Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/53208
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dc.contributor.authorMorris J.M.-
dc.contributor.authorLacey J.A.-
dc.contributor.authorStevens K.-
dc.contributor.authorKumar L.S.-
dc.contributor.authorWilmot M.-
dc.contributor.authorStrachan J.-
dc.contributor.authorEaston M.-
dc.contributor.authorHennessy D.-
dc.contributor.authorKorman, Tony-
dc.contributor.authorDaley A.J.-
dc.contributor.authorGibney K.B.-
dc.contributor.authorJenney A.W.J.-
dc.contributor.authorTong S.Y.C.-
dc.contributor.authorHowden B.P.-
dc.contributor.authorSherry N.L.-
dc.date.accessioned2025-02-17T05:17:08Z-
dc.date.available2025-02-17T05:17:08Z-
dc.date.copyright2025-
dc.date.issued2025-02-03en
dc.identifier.citationThe Lancet Regional Health - Western Pacific. 55(no pagination), 2025. Article Number: 101467. Date of Publication: 01 Feb 2025.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/53208-
dc.description.abstractBackground: Invasive group A Streptococcus (iGAS) cases have increased globally in 2022-2023, raising concerns within the medical and public health communities, including in Australia, while this impact is polyclonal in nature the worldwide spread and dominance of M1UK has been particularly concerning. Method(s): To investigate these changes and prepare to implement routine genomic surveillance of iGAS for public health purposes, we performed whole genome sequencing (WGS) on iGAS isolates from Victoria, Australia between 2017 and 2022. Genomic analyses were conducted to determine the epidemiology, genetic diversity, and population dynamics of iGAS. Finding(s): Analysis of 955 confirmed iGAS cases over a 6-year period revealed a polyclonal population. Fewer iGAS cases were noted between 2020 and 2021 in addition to genetic bottlenecks, likely reflecting the implementation of strict public health measures during the COVID pandemic, followed by a resurgence in cases post-COVID. Low levels of antimicrobial resistance were observed, primarily to macrolides and tetracyclines. Phylogenetic analysis identified a previously undescribed emm1 sub-lineage, designated M1Aus, detected in Australia (Victoria and Queensland), Belgium and the United Kingdom. In Victoria, M1Aus was the dominant emm1 variant in 2017 and 2018, more recently replaced by the M1UK lineage as the dominant variant, further demonstrating the worldwide impact of M1UK. Interpretation(s): This comprehensive genomic study of iGAS in Victoria, Australia provides valuable insights into the population dynamics, genetic diversity, and impact of pandemic public health measures on iGAS epidemiology. The identification of the M1Aus sub-lineage emphasises the need for continued genomic surveillance and monitoring of iGAS strains, particularly in the context of emerging global sub-lineages and shifts in population structure. Funding(s): MDU PHL-Department of Health, Victoria.NHMRC (GNT1196103 to BPH; Partnership Grant GNT1149991).Copyright © 2025 The Authors-
dc.publisherElsevier Ltd-
dc.relation.ispartofThe Lancet Regional Health - Western Pacific-
dc.subject.meshantibiotic resistance-
dc.subject.meshantibiotic sensitivity-
dc.subject.meshcoronavirus disease 2019-
dc.titleGenomic interrogation of invasive group A Streptococcus (iGAS) epidemiology and COVID-19 impacts in Victoria, Australia: a 6-year retrospective study.-
dc.typeArticle-
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional, or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1016/j.lanwpc.2025.101467-
dc.publisher.placeUnited Kingdom-
dc.identifier.institution(Morris, Kumar, Howden, Sherry) Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia-
dc.identifier.institution(Lacey, Stevens, Kumar, Wilmot, Howden, Sherry) Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia-
dc.identifier.institution(Strachan, Easton, Hennessy) Communicable Diseases, Epidemiology and Surveillance, Health Protection Branch, Department of Health Victoria, Australia-
dc.identifier.institution(Korman) Monash Infectious Diseases, Monash University and Monash Health, Clayton, VIC, Australia-
dc.identifier.institution(Daley) Department of Laboratory Services, Royal Children's Hospital, Parkville, VIC, Australia-
dc.identifier.institution(Daley) Murdoch Children's Research Institute, Parkville, VIC, Australia-
dc.identifier.institution(Daley) Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia-
dc.identifier.institution(Gibney, Tong) Department of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia-
dc.identifier.institution(Gibney, Tong) Victorian Infectious Disease Service, The Royal Melbourne Hospital, Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia-
dc.identifier.institution(Jenney) Microbiology Unit & Department of Infectious Diseases, Alfred Health, Melbourne, VIC, Australia-
dc.identifier.institution(Howden, Sherry) Department of Infectious Diseases & Immunology, Austin Health, Heidelberg, VIC, Australia-
dc.identifier.institution(Howden) Centre for Pathogen Genomics, University of Melbourne, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Korman) Monash Infectious Diseases, Monash University and Monash Health, Clayton, VIC, Australia-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.cerifentitytypePublications-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptPathology-
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