Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28696
Title: Optimising genomic approaches for identifying vancomycin-resistant Enterococcus faecium transmission in healthcare settings.
Austin Authors: Higgs, Charlie;Sherry, Norelle L ;Seemann, Torsten;Horan, Kristy;Walpola, Hasini;Kinsella, Paul;Bond, Katherine;Williamson, Deborah A;Marshall, Caroline;Kwong, Jason C ;Grayson, M Lindsay ;Stinear, Timothy P;Gorrie, Claire L;Howden, Benjamin P 
Affiliation: Victorian Infectious Diseases Service, The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia
Department of Microbiology, Royal Melbourne Hospital, Melbourne, VIC, Australia
Infectious Diseases
Department of Microbiology & Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia
Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology & Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia
Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital, The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia
Medicine (University of Melbourne)
Issue Date: 26-Jan-2022
Date: 2022
Publication information: Nature Communications 2022; 13(1): 509
Abstract: Vancomycin-resistant Enterococcus faecium (VREfm) is a major nosocomial pathogen. Identifying VREfm transmission dynamics permits targeted interventions, and while genomics is increasingly being utilised, methods are not yet standardised or optimised for accuracy. We aimed to develop a standardized genomic method for identifying putative VREfm transmission links. Using comprehensive genomic and epidemiological data from a cohort of 308 VREfm infection or colonization cases, we compared multiple approaches for quantifying genetic relatedness. We showed that clustering by core genome multilocus sequence type (cgMLST) was more informative of population structure than traditional MLST. Pairwise genome comparisons using split k-mer analysis (SKA) provided the high-level resolution needed to infer patient-to-patient transmission. The more common mapping to a reference genome was not sufficiently discriminatory, defining more than three times more genomic transmission events than SKA (3729 compared to 1079 events). Here, we show a standardized genomic framework for inferring VREfm transmission that can be the basis for global deployment of VREfm genomics into routine outbreak detection and investigation.
URI: https://ahro.austin.org.au/austinjspui/handle/1/28696
DOI: 10.1038/s41467-022-28156-4
ORCID: http://orcid.org/0000-0002-7789-8360
http://orcid.org/0000-0001-6046-610X
http://orcid.org/0000-0002-6167-9366
http://orcid.org/0000-0003-0150-123X
http://orcid.org/0000-0003-0237-1473
http://orcid.org/0000-0002-6298-7942
http://orcid.org/0000-0002-3261-3149
Journal: Nature Communications
PubMed URL: 35082278
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/35082278/
Type: Journal Article
Appears in Collections:Journal articles

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