Literature DB >> 20097818

Polymorphic mutation frequencies of clinical and environmental Stenotrophomonas maltophilia populations.

María Carmen Turrientes1, María Rosario Baquero, María Blanca Sánchez, Sylvia Valdezate, Esther Escudero, Gabrielle Berg, Rafael Cantón, Fernando Baquero, Juan Carlos Galán, José Luis Martínez.   

Abstract

Mutation frequencies were studied in 174 Stenotrophomonas maltophilia isolates from clinical and nonclinical environments by detecting spontaneous rifampin-resistant mutants in otherwise-susceptible populations. The distribution of mutation frequencies followed a pattern similar to that found for other bacterial species, with a modal value of 1 x 10(-8). Nevertheless, the proportion of isolates showing mutation frequencies below the modal value (hypomutators) was significantly higher for S. maltophilia than those so far reported in other organisms. Low mutation frequencies were particularly frequent among environmental S. maltophilia strains (58.3%), whereas strong mutators were found only among isolates with a clinical origin. These results indicate that clinical environments might select bacterial populations with high mutation frequencies, likely by second-order selection processes. In several of the strong-mutator isolates, functional-complementation assays with a wild-type allele of the mutS gene demonstrated that the mutator phenotype was due to the impairment of MutS activity. In silico analysis of the amino acid changes present in the MutS proteins of these hypermutator strains in comparison with the normomutator isolates suggests that the cause of the defect in MutS might be a H683P amino acid change.

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Year:  2010        PMID: 20097818      PMCID: PMC2838010          DOI: 10.1128/AEM.02817-09

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  78 in total

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Journal:  Genome Biol       Date:  2008-04-17       Impact factor: 13.583

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Review 6.  Achromobacter xylosoxidans and Stenotrophomonas maltophilia: Emerging Pathogens Well-Armed for Life in the Cystic Fibrosis Patients' Lung.

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7.  Spontaneous emergence of multiple drug resistance in tuberculosis before and during therapy.

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8.  The binding of triclosan to SmeT, the repressor of the multidrug efflux pump SmeDEF, induces antibiotic resistance in Stenotrophomonas maltophilia.

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