Trembizki Ella, Buckley Cameron, Donovan Basil, Chen Marcus, Guy Rebecca, Kaldor John, Lahra Monica M, Regan David G, Smith Helen, Ward James, Whiley David M
Queensland Paediatric Infectious Diseases (QPID) Laboratory, Queensland Children's Medical Research Institute, Brisbane, Queensland 4029, Australia UQ Child Health Research Centre, School of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia
Queensland Paediatric Infectious Diseases (QPID) Laboratory, Queensland Children's Medical Research Institute, Brisbane, Queensland 4029, Australia UQ Child Health Research Centre, School of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.
J Antimicrob Chemother. 2015 Dec;70(12):3244-9. doi: 10.1093/jac/dkv274. Epub 2015 Sep 3.
Surveillance for Neisseria gonorrhoeae azithromycin resistance is of growing importance given increasing use of ceftriaxone and azithromycin dual therapy for gonorrhoea treatment. In this study, we developed two real-time PCR methods for direct detection of two key N. gonorrhoeae 23S rRNA mutations associated with azithromycin resistance.
The real-time PCR assays, 2611-PCR and 2059-PCR, targeted the gonococcal 23S rRNA C2611T and A2059G mutations, respectively. A major design challenge was that gonococcal 23S rRNA sequences have high sequence homology with those of commensal Neisseria species. To limit the potential for cross-reaction, 'non-template' bases were utilized in primer sequences. The performance of the methods was initially assessed using a panel of gonococcal (n = 70) and non-gonococcal (n = 28) Neisseria species. Analytical specificity was further assessed by testing N. gonorrhoeae nucleic acid amplification test (NAAT)-negative clinical samples (n = 90), before being applied to N. gonorrhoeae NAAT-positive clinical samples (n = 306).
Cross-reactions with commensal Neisseria strains remained evident for both assays; however, cycle threshold (Ct) values were significantly delayed, indicating reduced sensitivity for non-gonococcal species. For the N. gonorrhoeae NAAT-negative clinical samples, 7/21 pharyngeal samples provided evidence of cross-reaction (Ct values >40 cycles); however, the remaining urogenital and rectal swab samples were negative. In total, the gonococcal 2611 and 2059 23S rRNA nucleotides were both successfully characterized in 266/306 (87%) of the N. gonorrhoeae NAAT-positive clinical specimens.
Real-time PCR detection of gonococcal 23S rRNA mutations directly from clinical samples is feasible and may enhance culture- and non-culture-based N. gonorrhoeae resistance surveillance.
鉴于头孢曲松和阿奇霉素联合治疗淋病的使用日益增加,监测淋病奈瑟菌对阿奇霉素的耐药性变得越来越重要。在本研究中,我们开发了两种实时荧光定量聚合酶链反应(PCR)方法,用于直接检测与阿奇霉素耐药相关的两个关键淋病奈瑟菌23S核糖体RNA(rRNA)突变。
实时荧光定量PCR检测方法,即2611-PCR和2059-PCR,分别针对淋病奈瑟菌23S rRNA的C2611T和A2059G突变。一个主要的设计挑战是淋病奈瑟菌23S rRNA序列与共生奈瑟菌属的序列具有高度的序列同源性。为了限制交叉反应的可能性,在引物序列中使用了“非模板”碱基。该方法的性能最初使用一组淋病奈瑟菌(n = 70)和非淋病奈瑟菌(n = 28)进行评估。在应用于淋病奈瑟菌核酸扩增试验(NAAT)阳性临床样本(n = 306)之前,通过检测淋病奈瑟菌NAAT阴性临床样本(n = 90)进一步评估分析特异性。
两种检测方法与共生奈瑟菌菌株的交叉反应仍然明显;然而,循环阈值(Ct)值明显延迟,表明对非淋病奈瑟菌属的敏感性降低。对于淋病奈瑟菌NAAT阴性临床样本,7/21份咽拭子样本提供了交叉反应的证据(Ct值>40个循环);然而,其余泌尿生殖系统和直肠拭子样本均为阴性。总共,在306份淋病奈瑟菌NAAT阳性临床标本中的266份(87%)中成功鉴定出淋病奈瑟菌2611和2059 23S rRNA核苷酸。
直接从临床样本中实时荧光定量PCR检测淋病奈瑟菌23S rRNA突变是可行的,可能会加强基于培养和非培养的淋病奈瑟菌耐药监测。