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Analysis of viral diversity of Dengue virus 1 and 2 following antibody neutralization by plasma from previously infected individuals

Grant number: 23/14976-1
Support Opportunities:Scholarships abroad - Research Internship - Doctorate
Effective date (Start): March 01, 2024
Effective date (End): August 31, 2024
Field of knowledge:Biological Sciences - Genetics - Molecular Genetics and Genetics of Microorganisms
Principal Investigator:Simone Kashima Haddad
Grantee:Debora Glenda Lima de La-Roque
Supervisor: Tulio de Paiva Nazareth Andrade de Oliveira
Host Institution: Hemocentro de Ribeirão Preto. Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da USP (HCMRP). Secretaria da Saúde (São Paulo - Estado). Ribeirão Preto , SP, Brazil
Research place: Stellenbosch University, South Africa  
Associated to the scholarship:22/16349-1 - Genomic surveillance and viral quasispecies reconstruction of dengue virus in an endemic region, BP.DR

Abstract

Dengue fever is caused by four distinct serotypes of the dengue virus (DENV), which are transmitted by Aedes mosquitoes. Approximately 390 million infections occur annually in tropical and subtropical countries. This infection is endemic in the northwest region of the State of São Paulo, with co-circulation of DENV1 and DENV2 serotypes. Around 25% of DENV infections progress to clinical manifestations, categorized as classic dengue or severe dengue. The primary factor leading to severe dengue is a secondary infection with a different DENV serotype. In RNA viruses like DENV, various subpopulations of similar but not identical genomes exist within the same host, called quasispecies. Previous studies showed that genomic diversity within the host is primarily observed in regions encoding viral envelope proteins. Therefore, we hypothesize that heterotypic antibodies may exert evolutionary pressure that worsens clinical outcomes in individuals infected with DENV by selecting quasispecies with best replication fitness. This project aims to investigate the selection of DENV strains influenced by antibodies present in the plasma of previously infected patients.

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