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Mutations on COVID-19 diagnostic targets

Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will...

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Autores principales: Wang, Rui, Hozumi, Yuta, Yin, Changchuan, Wei, Guo-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502284/
https://www.ncbi.nlm.nih.gov/pubmed/32966857
http://dx.doi.org/10.1016/j.ygeno.2020.09.028
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author Wang, Rui
Hozumi, Yuta
Yin, Changchuan
Wei, Guo-Wei
author_facet Wang, Rui
Hozumi, Yuta
Yin, Changchuan
Wei, Guo-Wei
author_sort Wang, Rui
collection PubMed
description Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. AVAILABILITY: Interactive real-time online Mutation Tracker.
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spelling pubmed-75022842020-09-21 Mutations on COVID-19 diagnostic targets Wang, Rui Hozumi, Yuta Yin, Changchuan Wei, Guo-Wei Genomics Original Article Effective, sensitive, and reliable diagnostic reagents are of paramount importance for combating the ongoing coronavirus disease 2019 (COVID-19) pandemic when there is neither a preventive vaccine nor a specific drug available for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It will cause a large number of false-positive and false-negative tests if currently used diagnostic reagents are undermined. Based on genotyping of 31,421 SARS-CoV-2 genome samples collected up to July 23, 2020, we reveal that essentially all of the current COVID-19 diagnostic targets have undergone mutations. We further show that SARS-CoV-2 has the most mutations on the targets of various nucleocapsid (N) gene primers and probes, which have been widely used around the world to diagnose COVID-19. To understand whether SARS-CoV-2 genes have mutated unevenly, we have computed the mutation rate and mutation h-index of all SARS-CoV-2 genes, indicating that the N gene is one of the most non-conservative genes in the SARS-CoV-2 genome. We show that due to human immune response induced APOBEC mRNA (C > T) editing, diagnostic targets should also be selected to avoid cytidines. Our findings might enable optimally selecting the conservative SARS-CoV-2 genes and proteins for the design and development of COVID-19 diagnostic reagents, prophylactic vaccines, and therapeutic medicines. AVAILABILITY: Interactive real-time online Mutation Tracker. Elsevier Inc. 2020-11 2020-09-20 /pmc/articles/PMC7502284/ /pubmed/32966857 http://dx.doi.org/10.1016/j.ygeno.2020.09.028 Text en © 2020 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Wang, Rui
Hozumi, Yuta
Yin, Changchuan
Wei, Guo-Wei
Mutations on COVID-19 diagnostic targets
title Mutations on COVID-19 diagnostic targets
title_full Mutations on COVID-19 diagnostic targets
title_fullStr Mutations on COVID-19 diagnostic targets
title_full_unstemmed Mutations on COVID-19 diagnostic targets
title_short Mutations on COVID-19 diagnostic targets
title_sort mutations on covid-19 diagnostic targets
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502284/
https://www.ncbi.nlm.nih.gov/pubmed/32966857
http://dx.doi.org/10.1016/j.ygeno.2020.09.028
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