This project has the long-term potential to exploit the differences in taste mechanisms between insects and mammals to develop new strategies to control insect disease vectors that infect hundreds of millions of people annually. In addition, this research explores unexpected similarities between insect and mammalian taste that are evolutionarily conserved. This project will exploit the vast array of tools provided by the fruit fly, Drosophila melanogaster, to address fundamental, longstanding questions in the field of contact chemosensation.
The aims will employ an usually diverse combination of approaches, including electrophysiology, Ca2+ imaging, behavior, molecular genetics and cell biological approaches.
Aim 1 tests the idea that there exists a signaling pathway that functions in the detection of low levels of bitter compounds, and which bears previously unrecognized similarity to mammalian sweet, bitter and umami taste transduction. The capacity to taste aversive compounds is essential for survival, and high levels of many noxious chemicals are detected through so-called ?gustatory receptors,? which are insect ligand-gated channels distinct from mammalian taste receptors. In addition, TRP channels are also employed to sense bitter compounds.
Aim 1 will test the idea that a G-protein coupled receptor (GPCR) couples to a TRP channel in bitter responsive gustatory receptor neurons, and enables flies to sense noxious chemicals at low levels. Thus, despite the striking differences in some mechanisms of taste reception between insects and humans, aim 1 is to define a GPCR/TRP dependent taste transduction pathway in an insect. However, the specific GPCRs that appear to initiate taste transduction in the fly are highly unexpected.
Aim 2 concerns a well-known and highly conserved behavior in which animals are attracted to low salt foods and reject foods with high salt.
The first aim leverages our recent discovery as to how low and high Na+ taste perceptions are differentially encoded in gustatory receptor cells, and thereby induce distinct behavioral responses. An ionotropic receptor (IR76b) is the low salt sensor, but the high salt receptor remains unknown.
Aim 2 is to define the high Na+ receptors, and address whether they form a multi- subunit cation channel. Another behaviorally conserved, but poorly characterized gustatory modality is Ca2+ taste.
Aim 3 is to reveal the enigmatic Ca2+ receptors that endow animals with the ability to taste Ca2+. Finally, aim 4 is to dissect the molecular and cellular mechanism through which food texture affects taste preferences. This would break important new ground since the molecular basis for food texture detection in animals is as yet completely unexplored.
Aim 4 will test the idea that the hardness of food is detected through the Drosophila homolog of ?transmembrane channel-like? (TMC) proteins, which in mammals are implicated as subunits of a channel complex in auditory hair cells. In summary, in those cases in which insect and human receptors are distinct, the differences can be exploited to develop strategies to control disease vectors. Conversely, focusing on flies also offers to reveal evolutionarily conserved gustatory detection mechanisms.

Public Health Relevance

An insect's sense of taste contributes to its decision to bite human hosts. The focus of the proposed work is to discover molecules that the fruit fly uniquely uses to taste chemicals, with the long-term goal of using these insights to develop new strategies to control the spread of insect-borne diseases. While there are some striking differences between insect and mammalian taste, the current proposal also explores some surprising molecular similarities between fly and human taste.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC007864-15
Application #
9953813
Study Section
Somatosensory and Chemosensory Systems Study Section (SCS)
Program Officer
Sullivan, Susan L
Project Start
2006-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
15
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Santa Barbara
Department
Miscellaneous
Type
Organized Research Units
DUNS #
094878394
City
Santa Barbara
State
CA
Country
United States
Zip Code
93106
Liu, Jiangqu; Sokabe, Takaaki; Montell, Craig (2018) A Temperature Gradient Assay to Determine Thermal Preferences of Drosophila Larvae. J Vis Exp :
Montell, Craig (2018) pHirst sour taste channels pHound? Science 359:991-992
Lee, Youngseok; Poudel, Seeta; Kim, Yunjung et al. (2018) Calcium Taste Avoidance in Drosophila. Neuron 97:67-74.e4
Luo, Junjie; Shen, Wei L; Montell, Craig (2017) TRPA1 mediates sensation of the rate of temperature change in Drosophila larvae. Nat Neurosci 20:34-41
Leung, Nicole Y; Montell, Craig (2017) Unconventional Roles of Opsins. Annu Rev Cell Dev Biol 33:241-264
Ni, Jinfei D; Baik, Lisa S; Holmes, Todd C et al. (2017) A rhodopsin in the brain functions in circadian photoentrainment in Drosophila. Nature 545:340-344
Huang, Jia; Liu, Weiwei; Qi, Yi-Xiang et al. (2016) Neuromodulation of Courtship Drive through Tyramine-Responsive Neurons in the Drosophila Brain. Curr Biol 26:2246-56
Zhang, Yali V; Aikin, Timothy J; Li, Zhengzheng et al. (2016) The Basis of Food Texture Sensation in Drosophila. Neuron 91:863-877
Shim, Jaewon; Lee, Youngseok; Jeong, Yong Taek et al. (2015) The full repertoire of Drosophila gustatory receptors for detecting an aversive compound. Nat Commun 6:8867
Liu, Chao; Montell, Craig (2015) Forcing open TRP channels: Mechanical gating as a unifying activation mechanism. Biochem Biophys Res Commun 460:22-5

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