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Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes

The human β-coronavirus SARS-CoV-2 epidemic started in late December 2019 in Wuhan, China. It causes Covid-19 disease which has become pandemic. Each of the five-known human β-coronaviruses has four major structural proteins (E, M, N and S) and 16 non-structural proteins encoded by ORF1a and ORF1b t...

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Autores principales: Emam, Mohamed, Oweda, Mariam, Antunes, Agostinho, El-Hadidi, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190378/
https://www.ncbi.nlm.nih.gov/pubmed/34118359
http://dx.doi.org/10.1016/j.virusres.2021.198472
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author Emam, Mohamed
Oweda, Mariam
Antunes, Agostinho
El-Hadidi, Mohamed
author_facet Emam, Mohamed
Oweda, Mariam
Antunes, Agostinho
El-Hadidi, Mohamed
author_sort Emam, Mohamed
collection PubMed
description The human β-coronavirus SARS-CoV-2 epidemic started in late December 2019 in Wuhan, China. It causes Covid-19 disease which has become pandemic. Each of the five-known human β-coronaviruses has four major structural proteins (E, M, N and S) and 16 non-structural proteins encoded by ORF1a and ORF1b together (ORF1ab) that are involved in virus pathogenicity and infectivity. Here, we performed detailed positive selection analyses for those six genes among the four previously known human β-coronaviruses and within 38 SARS-CoV-2 genomes to assess signatures of adaptive evolution using maximum likelihood approaches. Our results suggest that three genes (E, S and ORF1ab genes) are under strong signatures of positive selection among human β-coronavirus, influencing codons that are located in functional important protein domains. The E protein-coding gene showed signatures of positive selection in two sites, Asp 66 and Ser 68, located inside a putative transmembrane α-helical domain C-terminal part, which is preferentially composed by hydrophilic residues. Such Asp and Ser sites substitutions (hydrophilic residues) increase the stability of the transmembrane domain in SARS-CoV-2. Moreover, substitutions in the spike (S) protein S1 N-terminal domain have been found, all of them were located on the S protein surface, suggesting their importance in viral transmissibility and survival. Furthermore, evidence of strong positive selection was detected in three of the SARS-CoV-2 nonstructural proteins (NSP1, NSP3, NSP16), which are encoded by ORF1ab and play vital roles in suppressing host translation machinery, viral replication and transcription and inhibiting the host immune response. These results are insightful to assess the role of positive selection in the SARS-CoV-2 encoded proteins, which will allow to better understand the virulent pathogenicity of the virus and potentially identifying targets for drug or vaccine strategy design
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spelling pubmed-81903782021-06-10 Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes Emam, Mohamed Oweda, Mariam Antunes, Agostinho El-Hadidi, Mohamed Virus Res Article The human β-coronavirus SARS-CoV-2 epidemic started in late December 2019 in Wuhan, China. It causes Covid-19 disease which has become pandemic. Each of the five-known human β-coronaviruses has four major structural proteins (E, M, N and S) and 16 non-structural proteins encoded by ORF1a and ORF1b together (ORF1ab) that are involved in virus pathogenicity and infectivity. Here, we performed detailed positive selection analyses for those six genes among the four previously known human β-coronaviruses and within 38 SARS-CoV-2 genomes to assess signatures of adaptive evolution using maximum likelihood approaches. Our results suggest that three genes (E, S and ORF1ab genes) are under strong signatures of positive selection among human β-coronavirus, influencing codons that are located in functional important protein domains. The E protein-coding gene showed signatures of positive selection in two sites, Asp 66 and Ser 68, located inside a putative transmembrane α-helical domain C-terminal part, which is preferentially composed by hydrophilic residues. Such Asp and Ser sites substitutions (hydrophilic residues) increase the stability of the transmembrane domain in SARS-CoV-2. Moreover, substitutions in the spike (S) protein S1 N-terminal domain have been found, all of them were located on the S protein surface, suggesting their importance in viral transmissibility and survival. Furthermore, evidence of strong positive selection was detected in three of the SARS-CoV-2 nonstructural proteins (NSP1, NSP3, NSP16), which are encoded by ORF1ab and play vital roles in suppressing host translation machinery, viral replication and transcription and inhibiting the host immune response. These results are insightful to assess the role of positive selection in the SARS-CoV-2 encoded proteins, which will allow to better understand the virulent pathogenicity of the virus and potentially identifying targets for drug or vaccine strategy design Published by Elsevier B.V. 2021-09 2021-06-10 /pmc/articles/PMC8190378/ /pubmed/34118359 http://dx.doi.org/10.1016/j.virusres.2021.198472 Text en © 2021 Published by Elsevier B.V. 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
Emam, Mohamed
Oweda, Mariam
Antunes, Agostinho
El-Hadidi, Mohamed
Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title_full Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title_fullStr Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title_full_unstemmed Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title_short Positive selection as a key player for SARS-CoV-2 pathogenicity: Insights into ORF1ab, S and E genes
title_sort positive selection as a key player for sars-cov-2 pathogenicity: insights into orf1ab, s and e genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190378/
https://www.ncbi.nlm.nih.gov/pubmed/34118359
http://dx.doi.org/10.1016/j.virusres.2021.198472
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