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A 组链球菌组织嗜性表型的全基因组关联研究。

Whole-genome association study on tissue tropism phenotypes in group A Streptococcus.

机构信息

New York Medical College, Department of Microbiology & Immunology, Valhalla, NY 10595, USA.

出版信息

J Bacteriol. 2011 Dec;193(23):6651-63. doi: 10.1128/JB.05263-11. Epub 2011 Sep 23.

Abstract

Group A Streptococcus (GAS) has a rich evolutionary history of horizontal transfer among its core genes. Yet, despite extensive genetic mixing, GAS strains have discrete ecological phenotypes. To further our understanding of the molecular basis for ecological phenotypes, comparative genomic hybridization of a set of 97 diverse strains to a GAS pangenome microarray was undertaken, and the association of accessory genes with emm genotypes that define tissue tropisms for infection was determined. Of the 22 nonprophage accessory gene regions (AGRs) identified, only 3 account for all statistically significant linkage disequilibrium among strains having the genotypic biomarkers for throat versus skin infection specialists. Networked evolution and population structure analyses of loci representing each of the AGRs reveal that most strains with the skin specialist and generalist biomarkers form discrete clusters, whereas strains with the throat specialist biomarker are highly diverse. To identify coinherited and coselected accessory genes, the strength of genetic associations was determined for all possible pairwise combinations of accessory genes among the 97 GAS strains. Accessory genes showing very strong associations provide the basis for an evolutionary model, which reveals that a major transition between many throat and skin specialist haplotypes correlates with the gain or loss of genes encoding fibronectin-binding proteins. This study employs a novel synthesis of tools to help delineate the major genetic changes associated with key adaptive shifts in an extensively recombined bacterial species.

摘要

A 组链球菌 (GAS) 在其核心基因之间具有丰富的水平转移进化史。然而,尽管存在广泛的基因混合,GAS 菌株仍具有离散的生态表型。为了进一步了解生态表型的分子基础,对一组 97 种不同的菌株进行了比较基因组杂交,以检测 GAS 泛基因组微阵列,并确定与确定感染组织嗜性的 emm 基因型相关的辅助基因。在鉴定的 22 个非噬菌体辅助基因区 (AGRs) 中,只有 3 个与具有喉咙与皮肤感染专家的基因型生物标志物的菌株之间存在所有统计学显著的连锁不平衡有关。代表每个 AGR 的基因座的网络进化和群体结构分析表明,具有皮肤专家和通才生物标志物的大多数菌株形成离散的聚类,而具有喉咙专家生物标志物的菌株则高度多样化。为了鉴定共遗传和共选择的辅助基因,确定了 97 种 GAS 菌株中所有辅助基因之间可能的成对组合的遗传关联强度。显示非常强关联的辅助基因为进化模型提供了基础,该模型表明,许多喉咙和皮肤专家单倍型之间的主要转变与编码纤连蛋白结合蛋白的基因的获得或丢失相关。本研究采用了一种新的综合工具来帮助描绘与广泛重组细菌物种关键适应性转变相关的主要遗传变化。

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