Cargando…

Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens

On 31 December 2019, the World Health Organization was informed of a cluster of cases of pneumonia of unknown etiology in Wuhan, China. Subsequent investigations identified a novel coronavirus, now named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), from the affected patients. Highly...

Descripción completa

Detalles Bibliográficos
Autores principales: Chan, Jasper Fuk-Woo, Yip, Cyril Chik-Yan, To, Kelvin Kai-Wang, Tang, Tommy Hing-Cheung, Wong, Sally Cheuk-Ying, Leung, Kit-Hang, Fung, Agnes Yim-Fong, Ng, Anthony Chin-Ki, Zou, Zijiao, Tsoi, Hoi-Wah, Choi, Garnet Kwan-Yue, Tam, Anthony Raymond, Cheng, Vincent Chi-Chung, Chan, Kwok-Hung, Tsang, Owen Tak-Yin, Yuen, Kwok-Yung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180250/
https://www.ncbi.nlm.nih.gov/pubmed/32132196
http://dx.doi.org/10.1128/JCM.00310-20
_version_ 1783525783393796096
author Chan, Jasper Fuk-Woo
Yip, Cyril Chik-Yan
To, Kelvin Kai-Wang
Tang, Tommy Hing-Cheung
Wong, Sally Cheuk-Ying
Leung, Kit-Hang
Fung, Agnes Yim-Fong
Ng, Anthony Chin-Ki
Zou, Zijiao
Tsoi, Hoi-Wah
Choi, Garnet Kwan-Yue
Tam, Anthony Raymond
Cheng, Vincent Chi-Chung
Chan, Kwok-Hung
Tsang, Owen Tak-Yin
Yuen, Kwok-Yung
author_facet Chan, Jasper Fuk-Woo
Yip, Cyril Chik-Yan
To, Kelvin Kai-Wang
Tang, Tommy Hing-Cheung
Wong, Sally Cheuk-Ying
Leung, Kit-Hang
Fung, Agnes Yim-Fong
Ng, Anthony Chin-Ki
Zou, Zijiao
Tsoi, Hoi-Wah
Choi, Garnet Kwan-Yue
Tam, Anthony Raymond
Cheng, Vincent Chi-Chung
Chan, Kwok-Hung
Tsang, Owen Tak-Yin
Yuen, Kwok-Yung
author_sort Chan, Jasper Fuk-Woo
collection PubMed
description On 31 December 2019, the World Health Organization was informed of a cluster of cases of pneumonia of unknown etiology in Wuhan, China. Subsequent investigations identified a novel coronavirus, now named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), from the affected patients. Highly sensitive and specific laboratory diagnostics are important for controlling the rapidly evolving SARS-CoV-2-associated coronavirus disease 2019 (COVID-19) epidemic. In this study, we developed and compared the performance of three novel real-time reverse transcription-PCR (RT-PCR) assays targeting the RNA-dependent RNA polymerase (RdRp)/helicase (Hel), spike (S), and nucleocapsid (N) genes of SARS-CoV-2 with that of the reported RdRp-P2 assay, which is used in >30 European laboratories. Among the three novel assays, the COVID-19-RdRp/Hel assay had the lowest limit of detection in vitro (1.8 50% tissue culture infective doses [TCID(50)]/ml with genomic RNA and 11.2 RNA copies/reaction with in vitro RNA transcripts). Among 273 specimens from 15 patients with laboratory-confirmed COVID-19 in Hong Kong, 77 (28.2%) were positive by both the COVID-19-RdRp/Hel and RdRp-P2 assays. The COVID-19-RdRp/Hel assay was positive for an additional 42 RdRp-P2-negative specimens (119/273 [43.6%] versus 77/273 [28.2%]; P < 0.001), including 29/120 (24.2%) respiratory tract specimens and 13/153 (8.5%) non-respiratory tract specimens. The mean viral load of these specimens was 3.21 × 10(4) RNA copies/ml (range, 2.21 × 10(2) to 4.71 × 10(5) RNA copies/ml). The COVID-19-RdRp/Hel assay did not cross-react with other human-pathogenic coronaviruses and respiratory pathogens in cell culture and clinical specimens, whereas the RdRp-P2 assay cross-reacted with SARS-CoV in cell culture. The highly sensitive and specific COVID-19-RdRp/Hel assay may help to improve the laboratory diagnosis of COVID-19.
format Online
Article
Text
id pubmed-7180250
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-71802502020-04-27 Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens Chan, Jasper Fuk-Woo Yip, Cyril Chik-Yan To, Kelvin Kai-Wang Tang, Tommy Hing-Cheung Wong, Sally Cheuk-Ying Leung, Kit-Hang Fung, Agnes Yim-Fong Ng, Anthony Chin-Ki Zou, Zijiao Tsoi, Hoi-Wah Choi, Garnet Kwan-Yue Tam, Anthony Raymond Cheng, Vincent Chi-Chung Chan, Kwok-Hung Tsang, Owen Tak-Yin Yuen, Kwok-Yung J Clin Microbiol Virology On 31 December 2019, the World Health Organization was informed of a cluster of cases of pneumonia of unknown etiology in Wuhan, China. Subsequent investigations identified a novel coronavirus, now named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), from the affected patients. Highly sensitive and specific laboratory diagnostics are important for controlling the rapidly evolving SARS-CoV-2-associated coronavirus disease 2019 (COVID-19) epidemic. In this study, we developed and compared the performance of three novel real-time reverse transcription-PCR (RT-PCR) assays targeting the RNA-dependent RNA polymerase (RdRp)/helicase (Hel), spike (S), and nucleocapsid (N) genes of SARS-CoV-2 with that of the reported RdRp-P2 assay, which is used in >30 European laboratories. Among the three novel assays, the COVID-19-RdRp/Hel assay had the lowest limit of detection in vitro (1.8 50% tissue culture infective doses [TCID(50)]/ml with genomic RNA and 11.2 RNA copies/reaction with in vitro RNA transcripts). Among 273 specimens from 15 patients with laboratory-confirmed COVID-19 in Hong Kong, 77 (28.2%) were positive by both the COVID-19-RdRp/Hel and RdRp-P2 assays. The COVID-19-RdRp/Hel assay was positive for an additional 42 RdRp-P2-negative specimens (119/273 [43.6%] versus 77/273 [28.2%]; P < 0.001), including 29/120 (24.2%) respiratory tract specimens and 13/153 (8.5%) non-respiratory tract specimens. The mean viral load of these specimens was 3.21 × 10(4) RNA copies/ml (range, 2.21 × 10(2) to 4.71 × 10(5) RNA copies/ml). The COVID-19-RdRp/Hel assay did not cross-react with other human-pathogenic coronaviruses and respiratory pathogens in cell culture and clinical specimens, whereas the RdRp-P2 assay cross-reacted with SARS-CoV in cell culture. The highly sensitive and specific COVID-19-RdRp/Hel assay may help to improve the laboratory diagnosis of COVID-19. American Society for Microbiology 2020-04-23 /pmc/articles/PMC7180250/ /pubmed/32132196 http://dx.doi.org/10.1128/JCM.00310-20 Text en Copyright © 2020 Chan et al. This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Virology
Chan, Jasper Fuk-Woo
Yip, Cyril Chik-Yan
To, Kelvin Kai-Wang
Tang, Tommy Hing-Cheung
Wong, Sally Cheuk-Ying
Leung, Kit-Hang
Fung, Agnes Yim-Fong
Ng, Anthony Chin-Ki
Zou, Zijiao
Tsoi, Hoi-Wah
Choi, Garnet Kwan-Yue
Tam, Anthony Raymond
Cheng, Vincent Chi-Chung
Chan, Kwok-Hung
Tsang, Owen Tak-Yin
Yuen, Kwok-Yung
Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title_full Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title_fullStr Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title_full_unstemmed Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title_short Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens
title_sort improved molecular diagnosis of covid-19 by the novel, highly sensitive and specific covid-19-rdrp/hel real-time reverse transcription-pcr assay validated in vitro and with clinical specimens
topic Virology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180250/
https://www.ncbi.nlm.nih.gov/pubmed/32132196
http://dx.doi.org/10.1128/JCM.00310-20
work_keys_str_mv AT chanjasperfukwoo improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT yipcyrilchikyan improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT tokelvinkaiwang improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT tangtommyhingcheung improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT wongsallycheukying improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT leungkithang improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT fungagnesyimfong improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT nganthonychinki improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT zouzijiao improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT tsoihoiwah improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT choigarnetkwanyue improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT tamanthonyraymond improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT chengvincentchichung improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT chankwokhung improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT tsangowentakyin improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens
AT yuenkwokyung improvedmoleculardiagnosisofcovid19bythenovelhighlysensitiveandspecificcovid19rdrphelrealtimereversetranscriptionpcrassayvalidatedinvitroandwithclinicalspecimens