Combination Therapy for Mycoplasma genitalium, and New Insights Into the Utility of parC Mutant Detection to Improve Cure

Author:

Vodstrcil Lenka A123ORCID,Plummer Erica L12,Doyle Michelle1,Murray Gerald L456,Bodiyabadu Kaveesha456,Jensen Jorgen S7,Whiley David89,Sweeney Emma8,Williamson Deborah A1011,Chow Eric P F123,Fairley Christopher K12,Bradshaw Catriona S123

Affiliation:

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

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

3. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne , Melbourne, Victoria , Australia

4. Murdoch Children’s Research Institute , Parkville, Victoria , Australia

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

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

7. Research Unit for Reproductive Microbiology, Statens Serum Institut , Copenhagen , Denmark

8. The University of Queensland Centre for Clinical Research (UQ-CCR) , Queensland , Australia

9. Pathology Queensland Central Laboratory , Queensland , Australia

10. Department of Microbiology, Royal Melbourne Hospital , Melbourne , Australia and

11. Victorian Infectious Diseases Reference Laboratory, The Peter Doherty Institute for Infection and Immunity , Melbourne, Victoria , Australia

Abstract

Abstract Background Mycoplasma genitalium (MG) infection is challenging to cure because of rising antimicrobial resistance and limited treatment options. Methods This was a prospective evaluation of the efficacy and tolerability of resistance-guided combination antimicrobial therapy for MG treatment at Melbourne Sexual Health Centre (August 2019–December 2020). All patients received 7 days of doxycycline before combination therapy based on the macrolide-resistant profile. Macrolide-susceptible infections received combination doxycycline + azithromycin (1 g, day 1; 500 mg, days 2–4) and macrolide-resistant infections combination doxycycline + moxifloxacin (400 mg daily for 7 days). Adherence and adverse effects were recorded at test-of-cure, recommended 14–28 days after antimicrobial completion. Sequencing was performed to determine the prevalence of single nucleotide polymorphisms (SNPs) in the parC gene and their association with moxifloxacin treatment outcomes in macrolide-resistant infections. Results Of 100 patients with macrolide-susceptible MG treated with doxycycline + azithromycin, 93 were cured (93.0%; 95% confidence interval [CI], 86.1–97.1). Of 247 patients with macrolide-resistant MG receiving doxycycline + moxifloxacin, 210 were cured (85.0%; 95% CI, 80.0–89.2). parC sequencing was available for 164 (66%) macrolide-resistant infections; 29% had SNPs at parC S83 or D87 (23% S83I). The absence of SNPs at parC S83/D87 was associated with 98.3% cure (95% CI, 93.9–99.8) following doxycycline + moxifloxacin. The presence of the parC S83I-SNP was associated with failure in 62.5% (95% CI, 45.8–77.3). Side effects were common (40%–46%) and predominantly mild and gastrointestinal. Conclusions Combination doxycycline + azithromycin achieved high cure for macrolide-susceptible infections. However, in the context of a high prevalence of the parC S83I mutation (23%) in macrolide-resistant infections, doxycycline + moxifloxacin cured only 85%. Infections that were wild-type for S83/D87 experienced high cure following doxycycline + moxifloxacin, supporting the use of a parC-resistance/susceptibility testing strategy in clinical care.

Funder

Australian NHMRC Leadership Investigator Grants

Australian NHMRC Emerging Leadership Investigator Grants

Australian Research Council (ARC) Industrial Transformation Research Hub Grant

Victorian Medical Research Acceleration Fund grant

Queensland Advancing Clinical Research Fellowship

Queensland Government

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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