PLoS ONE (Jan 2014)

Sequential isolation in a patient of Raoultella planticola and Escherichia coli bearing a novel ISCR1 element carrying blaNDM-1.

  • Juan Li,
  • Ruiting Lan,
  • Yanwen Xiong,
  • Changyun Ye,
  • Min Yuan,
  • Xinfeng Liu,
  • Xia Chen,
  • Deshan Yu,
  • Bin Liu,
  • Wenchao Lin,
  • Xuemei Bai,
  • Yan Wang,
  • Qiangzheng Sun,
  • Yiting Wang,
  • Hongqing Zhao,
  • Qiong Meng,
  • Qiang Chen,
  • Ailan Zhao,
  • Jianguo Xu

DOI
https://doi.org/10.1371/journal.pone.0089893
Journal volume & issue
Vol. 9, no. 3
p. e89893

Abstract

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BACKGROUND: The gene for New Delhi metallo-β-lactamase 1 (NDM-1) has been reported to be transmitted via plasmids which are easily transferable and capable of wide distribution. We report the isolation of two NDM-1 producing strains and possible in vivo transfer of blaNDM-1 in a patient. METHODS: Clinical samples were collected for bacterial culture and antibiotic susceptibility testing from a patient during a 34-day hospitalization. The presence of blaNDM-1 was detected by PCR and sequencing. Plasmids of interest were sequenced. Medical records were reviewed for evidence of association between the administration of antibiotics and the acquisition of the NDM-1 resistance. RESULTS: A NDM-1 positive Raoultella planticola was isolated from blood on the ninth day of hospitalization without administration of any carbapenem antibiotics and a NDM-1 positive Escherichia coli was isolated from feces on the 29th day of hospitalization and eight days after imipenem administration. The blaNDM-1 was carried by a 280 kb plasmid pRpNDM1-1 in R. planticola and a 58 kb plasmid pEcNDM1-4 in E. coli. The two plasmids shared a 4812 bp NDM-1-ISCR1 element which was found to be excisable from the plasmid as a free form and transferrable in vitro to a NDM-1 negative plasmid from E. coli. CONCLUSION: blaNDM-1 was embedded in an ISCR1 complex class 1 integron as a novel 4812 bp NDM-1-ISCR1 element. The element was found to be able to self excise to become a free form, which may provide a new vehicle for NDM-1 dissemination. This mechanism could greatly accelerate the spread of NDM-1 mediated broad spectrum β-lactam resistance.