Cargando…

Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic

SARS-CoV-2, the causal agent of COVID 19, is a new human pathogen that appeared in Wuhan, late December 2019. SARS-CoV-2 is a positive sense RNA virus, having four structural and six accessory proteins including that encoded by ORF8 gene known to be one of the most hypervariable and rapidly evolving...

Descripción completa

Detalles Bibliográficos
Autores principales: Alkhansa, Ahmad, Lakkis, Ghayas, El Zein, Loubna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813478/
https://www.ncbi.nlm.nih.gov/pubmed/33490718
http://dx.doi.org/10.1016/j.genrep.2021.101024
_version_ 1783637856925777920
author Alkhansa, Ahmad
Lakkis, Ghayas
El Zein, Loubna
author_facet Alkhansa, Ahmad
Lakkis, Ghayas
El Zein, Loubna
author_sort Alkhansa, Ahmad
collection PubMed
description SARS-CoV-2, the causal agent of COVID 19, is a new human pathogen that appeared in Wuhan, late December 2019. SARS-CoV-2 is a positive sense RNA virus, having four structural and six accessory proteins including that encoded by ORF8 gene known to be one of the most hypervariable and rapidly evolving genes. Thus, global characterization of mutations in this gene is important for pathogenicity and diagnostics. 240 different nonsynonymous mutations and 2 deletions were identified in 45,400 ORF8 nucleotide sequences during six months pandemic with about half of these variants were deleterious for ORF8, and the quarter of them were located in conserved amino acids. Genetic diversity analysis showed two main regions that harbor L84S and S24L. L84S is by far the most predominant mutation, followed by S24L that appeared first in USA. Phylogenetic analysis of ORF8 variants revealed the appearance of small clades with that of L84S being closer to bats. This is the first study that revealed the global nonsynonymous mutations in ORF8 from January to June 2020.
format Online
Article
Text
id pubmed-7813478
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-78134782021-01-19 Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic Alkhansa, Ahmad Lakkis, Ghayas El Zein, Loubna Gene Rep Article SARS-CoV-2, the causal agent of COVID 19, is a new human pathogen that appeared in Wuhan, late December 2019. SARS-CoV-2 is a positive sense RNA virus, having four structural and six accessory proteins including that encoded by ORF8 gene known to be one of the most hypervariable and rapidly evolving genes. Thus, global characterization of mutations in this gene is important for pathogenicity and diagnostics. 240 different nonsynonymous mutations and 2 deletions were identified in 45,400 ORF8 nucleotide sequences during six months pandemic with about half of these variants were deleterious for ORF8, and the quarter of them were located in conserved amino acids. Genetic diversity analysis showed two main regions that harbor L84S and S24L. L84S is by far the most predominant mutation, followed by S24L that appeared first in USA. Phylogenetic analysis of ORF8 variants revealed the appearance of small clades with that of L84S being closer to bats. This is the first study that revealed the global nonsynonymous mutations in ORF8 from January to June 2020. Elsevier Inc. 2021-06 2021-01-17 /pmc/articles/PMC7813478/ /pubmed/33490718 http://dx.doi.org/10.1016/j.genrep.2021.101024 Text en © 2021 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 Article
Alkhansa, Ahmad
Lakkis, Ghayas
El Zein, Loubna
Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title_full Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title_fullStr Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title_full_unstemmed Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title_short Mutational analysis of SARS-CoV-2 ORF8 during six months of COVID-19 pandemic
title_sort mutational analysis of sars-cov-2 orf8 during six months of covid-19 pandemic
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813478/
https://www.ncbi.nlm.nih.gov/pubmed/33490718
http://dx.doi.org/10.1016/j.genrep.2021.101024
work_keys_str_mv AT alkhansaahmad mutationalanalysisofsarscov2orf8duringsixmonthsofcovid19pandemic
AT lakkisghayas mutationalanalysisofsarscov2orf8duringsixmonthsofcovid19pandemic
AT elzeinloubna mutationalanalysisofsarscov2orf8duringsixmonthsofcovid19pandemic