Insights gained from sequencing Australian non-invasive and invasive Streptococcus pyogenes isolates

Author:

Butler Trent A.J.1ORCID,Story Chloe2,Green Emily1,Williamson Kirsten M.3,Newton Peter2,Jenkins Frances4,Varadhan Hemalatha1,van Hal Sebastiaan54

Affiliation:

1. Microbiology, NSW Health Pathology, John Hunter Hospital, New Lambton Heights, New South Wales, Australia

2. Microbiology, NSW Health Pathology, Wollongong Hospital, Wollongong, New South Wales, Australia

3. Hunter New England Population Health, Hunter New England Local Health District, Newcastle, New South Wales, Australia

4. Department of Infectious Diseases and Microbiology, NSW Health Pathology, Royal Prince Alfred Hospital, Sydney, New South Wales 2050, Australia

5. Central Clinical School, University of Sydney, Sydney, New South Wales 2006, Australia

Abstract

Epidemiological data have indicated that invasive infections caused by the Gram-positive cocci Streptococcus pyogenes (group A streptococcus, GAS) have increased in many Australian states over the past two decades. In July 2022, invasive GAS (iGAS) infections became nationally notifiable in Australia via public-health agencies. Surveillance for S. pyogenes infections has been sporadic within the state of New South Wales (NSW). This has led to a lack of genetic data on GAS strains in circulation, particularly for non-invasive infections, which are the leading cause of GAS’s burden on the Australian healthcare system. To address this gap, we used whole-genome sequencing to analyse the genomes of 318  S . pyogenes isolates collected within two geographical regions of NSW. Invasive isolates were collected in 2007–2017, whilst non-invasive isolates were collected in 2019–2021. We found that at least 66 different emm-types were associated with clinical disease within NSW. There was no evidence of any Australian-specific clones in circulation. The M1UK variant of the emm1 global pandemic clone (M1global) has been detected in our isolates from 2013 onwards. We detected antimicrobial-resistance genes (mainly tetM, ermA or ermB genes) in less than 10 % of our 318 isolates, which were more commonly associated with non-invasive infections. Superantigen virulence gene carriage was reasonably proportionate between non-invasive and invasive infection isolates. Our study adds rich data on the genetic makeup of historical S. pyogenes infections within Australia. Ongoing surveillance of invasive and non-invasive GAS infections within NSW by whole-genome sequencing is warranted to inform on outbreaks, antimicrobial resistance and vaccine coverage.

Publisher

Microbiology Society

Subject

General Medicine

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