Guschin Alexander, Ryzhikh Pavel, Rumyantseva Tatiana, Gomberg Mikhail, Unemo Magnus
WHO Collaborating Centre for Gonorrhoea and other STIs, National Reference Laboratory for Pathogenic Neisseria, Örebro University Hospital, Örebro, Sweden.
BMC Infect Dis. 2015 Feb 3;15:40. doi: 10.1186/s12879-015-0781-7.
Azithromycin has been widely used for Mycoplasma genitalium treatment internationally. However, the eradication efficacy has substantially declined recent decade. In Russia, josamycin (another macrolide) is the recommended first-line treatment for M. genitalium infections, however, no data regarding treatment efficacy with josamycin and resistance in M. genitalium infections have been internationally published. We examined the M. genitalium prevalence in males attending an STI clinic in Moscow, Russia from December 2006 to January 2008, investigated treatment efficacy with josamycin in male urethritis, and monitored the M. genitalium DNA eradication dynamics and selection of macrolide resistance in M. genitalium during this treatment.
Microscopy and real-time PCRs were used to diagnose urethritis and non-viral STIs, respectively, in males (n = 320). M. genitalium positive patients were treated with recommended josamycin regimen and treatment efficacy was monitored using quantitative real-time PCR. Macrolide resistance mutations were identified using sequencing of the 23S rRNA gene.
Forty-seven (14.7%) males were positive for M. genitalium only and most (85.1%) of these had symptoms and signs of urethritis. Forty-six (97.9%) males agreed to participate in the treatment efficacy monitoring. All the pre-treatment M. genitalium specimens had wild-type 23S rRNA. The elimination of M. genitalium DNA was substantially faster in patients with lower pre-treatment M. genitalium load, and the total eradication rate was 43/46 (93.5%). Of the six patients with high pre-treatment M. genitalium load, three (50%) remained positive post-treatment and these positive specimens contained macrolide resistance mutations in the 23S rRNA gene, i.e., A2059G (n = 2) and A2062G (n = 1).
M. genitalium was a frequent cause of male urethritis in Moscow, Russia. The pre-treatment M. genitalium load might be an effective predictor of eradication efficacy with macrolides (and possibly additional antimicrobials) and selection of macrolide resistance. Additional in vivo and in vitro data are crucial to support the recommendation of using josamycin as first-line treatment for M. genitalium infections in Russia. It would be valuable to develop international M. genitalium management guidelines, and quantitative diagnostic PCRs determining also M. genitalium load and resistance mutations (for macrolides and ideally also moxifloxacin) should ideally be recommended.
阿奇霉素在国际上已被广泛用于治疗生殖支原体感染。然而,近十年来其根除效果已大幅下降。在俄罗斯,交沙霉素(另一种大环内酯类药物)是推荐用于治疗生殖支原体感染的一线药物,然而,关于交沙霉素治疗生殖支原体感染的疗效及耐药性的数据尚未在国际上发表。我们检测了2006年12月至2008年1月期间在俄罗斯莫斯科一家性传播感染诊所就诊的男性中生殖支原体的流行情况,研究了交沙霉素治疗男性尿道炎的疗效,并在此治疗过程中监测了生殖支原体DNA的根除动态及生殖支原体对大环内酯类药物耐药性的产生情况。
分别采用显微镜检查和实时荧光定量PCR诊断男性(n = 320)的尿道炎和非病毒性传播感染。生殖支原体阳性患者接受推荐的交沙霉素治疗方案,并使用定量实时荧光定量PCR监测治疗效果。通过对23S rRNA基因进行测序鉴定大环内酯类药物耐药突变。
47名(14.7%)男性仅生殖支原体呈阳性,其中大多数(85.1%)有尿道炎的症状和体征。46名(97.9%)男性同意参与治疗效果监测。所有治疗前的生殖支原体标本均具有野生型23S rRNA。治疗前生殖支原体载量较低的患者中,生殖支原体DNA的清除速度明显更快,总根除率为43/46(93.5%)。在6名治疗前生殖支原体载量较高的患者中,3名(50%)治疗后仍为阳性,这些阳性标本的23S rRNA基因中存在大环内酯类药物耐药突变,即A2059G(n = 2)和A2062G(n = 1)。
在俄罗斯莫斯科,生殖支原体是男性尿道炎的常见病因。治疗前生殖支原体载量可能是大环内酯类药物(可能还有其他抗菌药物)根除效果及大环内酯类药物耐药性产生的有效预测指标。需要更多的体内和体外数据来支持在俄罗斯将交沙霉素作为治疗生殖支原体感染的一线药物的推荐。制定国际生殖支原体管理指南将很有价值,理想情况下应推荐能够同时检测生殖支原体载量和耐药突变(针对大环内酯类药物,理想情况下还包括莫西沙星)的定量诊断PCR。