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2
High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi.高通量测序为伤寒沙门氏菌的基因组变异和进化提供了见解。
Nat Genet. 2008 Aug;40(8):987-93. doi: 10.1038/ng.195. Epub 2008 Jul 27.
3
Variation in virulence among clades of Escherichia coli O157:H7 associated with disease outbreaks.与疾病暴发相关的大肠杆菌O157:H7各进化枝间的毒力差异。
Proc Natl Acad Sci U S A. 2008 Mar 25;105(12):4868-73. doi: 10.1073/pnas.0710834105. Epub 2008 Mar 10.
4
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Microbiology (Reading). 2008 Feb;154(Pt 2):559-570. doi: 10.1099/mic.0.2007/013334-0.
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Recycling of Shiga toxin 2 genes in sorbitol-fermenting enterohemorrhagic Escherichia coli O157:NM.志贺毒素2基因在山梨醇发酵肠出血性大肠杆菌O157:NM中的循环利用
Appl Environ Microbiol. 2008 Jan;74(1):67-72. doi: 10.1128/AEM.01906-07. Epub 2007 Nov 2.
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Fim operon variation in the emergence of Enterohemorrhagic Escherichia coli: an evolutionary and functional analysis.肠出血性大肠杆菌出现过程中菌毛操纵子的变异:进化与功能分析
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Global genetic population structure of Bacillus anthracis.炭疽芽孢杆菌的全球遗传种群结构。
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Haplotype diversity in "source-sink" dynamics of Escherichia coli urovirulence.大肠杆菌尿路致病性“源-汇”动态中的单倍型多样性
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Greater diversity of Shiga toxin-encoding bacteriophage insertion sites among Escherichia coli O157:H7 isolates from cattle than in those from humans.来自牛的大肠杆菌O157:H7分离株中,志贺毒素编码噬菌体插入位点的多样性高于来自人类的分离株。
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通过主干串联基因组分析对大肠杆菌O157的出现和受限辐射进行的精确重建。

A precise reconstruction of the emergence and constrained radiations of Escherichia coli O157 portrayed by backbone concatenomic analysis.

作者信息

Leopold Shana R, Magrini Vincent, Holt Nicholas J, Shaikh Nurmohammad, Mardis Elaine R, Cagno Joseph, Ogura Yoshitoshi, Iguchi Atsushi, Hayashi Tetsuya, Mellmann Alexander, Karch Helge, Besser Thomas E, Sawyer Stanley A, Whittam Thomas S, Tarr Phillip I

机构信息

Department of Pediatrics, Washington University School of Medicine, 660 South Euclid Avenue, Saint Louis, MO 63110, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 May 26;106(21):8713-8. doi: 10.1073/pnas.0812949106. Epub 2009 May 13.

DOI:10.1073/pnas.0812949106
PMID:19439656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2689004/
Abstract

Single nucleotide polymorphisms (SNPs) in stable genome regions provide durable measurements of species evolution. We systematically identified each SNP in concatenations of all backbone ORFs in 7 newly or previously sequenced evolutionarily instructive pathogenic Escherichia coli O157:H7, O157:H(-), and O55:H7. The 1,113 synonymous SNPs demonstrate emergence of the largest cluster of this pathogen only in the last millennium. Unexpectedly, shared SNPs within circumscribed clusters of organisms suggest severely restricted survival and limited effective population sizes of pathogenic O157:H7, tenuous survival of these organisms in nature, source-sink evolutionary dynamics, or, possibly, a limited number of mutations that confer selective advantage. A single large segment spanning the rfb-gnd gene cluster is the only backbone region convincingly acquired by recombination as O157 emerged from O55. This concatenomic analysis also supports using SNPs to differentiate closely related pathogens for infection control and forensic purposes. However, constrained radiations raise the possibility of making false associations between isolates.

摘要

稳定基因组区域中的单核苷酸多态性(SNP)为物种进化提供了持久的测量方法。我们系统地鉴定了7种新测序或先前测序的具有进化指导意义的致病性大肠杆菌O157:H7、O157:H(-)和O55:H7中所有主干开放阅读框串联中的每个SNP。1113个同义SNP表明,这种病原体的最大集群仅在过去一千年中出现。出乎意料的是,生物受限集群内的共享SNP表明致病性O157:H7的生存受到严重限制,有效种群规模有限,这些生物在自然界中生存脆弱,存在源-汇进化动态,或者可能是少数赋予选择性优势的突变。当O157从O55中出现时,跨越rfb-gnd基因簇的单个大片段是唯一通过重组令人信服地获得的主干区域。这种串联基因组分析也支持使用SNP来区分密切相关的病原体,以用于感染控制和法医目的。然而,受限辐射增加了在分离株之间产生错误关联的可能性。