Targeting a reductive dehalogenase as a new strategy for controlling mosquito populations

Active Project Grant Awarded Last action

Award ID
R21AI188223
Recipient
Awarding agency
Obligated
$616,517

Award facts

Assistance listing
93.855 Allergy and Infectious Diseases Research
Completion date 99% complete
Place of performance
Baltimore, MD 21218, USA

Award details come from USAspending.gov.

Description

Abstract
Targeting a reductive dehalogenase as a new strategy for controlling mosquito populations the enzyme iodotyrosine deiodinase gained prominence from its role in salvaging iodide from iodotyrosine. This activity is necessary for generating the iodinated hormone thyroxine that is required for all vertebrates. Surprisingly, this enzyme was also found nearly ubiquitous in invertebrates that do not require iodide nor generate thyroxine. Initial studies have suggested that its ability to process a range of halotyrosines (x = i, BR, CL, not f) remains the same in fruit flies, but its biological role is quite different. The dehalogenase protects flies from the accumulation of endogenous halotyrosine that would otherwise suppress male fertility. Inhibition of the dehalogenase or accumulation of a halotyrosine in vivo significantly decreases fly populations by a mechanism orthogonal to those currently used to mitigate vector-borne disease. Homologs of the dehalogenase are present in most insects and offer a new and potent target for eliminating such vectors if the results from fruit flies extend to other invertebrates. The anopheles gambiae mosquito was selected as the test organism in our investigations due to its importance as a vector of malaria. Despite a vast amount of research and field work, this disease remains a health priority and its return has recently been reported in the united states. Knowledge gained from fruit flies now guides our experiments on the mosquito. Loss of fertility will be examined after alternative external exposure to halotyrosines and internal suppression of the dehalogenase by chemical and genetic strategies. Analytical chemistry will identify which halotyrosine is generated endogenously and whether halogenation targets tyrosine free in solution or tyrosyl residues within proteins. Initial efforts are also planned to identify the peroxidase responsible for halogenation to build a foundation for broad investigations in the future on the nature and function of an overlooked cycle of halogenation and dehalogenation in insects. The most immediate impact of these studies will derive from a newfound ability to limit mosquito populations and the diseases that they spread.

Transactions

Action Obligated Date
Amendment $194,441
Amendment $211,038
Original award $211,038

Quick answers

Who received award R21AI188223?

R21AI188223 was awarded to The Johns Hopkins University by National Institute of Allergy and Infectious Diseases (National Institutes of Health) on November 12, 2024.

How much is award R21AI188223 worth?

$616,517 has been obligated on R21AI188223.

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