Literature DB >> 11136463

The psp locus of Yersinia enterocolitica is required for virulence and for growth in vitro when the Ysc type III secretion system is produced.

A J Darwin1, V L Miller.   

Abstract

The phage shock protein locus (pspFpspABCDE) of Escherichia coli has proved to be something of an enigma since its discovery. The physiological functions of the psp locus, including those of the predicted effector protein PspA, are unknown. In a previous genetic screen, we determined that a Yersinia enterocolitica pspC mutant was severely attenuated for virulence. In this study, the psp locus of Y. enterocolitica was characterized further. The pspC gene of Y. enterocolitica was found to be important for normal growth when the Ysc type III secretion system was expressed in the laboratory. This growth defect was specifically caused by production of the secretin protein, YscC. Expression of the psp genes was induced when the type III secretion system was functional or when only the yscC gene was expressed. This induction of psp gene expression required a functional pspC gene. Most significantly, evidence suggests that the expression of at least one gene that is not part of the psp locus is regulated by Psp proteins. This unidentified gene (or genes) may also be important for growth when the type III secretion system is expressed. These conclusions are supported by the effects of various psp mutations on virulence. This is the first indication that Psp proteins might be involved in the regulation of genes besides the psp locus itself.

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Year:  2001        PMID: 11136463     DOI: 10.1046/j.1365-2958.2001.02235.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  50 in total

1.  Type III secretion chaperone-dependent regulation: activation of virulence genes by SicA and InvF in Salmonella typhimurium.

Authors:  K H Darwin; V L Miller
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

2.  Membrane association of PspA depends on activation of the phage-shock-protein response in Yersinia enterocolitica.

Authors:  Saori Yamaguchi; Erwan Gueguen; N Kaye Horstman; Andrew J Darwin
Journal:  Mol Microbiol       Date:  2010-10       Impact factor: 3.501

3.  Sigma54-dependent transcription activator phage shock protein F of Escherichia coli: a fragmentation approach to identify sequences that contribute to self-association.

Authors:  Patricia Bordes; Siva R Wigneshweraraj; Xiaodong Zhang; Martin Buck
Journal:  Biochem J       Date:  2004-03-15       Impact factor: 3.857

4.  A novel family of Escherichia coli toxin-antitoxin gene pairs.

Authors:  Jason M Brown; Karen Joy Shaw
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

5.  Temporal global changes in gene expression during temperature transition in Yersinia pestis.

Authors:  Vladimir L Motin; Anca M Georgescu; Joseph P Fitch; Pauline P Gu; David O Nelson; Shalini L Mabery; Janine B Garnham; Bahrad A Sokhansanj; Linda L Ott; Matthew A Coleman; Jeffrey M Elliott; Laura M Kegelmeyer; Andrew J Wyrobek; Thomas R Slezak; Robert R Brubaker; Emilio Garcia
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

6.  Phage shock proteins B and C prevent lethal cytoplasmic membrane permeability in Yersinia enterocolitica.

Authors:  N Kaye Horstman; Andrew J Darwin
Journal:  Mol Microbiol       Date:  2012-06-12       Impact factor: 3.501

7.  Improved system for construction and analysis of single-copy beta-galactosidase operon fusions in Yersinia enterocolitica.

Authors:  Michelle E Maxson; Andrew J Darwin
Journal:  Appl Environ Microbiol       Date:  2005-09       Impact factor: 4.792

8.  Multiple promoters control expression of the Yersinia enterocolitica phage-shock-protein A (pspA) operon.

Authors:  Michelle E Maxson; Andrew J Darwin
Journal:  Microbiology (Reading)       Date:  2006-04       Impact factor: 2.777

9.  Interactions between the Cytoplasmic Domains of PspB and PspC Silence the Yersinia enterocolitica Phage Shock Protein Response.

Authors:  Josué Flores-Kim; Andrew J Darwin
Journal:  J Bacteriol       Date:  2016-11-18       Impact factor: 3.490

10.  Analysis of the Yersinia enterocolitica PspBC proteins defines functional domains, essential amino acids and new roles within the phage-shock-protein response.

Authors:  Erwan Gueguen; Diana C Savitzky; Andrew J Darwin
Journal:  Mol Microbiol       Date:  2009-09-22       Impact factor: 3.501

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