Literature DB >> 26033734

Altered Competitive Fitness, Antimicrobial Susceptibility, and Cellular Morphology in a Triclosan-Induced Small-Colony Variant of Staphylococcus aureus.

Sarah Forbes1, Joe Latimer1, Abdulrahman Bazaid1, Andrew J McBain2.   

Abstract

Staphylococcus aureus can produce small-colony variants (SCVs) that express various phenotypes. While their significance is unclear, SCV propagation may be influenced by relative fitness, antimicrobial susceptibility, and the underlying mechanism. We have investigated triclosan-induced generation of SCVs in six S. aureus strains, including methicillin-resistant S. aureus (MRSA). Parent strains (P0) were repeatedly passaged on concentration gradients of triclosan using a solid-state exposure system to generate P10. P10 was subsequently passaged without triclosan to generate X10. Susceptibility to triclosan and 7 antibiotics was assessed at all stages. For S. aureus ATCC 6538, SCVs were further characterized by determining microbicide susceptibility and competitive fitness. Cellular morphology was examined using electron microscopy, and protein expression was evaluated through proteomics. Triclosan susceptibility in all SCVs (which could be generated from 4/6 strains) was markedly decreased, while antibiotic susceptibility was significantly increased in the majority of cases. An SCV of S. aureus ATCC 6538 exhibited significantly increased susceptibility to all tested microbicides. Cross-wall formation was impaired in this bacterium, while expression of FabI, a target of triclosan, and IsaA, a lytic transglycosylase involved in cell division, was increased. The P10 SCV was 49% less fit than P0. In summary, triclosan exposure of S. aureus produced SCVs in 4/6 test bacteria, with decreased triclosan susceptibility but with generally increased antibiotic susceptibility. An SCV derived from S. aureus ATCC 6538 showed reduced competitive fitness, potentially due to impaired cell division. In this SCV, increased FabI expression could account for reduced triclosan susceptibility, while IsaA may be upregulated in response to cell division defects.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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Year:  2015        PMID: 26033734      PMCID: PMC4505237          DOI: 10.1128/AAC.00352-15

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  43 in total

1.  A triclosan-resistant bacterial enzyme.

Authors:  R J Heath; C O Rock
Journal:  Nature       Date:  2000-07-13       Impact factor: 49.962

2.  BSAC standardized disc susceptibility testing method.

Authors:  J M Andrews
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3.  Membranotropic effects of the antibacterial agent Triclosan.

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Review 4.  Small colony variants of Staphylococci: a link to persistent infections.

Authors:  C von Eiff; R A Proctor; G Peters
Journal:  Berl Munch Tierarztl Wochenschr       Date:  2000-09       Impact factor: 0.328

5.  Triclosan resistance in methicillin-resistant Staphylococcus aureus expressed as small colony variants: a novel mode of evasion of susceptibility to antiseptics.

Authors:  Roger Bayston; Waheed Ashraf; Toni Smith
Journal:  J Antimicrob Chemother       Date:  2007-03-02       Impact factor: 5.790

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7.  Persistence of a Staphylococcus aureus small-colony variant under antibiotic pressure in vivo.

Authors:  Eric Brouillette; Alejandro Martinez; Bobbi J Boyll; Norris E Allen; François Malouin
Journal:  FEMS Immunol Med Microbiol       Date:  2004-05-01

8.  Thymidine-dependent small-colony variants of Staphylococcus aureus exhibit gross morphological and ultrastructural changes consistent with impaired cell separation.

Authors:  Barbara C Kahl; Gunnar Belling; Rudolf Reichelt; Mathias Herrmann; Richard A Proctor; Georg Peters
Journal:  J Clin Microbiol       Date:  2003-01       Impact factor: 5.948

9.  Physiological characterization of a heme-deficient mutant of Staphylococcus aureus by a proteomic approach.

Authors:  Christian Kohler; Christof von Eiff; Georg Peters; Richard A Proctor; Michael Hecker; Susanne Engelmann
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Journal:  Int J Med Microbiol       Date:  2007-04-06       Impact factor: 3.473

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3.  Functional mgrA Influences Genetic Changes within a Staphylococcus aureus Cell Population over Time.

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4.  Fatty Acid Supplementation Reverses the Small Colony Variant Phenotype in Triclosan-Adapted Staphylococcus aureus: Genetic, Proteomic and Phenotypic Analyses.

Authors:  Abdulrahman S Bazaid; Sarah Forbes; Gavin J Humphreys; Ruth G Ledder; Ronan O'Cualain; Andrew J McBain
Journal:  Sci Rep       Date:  2018-03-01       Impact factor: 4.379

5.  Anaerobiosis influences virulence properties of Pseudomonas aeruginosa cystic fibrosis isolates and the interaction with Staphylococcus aureus.

Authors:  Ross Pallett; Laura J Leslie; Peter A Lambert; Ivana Milic; Andrew Devitt; Lindsay J Marshall
Journal:  Sci Rep       Date:  2019-05-01       Impact factor: 4.379

6.  In Vitro Activity of the Bacteriophage Endolysin HY-133 against Staphylococcus aureus Small-Colony Variants and Their Corresponding Wild Types.

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Journal:  Int J Mol Sci       Date:  2019-02-07       Impact factor: 5.923

7.  Improving the Therapeutic Index of Smp24, a Venom-Derived Antimicrobial Peptide: Increased Activity against Gram-Negative Bacteria.

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8.  Extracellular DNA released by glycine-auxotrophic Staphylococcus epidermidis small colony variant facilitates catheter-related infections.

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Review 9.  Reduced Susceptibility and Increased Resistance of Bacteria against Disinfectants: A Systematic Review.

Authors:  Urška Rozman; Marko Pušnik; Sergej Kmetec; Darja Duh; Sonja Šostar Turk
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