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The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates

Coronavirus disease- 2019 (COVID-19) has rapidly become a major threat to humans due to its high infection rate and deaths caused worldwide. This disease is caused by an RNA virus, Severe Acquired Respiratory Syndrome –Corona Virus-2 (SARS-CoV-2). This class of viruses have a high rate of mutation t...

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Autor principal: Azad, Gajendra Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848562/
https://www.ncbi.nlm.nih.gov/pubmed/33553784
http://dx.doi.org/10.1016/j.heliyon.2021.e06167
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author Azad, Gajendra Kumar
author_facet Azad, Gajendra Kumar
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description Coronavirus disease- 2019 (COVID-19) has rapidly become a major threat to humans due to its high infection rate and deaths caused worldwide. This disease is caused by an RNA virus, Severe Acquired Respiratory Syndrome –Corona Virus-2 (SARS-CoV-2). This class of viruses have a high rate of mutation than DNA viruses that enables them to adapt and also evade host immune system. Here, we compared the first known Nucleocapsid Phosphoprotein (N protein) sequence of SARS-CoV-2 from China with the sequences from Indian COVID-19 patients to understand, if this virus is also mutating, as it is spreading to new locations. Our data revealed twenty mutations present among Indian isolates. Out of these, mutation at six positions led to changes in the secondary structure of N protein. Further, we also show that these mutations are primarily destabilising the protein structure. The candidate mutations identified in this study may help to speed up the understanding of variations occurring in SARS-CoV-2.
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spelling pubmed-78485622021-02-01 The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates Azad, Gajendra Kumar Heliyon Research Article Coronavirus disease- 2019 (COVID-19) has rapidly become a major threat to humans due to its high infection rate and deaths caused worldwide. This disease is caused by an RNA virus, Severe Acquired Respiratory Syndrome –Corona Virus-2 (SARS-CoV-2). This class of viruses have a high rate of mutation than DNA viruses that enables them to adapt and also evade host immune system. Here, we compared the first known Nucleocapsid Phosphoprotein (N protein) sequence of SARS-CoV-2 from China with the sequences from Indian COVID-19 patients to understand, if this virus is also mutating, as it is spreading to new locations. Our data revealed twenty mutations present among Indian isolates. Out of these, mutation at six positions led to changes in the secondary structure of N protein. Further, we also show that these mutations are primarily destabilising the protein structure. The candidate mutations identified in this study may help to speed up the understanding of variations occurring in SARS-CoV-2. Elsevier 2021-02-01 /pmc/articles/PMC7848562/ /pubmed/33553784 http://dx.doi.org/10.1016/j.heliyon.2021.e06167 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Azad, Gajendra Kumar
The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title_full The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title_fullStr The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title_full_unstemmed The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title_short The molecular assessment of SARS-CoV-2 Nucleocapsid Phosphoprotein variants among Indian isolates
title_sort molecular assessment of sars-cov-2 nucleocapsid phosphoprotein variants among indian isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848562/
https://www.ncbi.nlm.nih.gov/pubmed/33553784
http://dx.doi.org/10.1016/j.heliyon.2021.e06167
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