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利用寡核苷酸微阵列同时检测埃博拉病毒及与出血热相关的病原体

Simultaneous Detection of Ebola Virus and Pathogens Associated With Hemorrhagic Fever by an Oligonucleotide Microarray.

作者信息

Yao Wenwu, Yang Zhangnv, Lou Xiuyu, Mao Haiyan, Yan Hao, Zhang Yanjun

机构信息

Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, China.

出版信息

Front Microbiol. 2021 Jul 30;12:713372. doi: 10.3389/fmicb.2021.713372. eCollection 2021.

DOI:10.3389/fmicb.2021.713372
PMID:34394063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8363200/
Abstract

Ebola virus infection causes severe hemorrhagic fever, and its mortality rates varied from 25 to 90% in the previous outbreaks. The highly infectious and lethal nature of this virus highlights the need for reliable and sensitive diagnostic methods to distinguish it from other diseases present with similar clinical symptoms. Based on multiplex polymerase chain reaction (PCR) and oligonucleotide microarray technology, a cost-effective, multipathogen and high-throughput method was developed for simultaneous detection of Ebola virus and other pathogens associated with hemorrhagic fever, including Marburg virus, Lassa fever virus, Junin virus, Machupo virus, Rift Valley fever virus, Crimean-Congo hemorrhagic fever virus, malaria parasite, hantavirus, severe fever with thrombocytopenia syndrome virus, dengue virus, yellow fever virus, Chikungunya virus, influenza A virus, and influenza B virus. This assay had an excellent specificity for target pathogens, without overlap signal between the probes. The limit of detection was approximately 10 pathogen copies/μl. A total of 60 positive nucleic acid samples for different pathogens were detected, a concordance of 100% was observed between microarray assay and real-time PCR analysis. Consequently, the described oligonucleotide microarray may be specific and sensitive assay for diagnosis and surveillance of infections caused by Ebola virus and other species of hemorrhagic fever pathogens.

摘要

埃博拉病毒感染可导致严重的出血热,在前几次疫情爆发中,其死亡率在25%至90%之间。这种病毒具有高度传染性和致命性,这凸显了需要可靠且灵敏的诊断方法,以将其与具有相似临床症状的其他疾病区分开来。基于多重聚合酶链反应(PCR)和寡核苷酸微阵列技术,开发了一种经济高效、可同时检测多种病原体且高通量的方法,用于同时检测埃博拉病毒以及其他与出血热相关的病原体,包括马尔堡病毒、拉沙热病毒、胡宁病毒、马丘波病毒、裂谷热病毒、克里米亚-刚果出血热病毒、疟原虫、汉坦病毒、严重发热伴血小板减少综合征病毒、登革病毒、黄热病毒、基孔肯雅病毒、甲型流感病毒和乙型流感病毒。该检测方法对目标病原体具有出色的特异性,各探针之间无信号重叠。检测限约为10个病原体拷贝/微升。共检测了60份不同病原体的阳性核酸样本,微阵列检测与实时PCR分析之间的一致性为100%。因此,所描述的寡核苷酸微阵列可能是用于诊断和监测由埃博拉病毒及其他出血热病原体引起的感染的特异性和灵敏性检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/3709cd938b54/fmicb-12-713372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/9b7e6299aa4c/fmicb-12-713372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/b118f7e76496/fmicb-12-713372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/3709cd938b54/fmicb-12-713372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/9b7e6299aa4c/fmicb-12-713372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/b118f7e76496/fmicb-12-713372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f15/8363200/3709cd938b54/fmicb-12-713372-g003.jpg

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