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Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic

PURPOSE: To assess, if the SARS-CoV-2 mutate in a similar pattern globally or has a specific pattern in any given population. RESULTS: We report, the insertion of TTT at 11085, which adds an extra amino acid, F to the NSP6 at amino acid position 38. The highest occurrence of TTT insertion at 11,085...

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Autores principales: Khalid, Mohammad, Murphy, David, Shoai, Maryam, George-William, Jonahunnatha Nesson, Al-ebini, Yousef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635256/
https://www.ncbi.nlm.nih.gov/pubmed/36343703
http://dx.doi.org/10.1016/j.gene.2022.147020
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author Khalid, Mohammad
Murphy, David
Shoai, Maryam
George-William, Jonahunnatha Nesson
Al-ebini, Yousef
author_facet Khalid, Mohammad
Murphy, David
Shoai, Maryam
George-William, Jonahunnatha Nesson
Al-ebini, Yousef
author_sort Khalid, Mohammad
collection PubMed
description PURPOSE: To assess, if the SARS-CoV-2 mutate in a similar pattern globally or has a specific pattern in any given population. RESULTS: We report, the insertion of TTT at 11085, which adds an extra amino acid, F to the NSP6 at amino acid position 38. The highest occurrence of TTT insertion at 11,085 position was found in UK derived samples (65.97%). The second and third highest occurrence of the mutation were found in Australia (8.3%) and USA (4.16%) derived samples, respectively. Another important discovery of this study is the C27945T mutation, which translates into the termination of ORF-8 after 17 amino acids, reveals that the SARS-CoV-2 can replicate without the intact ORF-8 protein. We found that the 97% of C27945T mutation of global occurrence, occurred in Europe and the USA derived samples. CONCLUSIONS: Two of the reported mutations (11085TTT insertion and C27945T nonsense), which seemed to reduce Type I interferon response are linked to specific geographical locations of the host and implicate region-specific mutations in the virus. The findings of this study signify that SARS-CoV-2 has the potential to adapt differently to different populations.
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spelling pubmed-96352562022-11-04 Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic Khalid, Mohammad Murphy, David Shoai, Maryam George-William, Jonahunnatha Nesson Al-ebini, Yousef Gene Article PURPOSE: To assess, if the SARS-CoV-2 mutate in a similar pattern globally or has a specific pattern in any given population. RESULTS: We report, the insertion of TTT at 11085, which adds an extra amino acid, F to the NSP6 at amino acid position 38. The highest occurrence of TTT insertion at 11,085 position was found in UK derived samples (65.97%). The second and third highest occurrence of the mutation were found in Australia (8.3%) and USA (4.16%) derived samples, respectively. Another important discovery of this study is the C27945T mutation, which translates into the termination of ORF-8 after 17 amino acids, reveals that the SARS-CoV-2 can replicate without the intact ORF-8 protein. We found that the 97% of C27945T mutation of global occurrence, occurred in Europe and the USA derived samples. CONCLUSIONS: Two of the reported mutations (11085TTT insertion and C27945T nonsense), which seemed to reduce Type I interferon response are linked to specific geographical locations of the host and implicate region-specific mutations in the virus. The findings of this study signify that SARS-CoV-2 has the potential to adapt differently to different populations. Elsevier B.V. 2023-01-30 2022-11-04 /pmc/articles/PMC9635256/ /pubmed/36343703 http://dx.doi.org/10.1016/j.gene.2022.147020 Text en © 2022 Elsevier B.V. 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
Khalid, Mohammad
Murphy, David
Shoai, Maryam
George-William, Jonahunnatha Nesson
Al-ebini, Yousef
Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title_full Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title_fullStr Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title_full_unstemmed Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title_short Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic
title_sort geographical distribution of host's specific sars-cov-2 mutations in the early phase of the covid-19 pandemic
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635256/
https://www.ncbi.nlm.nih.gov/pubmed/36343703
http://dx.doi.org/10.1016/j.gene.2022.147020
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