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Last Updated: 18/06/2024

Identification of genomic components that predict transmission of the malaria parasite in different vector species

Objectives

To understand how malaria parasite transmission through the mosquito vector drives selection on the parasite.

Principal Investigators / Focal Persons

Virginia Howick

Rationale and Abstract

The malaria parasite (Plasmodium falciparum) has a complex life cycle in which it must transit through multiple environments in a vertebrate host and mosquito vector. Transmission begins with ingestion of an infectious blood meal by one of 40 potential Anopheles mosquito species capable of transmitting the disease. This initiates the most extreme population bottleneck in the life cycle in which the parasite must rapidly undergo fertilisation, develop into an invasive form and transit through the midgut epithelium. The hypothesis is that parasites have adapted to their local vector community composition, and this shapes their ability to infect sympatric and allopatric vector species. Using large-scale transmissibility assays and single-cell RNA-sequencing, genomic and transcriptomic vector-dependent signatures of transmission will be identified. Then the study will generate allelic-replacement parasites to unambiguously attribute phenotypic variation in species-specific transmission to specific loci in the parasite. Comprehensively understanding how vector communities shape parasite populations will guide future interventions and vector control programs by providing information that will allow for strategies to be locally tailored based on parasite genomic-surveillance and entomological surveys.

Date

Aug 2020 — Jul 2025

Total Project Funding

$1.41M

Funding Details
Wellcome Trust, United Kingdom

Grant ID: 220185/Z/20/Z
GBP 1.06M
Project Site

United Kingdom

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