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 |
Show full item record
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.