| Title | Gustatory avoidance of fatty acids by depends on an arthropod-specific TRP channel |
| Publication Type | Journal Article |
| Year of Publication | 2026 |
| Authors | Dhakal S, Bontempo AE, Singh R, Dhavan P, Montell C |
| Journal | Proc Natl Acad Sci U S A |
| Volume | 123 |
| Pagination | e2522818123 |
| Date Published | 2026 Feb 17 |
| ISSN | 1091-6490 |
| Keywords | Aedes, Animals, Drosophila melanogaster, Drosophila Proteins, Fatty Acids, Insect Proteins, Taste, Transient Receptor Potential Channels |
| Abstract | Mosquito-disease vectors, such as , use their sense of taste before deciding whether to consume a blood meal, or fly away. However, the molecular mechanisms controlling gustatory decisions in mosquitoes are largely unknown. The transient receptor potential (TRP) channel, Painless1 (Pain1), is an intriguing candidate for participating in taste since transcripts are detected in gustatory receptor neurons (GRNs). The homolog, () is also expressed in GRNs, where it is required for sensing allyl-isothiocyanate. Here, to identify additional gustatory roles for homologs, we first focused on , which is widely expressed in multiple GRN classes. We demonstrated that mutations eliminated gustatory attraction to low fatty acids levels, repulsion to high levels, and fatty acid-induced action potentials. The attraction and repulsion depended on expression in different GRN classes. In contrast to , when contacts fatty acids, they induce gustatory rejection only. is expressed in taste organs, and is required for gustatory avoidance of fatty acids, and for fatty acid-induced action potentials. Given that Pain homologs are found in insects but not vertebrates, Pain1 represents an intriguing target for developing repellents to diminish biting, and transmission of infectious agents by mosquito disease vectors. |
| DOI | 10.1073/pnas.2522818123 |
| Alternate Journal | Proc Natl Acad Sci U S A |
| PubMed ID | 41662530 |
| PubMed Central ID | PMC12912979 |
| Grant List | R01 AI165575 / AI / NIAID NIH HHS / United States R01 DC007864 / DC / NIDCD NIH HHS / United States R01 DC016278 / DC / NIDCD NIH HHS / United States |
