Mycoplasma genitalium molecular typing in men with non-gonococcal urethritis discriminates between phylogenetic clusters based on sexual preference and antibiotic resistance.

Nikki Adriaens, Fenna M Bouwman, Sylvia M Bruisten, Clarissa E Vergunst, Alje P van Dam, Tessa A Doelman, Brenda M Westerhuis
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Abstract

Introduction. Mycoplasma genitalium is a sexually transmitted bacterium associated with non-gonococcal urethritis (NGU) in men. The rising macrolide and fluoroquinolone resistance in M. genitalium has become a public health concern, requiring close surveillance.Gap statement. MgpB/MG309 typing is commonly used to study genotype distribution and resistance patterns of M. genitalium in men who have sex with men (MSM); however, data for men who have sex with women (MSW) are limited.Aim. The aim of this study was to explore the epidemiology of M. genitalium based on mgpB/MG309 molecular typing in isolates from men diagnosed with NGU, comparing MSM and MSW. Additionally, antibiotic resistance was evaluated to assess associations between the mgpB/MG309 genotypes, antimicrobial resistance profiles, and epidemiological determinants.Methodology. A subset of previously collected M. genitalium isolates from men diagnosed with NGU in Amsterdam, the Netherlands, between May 2018 and November 2019 was analysed. Molecular typing was performed by sequencing relevant regions of the mgpB and MG309 loci. Macrolide resistance was assessed by detecting mutations in the 23S rRNA gene via quantitative polymerase chain reaction, while fluoroquinolone resistance was determined through sequencing parC and gyrA.Results. A total of 62 M. genitalium samples were analysed from 33 MSM and 29 MSW. The overall macrolide and fluoroquinolone resistance was 75.8% and 24.2 %, respectively. At the mgpB locus, 24 sequence types (STs) were identified, with ST4 most prevalent in MSM and ST2 in MSW. The MG309 locus revealed 12 distinct short tandem repeat numbers, with repeat 10 being most common in both groups. Phylogenetic analysis based on mgpB sequences revealed two clusters: cluster A included significantly more MSW, whereas cluster B predominantly comprised MSM (P<0.001). Macrolide and fluoroquinolone resistance was significantly higher in cluster B compared with cluster A (P<0.01 and P<0.05, respectively).Conclusion. Molecular typing of M. genitalium revealed two clusters that differed by sexual preference and antibiotic resistance, highlighting the importance of surveillance of resistance across genotypes. The findings suggest multiclonal spread of resistance through independent mutations. Future studies using next-generation sequencing are needed to further explore the links between sexual transmission and genetic diversity in M. genitalium.

非淋球菌性尿道炎男性生殖器支原体分子分型可根据性偏好和抗生素耐药性区分系统发育簇。
介绍。生殖支原体是一种与男性非淋球菌性尿道炎(NGU)相关的性传播细菌。生殖支原体不断上升的大环内酯类和氟喹诺酮类耐药性已成为一个公共卫生问题,需要密切监测。差距的声明。MgpB/MG309分型是研究男男性行为人群中生殖支原体基因型分布和耐药模式的常用方法;然而,男性与女性发生性行为(MSW)的数据有限。本研究的目的是通过mgpB/MG309分子分型方法对NGU男性分离株的生殖支原体进行流行病学研究,并对MSM和MSW进行比较。此外,还评估了抗生素耐药性,以评估mgpB/MG309基因型、抗生素耐药性谱和流行病学决定因素之间的关系。对2018年5月至2019年11月期间从荷兰阿姆斯特丹诊断为NGU的男性中收集的生殖支原体分离株进行了分析。通过测序mgpB和MG309位点的相关区域进行分子分型。采用定量聚合酶链反应检测23S rRNA基因突变,检测大环内酯类药物耐药性;采用parC和gyra测序检测氟喹诺酮类药物耐药性。从33名男男性行为者和29名城市妇女中共分析了62份生殖器分枝杆菌样本。大环内酯类药物和氟喹诺酮类药物的总体耐药率分别为75.8%和24.2%。在mgpB位点,共鉴定出24种序列类型(STs),其中ST4在男男性行为中最常见,ST2在都市女性中最常见。MG309基因座显示12个不同的短串联重复序列,其中重复10在两组中最常见。基于mgpB序列的系统发育分析显示,A类含有较多的MSW,而B类以MSM为主(ppp结论)。生殖支原体的分子分型揭示了两个不同性别偏好和抗生素耐药性的集群,突出了跨基因型耐药性监测的重要性。研究结果表明,耐药性通过独立突变进行多克隆传播。未来的研究需要使用下一代测序来进一步探索生殖支原体性传播与遗传多样性之间的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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