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. 2020 May;47(5):321-325.
doi: 10.1097/OLQ.0000000000001148.

High Prevalence of Vaginal and Rectal Mycoplasma genitalium Macrolide Resistance Among Female Sexually Transmitted Disease Clinic Patients in Seattle, Washington

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High Prevalence of Vaginal and Rectal Mycoplasma genitalium Macrolide Resistance Among Female Sexually Transmitted Disease Clinic Patients in Seattle, Washington

Christine M Khosropour et al. Sex Transm Dis. 2020 May.

Abstract

Background: Rectal Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (GC) are increasingly recognized as common infections among women. Little is known about the prevalence of rectal Mycoplasma genitalium (MG), rectal MG/CT/GC coinfection, or MG antimicrobial resistance patterns among women.

Methods: In 2017 to 2018, we recruited women at high risk for CT from Seattle's municipal sexually transmitted disease clinic. Participants self-collected vaginal and rectal specimens for CT/GC nucleic acid amplification testing. We retrospectively tested samples for vaginal and rectal MG using nucleic acid amplification testing and tested MG-positive specimens for macrolide resistance-mediating mutations (MRM) and ParC quinolone resistance-associated mutations (QRAMs).

Results: Of 50 enrolled women, 13 (26%) tested positive for MG, including 10 (20%) with vaginal MG and 11 (22%) with rectal MG; 8 (62%) had concurrent vaginal/rectal MG. Five (38%) were coinfected with CT, none with GC. Only 2 of 11 women with rectal MG reported anal sex in the prior year. Of MG-positive specimens, 100% of rectal and 89% of vaginal specimens had an MRM. There were no vaginal or rectal MG-positive specimens with ParC QRAMs previously associated with quinolone failure. Five MG-infected women received azithromycin for vaginal CT, 4 of whom had a MG MRM detected in their vaginal and/or rectal specimens.

Conclusions: We observed a high prevalence of macrolide-resistant vaginal and rectal MG among a population of women at high risk for CT. This study highlights how the use of antimicrobials designed to treat an identified infection-in this case, CT-could influence treatment outcomes and antimicrobial susceptibility in other unidentified infections.

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Conflict of interest statement

CONFLICT OF INTERESTS

CMK, MRG, LAB, OOS, and LEM have received donations of specimen collection kits and reagents from Hologic, Inc. LEM and MRG have also engaged in contract work with Hologic, Inc. JSJ has received speaker’s fees from Hologic, Cepheid, BD, and SpeeDx and serves on the scientific advisory board of Roche Molecular Systems, Abbott Molecular Inc., and Cepheid. The Statens Serum Institut has received remuneration for contract work from SpeeDx, Hologic, NYtor, Diagenode, Nabriva, and GlaxoSmithKline. MRG has received research support from GSK. JCD has conducted research unrelated to this work through grants to the University of Washington from Hologic, Curatek and Quidel. All other authors declare that they have no conflicts of interest.

References

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