Intra-host dengue virus genetic diversity among primary and secondary infections in Laos
- Funded by Wellcome Trust
- Total publications:0 publications
Grant number: 222119/Z/20/Z
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Key facts
Disease
DengueStart & end year
20212023Known Financial Commitments (USD)
$166,748.28Funder
Wellcome TrustPrincipal Investigator
Dr. Vilayouth PhimolsannusithResearch Location
Lao People's Democratic RepublicLead Research Institution
University of OxfordResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen genomics, mutations and adaptations
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Not applicable
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
There are an estimated 100-400 million cases of dengue worldwide per year with the highest burden of disease in Asia. The virus (DENV) is a positive-sense single stranded RNA virus belonging to the genus Flavivirus. There are four serotypes: DENV1 to DENV4. Dengue virus RNA dependent RNA polymerase has no proof-reading activity, resulting in accumulation of mutations at each replication cycle. Therefore, within an infected individual, there is diversification of the DENV genome sequence leading to the presence of intra- host genetic variants (quasispecies), which may then lead, under selective pressure, to the emergence of a new strain of higher virulence. Previous findings suggested that immune pressure drives intra-host diversity. My research will explore whether serotype-specific past immunity influences intra-host DENV genetic diversity during acute infection. Objectives: - To describe intra host DENV genetic diversity in patients with primary and secondary infections - To compare quasispecies profiles between primary and secondary infections - To compare quasispecies profiles in secondary infections between two patient groups previously exposed to a different serotype. Impact : We expect the findings of this project would permit a better understanding of processes leading to viral genetic variation, and could eventually be useful for improving viral surveillance systems and epidemic forecasting.