Regulatory cascade controls virulence in Vibrio cholerae.
- 15 June 1991
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 88 (12) , 5403-5407
- https://doi.org/10.1073/pnas.88.12.5403
Abstract
Expression of more than 17 virulence genes in Vibrio cholerae is under the coordinate control of the ToxR protein. ToxR is a transmembrane protein that binds to and activates the promoter of the operon encoding cholera toxin. As yet, the ability of ToxR to activate directly other genes in this regulon has not been demonstrated. We have cloned a gene called toxT from V. cholerae 569B; the toxT gene product, like ToxR, can activate the ctx promoter in Escherichia coli. In addition, expression of other genes identified as members of the ToxR regulon (tcpA, tcpI, aldA, and tagA) can be activated in E. coli by the toxT gene product but not by ToxR. When expressed from a constitutive promoter, the toxT gene product partially suppresses the ToxR- phenotype of a toxR deletion mutant of V. cholerae. The level of toxT mRNA is greatly reduced in a toxR mutant of V. cholerae. In addition, growth conditions under which the ToxR regulon is not expressed also repress the synthesis of toxT mRNA. These results suggest that ToxR controls transcription of toxT, whose product in turn is directly responsible for activation of several virulence genes under ToxR control.Keywords
This publication has 27 references indexed in Scilit:
- New attenuated derivatives of Vibrio choleraeResearch in Microbiology, 1990
- Cholera toxin transcriptional activator ToxR is a transmembrane DNA binding proteinPublished by Elsevier ,1987
- TnphoA: a transposon probe for protein export signals.Proceedings of the National Academy of Sciences, 1985
- Synthesis of cholera toxin is positively regulated at the transcriptional level by toxR.Proceedings of the National Academy of Sciences, 1984
- Cholera toxin genes: nucleotide sequence, deletion analysis and vaccine developmentNature, 1983
- Construction of a broad host range cosmid cloning vector and its use in the genetic analysis of Rhizobium mutantsGene, 1982
- Evidence for two functional gal promoters in intact Escherichia coli cells.Journal of Biological Chemistry, 1981
- Cascades of sigma factorsCell, 1981
- Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.Proceedings of the National Academy of Sciences, 1980
- Recombination genes on the Escherichia coli sex factor specific for transposable elements.Proceedings of the National Academy of Sciences, 1980