Chen Yi, He Hui, Pan Ping, He Songzhe, Dong Xueyan, Chen Yueming, Wang Shuying, Yu Daojun
Affiliated First Hospital of Hangzhou, Zhejiang Chinese Medical University, Hangzhou, PR China.
Department of Clinical Laboratory, Hangzhou First People's Hospital, Hangzhou, PR China.
J Med Microbiol. 2016 Jul;65(7):590-595. doi: 10.1099/jmm.0.000266. Epub 2016 Apr 19.
Acute respiratory infections (ARIs) cause substantial morbidity and mortality worldwide. The causes of ARI are dynamic, and co-infections of Mycoplasma pneumoniae, Epstein-Barr virus and human cytomegalovirus are recently developed causes of ARI. Here, we established a quadruplex quantitative PCR (qPCR) method to rapidly identify and simultaneously detect a single infection or co-infection of these three pathogens and an internal control in a single tube using AllGlo probes. The analysis demonstrated a wide linear range of detection from 101 to 108 copies per test and a low coefficient of variation of less than 5 %. The amplification efficiencies were all close to 1, and the correlation coefficients (r2) were all greater than 0.99. We found no significant difference in a comparative reagent test (P >0.05). Moreover, the results of tests on clinical samples using AllGlo quadruplex qPCR and TaqMan uniplex qPCR were in near-perfect agreement (κ =0.97). Clinically, the availability of this method will enable better differential diagnosis, disease surveillance and controlled outcomes.
急性呼吸道感染(ARI)在全球范围内导致大量发病和死亡。ARI的病因是动态变化的,肺炎支原体、EB病毒和人巨细胞病毒的合并感染是ARI最近出现的病因。在此,我们建立了一种四重定量PCR(qPCR)方法,使用AllGlo探针在单个管中快速鉴定并同时检测这三种病原体的单一感染或合并感染以及一个内部对照。分析表明检测的线性范围很宽,每次检测从10¹到10⁸拷贝,变异系数低至小于5%。扩增效率均接近1,相关系数(r²)均大于0.99。我们发现在比较试剂测试中没有显著差异(P>0.05)。此外,使用AllGlo四重qPCR和TaqMan单重qPCR对临床样本进行检测的结果几乎完全一致(κ=0.97)。临床上,这种方法的可用性将有助于更好地进行鉴别诊断、疾病监测并控制结果。