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Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis

BACKGROUND: The methicillin-resistant Staphylococcus aureus clone USA300 contains a novel mobile genetic element, arginine catabolic mobile element (ACME), that contributes to its enhanced capacity to grow and survive within the host. Although ACME appears to have been transferred into USA300 from S...

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Autores principales: Miragaia, Maria, de Lencastre, Herminia, Perdreau-Remington, Francoise, Chambers, Henry F., Higashi, Julie, Sullam, Paul M., Lin, Jessica, Wong, Kester I., King, Katherine A., Otto, Michael, Sensabaugh, George F., Diep, Binh An
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768820/
https://www.ncbi.nlm.nih.gov/pubmed/19893740
http://dx.doi.org/10.1371/journal.pone.0007722
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author Miragaia, Maria
de Lencastre, Herminia
Perdreau-Remington, Francoise
Chambers, Henry F.
Higashi, Julie
Sullam, Paul M.
Lin, Jessica
Wong, Kester I.
King, Katherine A.
Otto, Michael
Sensabaugh, George F.
Diep, Binh An
author_facet Miragaia, Maria
de Lencastre, Herminia
Perdreau-Remington, Francoise
Chambers, Henry F.
Higashi, Julie
Sullam, Paul M.
Lin, Jessica
Wong, Kester I.
King, Katherine A.
Otto, Michael
Sensabaugh, George F.
Diep, Binh An
author_sort Miragaia, Maria
collection PubMed
description BACKGROUND: The methicillin-resistant Staphylococcus aureus clone USA300 contains a novel mobile genetic element, arginine catabolic mobile element (ACME), that contributes to its enhanced capacity to grow and survive within the host. Although ACME appears to have been transferred into USA300 from S. epidermidis, the genetic diversity of ACME in the latter species remains poorly characterized. METHODOLOGY/PRINCIPAL FINDINGS: To assess the prevalence and genetic diversity of ACME, 127 geographically diverse S. epidermidis isolates representing 86 different multilocus sequence types (STs) were characterized. ACME was found in 51% (65/127) of S. epidermidis isolates. The vast majority (57/65) of ACME-containing isolates belonged to the predominant S. epidermidis clonal complex CC2. ACME was often found in association with different allotypes of staphylococcal chromosome cassette mec (SCCmec) which also encodes the recombinase function that facilities mobilization ACME from the S. epidermidis chromosome. Restriction fragment length polymorphism, PCR scanning and DNA sequencing allowed for identification of 39 distinct ACME genetic variants that differ from one another in gene content, thereby revealing a hitherto uncharacterized genetic diversity within ACME. All but one ACME variants were represented by a single S. epidermidis isolate; the singular variant, termed ACME-I.02, was found in 27 isolates, all of which belonged to the CC2 lineage. An evolutionary model constructed based on the eBURST algorithm revealed that ACME-I.02 was acquired at least on 15 different occasions by strains belonging to the CC2 lineage. CONCLUSIONS/SIGNIFICANCE: ACME-I.02 in diverse S. epidermidis isolates were nearly identical in sequence to the prototypical ACME found in USA300 MRSA clone, providing further evidence for the interspecies transfer of ACME from S. epidermidis into USA300.
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spelling pubmed-27688202009-11-06 Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis Miragaia, Maria de Lencastre, Herminia Perdreau-Remington, Francoise Chambers, Henry F. Higashi, Julie Sullam, Paul M. Lin, Jessica Wong, Kester I. King, Katherine A. Otto, Michael Sensabaugh, George F. Diep, Binh An PLoS One Research Article BACKGROUND: The methicillin-resistant Staphylococcus aureus clone USA300 contains a novel mobile genetic element, arginine catabolic mobile element (ACME), that contributes to its enhanced capacity to grow and survive within the host. Although ACME appears to have been transferred into USA300 from S. epidermidis, the genetic diversity of ACME in the latter species remains poorly characterized. METHODOLOGY/PRINCIPAL FINDINGS: To assess the prevalence and genetic diversity of ACME, 127 geographically diverse S. epidermidis isolates representing 86 different multilocus sequence types (STs) were characterized. ACME was found in 51% (65/127) of S. epidermidis isolates. The vast majority (57/65) of ACME-containing isolates belonged to the predominant S. epidermidis clonal complex CC2. ACME was often found in association with different allotypes of staphylococcal chromosome cassette mec (SCCmec) which also encodes the recombinase function that facilities mobilization ACME from the S. epidermidis chromosome. Restriction fragment length polymorphism, PCR scanning and DNA sequencing allowed for identification of 39 distinct ACME genetic variants that differ from one another in gene content, thereby revealing a hitherto uncharacterized genetic diversity within ACME. All but one ACME variants were represented by a single S. epidermidis isolate; the singular variant, termed ACME-I.02, was found in 27 isolates, all of which belonged to the CC2 lineage. An evolutionary model constructed based on the eBURST algorithm revealed that ACME-I.02 was acquired at least on 15 different occasions by strains belonging to the CC2 lineage. CONCLUSIONS/SIGNIFICANCE: ACME-I.02 in diverse S. epidermidis isolates were nearly identical in sequence to the prototypical ACME found in USA300 MRSA clone, providing further evidence for the interspecies transfer of ACME from S. epidermidis into USA300. Public Library of Science 2009-11-06 /pmc/articles/PMC2768820/ /pubmed/19893740 http://dx.doi.org/10.1371/journal.pone.0007722 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Miragaia, Maria
de Lencastre, Herminia
Perdreau-Remington, Francoise
Chambers, Henry F.
Higashi, Julie
Sullam, Paul M.
Lin, Jessica
Wong, Kester I.
King, Katherine A.
Otto, Michael
Sensabaugh, George F.
Diep, Binh An
Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title_full Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title_fullStr Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title_full_unstemmed Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title_short Genetic Diversity of Arginine Catabolic Mobile Element in Staphylococcus epidermidis
title_sort genetic diversity of arginine catabolic mobile element in staphylococcus epidermidis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768820/
https://www.ncbi.nlm.nih.gov/pubmed/19893740
http://dx.doi.org/10.1371/journal.pone.0007722
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