Identification of genotypic variants and its proteomic mutations of Brazilian SARS-CoV-2 isolates.


Journal

Virus research
ISSN: 1872-7492
Titre abrégé: Virus Res
Pays: Netherlands
ID NLM: 8410979

Informations de publication

Date de publication:
02 01 2022
Historique:
received: 06 10 2021
revised: 25 10 2021
accepted: 26 10 2021
pubmed: 7 11 2021
medline: 15 12 2021
entrez: 6 11 2021
Statut: ppublish

Résumé

The second wave of COVID-19 caused by severe acute respiratory syndrome virus (SARS-CoV-2) is rapidly spreading over the world. Mechanisms behind the flee from current antivirals are still unclear due to the continuous occurrence of SARS-CoV-2 genetic variants. Brazil is the world's second-most COVID-19 affected country. In the present study, we identified the genomic and proteomic variants of Brazilian SARS-CoV-2 isolates. We identified 16 different genotypic variants were found among the 27 isolates. The genotypes of three isolates such as Bra/1236/2021 (G15), Bra/MASP2C844R2/2020 (G11), and Bra/RJ-DCVN5/2020 (G9) have a unique mutant in NSP4 (S184N), 2'O-Mutase (R216N), membrane protein (A2V) and Envelope protein (V5A). A mutation in RdRp of SARS-CoV-2, particularly the change of Pro-to Leu-at 323 resulted in the stabilization of the structure in BRA/CD1739-P4/2020. NSP4, NSP5 protein mutants are more virulent in genotype 15 and 16. A fast protein folding rate changes the structural stability and leads to escape for current antivirals. Thus, our findings help researchers to develop the best potent antivirals based on the new mutant of Brazilian isolates.

Identifiants

pubmed: 34740719
pii: S0168-1702(21)00325-7
doi: 10.1016/j.virusres.2021.198618
pmc: PMC8563081
pii:
doi:

Substances chimiques

Coronavirus Nucleocapsid Proteins 0
NSP4 protein, SARS-CoV-2 0
Phosphoproteins 0
Spike Glycoprotein, Coronavirus 0
Viral Nonstructural Proteins 0
nucleocapsid phosphoprotein, SARS-CoV-2 0
spike protein, SARS-CoV-2 0
Coronavirus RNA-Dependent RNA Polymerase EC 2.7.7.48
NSP12 protein, SARS-CoV-2 EC 2.7.7.48
3C-like proteinase, SARS-CoV-2 EC 3.4.22.-
Coronavirus 3C Proteases EC 3.4.22.28

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

198618

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

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Auteurs

Ragothaman Prathiviraj (R)

Department of Microbiology, Pondicherry University, Puducherry 605014, India.

Paulchamy Chellapandi (P)

Department of Bioinformatics, Bharathidasan University, Tiruchirappalli 620024, India.

Ajima Begum (A)

National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi 110067, India.

George Seghal Kiran (GS)

Department of Food Science and Technology, Pondicherry University, Puducherry 605014, India.

Joseph Selvin (J)

Department of Microbiology, Pondicherry University, Puducherry 605014, India.

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Classifications MeSH