Literature DB >> 8682766

Starvation- and Stationary-phase-induced resistance to the antimicrobial peptide polymyxin B in Salmonella typhimurium is RpoS (sigma(S)) independent and occurs through both phoP-dependent and -independent pathways.

G I McLeod1, M P Spector.   

Abstract

A common stress encountered by Salmonella serovars involves exposure to membrane-permeabilizing antimicrobial peptides and proteins such as defensins, cationic antibacterial proteins, and polymyxins. We wanted to determine if starvation induces cross-resistance to the membrane-permeabilizing antimicrobial peptide polymyxin B (PmB). We report here that starved and stationary-phase (Luria-Bertani [LB] medium) cells exhibited ca. 200- to 1,500-fold-higher (cross-)resistance to a 60-min PmB challenge than log-phase cells. Genetic analysis indicates that this PmB resistance involves both phoP-dependent and -independent pathways. Furthermore, both pathways were sigma(S) independent, indicating that they are different from other known sigma(S) -dependent cross-resistance mechanisms. Additionally, both pathways were important for PmB resistance early during C starvation and for cells in stationary phase in LB medium. However, only the phoP-independent pathway was important for P-starvation-induced PmB resistance and the sustained PmB resistance seen in 24-h-C-starved (and N-starved) or stationary-phase cells in LB medium. The results indicate the presence of an rpoS- and phoP-independent pathway important to starvation- and stationary-phase-induced resistance to membrane-permeabilizing antimicrobial agents.

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Year:  1996        PMID: 8682766      PMCID: PMC178147          DOI: 10.1128/jb.178.13.3683-3688.1996

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


  34 in total

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2.  Global control in Salmonella typhimurium: two-dimensional electrophoretic analysis of starvation-, anaerobiosis-, and heat shock-inducible proteins.

Authors:  M P Spector; Z Aliabadi; T Gonzalez; J W Foster
Journal:  J Bacteriol       Date:  1986-10       Impact factor: 3.490

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Authors:  M Givskov; L Eberl; S Møller; L K Poulsen; S Molin
Journal:  J Bacteriol       Date:  1994-01       Impact factor: 3.490

4.  Characterization of defensin resistance phenotypes associated with mutations in the phoP virulence regulon of Salmonella typhimurium.

Authors:  S I Miller; W S Pulkkinen; M E Selsted; J J Mekalanos
Journal:  Infect Immun       Date:  1990-11       Impact factor: 3.441

5.  A two-component regulatory system (phoP phoQ) controls Salmonella typhimurium virulence.

Authors:  S I Miller; A M Kukral; J J Mekalanos
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

6.  Starvation proteins in Escherichia coli: kinetics of synthesis and role in starvation survival.

Authors:  R G Groat; J E Schultz; E Zychlinsky; A Bockman; A Matin
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Authors:  T Nyström; R M Olsson; S Kjelleberg
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9.  Starvation-inducible loci of Salmonella typhimurium: regulation and roles in starvation-survival.

Authors:  M P Spector; C L Cubitt
Journal:  Mol Microbiol       Date:  1992-06       Impact factor: 3.501

10.  Molecular genetic analysis of a locus required for resistance to antimicrobial peptides in Salmonella typhimurium.

Authors:  C Parra-Lopez; M T Baer; E A Groisman
Journal:  EMBO J       Date:  1993-11       Impact factor: 11.598

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  20 in total

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6.  Regulation of polymyxin resistance and adaptation to low-Mg2+ environments.

Authors:  E A Groisman; J Kayser; F C Soncini
Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

7.  Role of antibiotic penetration limitation in Klebsiella pneumoniae biofilm resistance to ampicillin and ciprofloxacin.

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8.  Inorganic polyphosphate is essential for long-term survival and virulence factors in Shigella and Salmonella spp.

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

9.  Escherichia coli biofilms formed under low-shear modeled microgravity in a ground-based system.

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10.  A new approach for the discovery of antibiotics by targeting non-multiplying bacteria: a novel topical antibiotic for staphylococcal infections.

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