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1.
J Neurosci ; 41(50): 10222-10246, 2021 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-34753739

RESUMO

Food choice, in animals, has been known to change with internal nutritional state and also with variable dietary conditions. To better characterize mechanisms of diet-induced plasticity of food preference in Drosophila melanogaster, we synthesized diets with macronutrient imbalances and examined how food choice and taste sensitivity were modified in flies that fed on these diets. We found that dietary macronutrient imbalances caused compensatory behavioral shifts in both sexes to increase preference for the macronutrient that was scant in the food source, and simultaneously reduce preference for the macronutrient that was enriched. Further analysis with females revealed analogous changes in sweet taste responses in labellar neurons, with increased sensitivity on sugar-reduced diet and decreased sensitivity on sugar-enriched diet. Interestingly, we found differences in the onset of changes in taste sensitivity and behavior, which occur over 1-4 d, in response to dietary sugar reduction or enrichment. To investigate molecular mechanisms responsible for diet-induced taste modulation, we used candidate gene and transcriptome analyses. Our results indicate that signaling via Dop2R is involved in increasing cellular and behavioral sensitivity to sugar as well as in decreasing behavioral sensitivity to amino acids on dietary sugar reduction. On the other hand, cellular and behavioral sensitivity to sugar relies on dilp5 and a decrease in sugar preference following dietary sugar abundance was correlated with downregulation of dilp5 Together, our results suggest that feeding preference for sugar and amino acid can be modulated independently to facilitate food choice that accounts for prior dietary experience.SIGNIFICANCE STATEMENT Animals adjust their feeding preferences based on prior dietary experiences. Here, we find that upon dietary macronutrient deprivation, flies undergo compensatory changes in food preference. The altered preference correlates with changes in peripheral taste sensitivity. While Dop2R mediates changes following dietary sugar reduction, downregulation of dilp5 is associated with changes caused by a sugar-enriched diet. This study contributes to a better understanding of neurophysiological plasticity of the taste system in flies, and its role in facilitating adjustment of foraging behavior based on nutritional requirements.


Assuntos
Drosophila melanogaster/fisiologia , Preferências Alimentares/fisiologia , Nutrientes , Transdução de Sinais/fisiologia , Animais , Proteínas de Drosophila/metabolismo , Comportamento Alimentar/fisiologia , Feminino , Insulinas/metabolismo , Masculino , Receptores de Dopamina D1/metabolismo
2.
Cell Rep ; 18(3): 737-750, 2017 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-28099851

RESUMO

Amino acid taste is expected to be a universal property among animals. Although sweet, bitter, salt, and water tastes have been well characterized in insects, the mechanisms underlying amino acid taste remain elusive. From a Drosophila RNAi screen, we identify an ionotropic receptor, Ir76b, as necessary for yeast preference. Using calcium imaging, we identify Ir76b+ amino acid taste neurons in legs, overlapping partially with sweet neurons but not those that sense other tastants. Ir76b mutants have reduced responses to amino acids, which are rescued by transgenic expression of Ir76b and a mosquito ortholog AgIr76b. Co-expression of Ir20a with Ir76b is sufficient for conferring amino acid responses in sweet-taste neurons. Notably, Ir20a also serves to block salt response of Ir76b. Our study establishes the role of a highly conserved receptor in amino acid taste and suggests a mechanism for mutually exclusive roles of Ir76b in salt- and amino-acid-sensing neurons.


Assuntos
Aminoácidos/farmacologia , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/fisiologia , Receptores Ionotrópicos de Glutamato/metabolismo , Canais de Sódio/metabolismo , Paladar/efeitos dos fármacos , Animais , Animais Geneticamente Modificados/fisiologia , Sequência de Bases , Comportamento Animal/efeitos dos fármacos , Sistemas CRISPR-Cas/genética , Cálcio/metabolismo , Proteínas de Drosophila/antagonistas & inibidores , Proteínas de Drosophila/deficiência , Proteínas de Drosophila/genética , Drosophila melanogaster/efeitos dos fármacos , Feminino , Masculino , Microscopia Confocal , Neurônios/metabolismo , Neurônios/patologia , Fenótipo , Interferência de RNA , Receptores Ionotrópicos de Glutamato/antagonistas & inibidores , Receptores Ionotrópicos de Glutamato/genética , Canais de Sódio/genética , Cloreto de Sódio/farmacologia , Açúcares/farmacologia , Paladar/fisiologia
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