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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2006-6-26
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pubmed:abstractText |
In this report we have examined the role of the regulatory alarmone (p)ppGpp on expression of virulence determinants of uropathogenic Escherichia coli strains. The ability to form biofilms is shown to be markedly diminished in (p)ppGpp-deficient strains. We present evidence (i) that (p)ppGpp tightly regulates expression of the type 1 fimbriae in both commensal and pathogenic E. coli isolates by increasing the subpopulation of cells that express the type 1 fimbriae; and (ii) that the effect of (p)ppGpp on the number of fimbrial expressing cells can ultimately be traced to its role in transcription of the fimB recombinase gene, whose product mediates inversion of the fim promoter to the productive (ON) orientation. Primer extension analysis suggests that the effect of (p)ppGpp on transcription of fimB occurs by altering the activity of only one of the two fimB promoters. Furthermore, spontaneous mutants with properties characteristic of ppGpp(0) suppressors restore fimB transcription and consequent downstream effects in the absence of (p)ppGpp. Consistently, the rpoB3770 allele also fully restores transcription of fimB in a ppGpp(0) strain and artificially elevated levels of FimB bypass the need for (p)ppGpp for type 1 fimbriation. Our findings suggest that the (p)ppGpp-stimulated expression of type 1 fimbriae may be relevant during the interaction of pathogenic E. coli with the host.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Nucleotidyltransferases,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Escherichia coli Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Fimbriae Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Pentaphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Tetraphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/H-NS protein, bacteria,
http://linkedlifedata.com/resource/pubmed/chemical/Integrases,
http://linkedlifedata.com/resource/pubmed/chemical/NanR protein, E coli,
http://linkedlifedata.com/resource/pubmed/chemical/Sigma Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Site-specific recombinase,
http://linkedlifedata.com/resource/pubmed/chemical/fimB protein, E coli,
http://linkedlifedata.com/resource/pubmed/chemical/fimbrillin,
http://linkedlifedata.com/resource/pubmed/chemical/sigma factor KatF protein, Bacteria
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0950-382X
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
60
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1520-33
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16796685-Agglutination,
pubmed-meshheading:16796685-Bacterial Proteins,
pubmed-meshheading:16796685-Biofilms,
pubmed-meshheading:16796685-DNA Nucleotidyltransferases,
pubmed-meshheading:16796685-DNA-Binding Proteins,
pubmed-meshheading:16796685-Escherichia coli,
pubmed-meshheading:16796685-Escherichia coli Proteins,
pubmed-meshheading:16796685-Fimbriae, Bacterial,
pubmed-meshheading:16796685-Fimbriae Proteins,
pubmed-meshheading:16796685-Gene Expression Regulation, Bacterial,
pubmed-meshheading:16796685-Guanosine Pentaphosphate,
pubmed-meshheading:16796685-Guanosine Tetraphosphate,
pubmed-meshheading:16796685-Integrases,
pubmed-meshheading:16796685-Mutation,
pubmed-meshheading:16796685-Promoter Regions, Genetic,
pubmed-meshheading:16796685-Sigma Factor,
pubmed-meshheading:16796685-Suppression, Genetic,
pubmed-meshheading:16796685-Transcription, Genetic,
pubmed-meshheading:16796685-Urologic Diseases,
pubmed-meshheading:16796685-Yeasts
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pubmed:year |
2006
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pubmed:articleTitle |
(p)ppGpp regulates type 1 fimbriation of Escherichia coli by modulating the expression of the site-specific recombinase FimB.
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pubmed:affiliation |
Department of Molecular Biology, Umeå University, S-90187 Umeå, Sweden.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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