Zhou Qian, Liu Jingwei, Chen Shaochun, Xu Wenqi, Han Yan, Yin Yueping
National Center for STD Control, Chinese Center for Disease Control and Prevention, Department of Reference STD Lab, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China.
Antibiotics (Basel). 2021 Aug 24;10(9):1027. doi: 10.3390/antibiotics10091027.
is now recognized as a commonly reported sexually transmitted pathogen, and the increasing drug resistance of has become a serious public health problem. The accuracy of molecular detection for detecting moderate-level azithromycin resistance is not well-established. We summarized the data from studies of the 23S rRNA mutation at position 2611 with azithromycin resistance to determine the relationship between the mutation and resistance.
In this systematic review and meta-analysis, two researchers independently searched six databases for studies with data for the azithromycin minimum inhibitory concentrations (MICs) and the 23S rRNA mutation C2611T of each isolate. Since the breakpoint of moderate-level resistance to azithromycin (ML-AzmR) was not determined, we divided the moderate level into two groups according to the range of MICs (moderate resistance limited to 2-128 mg/L or 4-128 mg/L) for data extraction. A random-effects model was used to calculate the pooled sensitivity rate, the specificity rate, the pooled positive likelihood ratio (PLR), the negative likelihood ratio (NLR), and the diagnostic odds ratio (DOR). Meta-regression analyses by detection method, isolates sampling (a random sample or not), location, and sample size were performed to explore the possible causes of heterogeneity. The potential publication bias of the included studies was conducted by the Deeks' test. We included 20 studies in our study: 20 studies have data of with MICs between 2 and 128 mg/L with mutation or without mutation at position 2611(4759 samples), and 14 studies have data of with MICs between 4 and 128 mg/L (3367 samples). In the group with the moderate level of 2-128 mg/L, the pooled sensitivity rate of the molecular assays was determined to be 71.9% (95% CI, 67.6-74%), the pooled specificity rate was 98.7% (95% CI, 98.2-99.0%), and the DOR ranged from 55.0 to 351.3 (mean, 139.1). In the 4-128 mg/L group, the pooled sensitivity rate was 91.9% (95% CI, 88.9-94.2%), the pooled specificity rate was 95.9% (95% CI, 95.1-96.6%), and the DOR ranged from 41.9 to 364.1 (mean, 123.6).
Through this meta-analysis, we found that the C2611T mutation of 23S rRNA is valuable for the molecular diagnostic of moderate-level azithromycin resistance (ML-AzmR) in , especially when the moderate level is set at 4-128 mg/L. This rapid molecular detection method can be used for the rapid identification of ML-AzmR isolates in the clinic.
现已被公认为一种常见的性传播病原体,其耐药性不断增加已成为一个严重的公共卫生问题。检测中度阿奇霉素耐药性的分子检测准确性尚未完全确立。我们总结了关于2611位23S rRNA突变与阿奇霉素耐药性的研究数据,以确定该突变与耐药性之间的关系。
在这项系统评价和荟萃分析中,两名研究人员独立检索了六个数据库,以查找有关每种分离株阿奇霉素最低抑菌浓度(MIC)和23S rRNA突变C2611T的数据。由于中度阿奇霉素耐药(ML-AzmR)的断点尚未确定,我们根据MIC范围(中度耐药限于2-128mg/L或4-128mg/L)将中度水平分为两组进行数据提取。采用随机效应模型计算合并敏感度、特异度、合并阳性似然比(PLR)、阴性似然比(NLR)和诊断比值比(DOR)。通过检测方法、分离株采样(是否为随机样本)、地点和样本量进行Meta回归分析,以探讨异质性的可能原因。采用Deeks检验对纳入研究的潜在发表偏倚进行评估。我们的研究纳入了20项研究:20项研究有2611位有突变或无突变且MIC在2至128mg/L之间的分离株数据(4759个样本),14项研究有MIC在4至128mg/L之间的分离株数据(3367个样本)。在2-128mg/L的中度水平组中,分子检测的合并敏感度为71.9%(95%CI,67.6-74%),合并特异度为98.7%(95%CI,98.2-99.0%),DOR范围为55.0至351.3(均值,139.1)。在4-128mg/L组中,合并敏感度为91.9%(95%CI,88.9-94.2%),合并特异度为95.9%(95%CI,95.1-96.6%),DOR范围为41.9至364.1(均值,123.6)。
通过这项荟萃分析,我们发现23S rRNA的C2611T突变对沙眼衣原体中度阿奇霉素耐药(ML-AzmR)的分子诊断有价值,特别是当中度水平设定为4-128mg/L时。这种快速分子检测方法可用于临床快速鉴定ML-AzmR分离株。