Molecular epidemiology of SARS‐CoV‐2 variants in circulation in the state of Maranhão, Brazil

Author:

de Sousa Luis Artur Ferreira12ORCID,Ferreira Lucas Salomão de Sousa2,Lobato Luis Felipe Lima23,Ferreira Hivylla Lorrana dos Santos2,Sousa Lucas Henrique dos Santos2,Santos Valdenice Ferreira dos4,Nunes Paulo Ricardo Silva2,Maramaldo Carlos Eduardo Campos2,Neto Sebastião Silveira2,Sampaio Hellen Lobato1,Silva Fabiano Vieira da23,Brito Marcelo da Costa2,Lima Washington Kleber Rodrigues45,Lima Claudia Zeneida Gomes Parente Alves5,Neto Lidio Gonçalves Lima12

Affiliation:

1. Virology Laboratory, Postgraduation Program in Microbial Biology CEUMA University, UniCEUMA São Luís Maranhão Brazil

2. Oswaldo Cruz Institute/Central Public Health Laboratory of Maranhão—IOC/LACEN‐MA São Luís Maranhão Brazil

3. Postgraduation Program in Tropical Medicine—IOC/FIOCRUZ‐RJ Rio de Janeiro Brazil

4. Post‐graduate Programme in Biodiversity and Biotechnology (BIONORTE) CEUMA University, UniCEUMA São Luís Maranhão Brazil

5. UniCEUMA CEUMA University São Luís Maranhão Brazil

Abstract

AbstractSevere acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) is a coronavirus belonging to the beta CoV genus, responsible for SARS in humans, which became known as COVID‐19. The emergence of variants of this virus is related to the presence of cases of reinfection, reduced vaccine effectiveness and greater transmission of the virus. Objective: In this study, we evaluated the molecular epidemiology of SARS‐CoV‐2 lineages circulating in the state of Maranhão. This is a cross‐sectional and retrospective epidemiological study of genomic surveillance of SARS‐CoV‐2. The study comprised of 338 genomes sequenced by the Next Generation Sequencing technique on Illumina's Miseq equipment, submitted to Global Initiative on Sharing Avian Influenza Data, 190 (56.2%) are from samples of female and 148 (43.8%) from male patients. Sequencing performed covered samples of patients aged between 1 and 108 years, with emphasis on the age groups from 30 to 39 years with 15.0% of sequenced genomes and 20 to 29 years with 12.4%. As for the distribution of sequenced genomes by health macro‐regions, 285 (84.3%) are from cities in the northern macro‐region. We evidenced the circulation of 29 lineages and sub‐lineages, four of which belonging to the Delta variant (AY.43, AY.99.1, AY.99.2 and AY.101 responsible for 4.5% of the genomes) and the others belonging to the Omicron variant, with emphasis on: BA.1 and sub‐lineages (42.8%); BA.4, BA.5 and sub‐lineages (5.3% and 41.1%); the sub‐lineages DL.1 and BQ.1 (5% and 2%). A strong genomic surveillance system allows the study of the natural history of the disease, when there is a resurgence of SARS‐CoV‐2 cases.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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