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开发两种多重实时荧光定量PCR检测方法,用于同时检测和区分猴痘病毒IIa、IIb和I分支以及B.1谱系。

Development of two multiplex real-time PCR assays for simultaneous detection and differentiation of monkeypox virus IIa, IIb, and I clades and the B.1 lineage.

作者信息

Huo Shuting, Chen Yuda, Lu Roujian, Zhang Zhongxian, Zhang Gaoqian, Zhao Li, Deng Yao, Wu Changcheng, Tan Wenjie

机构信息

NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China.

School of Public Health, Baotou Medical College, Baotou 014030, China.

出版信息

Biosaf Health. 2022 Dec;4(6):392-398. doi: 10.1016/j.bsheal.2022.10.005. Epub 2022 Nov 4.

Abstract

An ongoing multi-country outbreak of monkeypox was reported in May 2022 with several deaths, affecting 107 countries of all six World Health Organization (WHO) regions. The WHO has declared the current monkeypox outbreak to be a Public Health Emergency of International Concern. It is, thus, necessary to rapidly and accurately detect and distinguish different monkeypox virus (MPXV) clades. We designed primers and probes based on the alignment of 138 complete genomes of poxviruses. In Panel 1, we mixed one pair of primers and three probes to detect and differentiate the MPXV Western Africa (IIa, IIb clade) and Congo Basin (I clade) and other orthopoxviruses. In Panel 2, we mixed one pair of primers and two probes to detect the 2022 MPXV (B.1 lineage and its descendant lineages). In addition, we tested the specificity and sensitivity of the assay using real-time PCR. In Panel 1, the assay reproducibly identified various concentrations of two plasmids of the monkeypox virus, whereas other orthopoxviruses did not cross-react. In Panel 2, the probe annealed well to MPXV B.1 and showed the expected linearity. These two multiple real-time assays are inclusive and highly specific for identifying different clades of MPXV.

摘要

2022年5月报告了一场正在多个国家爆发的猴痘疫情,造成数人死亡,疫情影响了世界卫生组织(WHO)所有六个区域的107个国家。WHO已宣布当前的猴痘疫情为国际关注的突发公共卫生事件。因此,有必要快速、准确地检测和区分不同的猴痘病毒(MPXV)进化枝。我们基于138个痘病毒完整基因组的比对设计了引物和探针。在实验1中,我们混合了一对引物和三种探针,以检测和区分MPXV西非株(IIa、IIb进化枝)和刚果盆地株(I进化枝)以及其他正痘病毒。在实验2中,我们混合了一对引物和两种探针,以检测2022年的MPXV(B.1谱系及其后代谱系)。此外,我们使用实时PCR检测了该检测方法的特异性和灵敏度。在实验1中,该检测方法可重复识别不同浓度的两种猴痘病毒质粒,而其他正痘病毒没有交叉反应。在实验2中,探针与MPXV B.1退火良好,并显示出预期的线性关系。这两种多重实时检测方法对于识别MPXV的不同进化枝具有全面性和高度特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e6/9633113/35557d3ca629/gr1_lrg.jpg

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