<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Zhou Y</dc:creator>
  <dc:creator>Tang Y</dc:creator>
  <dc:creator>Fu P</dc:creator>
  <dc:creator>Tian D</dc:creator>
  <dc:creator>Yu L</dc:creator>
  <dc:creator>Huang Y</dc:creator>
  <dc:creator>Li G</dc:creator>
  <dc:creator>Li M</dc:creator>
  <dc:creator>Wang Y</dc:creator>
  <dc:creator>Yang Z</dc:creator>
  <dc:creator>Xu X</dc:creator>
  <dc:creator>Yin Z</dc:creator>
  <dc:creator>Zhou D</dc:creator>
  <dc:creator>Poirel L</dc:creator>
  <dc:creator>Jiang X</dc:creator>
  <dc:date>2020</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae (KPC-KP) have disseminated worldwide and emerged as major threats to public health. Of epidemiological significance, the international pandemic of KPC-KP is primarily associated with CG258 isolates and blaKPC-IncF plasmids. CRISPR-Cas system is an adaptive immune system that can hinder gene expansion driven by horizontal gene transfer. Because of blaKPC-IncF plasmids are favored by CG258 K. pneumoniae, it was of interest to examine the co-distribution of CRISPR and blaKPC-IncF plasmids in such isolates. We collected 459 clinical K. pneumoniae isolates in China and collected 203 global whole-genome sequences in GenBank to determine the prevalence of CRISPR-Cas systems. We observed that CRISPR-Cas system was significantly scarce in the CG258 lineage and blaKPC-positive isolates. Furthermore, the results of conjugation and plasmid stability assay fully demonstrated the CRIPSR-Cas system in K. pneumoniae could effectively hindered blaKPC-IncF plasmids invasion and existence. Notably, most blaKPC-IncF plasmids were also proved to be good targets of CRISPR owing to carry matched and functional protospacers and PAMs. Overall, our work suggests that type I-E CRISPR-Cas systems could impact the spread of blaKPC in K. pneumoniae populations, and the scarcity of CRISPR-Cas system was one of potential factors leading to the propagation of blaKPC-IncF plasmids in CG258 K. pneumoniae.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/139267</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1080/22221751.2020.1763209</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/32393110</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Emerging microbes &amp; infections. - 2020</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">CRISPR-Cas</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Klebsiella pneumoniae clonal complex 258</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">carbapenem resistance</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">horizontal gene transfer</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">plasmids</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">The type I-E CRISPR-Cas system influences the acquisition of blaKPC-IncF plasmid in Klebsiella pneumonia.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
