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本文引用的文献

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Genome plasticity in pathogenic and nonpathogenic enterobacteria.致病性和非致病性肠道杆菌的基因组可塑性
Curr Top Microbiol Immunol. 2002;264(1):157-75.
2
Extraintestinal Escherichia coli as a model system for the study of pathogenicity islands.肠外大肠杆菌作为研究致病岛的模型系统。
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Whole genome plasticity in pathogenic bacteria.致病细菌的全基因组可塑性
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Identification of DNA sequences from a second pathogenicity island of uropathogenic Escherichia coli CFT073: probes specific for uropathogenic populations.从尿路致病性大肠杆菌CFT073的第二个致病岛鉴定DNA序列:针对尿路致病性菌群的特异性探针。
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Ongoing horizontal and vertical transmission of virulence genes and papA alleles among Escherichia coli blood isolates from patients with diverse-source bacteremia.来自不同来源菌血症患者的大肠杆菌血液分离株中,毒力基因和papA等位基因持续进行水平和垂直传播。
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S-Fimbria-encoding determinant sfa(I) is located on pathogenicity island III(536) of uropathogenic Escherichia coli strain 536.编码S菌毛的决定簇sfa(I)位于尿路致病性大肠杆菌菌株536的致病岛III(536)上。
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Inhibition of Shigella flexneri-induced transepithelial migration of polymorphonuclear leucocytes by cadaverine.尸胺对福氏志贺菌诱导的多形核白细胞跨上皮迁移的抑制作用。
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afa-8 Gene cluster is carried by a pathogenicity island inserted into the tRNA(Phe) of human and bovine pathogenic Escherichia coli isolates.afa-8基因簇由一个插入人源和牛源致病性大肠杆菌分离株的tRNA(苯丙氨酸)中的致病岛携带。
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尿路致病性大肠杆菌菌株536的四个致病岛(PAI I(536)至PAI IV(536))的遗传结构与分布

Genetic structure and distribution of four pathogenicity islands (PAI I(536) to PAI IV(536)) of uropathogenic Escherichia coli strain 536.

作者信息

Dobrindt Ulrich, Blum-Oehler Gabriele, Nagy Gabor, Schneider György, Johann André, Gottschalk Gerhard, Hacker Jörg

机构信息

Institut für Molekulare Infektionsbiologie, Universität Würzburg, D-97070 Würzburg, Germany.

出版信息

Infect Immun. 2002 Nov;70(11):6365-72. doi: 10.1128/IAI.70.11.6365-6372.2002.

DOI:10.1128/IAI.70.11.6365-6372.2002
PMID:12379716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC130402/
Abstract

For the uropathogenic Escherichia coli strain 536 (O6:K15:H31), the DNA sequences of three pathogenicity islands (PAIs) (PAI I(536) to PAI III(536)) and their flanking regions (about 270 kb) were determined to further characterize the virulence potential of this strain. PAI I(536) to PAI III(536) exhibit features typical of PAIs, such as (i) association with tRNA-encoding genes; (ii) G+C content differing from that of the host genome; (iii) flanking repeat structures; (iv) a mosaic-like structure comprising a multitude of functional, truncated, and nonfunctional putative open reading frames (ORFs) with known or unknown functions; and (v) the presence of many fragments of mobile genetic elements. PAI I(536) to PAI III(536) range between 68 and 102 kb in size. Although these islands contain several ORFs and known virulence determinants described for PAIs of other extraintestinal pathogenic E. coli (ExPEC) isolates, they also consist of as-yet-unidentified ORFs encoding putative virulence factors. The genetic structure of PAI IV(536), which represents the core element of the so-called high-pathogenicity island encoding a siderophore system initially identified in pathogenic yersiniae, was further characterized by sample sequencing. For the first time, multiple PAI sequences (PAI I(536) to PAI IV(536)) in uropathogenic E. coli were studied and their presence in several wild-type E. coli isolates was extensively investigated. The results obtained suggest that these PAIs or at least large fragments thereof are detectable in other pathogenic E. coli isolates. These results support our view that the acquisition of large DNA regions, such as PAIs, by horizontal gene transfer is an important factor for the evolution of bacterial pathogens.

摘要

对于尿路致病性大肠杆菌菌株536(O6:K15:H31),测定了三个致病岛(PAIs)(PAI I(536)至PAI III(536))及其侧翼区域(约270 kb)的DNA序列,以进一步表征该菌株的毒力潜力。PAI I(536)至PAI III(536)表现出PAIs的典型特征,例如:(i)与编码tRNA的基因相关;(ii)G+C含量与宿主基因组不同;(iii)侧翼重复结构;(iv)由众多具有已知或未知功能的功能性、截短的和无功能的推定开放阅读框(ORFs)组成的镶嵌样结构;以及(v)存在许多移动遗传元件片段。PAI I(536)至PAI III(536)的大小在68至102 kb之间。尽管这些岛包含几个ORFs和其他肠道外致病性大肠杆菌(ExPEC)分离株的PAIs中描述的已知毒力决定因素,但它们也由编码推定毒力因子的尚未鉴定的ORFs组成。通过样本测序进一步表征了PAI IV(536)的遗传结构,PAI IV(536)代表了所谓高致病性岛的核心元件,该岛编码最初在致病性耶尔森氏菌中鉴定的铁载体系统。首次研究了尿路致病性大肠杆菌中的多个PAI序列(PAI I(来自536)至PAI IV(536)),并广泛调查了它们在几种野生型大肠杆菌分离株中的存在情况。获得的结果表明,这些PAIs或其至少大片段在其他致病性大肠杆菌分离株中是可检测到的。这些结果支持了我们的观点,即通过水平基因转移获得大的DNA区域,如PAIs,是细菌病原体进化的一个重要因素。