Evolutionary origins of the emergent ST796 clone of vancomycin resistant Enterococcus faecium

Andrew H. Buultjens, Margaret M.C. Lam, Susan Ballard, Ian R. Monk, Andrew A. Mahony, Elizabeth A. Grabsch, M. Lindsay Grayson, Stanley Pang, Geoffrey W. Coombs, J. Owen Robinson, Torsten Seemann, Paul D.R. Johnson, Benjamin P. Howden, Timothy P. Stinear

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18 Citations (Scopus)

Abstract

From early 2012, a novel clone of vancomycin resistant Enterococcus faecium (assigned the multi locus sequence type ST796) was simultaneously isolated from geographically separate hospitals in south eastern Australia and New Zealand. Here we describe the complete genome sequence of Ef_aus0233, a representative ST796 E. faecium isolate. We used PacBio single molecule real-time sequencing to establish a high quality, fully assembled genome comprising a circular chromosome of 2,888,087 bp and five plasmids. Comparison of Ef_aus0233 to other E. faecium genomes shows Ef_aus0233 is a member of the epidemic hospital-adapted lineage and has evolved from an ST555- like ancestral progenitor by the accumulation or modification of five mosaic plasmids and five putative prophage, acquisition of two cryptic genomic islands, accrued chromosomal single nucleotide polymorphisms and a 80 kb region of recombination, also gaining Tn1549 and Tn916, transposons conferring resistance to vancomycin and tetracycline respectively. The genomic dissection of this new clone presented here underscores the propensity of the hospital E. faecium lineage to change, presumably in response to the specific conditions of hospital and healthcare environments.

Original languageEnglish
Article numbere2916
Number of pages22
JournalPeerJ
Volume2017
Issue number1
DOIs
Publication statusPublished - 1 Jan 2017
Externally publishedYes

Keywords

  • Accessory genome
  • Antibiotic resistance
  • Comparative genomics
  • Enterococcus faecium
  • Evolution
  • Genome sequence
  • Hospital adapted
  • PacBio
  • Recombination
  • Vancomycin resistant

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