The virR/virS locus regulates the transcription of genes encoding extracellular toxin production in Clostridium perfringens

被引:103
作者
BaThein, W
Lyristis, M
Ohtani, K
Nisbet, IT
Hayashi, H
Rood, JI
Shimizu, T
机构
[1] UNIV TSUKUBA,INST BASIC MED SCI,DEPT MICROBIOL,TSUKUBA,IBARAKI 305,JAPAN
[2] MONASH UNIV,DEPT MICROBIOL,CLAYTON,VIC 3168,AUSTRALIA
[3] CSL LTD,PARKVILLE,VIC 3052,AUSTRALIA
关键词
D O I
10.1128/jb.178.9.2514-2520.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Extracellular toxin production in Clostridium perfringens is positively regulated by the two-component regulatory genes virR and virS, Northern (RNA) blots carried out with RNA preparations from the wild-type strain 13 and the isogenic virR and virS mutants TS133 and JIR4000 showed that the virR and virS genes composed an operon and were transcribed as a single 2,1-kb mRNA molecule, Primer extension analysis led to the identification of two promoters upstream of virR, Hybridization analysis of the mutants and their complemented derivatives showed that the virR/virS system positively regulated the production of alpha-toxin (or phospholipase C), theta-toxin (perfringolysin O), and kappa-toxin (collagenase) at the transcriptional level, However, the modes of regulation of these genes were shown to differ, The theta-toxin structural gene, pfoA, had both a major and a very minor promoter, with the major promoter being virR/virS dependent, The coLA gene, which encodes the kappa-toxin, had two major promoters, only one of which was virR/virS-dependent. In contrast, the alpha-toxin structural gene, pie, had only one promoter, which was shown to be partially regulated by the virR and virS genes. Comparative analysis of the virR/virS-dependent promoters did not reveal any common sequence motifs that could represent VirR-binding sites. It was concluded that either the virR/virS system modulates its effects via secondary regulatory genes that are specific for each toxin structural gene or the VirR protein does not have a single consensus binding sequence.
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页码:2514 / 2520
页数:7
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