Author: Yan, Ying; Chang, Le; Wang, Lunan
Title: Laboratory testing of SARSâ€CoV, MERSâ€CoV, and SARSâ€CoVâ€2 (2019â€nCoV): Current status, challenges, and countermeasures Cord-id: 1huoe4dp Document date: 2020_4_17
ID: 1huoe4dp
Snippet: Emerging and reemerging infectious diseases are global public concerns. With the outbreak of unknown pneumonia in Wuhan, China in December 2019, a new coronavirus, SARSâ€CoVâ€2 has been attracting tremendous attention. Rapid and accurate laboratory testing of SARSâ€CoVâ€2 is essential for early discovery, early reporting, early quarantine, early treatment, and cutting off epidemic transmission. The genome structure, transmission, and pathogenesis of SARSâ€CoVâ€2 are basically similar to SA
Document: Emerging and reemerging infectious diseases are global public concerns. With the outbreak of unknown pneumonia in Wuhan, China in December 2019, a new coronavirus, SARSâ€CoVâ€2 has been attracting tremendous attention. Rapid and accurate laboratory testing of SARSâ€CoVâ€2 is essential for early discovery, early reporting, early quarantine, early treatment, and cutting off epidemic transmission. The genome structure, transmission, and pathogenesis of SARSâ€CoVâ€2 are basically similar to SARSâ€CoV and MERSâ€CoV, the other two betaâ€CoVs of medical importance. During the SARSâ€CoV and MERSâ€CoV epidemics, a variety of molecular and serological diagnostic assays were established and should be referred to for SARSâ€CoVâ€2. In this review, by summarizing the articles and guidelines about specimen collection, nucleic acid tests (NAT) and serological tests for SARSâ€CoV, MERSâ€CoV, and SARSâ€CoVâ€2, several suggestions are put forward to improve the laboratory testing of SARSâ€CoVâ€2. In summary, for NAT: collecting stool and blood samples at later periods of illness to improve the positive rate if lower respiratory tract specimens are unavailable; increasing template volume to raise the sensitivity of detection; putting samples in reagents containing guanidine salt to inactivate virus as well as protect RNA; setting proper positive, negative and inhibition controls to ensure highâ€quality results; simultaneously amplifying human RNase P gene to avoid falseâ€negative results. For antibody test, diverse assays targeting different antigens, and collecting paired samples are needed.
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