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Published on: June 24, 2019
Infectious cDNA clones of two strains of Mayaro virus for studies on viral pathogenesis and vaccine development
Christina Chuong1, Tyler A Bates1, James Weger-Lucarelli1
1Department of Biomedical Sciences and Pathobiology, Virginia Tech, VA-MD Regional College of Veterinary Medicine, Blacksburg, VA, USA.
Abstract:
Mayaro virus (MAYV; family Togaviridae, genus Alphavirus) is an emerging global threat that can cause severe clinical manifestations similar to Zika, dengue, and chikungunya viruses. Currently, there is a lack of molecular tools to enable a better understanding of the transmission and pathogenesis of MAYV. Here, we detail the development and characterization of infectious clones of two strains of MAYV that produce infectious virus and replicate in mammalian and mosquito cells similarly to wild-type virus. Additionally, clone-derived viruses produced identical infection rates and phenotypes in CD-1 mice compared to the parental strains. This infectious clone system will provide a resource to the research community to analyze MAYV genetic determinants of virulence, determine vector competence, and develop vaccines.
Insights
Researchers developed infectious clones for Mayaro virus (MAYV), an emerging threat. These tools enable studying MAYV
Area of Science:
- Virology
- Molecular Biology
- Public Health
Background:
- Mayaro virus (MAYV) is an emerging alphavirus with severe clinical manifestations.
- Existing molecular tools are insufficient for understanding MAYV transmission and pathogenesis.
- MAYV shares similarities with other significant arboviruses like Zika, dengue, and chikungunya.
Purpose of the Study:
- To develop and characterize infectious clones of Mayaro virus (MAYV).
- To create a molecular resource for studying MAYV virulence, transmission, and vaccine development.
Main Methods:
- Development of infectious cDNA clones for two MAYV strains.
- Characterization of clone-derived viruses in mammalian (CD-1 mice) and mosquito cell lines.
- Assessment of viral replication, infection rates, and phenotypes.
Main Results:
- Infectious MAYV was produced from the developed clones.
- Clone-derived viruses replicated similarly to wild-type MAYV in mammalian and mosquito cells.
- Infection rates and phenotypes of clone-derived viruses matched parental strains in mice.
Conclusions:
- The developed infectious clone system is a valuable resource for MAYV research.
- This system will facilitate analysis of MAYV genetic determinants of virulence.
- It will aid in determining MAYV vector competence and in developing novel vaccines.
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