Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.
CAS Key Laboratory of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China.
Virol Sin. 2021 Aug;36(4):746-754. doi: 10.1007/s12250-021-00354-2. Epub 2021 Feb 26.
Human herpesviruses are double-stranded DNA viruses that are classified into nine species. More than 90% of adults are ever infected with one or more herpesviruses. The symptoms of infection with different herpesviruses are diverse ranging from mild or asymptomatic infections to deadly diseases such as aggressive lymphomas and sarcomas. Timely and accurate detection of herpesvirus infection is critical for clinical management and treatment. In this study, we established a single-tube nonuple qPCR assay for detection of all nine herpesviruses using a 2-D multiplex qPCR method with a house-keeping gene as the internal control. The novel assay can detect and distinguish different herpesviruses with 30 to 300 copies per 25 µL single-tube reaction, and does not cross-react with 20 other human viruses, including DNA and RNA viruses. The robustness of the novel assay was evaluated using 170 clinical samples. The novel assay showed a high consistency (100%) with the single qPCR assay for HHVs detection. The features of simple, rapid, high sensitivity, specificity, and low cost make this assay a high potential to be widely used in clinical diagnosis and patient treatment.
人类疱疹病毒是双链 DNA 病毒,分为九种。超过 90%的成年人曾感染过一种或多种疱疹病毒。不同疱疹病毒感染的症状多种多样,从轻度或无症状感染到致命疾病,如侵袭性淋巴瘤和肉瘤。及时准确地检测疱疹病毒感染对于临床管理和治疗至关重要。在这项研究中,我们使用 2-D 多重 qPCR 方法建立了一种单管九重 qPCR 检测方法,以管家基因作为内参,用于检测所有九种疱疹病毒。新型检测方法可以检测和区分不同的疱疹病毒,每个 25µL 单管反应的检测限为 30 至 300 拷贝,并且与包括 DNA 和 RNA 病毒在内的 20 种其他人类病毒无交叉反应。使用 170 个临床样本评估了新型检测方法的稳健性。新型检测方法与 HHVs 的单 qPCR 检测方法具有高度一致性(100%)。该检测方法具有简单、快速、高灵敏度、特异性和低成本的特点,具有广泛应用于临床诊断和患者治疗的巨大潜力。