Literature DB >> 33647020

Nucleic acid visualization assay for Middle East Respiratory Syndrome Coronavirus (MERS-CoV) by targeting the UpE and N gene.

Pei Huang1,2, Hongli Jin2,3, Yongkun Zhao2, Entao Li2,4, Feihu Yan2, Hang Chi2, Qi Wang2,5, Qiuxue Han2,6, Ruo Mo1,2, Yumeng Song3, Jinhao Bi1,2, Cuicui Jiao3, Wujian Li2,3, Hongbin He7, Hongmei Wang7, Aimin Ma8, Na Feng2, Jianzhong Wang1, Tiecheng Wang2, Songtao Yang2, Yuwei Gao2, Xianzhu Xia2, Hualei Wang3.   

Abstract

Since its first emergence in 2012, cases of infection with Middle East respiratory syndrome coronavirus (MERS-CoV) have continued to occur. At the end of January 2020, 2519 laboratory confirmed cases with a case-fatality rate of 34.3% have been reported. Approximately 84% of human cases have been reported in the tropical region of Saudi Arabia. The emergence of MERS-CoV has highlighted need for a rapid and accurate assay to triage patients with a suspected infection in a timely manner because of the lack of an approved vaccine or an effective treatment for MERS-CoV to prevent and control potential outbreaks. In this study, we present two rapid and visual nucleic acid assays that target the MERS-CoV UpE and N genes as a panel that combines reverse transcription recombinase polymerase amplification with a closed vertical flow visualization strip (RT-RPA-VF). This test panel was designed to improve the diagnostic accuracy through dual-target screening after referencing laboratory testing guidance for MERS-CoV. The limit of detection was 1.2×101 copies/μl viral RNA for the UpE assay and 1.2 copies/μl viral RNA for the N assay, with almost consistent with the sensitivity of the RT-qPCR assays. The two assays exhibited no cross-reactivity with multiple CoVs, including the bat severe acute respiratory syndrome related coronavirus (SARSr-CoV), the bat coronavirus HKU4, and the human coronaviruses 229E, OC43, HKU1 and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Furthermore, the panel does not require sophisticated equipment and provides rapid detection within 30 min. This panel displays good sensitivity and specificity and may be useful to rapidly detect MERS-CoV early during an outbreak and for disease surveillance.

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Year:  2021        PMID: 33647020      PMCID: PMC7951983          DOI: 10.1371/journal.pntd.0009227

Source DB:  PubMed          Journal:  PLoS Negl Trop Dis        ISSN: 1935-2727


  35 in total

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Journal:  Analyst       Date:  2018-12-17       Impact factor: 4.616

2.  Identification of diverse alphacoronaviruses and genomic characterization of a novel severe acute respiratory syndrome-like coronavirus from bats in China.

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Journal:  Am J Trop Med Hyg       Date:  2017-12-14       Impact factor: 2.345

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Journal:  Lancet Infect Dis       Date:  2020-02-18       Impact factor: 25.071

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Journal:  PLoS Curr       Date:  2013-12-12

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Journal:  Transbound Emerg Dis       Date:  2014-01-24       Impact factor: 5.005

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Journal:  BMJ Glob Health       Date:  2019-02-01

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Authors:  Rakan I Nazer
Journal:  Ann Thorac Surg       Date:  2017-08       Impact factor: 4.330

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  1 in total

Review 1.  Current diagnostic approaches to detect two important betacoronaviruses: Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).

Authors:  Zhi Xiong Chong; Winnie Pui Pui Liew; Hui Kian Ong; Chean Yeah Yong; Chong Seng Shit; Wan Yong Ho; Stephanie Y L Ng; Swee Keong Yeap
Journal:  Pathol Res Pract       Date:  2021-07-24       Impact factor: 3.250

  1 in total

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