parC Variants in Mycoplasma genitalium: Trends over Time and Association with Moxifloxacin Failure

Author:

Murray Gerald L.123ORCID,Bodiyabadu Kaveesha123,Vodstrcil Lenka A.45,Machalek Dorothy A.126,Danielewski Jennifer12,Plummer Erica L.1245,Garland Suzanne M.123,Whiley David M.78,Sweeney Emma L.7ORCID,Bradshaw Catriona S.459

Affiliation:

1. Centre for Women’s Infectious Diseases, The Royal Women’s Hospital, Parkville, Victoria, Australia

2. Molecular Microbiology Research Group, Murdoch Children’s Research Institute, Parkville, Victoria, Australia

3. Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Victoria, Australia

4. Melbourne Sexual Health Centre, Alfred Health, Carlton, Victoria, Australia

5. Central Clinical School, Monash University, Melbourne, Victoria, Australia

6. The Kirby Institute, University of New South Wales, Kensington, Sydney, New South Wales, Australia

7. The University of Queensland Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia

8. Pathology Queensland Central Laboratory, Brisbane, Queensland, Australia

9. Melbourne School of Population and Global Health, University of Melbourne, Parkville, Victoria, Australia

Abstract

Prevalence, trends, and treatment outcome estimates were generated for parC variants in macrolide-resistant Mycoplasma genitalium . Among 539 cases, the most common amino acid change was S83I, which increased from 13% in 2012 to 2013, to 23% in 2019 to 2020 ( P trend  = 0.046).

Funder

Australian Resarch Council Research Hub to Combat Antimicrobial Resistance

Department of Health | National Health and Medical Research Council

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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