建立同时检测和分化猴痘病毒IIa、IIb、I支和b1支的两种多重实时PCR方法

IF 3.5 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Shuting Huo , Yuda Chen , Roujian Lu , Zhongxian Zhang , Gaoqian Zhang , Li Zhao , Yao Deng , Changcheng Wu , Wenjie Tan
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引用次数: 12

摘要

2022年5月报告了一场正在多国暴发的猴痘疫情,造成数人死亡,影响到世界卫生组织(世卫组织)所有六个区域的107个国家。世界卫生组织宣布目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)分支。我们基于138个痘病毒全基因组的比对设计了引物和探针。在Panel 1中,我们混合了一对引物和三个探针来检测和区分MPXV西非(IIa, IIb支系)和刚果盆地(I支系)和其他正痘病毒。在Panel 2中,我们混合了一对引物和两个探针来检测2022 MPXV (B.1谱系及其后代谱系)。此外,我们使用实时PCR测试了该检测的特异性和敏感性。在图1中,该试验可重复地鉴定出猴痘病毒的两种质粒的不同浓度,而其他正痘病毒则没有交叉反应。在面板2中,探针退火到MPXV B.1并显示出预期的线性。这两种多重实时检测方法具有包容性和高度特异性,可用于识别MPXV的不同分支。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
Biosafety and Health
Biosafety and Health Medicine-Infectious Diseases
CiteScore
7.60
自引率
0.00%
发文量
116
审稿时长
66 days
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