NHC Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Key Laboratory of Respiratory Disease Pathogenomics, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Microb Biotechnol. 2021 Mar;14(2):668-676. doi: 10.1111/1751-7915.13724. Epub 2020 Dec 5.
Chlamydia trachomatis is the most common sexually transmitted pathogen globally, causing serious health problems and representing a burden on public health. A new variant of C. trachomatis (nvCT) that carries mutations (C1514T, C1515T and G1523A) in the 23S rRNA gene has eluded detection in Aptima Combo 2 assays. This has led to false negatives in diagnostics tests and poses a challenge for C. trachomatis diagnostics on a global level. In this study, we developed a simple and cost-effective assay to identify C. trachomatis, with a potential application to screen for nvCT. We developed a screening assay based on high-resolution melting (HRM), targeting the 23S rRNA gene and cryptic plasmid. To evaluate the performance of the assay, 404 archived C. trachomatis DNA specimens and 570 extracted clinical specimens were analysed. Our HRM assay not only identified C. trachomatis in clinical specimens, but also correctly differentiated nvCT carrying C1514T, C1515T and G1523A mutations from the wild-type. We observed no cross-reactions with other clinically related agents, and the limit of detection was 11.26 (95% CI; 7.61-31.82) copies per reaction. Implementation of this screening assay could reduce detection times and costs for C. trachomatis diagnoses, and facilitate increased research on the presence and monitoring of nvCT.
沙眼衣原体是全球最常见的性传播病原体,可导致严重的健康问题,给公共卫生带来负担。一种新的沙眼衣原体变体(nvCT)在 23S rRNA 基因中携带突变(C1514T、C1515T 和 G1523A),逃避了 Aptima Combo 2 检测。这导致诊断测试出现假阴性,对全球范围内的沙眼衣原体诊断构成挑战。在这项研究中,我们开发了一种简单且具有成本效益的检测方法来识别沙眼衣原体,该方法有可能用于筛查 nvCT。我们开发了一种基于高分辨率熔解(HRM)的筛选检测方法,针对 23S rRNA 基因和隐秘质粒。为了评估该检测方法的性能,我们分析了 404 个存档的沙眼衣原体 DNA 标本和 570 个提取的临床标本。我们的 HRM 检测方法不仅能够在临床标本中识别沙眼衣原体,还能够正确区分携带 C1514T、C1515T 和 G1523A 突变的 nvCT 与野生型。我们没有观察到与其他临床相关制剂的交叉反应,检测限为 11.26(95%CI;7.61-31.82)个拷贝/反应。该筛查检测方法的实施可以减少沙眼衣原体诊断的检测时间和成本,并促进对 nvCT 的存在和监测的研究。