Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5705
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dc.contributor.authorForde, Brian M.-
dc.contributor.authorBergh, Haakon-
dc.contributor.authorCuddihy, Thom-
dc.contributor.authorHajkowicz, Krispin-
dc.contributor.authorHurst, Trish-
dc.contributor.authorPlayford, E. Geoffrey-
dc.contributor.authorHenderson, Belinda C.-
dc.contributor.authorRunnegar, Naomi-
dc.contributor.authorClark, Julia-
dc.contributor.authorJennison, Amy V.-
dc.contributor.authorMoss, Susan-
dc.contributor.authorHume, Anna-
dc.contributor.authorLeroux, Hugo-
dc.contributor.authorBeatson, Scott A.-
dc.contributor.authorPaterson, David L.-
dc.contributor.authorHarris, Patrick N. A.-
dc.date.accessioned2024-06-20T00:27:04Z-
dc.date.available2024-06-20T00:27:04Z-
dc.date.issued2023-
dc.identifier.citationClinical Infectious Diseases, 2023 (76) 3 p.e1277-e1284en
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/5705-
dc.description.abstractBackground Prospective whole-genome sequencing (WGS)-based surveillance may be the optimal approach to rapidly identify transmission of multi-drug resistant (MDR) bacteria in the healthcare setting. Methods We prospectively collected methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), carbapenem-resistant Acinetobacter baumannii (CRAB), extended-spectrum beta-lactamase (ESBL-E), and carbapenemase-producing Enterobacterales (CPE) isolated from blood cultures, sterile sites, or screening specimens across three large tertiary referral hospitals (2 adult, 1 paediatric) in Brisbane, Australia. WGS was used to determine in silico multi-locus sequence typing (MLST) and resistance gene profiling via a bespoke genomic analysis pipeline. Putative transmission events were identified by comparison of core genome single nucleotide polymorphisms (SNPs). Relevant clinical meta-data were combined with genomic analyses via customised automation, collated into hospital-specific reports regularly distributed to infection control teams. Results Over 4 years (April 2017 to July 2021) 2660 isolates were sequenced. This included MDR gram-negative bacilli (n = 293 CPE, n = 1309 ESBL), MRSA (n = 620), and VRE (n = 433). A total of 379 clinical reports were issued. Core genome SNP data identified that 33% of isolates formed 76 distinct clusters. Of the 76 clusters, 43 were contained to the 3 target hospitals, suggesting ongoing transmission within the clinical environment. The remaining 33 clusters represented possible inter-hospital transmission events or strains circulating in the community. In 1 hospital, proven negligible transmission of non-multi-resistant MRSA enabled changes to infection control policy. Conclusions Implementation of routine WGS for MDR pathogens in clinical laboratories is feasible and can enable targeted infection prevention and control interventions.-
dc.titleClinical Implementation of Routine Whole-genome Sequencing for Hospital Infection Control of Multi-drug Resistant Pathogens-
dc.identifier.doi10.1093/cid/ciac726-
dc.relation.urlhttps://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=ccm&AN=161829825&site=ehost-live-
dc.identifier.journaltitleClinical Infectious Diseases-
dc.identifier.risid4406-
dc.description.pagese1277-e1284-
dc.description.volume76-
dc.description.issue3-
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Sites:Children's Health Queensland Publications
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