Literature DB >> 9371470

Influence of genes encoding proton-translocating enzymes on suppression of Salmonella typhimurium growth and colonization.

L Zhang-Barber1, A K Turner, G Martin, G Frankel, G Dougan, P A Barrow.   

Abstract

Twenty-four-hour-old, aerobically grown, Luria-Bertani broth cultures of Salmonella typhimurium F98 suppressed the growth of a spectinomycin-resistant (Spcr) derivative of the same strain inoculated at 10(3) CFU ml(-1). This growth suppression is genus specific and RpoS independent, and it is not solely a result of nutrient depletion (P. A. Barrow, M. A. Lovell, and L. Zhang-Barber, J. Bacteriol. 178:3072-3076, 1996). Mutations in three genes are shown here to significantly reduce growth suppression under these conditions. The mutations were located in the nuo, cyd, and unc operons, which code for the NADH dehydrogenase I, cytochrome d oxidase, and F0F1 proton-translocating ATPase complexes, respectively. When cultures were grown under strictly anaerobic conditions, only the unc mutant did not suppress growth. Prior colonization of the alimentary tract of newly hatched chickens with the S. typhimurium F98 wild type or nuo or cyd mutants suppressed colonization by an S. typhimurium F98 Spcr derivative inoculated 24 h later. In contrast, the S. typhimurium unc mutant did not suppress colonization. The nuo and unc mutants showed poorer growth on certain carbon sources. The data support the hypothesis that growth suppression operates because of the absence of a utilizable carbon source or electron acceptor.

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Year:  1997        PMID: 9371470      PMCID: PMC179664          DOI: 10.1128/jb.179.22.7186-7190.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  25 in total

1.  Growth suppression in early-stationary-phase nutrient broth cultures of Salmonella typhimurium and Escherichia coli is genus specific and not regulated by sigma S.

Authors:  P A Barrow; M A Lovell; L Z Barber
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

2.  Stabilization of a HemA-LacZ hybrid protein against proteolysis during carbon starvation in atp mutants of Salmonella typhimurium.

Authors:  C D Archer; J Jin; T Elliott
Journal:  J Bacteriol       Date:  1996-04       Impact factor: 3.490

3.  Cytochrome o (cyoABCDE) and d (cydAB) oxidase gene expression in Escherichia coli is regulated by oxygen, pH, and the fnr gene product.

Authors:  P A Cotter; V Chepuri; R B Gennis; R P Gunsalus
Journal:  J Bacteriol       Date:  1990-11       Impact factor: 3.490

4.  Further studies on the inhibition of colonization of the chicken alimentary tract with Salmonella typhimurium by pre-colonization with an avirulent mutant.

Authors:  A Berchieri; P A Barrow
Journal:  Epidemiol Infect       Date:  1990-06       Impact factor: 2.451

5.  Salmonella typhimurium loci involved in survival within macrophages.

Authors:  A J Bäumler; J G Kusters; I Stojiljkovic; F Heffron
Journal:  Infect Immun       Date:  1994-05       Impact factor: 3.441

6.  Mutants defective in the energy-conserving NADH dehydrogenase of Salmonella typhimurium identified by a decrease in energy-dependent proteolysis after carbon starvation.

Authors:  C D Archer; X Wang; T Elliott
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-01       Impact factor: 11.205

7.  Escherichia coli mutants lacking NADH dehydrogenase I have a competitive disadvantage in stationary phase.

Authors:  M M Zambrano; R Kolter
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

8.  Mutations in NADH:ubiquinone oxidoreductase of Escherichia coli affect growth on mixed amino acids.

Authors:  B M Prüss; J M Nelms; C Park; A J Wolfe
Journal:  J Bacteriol       Date:  1994-04       Impact factor: 3.490

9.  arc-dependent thermal regulation and extragenic suppression of the Escherichia coli cytochrome d operon.

Authors:  D Wall; J M Delaney; O Fayet; B Lipinska; T Yamamoto; C Georgopoulos
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

10.  Host specificity of Salmonella infection in chickens and mice is expressed in vivo primarily at the level of the reticuloendothelial system.

Authors:  P A Barrow; M B Huggins; M A Lovell
Journal:  Infect Immun       Date:  1994-10       Impact factor: 3.441

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Authors:  Vitaliy B Borisov; Robert B Gennis; James Hemp; Michael I Verkhovsky
Journal:  Biochim Biophys Acta       Date:  2011-07-01

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Authors:  S Hudault; J Guignot; A L Servin
Journal:  Gut       Date:  2001-07       Impact factor: 23.059

3.  Salmonella enterica serovar typhimurium colonizing the lumen of the chicken intestine grows slowly and upregulates a unique set of virulence and metabolism genes.

Authors:  P C Harvey; M Watson; S Hulme; M A Jones; M Lovell; A Berchieri; J Young; N Bumstead; P Barrow
Journal:  Infect Immun       Date:  2011-07-18       Impact factor: 3.441

4.  Contribution of proton-translocating proteins to the virulence of Salmonella enterica serovars Typhimurium, Gallinarum, and Dublin in chickens and mice.

Authors:  A K Turner; L Z Barber; P Wigley; S Muhammad; M A Jones; M A Lovell; S Hulme; P A Barrow
Journal:  Infect Immun       Date:  2003-06       Impact factor: 3.441

5.  Molecular characterization of benzimidazole resistance in Helicobacter pylori.

Authors:  Scott D Mills; Wei Yang; Kathleen MacCormack
Journal:  Antimicrob Agents Chemother       Date:  2004-07       Impact factor: 5.191

6.  Cytochrome bd Displays Significant Quinol Peroxidase Activity.

Authors:  Sinan Al-Attar; Yuanjie Yu; Martijn Pinkse; Jo Hoeser; Thorsten Friedrich; Dirk Bald; Simon de Vries
Journal:  Sci Rep       Date:  2016-06-09       Impact factor: 4.379

Review 7.  Terminal Respiratory Oxidases: A Targetables Vulnerability of Mycobacterial Bioenergetics?

Authors:  Sapna Bajeli; Navin Baid; Manjot Kaur; Ganesh P Pawar; Vinod D Chaudhari; Ashwani Kumar
Journal:  Front Cell Infect Microbiol       Date:  2020-11-23       Impact factor: 5.293

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