浆凝固的能力是一个关键的致病性和诊断特征。在这里,我们对葡萄球菌的凝固酶阳性及其进化遗传基础进行了全面分析。我们证明,血管性血友病结合蛋白而不是葡萄球菌凝固酶是葡萄球菌的原型凝血因子,基因在葡萄球菌的进化过程中已经独立获得了多次。随后,经历了适应性多样化,以促进宿主特异性功能。我们的研究结果为葡萄球菌属中致病性的进化以及定义诊断表型的遗传基础提供了重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/8386474/5c400430fed4/msphere.00381-21-f001.jpg

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