Evolutionary origins of the emergent ST796 clone of vancomycin resistantEnterococcus faecium

Author:

Buultjens Andrew H.1,Lam Margaret M.C.1,Ballard Susan2,Monk Ian R.1,Mahony Andrew A.3,Grabsch Elizabeth A.3,Grayson M. Lindsay3,Pang Stanley45,Coombs Geoffrey W.45,Robinson J. Owen46,Seemann Torsten7,Johnson Paul D.R.38,Howden Benjamin P.2,Stinear Timothy P.1

Affiliation:

1. Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

2. Microbiology Diagnostic Unit, Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

3. Infectious Diseases Department, Austin Health, Heidelberg, Victoria, Australia

4. School of Veterinary and Life Sciences, Murdoch University, Murdoch, Western Australia, Australia

5. Department of Microbiology, Pathwest Laboratory Medicine-WA, Fiona Stanley Hospital, Murdoch, Western Australia, Australia

6. Department of Infectious Diseases, Fiona Stanley Hospital, Murdoch, Western Australia, Australia

7. Victorian Life Sciences Computation Initiative, University of Melbourne, Carlton, Victoria, Australia

8. Department of Medicine, University of Melbourne, Heidelberg, Victoria, Australia

Abstract

From early 2012, a novel clone of vancomycin resistantEnterococcus 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 ST796E. faeciumisolate. 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 otherE. faeciumgenomes 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 Tn1549and Tn916, transposons conferring resistance to vancomycin and tetracycline respectively. The genomic dissection of this new clone presented here underscores the propensity of the hospitalE. faeciumlineage to change, presumably in response to the specific conditions of hospital and healthcare environments.

Funder

National Health and Medical Research Council (NHMRC) of Australia

NHMRC fellowships

VLSCI Life Sciences Computation Centre

Australian Postgraduate Award

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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