Baudry B, Maurelli A T, Clerc P, Sadoff J C, Sansonetti P J
Service des Entérobactéries, Unité INSERM 199, Institut Pasteur, Paris, France.
J Gen Microbiol. 1987 Dec;133(12):3403-13. doi: 10.1099/00221287-133-12-3403.
We have previously cloned a 44 kb fragment from the virulence plasmid of Shigella flexneri serotype 5 strain M90T which is capable of restoring invasiveness to an avirulent, plasmidless mutant. This report presents a genetic and physical analysis of Tn5 mutations in recombinant clone pHS4108. Tn5 mutagenesis allowed identification of at least five regions implicated in the entry phenotype. These regions were located on a 20 kb portion of pHS4108. Expression of the insertion mutants was studied by immunoblots using the serum of a convalescent monkey infected by S. flexneri 2a, which recognized four plasmid-associated polypeptides. We propose that the four immunogenic polypeptides, a, b, c, and d, are encoded an operon.
我们先前从福氏志贺菌5型菌株M90T的毒力质粒中克隆了一个44 kb的片段,该片段能够恢复无毒性、无质粒突变体的侵袭力。本报告介绍了重组克隆pHS4108中Tn5突变的遗传和物理分析。Tn5诱变可鉴定出至少五个与侵入表型有关的区域。这些区域位于pHS4108的20 kb部分。利用感染了福氏志贺菌2a的恢复期猴子的血清进行免疫印迹,研究了插入突变体的表达,该血清可识别四种质粒相关多肽。我们认为,四种免疫原性多肽a、b、c和d由一个操纵子编码。