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分离表达菌毛突变体的简易方法。

SIMPLE approach for isolating mutants expressing fimbriae.

作者信息

Nuccio Sean-Paul, Chessa Daniela, Weening Eric H, Raffatellu Manuela, Clegg Steven, Bäumler Andreas J

机构信息

Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, Davis, CA 95616-8645, USA.

出版信息

Appl Environ Microbiol. 2007 Jul;73(14):4455-62. doi: 10.1128/AEM.00148-07. Epub 2007 May 25.

DOI:10.1128/AEM.00148-07
PMID:17526787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1932825/
Abstract

Genomes of members of the family Enterobacteriaceae contain large repertoires of putative fimbrial operons. Since many of these operons are poorly expressed in vitro, a convenient method for inducing elaboration of the encoded fimbriae would greatly facilitate their functional characterization. Here we describe a new technique for identifying fimbriated bacteria from a library of transposon mutants by screening with immunomagnetic particles for ligand expression (SIMPLE). The SIMPLE method was applied to identify the T-POP mutants of Salmonella enterica serotype Typhimurium carrying on their surfaces filaments composed of PefA, the major subunit product of a fimbrial operon (pef) that is not expressed during growth in Luria-Bertani broth. Four such mutants were identified from a library of 24,000 mutants, each of which carried a T-POP insertion within the hns gene, which encodes a global silencer of horizontally acquired genes. Our data suggest that the SIMPLE method is an effective approach for isolating fimbriated bacteria, which can be readily applied to fimbrial operons identified by whole-genome sequencing.

摘要

肠杆菌科成员的基因组包含大量假定的菌毛操纵子。由于其中许多操纵子在体外表达不佳,一种诱导所编码菌毛形成的便捷方法将极大地促进其功能表征。在此,我们描述了一种新技术,即通过用免疫磁珠筛选配体表达,从转座子突变体文库中鉴定菌毛化细菌(SIMPLE)。将SIMPLE方法应用于鉴定鼠伤寒沙门氏菌血清型鼠伤寒的T-POP突变体,这些突变体表面带有由菌毛操纵子(pef)的主要亚基产物PefA组成的细丝,该操纵子在Luria-Bertani肉汤中生长期间不表达。从24000个突变体文库中鉴定出四个这样的突变体,每个突变体在编码水平获得基因的全局沉默子的hns基因内携带一个T-POP插入。我们的数据表明,SIMPLE方法是分离菌毛化细菌的有效方法,可轻松应用于通过全基因组测序鉴定的菌毛操纵子。

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