Centre for Women's Infectious Diseases, The Royal Women's Hospital, Parkville, VIC, Australia; The Kirby Institute, University of New South Wales, Kensington, Sydney, NSW, Australia; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
Melbourne Sexual Health Centre, Alfred Health, Melbourne, VIC, Australia; Central Clinical School, Monash University, Melbourne, VIC, Australia; China-Australia Joint Research Center for Infectious Diseases, School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Lancet Infect Dis. 2020 Nov;20(11):1302-1314. doi: 10.1016/S1473-3099(20)30154-7. Epub 2020 Jul 2.
Mycoplasma genitalium is now recognised as an important bacterial sexually transmitted infection. We summarised data from studies of mutations associated with macrolide and fluoroquinolone resistance in M genitalium to establish the prevalence of resistance. We also investigated temporal trends in resistance and aimed to establish the association between resistance and geographical location.
In this systematic review and meta-analysis, we searched PubMed, Embase, and MEDLINE for studies that included data for the prevalence of mutations associated with macrolide and fluoroquinolone resistance in M genitalium published in any language up to Jan 7, 2019. We defined prevalence as the proportion of M genitalium samples positive for key mutations associated with azithromycin resistance (23S rRNA gene, position 2058 or 2059) or moxifloxacin resistance (S83R, S83I, D87N, or D87Y in parC), or both, among all M genitalium samples that were successfully characterised. We used random-effects meta-analyses to calculate summary estimates of prevalence. Subgroup and meta-regression analyses by WHO region and time period were done. This study was registered with PROSPERO, number CRD42016050370.
Overall, 59 studies from 21 countries met the inclusion criteria for our study: 57 studies of macrolide resistance (8966 samples), 25 of fluoroquinolone resistance (4003 samples), and 22 of dual resistance to macrolides and fluoroquinolones (3280 samples). The summary prevalence of mutations associated with macrolide resistance among M genitalium samples was 35·5% (95% CI 28·8-42·5); prevalence increased from 10·0% (95% CI 2·6-20·1%) before 2010, to 51·4% (40·3-62·4%) in 2016-17 (p<0·0001). Prevalence of mutations associated with macrolide resistance was significantly greater in samples in the WHO Western Pacific and Americas regions than in those from the WHO European region. The overall prevalence of mutations associated with fluoroquinolone resistance in M genitalium samples was 7·7% (95% CI 4·5-11·4%). Prevalence did not change significantly over time, but was significantly higher in the Western Pacific region than in the European region. Overall, the prevalence of both mutations associated with macrolide resistance and those associated with fluoroquinolone resistance among M genitalium samples was 2·8% (1·3-4·7%). The prevalence of dual resistance did not change significantly over time, and did not vary significantly by geographical region.
Global surveillance and measures to optimise the efficacy of treatments-including resistance-guided strategies, new antimicrobials, and antimicrobial combination approaches-are urgently needed to ensure cure in a high proportion of M genitalium infections and to prevent further spread of resistant strains.
Australian National Health and Medical Research Council.
支原体生殖器现在被认为是一种重要的细菌性性传播感染。我们总结了与支原体生殖器中环丙沙星和大环内酯类耐药相关的突变研究数据,以确定耐药的流行率。我们还研究了耐药的时间趋势,并旨在确定耐药与地理位置之间的关系。
在这项系统评价和荟萃分析中,我们检索了 PubMed、Embase 和 MEDLINE,以获取截至 2019 年 1 月 7 日发表的任何语言的与支原体生殖器中环丙沙星和大环内酯类耐药相关的突变流行率研究数据。我们将流行率定义为所有成功鉴定的支原体生殖器样本中,与阿奇霉素耐药相关的关键突变(23S rRNA 基因,位置 2058 或 2059)或与莫西沙星耐药相关的突变(S83R、S83I、D87N 或 D87Y 在 parC)阳性的支原体生殖器样本比例。我们使用随机效应荟萃分析计算流行率的综合估计值。按世界卫生组织(WHO)区域和时间进行亚组和荟萃回归分析。本研究在 PROSPERO 注册,注册号为 CRD42016050370。
共有来自 21 个国家的 59 项研究符合我们的研究标准:57 项大环内酯类耐药研究(8966 个样本)、25 项氟喹诺酮类耐药研究(4003 个样本)和 22 项大环内酯类和氟喹诺酮类双重耐药研究(3280 个样本)。支原体生殖器样本中与大环内酯类耐药相关的突变的综合流行率为 35.5%(95%CI,28.8-42.5);耐药率从 2010 年之前的 10.0%(95%CI,2.6-20.1%)增加到 2016-2017 年的 51.4%(40.3-62.4%)(p<0.0001)。与大环内酯类耐药相关的突变的流行率在世界卫生组织西太平洋和美洲地区的样本中明显高于欧洲地区的样本。支原体生殖器样本中与氟喹诺酮类耐药相关的突变的总体流行率为 7.7%(95%CI,4.5-11.4%)。耐药率随时间变化无显著变化,但在西太平洋地区明显高于欧洲地区。总的来说,与大环内酯类耐药相关的突变和与氟喹诺酮类耐药相关的突变在支原体生殖器样本中的总体流行率为 2.8%(1.3-4.7%)。支原体生殖器中双重耐药的流行率随时间变化无显著变化,且在地理区域上无显著差异。
迫切需要进行全球监测并采取措施优化治疗效果,包括耐药指导策略、新抗菌药物和抗菌药物联合应用,以确保在大多数支原体生殖器感染中治愈,并防止耐药菌株进一步传播。
澳大利亚国家卫生和医学研究理事会。