<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="http://hdl.handle.net/10362/3734">
    <title>DSpace Collection:</title>
    <link>http://hdl.handle.net/10362/3734</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://hdl.handle.net/10362/5855" />
      </rdf:Seq>
    </items>
    <dc:date>2013-05-18T05:54:53Z</dc:date>
  </channel>
  <item rdf:about="http://hdl.handle.net/10362/5855">
    <title>Genetic diversity of arginine catabolic mobile element in Staphylococcus epidermidis</title>
    <link>http://hdl.handle.net/10362/5855</link>
    <description>Title: Genetic diversity of arginine catabolic mobile element in Staphylococcus epidermidis
Authors: Miragaia, M; de Lencastre, H; Perdreau-Remington, F; Chambers, HF; Higashi, J; Sullam, PM; Lin, J; Wong, KI; King, KA; Otto, M; Sensabaugh, GF; Diep, BA
Abstract: Background: The methicillin-resistant Staphylococcus aureus clone USA300&#xD;
contains a novel mobile genetic element, arginine catabolic mobile element&#xD;
( ACME), that contributes to its enhanced capacity to grow and survive within&#xD;
the host. Although ACME appears to have been transferred into USA300 from S.&#xD;
epidermidis, the genetic diversity of ACME in the latter species remains poorly&#xD;
characterized. Methodology/Principal Findings: To assess the prevalence and&#xD;
genetic diversity of ACME, 127 geographically diverse S. epidermidis isolates&#xD;
representing 86 different multilocus sequence types (STs) were characterized.&#xD;
ACME was found in 51% (65/127) of S. epidermidis isolates. The vast majority&#xD;
(57/65) of ACME-containing isolates belonged to the predominant S. epidermidis&#xD;
clonal complex CC2. ACME was often found in association with different allotypes&#xD;
of staphylococcal chromosome cassette mec (SCCmec) which also encodes the&#xD;
recombinase function that facilities mobilization ACME from the S. epidermidis&#xD;
chromosome. Restriction fragment length polymorphism, PCR scanning and DNA&#xD;
sequencing allowed for identification of 39 distinct ACME genetic variants that&#xD;
differ from one another in gene content, thereby revealing a hitherto&#xD;
uncharacterized genetic diversity within ACME. All but one ACME variants were&#xD;
represented by a single S. epidermidis isolate; the singular variant, termed&#xD;
ACME-I.02, was found in 27 isolates, all of which belonged to the CC2 lineage.&#xD;
An evolutionary model constructed based on the eBURST algorithm revealed that&#xD;
ACME-I.02 was acquired at least on 15 different occasions by strains belonging&#xD;
to the CC2 lineage. Conclusions/Significance: ACME-I.02 in diverse S.&#xD;
epidermidis isolates were nearly identical in sequence to the prototypical ACME&#xD;
found in USA300 MRSA clone, providing further evidence for the interspecies&#xD;
transfer of ACME from S. epidermidis into USA300.
Description: PLos One, 4(11): ARTe7722</description>
    <dc:date>2009-01-01T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

