Chromosome scale genome assemblies for Culex pipiens mosquitoes
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 1R21AI156280-01
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Key facts
Disease
West Nile Virus InfectionStart & end year
20202022Known Financial Commitments (USD)
$227,369Funder
National Institutes of Health (NIH)Principal Investigator
RESEARCH SCIENTIST Maria SharakhovaResearch Location
United States of AmericaLead Research Institution
VIRGINIA POLYTECHNIC INST AND ST UNIVResearch Priority Alignment
N/A
Research Category
Animal and environmental research and research on diseases vectors
Research Subcategory
Vector biology
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
PROJECT SUMMARY Mosquitoes from the Cx. pipiens complex are principal vectors of lymphatic filariasis worms and encephalitis viruses, including West Nile virus, which is now the most common arboviral disease in the USA. To facilitate the development of advanced genome-based strategies for vector control, high-quality genome assemblies, based on third-generation sequencing technologies, were developed for species of the Anopheles gambiae complex, as well as for Aedes aegypti and Aedes albopictus. However, the genome assembly for Cx. pipiens, the type species in the complex, is still missing. Our project will develop high-quality genome assemblies for two members of the complex, Cx. p. pipiens and Cx. p. molestus. Ecological, behavioral, and physiological differences between closely related taxa are often associated with chromosomal inversions. However, very few chromosomal inversions have been described in Culex mosquitoes due to the inferior quality of their polytene chromosomes. Our project will test whether any of the chromosomal rearrangements are taxa-specific or related to local adaptation of Cx. pipiens mosquitoes to the environment. Specific aims for this project are to: 1) develop high-quality genome assemblies for Cx. p. pipiens and Cx. p. molestus; 2) create physical maps of the genomes of Cx. p. pipiens and Cx. p. molestus; and 3) identify chromosomal rearrangements in Cx. p. pipiens and Cx. p. molestus. We will utilize the cutting-edge genomic technologies of Oxford Nanopore Technology sequencing, BioNano optical mapping, Hi-C scaffolding, and cDNA-based physical mapping. The Hi-C approach and fluorescence in situ hybridization will be used to identify chromosomal inversions in Cx. p. pipiens and Cx. p. molestus. We envision that development of high- quality genome assemblies for two members of the Cx. pipiens complex, and identification of their chromosomal rearrangements, will further stimulate the development of new strategies for vector control.