Literature DB >> 7867068

Ectopic expression of the flagellar regulon alters development of the Bordetella-host interaction.

B J Akerley1, P A Cotter, J F Miller.   

Abstract

Signal transduction molecules within the two-component family represent a conserved adaptation for the control of genes involved in pathogenesis. The Bordetella virulence control locus, bvgAS, activates and represses gene expression in response to environmental signals. While infection requires virulence gene activation, the role of gene repression during infection is not understood. By altering regulatory genes and reversing regulatory connections, we found evidence that the BvgAS-repressed genes responsible for motility are neither required nor expressed during colonization of the host. Expression of this Bvg- phase-specific phenotype in the Bvg+ growth phase resulted in a defect in tracheal colonization. Therefore, BvgAS promotes virulence both by activating genes required for colonization and by repressing genes that inhibit the development of infection.

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Year:  1995        PMID: 7867068     DOI: 10.1016/0092-8674(95)90515-4

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  126 in total

1.  Differential regulation of Bvg-activated virulence factors plays a role in Bordetella pertussis pathogenicity.

Authors:  S M Kinnear; R R Marques; N H Carbonetti
Journal:  Infect Immun       Date:  2001-04       Impact factor: 3.441

2.  Multiple control of flagellum biosynthesis in Escherichia coli: role of H-NS protein and the cyclic AMP-catabolite activator protein complex in transcription of the flhDC master operon.

Authors:  O Soutourina; A Kolb; E Krin; C Laurent-Winter; S Rimsky; A Danchin; P Bertin
Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

3.  Helicobacter pylori uses motility for initial colonization and to attain robust infection.

Authors:  Karen M Ottemann; Andrew C Lowenthal
Journal:  Infect Immun       Date:  2002-04       Impact factor: 3.441

4.  Transcriptional regulation of the esp genes of enterohemorrhagic Escherichia coli.

Authors:  F Beltrametti; A U Kresse; C A Guzmán
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

5.  Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei.

Authors:  A A Al Mamun; A Tominaga; M Enomoto
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

6.  Differential modulation of Bordetella pertussis virulence genes as evidenced by DNA microarray analysis.

Authors:  D Hot; R Antoine; G Renauld-Mongénie; V Caro; B Hennuy; E Levillain; L Huot; G Wittmann; D Poncet; F Jacob-Dubuisson; C Guyard; F Rimlinger; L Aujame; E Godfroid; N Guiso; M-J Quentin-Millet; Y Lemoine; C Locht
Journal:  Mol Genet Genomics       Date:  2003-05-24       Impact factor: 3.291

7.  Contribution of Bordetella bronchiseptica filamentous hemagglutinin and pertactin to respiratory disease in swine.

Authors:  Tracy L Nicholson; Susan L Brockmeier; Crystal L Loving
Journal:  Infect Immun       Date:  2009-02-23       Impact factor: 3.441

8.  The BfeR regulator mediates enterobactin-inducible expression of Bordetella enterobactin utilization genes.

Authors:  Mark T Anderson; Sandra K Armstrong
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

9.  MgrA, an orthologue of Mga, Acts as a transcriptional repressor of the genes within the rlrA pathogenicity islet in Streptococcus pneumoniae.

Authors:  Carolyn Hemsley; Elizabeth Joyce; David L Hava; Amita Kawale; Andrew Camilli
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

10.  Contribution of regulation by the bvg locus to respiratory infection of mice by Bordetella pertussis.

Authors:  T J Merkel; S Stibitz; J M Keith; M Leef; R Shahin
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

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