Visual olfactory learning in mosquitoes

Active Project Grant Awarded Last action

Award ID
F31AI191763
Recipient
Awarding agency
Obligated
$198,728

Award facts

Assistance listing
93.855 Allergy and Infectious Diseases Research
Completion date 34% complete
Originally
Place of performance
Seattle, WA 98195, USA

Award details come from USAspending.gov.

About this award

The National Institute of Allergy and Infectious Diseases awarded the University of Washington $198,728 on February 25, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to investigate visual-olfactory learning and integration in the yellow fever mosquito, Aedes aegypti.

The research addresses how mosquitoes combine visual and olfactory sensory cues to locate and feed on hosts. Specific Aim 1 examines multimodal learning and memory of visual and olfactory stimuli through aversive conditioning using a two-choice T-maze assay and a free-flight blood-feeding choice assay, alongside neurogenetic sensory knockout lines to characterize interplay between olfactory and visual inputs. The work tests the hypothesis that olfaction drives learning performance while visual stimuli enhance responses. Specific Aim 2 investigates how the mosquito mushroom body—a sensory learning and integration center in the insect brain—encodes learned and unlearned host-related visual and olfactory stimuli, using two-photon calcium imaging to record neural activity in mushroom body Kenyon cells and dopaminergic neurons.

The University of Washington Office of Sponsored Programs serves as the recipient, with performance in Seattle, Washington. The period of performance extends from February 25, 2026, through February 15, 2028. The award is a project grant, classified as assistance funding.

Description

Abstract
Mosquitoes rely on a combination of sensory cues to locate their hosts, including olfactory, heat, and visual stimuli. Previous studies have shown that olfactory cues play a crucial role in mosquito behavior, but emerging evidence suggests that visual cues are also important, particularly in the final stages of host localization. While significant research has focused on the role of olfaction in mosquito host-seeking behavior, the contribution of vision remains less understood. This proposed research seeks to address this GAP by investigating our working hypothesis that bimodal visual-olfactory stimuli elicit more robust behavioral and neural responses from mosquitoes - eventually leading to altered blood-feeding choices. We will test several hypotheses regarding the role of visual and olfactory integration in mosquito behavior and neural processing. Specific aim 1 investigates the multimodal learning and memory of visual and olfactory stimuli, including host-related cues, in the yellow fever mosquito, aedes aegypti. This aim will utilize an aversive conditioning paradigm with two testing assays - a two-choice T- maze and a free-flight blood-feeding choice assay, in addition to neurogenetic sensory knockout lines to characterize the interplay between olfactory and visual inputs in mosquito responses. We will determine how aversive learning affects mosquito attraction towards human host odorants and visual wavelengths (1A) and will test the hypothesis that olfaction is the primary driver of learning performance, with visual stimuli enhancing those responses (1B). Specific aim 2 will investigate the encoding of learned and unlearned host-related visual and olfactory stimuli in the a. Aegypti mushroom body (MB), an crucial sensory learning and integration center in the insect brain. Using 2-photon calcium imaging, we will record neural activity in the mushroom body kenyon cells and dopaminergic neurons in response to olfactory, visual, and bimodal stimuli. This aim will test the hypotheses that KCS exhibit increased activity in response to host-related cues (2A) and that PPL1 dopaminergic neurons will increase their activity following aversive associative conditioning (2B). This comprehensive examination of visual-olfactory sensory encoding in a vector species will significantly advance our understanding of the neural bases of mosquito learning and its implications for host selection. Additionally, the completion of the proposed aims will provide the first evidence of visual-spectral learning in mosquitoes and the first recordings from the mosquito MB. Carrying out these experiments will provide me with training in calcium imaging, neurogenetic techniques, and data analytical approaches. We are confident that the collaborative environment at the university of washington, along with my mentor's experience in training successful scientists, puts me in an ideal position to achieve these aims and gain the necessary training for my future career.

Transactions

Action Obligated Date
Amendment $50,114
Amendment $49,538
Amendment $49,538
Amendment $0
Amendment $49,538
Original award $0

Quick answers

Who received award F31AI191763?

F31AI191763 was awarded to University Of Washington by National Institute of Allergy and Infectious Diseases (National Institutes of Health) on February 25, 2026.

How much is award F31AI191763 worth?

$198,728 has been obligated on F31AI191763.

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