Cargando…

Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients

The etiologic agent SARS-CoV-2 has caused the outbreak of COVID-19 which is spread widely around the world. It is vital to uncover and investigate the full genome sequence of SARS-CoV-2 throughout the world to track changes in this virus. To this purpose, SARS-CoV-2 full genome sequence profiling of...

Descripción completa

Detalles Bibliográficos
Autores principales: Salehi, Najmeh, Amiri-Yekta, Amir, Totonchi, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481902/
https://www.ncbi.nlm.nih.gov/pubmed/32779445
http://dx.doi.org/10.22074/cellj.2020.7524
_version_ 1783580704516341760
author Salehi, Najmeh
Amiri-Yekta, Amir
Totonchi, Mehdi
author_facet Salehi, Najmeh
Amiri-Yekta, Amir
Totonchi, Mehdi
author_sort Salehi, Najmeh
collection PubMed
description The etiologic agent SARS-CoV-2 has caused the outbreak of COVID-19 which is spread widely around the world. It is vital to uncover and investigate the full genome sequence of SARS-CoV-2 throughout the world to track changes in this virus. To this purpose, SARS-CoV-2 full genome sequence profiling of 20 patients in Iran and different countries that already had a travel history to Iran or contacts with Iranian cases were provided from the GISAID database. The bioinformatics analysis showed 44 different nucleotide mutations that caused 26 nonsynonymous mutations in protein sequences with regard to the reference full genome of the SARS-CoV-2 sequence (NC_045512.2). R207C, V378I, M2796I, L3606F, and A6407V in ORF1ab were common mutations in these sequences. Also, some of the detected mutations only were found in Iranian data in comparison with all the available sequences of SARS-CoV-2. The position of S protein mutations showed they were far from the binding site of this protein with angiotensin-converting enzyme-2 (ACE2) as the host cell receptor. These results can be helpful to design specific diagnostic tests, trace the SARS-CoV-2 sequence changes in Iran, and explore therapeutic drugs and vaccines.
format Online
Article
Text
id pubmed-7481902
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Royan Institute
record_format MEDLINE/PubMed
spelling pubmed-74819022020-09-15 Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients Salehi, Najmeh Amiri-Yekta, Amir Totonchi, Mehdi Cell J Short Communication The etiologic agent SARS-CoV-2 has caused the outbreak of COVID-19 which is spread widely around the world. It is vital to uncover and investigate the full genome sequence of SARS-CoV-2 throughout the world to track changes in this virus. To this purpose, SARS-CoV-2 full genome sequence profiling of 20 patients in Iran and different countries that already had a travel history to Iran or contacts with Iranian cases were provided from the GISAID database. The bioinformatics analysis showed 44 different nucleotide mutations that caused 26 nonsynonymous mutations in protein sequences with regard to the reference full genome of the SARS-CoV-2 sequence (NC_045512.2). R207C, V378I, M2796I, L3606F, and A6407V in ORF1ab were common mutations in these sequences. Also, some of the detected mutations only were found in Iranian data in comparison with all the available sequences of SARS-CoV-2. The position of S protein mutations showed they were far from the binding site of this protein with angiotensin-converting enzyme-2 (ACE2) as the host cell receptor. These results can be helpful to design specific diagnostic tests, trace the SARS-CoV-2 sequence changes in Iran, and explore therapeutic drugs and vaccines. Royan Institute 2020 2020-09-08 /pmc/articles/PMC7481902/ /pubmed/32779445 http://dx.doi.org/10.22074/cellj.2020.7524 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Salehi, Najmeh
Amiri-Yekta, Amir
Totonchi, Mehdi
Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title_full Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title_fullStr Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title_full_unstemmed Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title_short Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients
title_sort profiling of initial available sars-cov-2 sequences from iranian related covid-19 patients
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481902/
https://www.ncbi.nlm.nih.gov/pubmed/32779445
http://dx.doi.org/10.22074/cellj.2020.7524
work_keys_str_mv AT salehinajmeh profilingofinitialavailablesarscov2sequencesfromiranianrelatedcovid19patients
AT amiriyektaamir profilingofinitialavailablesarscov2sequencesfromiranianrelatedcovid19patients
AT totonchimehdi profilingofinitialavailablesarscov2sequencesfromiranianrelatedcovid19patients