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. 2022 Aug 6;10(8):1587.
doi: 10.3390/microorganisms10081587.

Molecular Typing Reveals Distinct Mycoplasma genitalium Transmission Networks among a Cohort of Men Who Have Sex with Men and a Cohort of Women in France

Affiliations

Molecular Typing Reveals Distinct Mycoplasma genitalium Transmission Networks among a Cohort of Men Who Have Sex with Men and a Cohort of Women in France

Jennifer Guiraud et al. Microorganisms. .

Abstract

Mycoplasma genitalium causes sexually transmitted infecti.ons in men and women. Treatment failures to macrolides and fluoroquinolones have been reported worldwide. Although the mgpB typing method has often been used in M. genitalium-infected men who have sex with men (MSM), limited typing data are available for M. genitalium-infected women. In this study, we aimed to investigate the genetic relationship between M. genitalium strains and their antibiotic resistance profile in a cohort of MSM (86.2% on HIV preexposure prophylaxis [PrEP], 13.8% HIV positive) and a large cohort of women using mgpB/MG309 typing. The mgpB types were determined in 374 samples from 305 women and 65 MSM. Three MSM and one woman had two concurrent or subsequent samples. Macrolide and fluoroquinolone resistance-associated mutations were searched in the 23S rRNA as well as parC and gyrA genes. The mgpB phylogenetic construction revealed three large clusters that differed according to sexual practices and geographical origin of patients. The prevalence of macrolide and fluoroquinolone resistance was significantly higher in MSM compared with women (95.4% vs. 14.1% and 30.6% vs. 7.2%, p < 0.001, respectively). The macrolide resistance spread was polyclonal in both populations, but clonal diffusion of two dual-resistant types was observed in PrEP users in association with high antibiotic pressure and dense connectivity in this population.

Keywords: MG309; Mycoplasma genitalium; antimicrobial resistance; fluoroquinolones; macrolides; mgpB; sexually transmitted infection; typing.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Maximum likelihood tree based on the mgpB type of the 374 M. genitalium strains collected from 305 women and 65 MSM. The tree was constructed using a T92 G+I model. Branch support values were generated from 1000 bootstrap replicates. The sequence of the M. genitalium G37 strain was used as a reference. The phylogenetic tree was annotated with (from the centre to the outside) the strain name, the cohort, the individual geographical origin, the sampling site, the mgpB sequence type (from 1 to 323), the MG309-STR type of the strain (from 8 to 20, if available), and the macrolide and fluoroquinolone resistance profile of the strain (if available). Clusters A, B, and C are represented by branches and strain names in purple, red, and green, respectively. Concurrent or subsequent samples from four patients are highlighted. HIV-positive patients are symbolized by a black star. For better reading, a clearer figure is available as supplementary data file (Figure S1).

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