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1
Characterization of plasmids encoding the adherence factor of enteropathogenic Escherichia coli.编码肠致病性大肠杆菌黏附因子的质粒的特性分析
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2
Properties of adherence factor plasmids of enteropathogenic Escherichia coli and the effect of host strain on expression of adherence to HEp-2 cells.致病性大肠杆菌黏附因子质粒的特性及宿主菌株对其黏附HEp-2细胞表达的影响。
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3
Nucleotide sequence analysis of enteropathogenic Escherichia coli (EPEC) adherence factor probe and development of PCR for rapid detection of EPEC harboring virulence plasmids.肠致病性大肠杆菌(EPEC)黏附因子探针的核苷酸序列分析及用于快速检测携带毒力质粒的EPEC的PCR技术的开发。
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4
Role of plasmid-encoded adherence factors in adhesion of enteropathogenic Escherichia coli to HEp-2 cells.质粒编码的黏附因子在肠致病性大肠杆菌黏附到HEP - 2细胞中的作用。
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本文引用的文献

1
Detection of enterotoxigenic Escherichia coli by DNA colony hybridization.通过DNA菌落杂交法检测产肠毒素大肠杆菌
J Infect Dis. 1980 Dec;142(6):892-8. doi: 10.1093/infdis/142.6.892.
2
Pathogenesis of escherichia coli gastroenteritis in man--another mechanism.人类大肠杆菌性胃肠炎的发病机制——另一种机制
N Engl J Med. 1980 Jan 10;302(2):99-101. doi: 10.1056/NEJM198001103020207.
3
An ultrastructural study of enteropathogenic Escherichia coli infection in human infants.人类婴儿肠道致病性大肠杆菌感染的超微结构研究。
Ultrastruct Pathol. 1983 Jun;4(4):291-304. doi: 10.3109/01913128309140582.
4
Plasmid-mediated adhesion in enteropathogenic Escherichia coli.质粒介导的致病性大肠杆菌黏附作用
J Pediatr Gastroenterol Nutr. 1983;2(3):534-8. doi: 10.1097/00005176-198302030-00023.
5
From the National Institute of Allergy and Infectious Diseases. Summary of a workshop on enteropathogenic Escherichia coli.来自美国国立过敏与传染病研究所。肠道致病性大肠杆菌研讨会总结。
J Infect Dis. 1983 Jun;147(6):1108-18. doi: 10.1093/infdis/147.6.1108.
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Variability in DNA sequence of closely related nosocomial gentamicin-resistant plasmids.
J Infect Dis. 1983 Dec;148(6):1013-8. doi: 10.1093/infdis/148.6.1013.
7
Characterization of virulence plasmids and plasmid-associated outer membrane proteins in Shigella flexneri, Shigella sonnei, and Escherichia coli.福氏志贺菌、宋内志贺菌和大肠杆菌中毒力质粒及质粒相关外膜蛋白的特性分析
Infect Immun. 1983 Apr;40(1):340-50. doi: 10.1128/iai.40.1.340-350.1983.
8
Genetic transfer of a mucosal adherence factor (R1) from an enteropathogenic Escherichia coli strain into a Shigella flexneri strain and the phenotypic suppression of this adherence factor.将一种黏膜黏附因子(R1)从一株肠致病性大肠杆菌转移至一株福氏志贺菌,并对该黏附因子进行表型抑制。
J Infect Dis. 1983 Apr;147(4):711-23. doi: 10.1093/infdis/147.4.711.
9
Isolation of a temperature-sensitive derivative of RP1.RP1温度敏感衍生物的分离
Plasmid. 1980 May;3(3):343-7. doi: 10.1016/0147-619x(80)90047-5.
10
A complementation analysis of the restriction and modification of DNA in Escherichia coli.大肠杆菌中DNA限制与修饰的互补分析。
J Mol Biol. 1969 May 14;41(3):459-72. doi: 10.1016/0022-2836(69)90288-5.

编码肠致病性大肠杆菌黏附因子的质粒的特性分析

Characterization of plasmids encoding the adherence factor of enteropathogenic Escherichia coli.

作者信息

Nataro J P, Maher K O, Mackie P, Kaper J B

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore 21201.

出版信息

Infect Immun. 1987 Oct;55(10):2370-7. doi: 10.1128/iai.55.10.2370-2377.1987.

DOI:10.1128/iai.55.10.2370-2377.1987
PMID:2888732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC260715/
Abstract

Volunteer studies have shown that a 60-megadalton plasmid is required for full virulence of the human enteropathogenic Escherichia coli (EPEC) strain E2348/69 (O127:H6). The plasmid, designated pMAR2, encodes localized adherence to HEp-2 cells in tissue culture via the adhesin known as the EPEC adherence factor (EAF). Using a DNA probe for the EAF, we have previously shown that these genes are specific for EPEC and are usually encoded on plasmids ranging from 55 to 65 megadaltons. In this study, Southern blot analysis and S1 nuclease homology determination reveal a high degree of sequence conservation among these plasmids, despite some variation in restriction maps. Phenotypic characterization of the prototype EAF plasmid pMAR2 reveals that the plasmid belongs to the group IncFII and is negative for alpha-hemolysin, colicin, and aerobactin synthesis, as well as biochemical markers and antibiotic resistance. Regions encoding adherence to HEp-2 cells were localized by Tn801 insertion mutagenesis. Adherence genes were then cloned as two distinct plasmid regions which confer the adherence phenotype only when complementing each other in trans.

摘要

志愿者研究表明,人肠道致病性大肠杆菌(EPEC)菌株E2348/69(O127:H6)的完全毒力需要一个60兆道尔顿的质粒。该质粒命名为pMAR2,通过被称为EPEC黏附因子(EAF)的黏附素编码在组织培养中对HEp-2细胞的局部黏附。使用针对EAF的DNA探针,我们之前已经表明这些基因对EPEC具有特异性,并且通常编码在大小从55到65兆道尔顿的质粒上。在本研究中,Southern印迹分析和S1核酸酶同源性测定揭示了这些质粒之间高度的序列保守性,尽管限制酶切图谱存在一些差异。原型EAF质粒pMAR2的表型特征表明,该质粒属于IncFII组,并且α-溶血素、大肠杆菌素和气杆菌素合成以及生化标记和抗生素抗性均为阴性。通过Tn801插入诱变确定了编码对HEp-2细胞黏附的区域。然后将黏附基因克隆为两个不同的质粒区域,这两个区域只有在反式互补时才赋予黏附表型。