Structural analysis of SARS-Cov-2 nonstructural protein 1 polymorphisms found in the Brazilian Amazon. Issue 21 (November 2021)

• Record Type: Journal Article
• Authors: Zanchi, Fernando Berton; Mariúba, Luis André; Nascimento, Valdinete; Souza, Victor; Corado, André; Nascimento, Fernanda; Costa, Ágatha Kelly; Duarte, Débora; Silva, George; Mejía, Matilde; Pessoa, Karina; Gonçalves, Luciana; Brandão, Maria Júlia; Jesus, Michele; Glória, Juliane; Silva, Marineide; Mattos, Tirza; da Costa, Cristiano; Naveca, Felipe Gomes
• Is Part Of: Experimental biology and medicine. Volume 246:Issue 21(2021)
• Page Start: 2332
• Page End: 2337
• Publication Date: 2021-11
• Subjects: SARS-CoV-2 -- COVID-19 -- coronavirus -- polymorphism -- NSP1 -- 3D structure modeling; Physiology -- Periodicals; Biology, Experimental -- Periodicals; Medicine, Experimental -- Periodicals; 610.72
• DOI: 10.1177/15353702211021348
• Languages: English
• ISSNs: 1535-3702

Abstract

The coronavirus disease COVID-19 has been the cause of millions of deaths worldwide. Among the SARS-CoV-2 proteins, the non-structural protein 1 (NSP1) has great importance during the virus infection process and is present in both alpha and beta-CoVs. Therefore, monitoring of NSP1 polymorphisms is crucial in order to understand their role during infection and virus-induced pathogenicity. Herein, we analyzed how mutations detected in the circulating SARS-CoV-2 in the population of the city of Manaus, Amazonas state, Brazil could modify the tertiary structure of the NSP1 protein. Three mutations were detected in the SARS-CoV-2 NSP1 gene: deletion of the amino acids KSF from positions 141 to 143 (delKSF), SARS-CoV-2, lineage B.1.195; and two substitutions, R29H and R43C, SARS-CoV-2 lineage B.1.1.28 and B.1.1.33, respectively. The delKSF was found in 47 samples, whereas R29H and R43C were found in two samples, one for each mutation. The NSP1 structures carrying the mutations R43C and R29H on the N-terminal portion (e.g. residues 10 to 127) showed minor backbone divergence compared to the Wuhan model. However, the NSP1 C-terminal region (residues 145 to 180) was severely affected in the delKSF and R29H mutants. The intermediate variable region (residues 144 to 148) leads to changes in the C-terminal region, particularly in the delKSF structure. New investigations must be carried out to analyze how these changes affect NSP1 activity during the infection. Our results reinforce the need for continuous genomic surveillance of SARS-CoV-2 to better understand virus evolution and assess the potential impact of the viral mutations on the approved vaccines and future therapies.