Abstract

Mycoplasma genitalium causes a sexually transmitted infection that sometimes persists or recurs despite adequate antibiotic treatment. Between 2014 and 2018, molecular typing was applied to 75 M. genitalium-positive samples from 48 patients with repeated infection and/or couples/groups of other infected sexual contacts. MG191 adhesin, MG309 lipoprotein, and the rRNA operon were amplified, sequenced, and typed using phylogenetic, variable number tandem repeat, and single-nucleotide polymorphism analysis, respectively. Amplicons were obtained in 74/75 samples, and the combination of locus patterns gave 44 different genetic profiles (discriminatory index of 0.987), with 43 considering only MG191 and MG309. Interestingly, 15/17 patients who presented a first sample sensitive and a second resistant to macrolides had the same genetic variant in the samples (persistence of the same strain). In 2/17 patients, discordant variants (one mixed infection and one recurrence due to incomplete contact tracing) were detected. In 31 additional not related and randomly distributed samples, MG191 typing obtained 23 different genotypes, with no appreciable clustering over time. The typing method allowed persistent and recurrent infections to be distinguished, indicating that macrolide resistance-associated mutations mostly developed during treatment. To detect these secondary resistant strains, prevent reinfections, and improve the control of M. genitalium infections, tests of cure and contact tracing of sexual partners should be mandatory.

Highlights

  • Mycoplasma genitalium is a leading cause of sexually transmitted infections (STIs), which can sometimes be persistent and/or recurrent due to treatment failure or reinfection, urethritis, cervicitis and pelvic inflammatory disease, among others

  • Treatment of non-gonococcal urethritis with oral azithromycin 1 g has been associated with variable and growing rates of macrolide resistance in M. genitalium [1,2]

  • The samples received for the microbiological diagnosis of patients with suspected STIs were analysed daily using a real-time nucleic acid amplification test (RT-nucleic acid amplification techniques (NAAT)) that simultaneously detects DNA of M. genitalium and six other microorganisms associated with STIs (AllplexTM STI Essential Assay, Seegene)

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Summary

Introduction

Mycoplasma genitalium is a leading cause of sexually transmitted infections (STIs), which can sometimes be persistent and/or recurrent due to treatment failure or reinfection, urethritis, cervicitis and pelvic inflammatory disease, among others. The characteristics of this bacterial species (notably, a small genome and no cell wall) make its isolation from culture media difficult and slow, and nucleic acid amplification techniques (NAAT) are used for its detection. Treatment of non-gonococcal urethritis with oral azithromycin 1 g has been associated with variable and growing rates of macrolide resistance in M. genitalium [1,2]. For comprehensive management of this infection, sexual partners should be tested (and as appropriate, treated), and tests of cure (TOC) performed after 3 weeks

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