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通过主要菌毛亚基基因(fedA)的单链构象多态性分析区分F18ab+和F18ac+大肠杆菌。

Differentiation of F18ab+ from F18ac+ Escherichia coli by single-strand conformational polymorphism analysis of the major fimbrial subunit gene (fedA).

作者信息

Bosworth B T, Dean-Nystrom E A, Casey T A, Neibergs H L

机构信息

Enteric Diseases and Food Safety Research Unit, National Animal Disease Center, USDA Agricultural Research Service, Ames, Iowa 50010, USA.

出版信息

Clin Diagn Lab Immunol. 1998 May;5(3):299-302. doi: 10.1128/CDLI.5.3.299-302.1998.

Abstract

Toxin-producing Escherichia coli expressing F18 fimbriae colonizes the small intestines of weaned pigs and causes diarrhea, edema disease, or both. The F18 family is composed of two antigenic variants, F18ab and F18ac. Because many strains do not express F18 fimbriae in vitro, identification and differentiation of these two variants are difficult. Single-strand conformational polymorphism (SSCP) analysis is a rapid method for identifying genetic mutations and polymorphisms. The F18 major fimbrial subunit genes (fedA) of 138 strains were amplified by PCR, and genetic differences were detected by SSCP analysis. The SSCP analysis of the fedA gene differentiated F18ab+ strains from F18ac+ strains. Most strains classified as F18ab+ by SSCP analysis contained Shiga toxin 2e and enterotoxin genes. Most strains classified as F18ac+ by SSCP analysis contained only enterotoxin genes. The SSCP analysis was a useful method for predicting the antigenicity of F18+ E. coli and could also be used for analysis of other virulence genes in E. coli and other pathogenic bacteria.

摘要

表达F18菌毛的产毒素大肠杆菌定殖于断奶仔猪的小肠,可引起腹泻、水肿病或两者皆有。F18家族由两种抗原变体F18ab和F18ac组成。由于许多菌株在体外不表达F18菌毛,因此这两种变体的鉴定和区分较为困难。单链构象多态性(SSCP)分析是一种鉴定基因突变和多态性的快速方法。通过PCR扩增了138株菌株的F18主要菌毛亚基基因(fedA),并通过SSCP分析检测遗传差异。fedA基因的SSCP分析可区分F18ab+菌株和F18ac+菌株。通过SSCP分析归类为F18ab+的大多数菌株含有志贺毒素2e和肠毒素基因。通过SSCP分析归类为F18ac+的大多数菌株仅含有肠毒素基因。SSCP分析是预测F18+大肠杆菌抗原性的有用方法,也可用于分析大肠杆菌和其他病原菌中的其他毒力基因。

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Presence of F18ac (2134P) fimbriae on 4P- Escherichia coli isolates from weaned pigs with diarrhea.
J Vet Diagn Invest. 1997 Jan;9(1):77-9. doi: 10.1177/104063879700900114.

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