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At an earlier developmental stage, Drosophila larvae display simple and robust olfactory-mediated chemotactic behavior controlled by 21 olfactory neurons expressing a repertoire of 25 odorant receptor genes. We have used a genetic approach to study odor coding in this simple animal by ablating specific sensory neurons and the receptors expressed in them, or by constructing animals with only a single functional olfactory neuron. By combining behavioral analysis with calcium imaging, we are attempting to understand the neural basis of olfactory behavior in this animal.
It is a widespread observation that mosquitoes prefer some people over others.
In our well-controlled laboratory setting, we found that this is also true — mosquitoes go crazy when offered a whiff of certain human subjects, while they find the smell of other subjects only mildly compelling. Many hypotheses have been put forth, both anecdotally and scientifically, to attempt to explain these large differences in mosquito attraction, but none fully explain the cues mosquitoes use to choose between individuals.
We are currently conducting studies with human subjects from the New York City area to seek out better answers to this question. In these studies, we are determining how attractive subjects are to mosquitoes in our laboratory setting (using an olfactometer, pictured on the right) and then searching for physiological correlates of this behavior. Understanding what drives mosquitoes to target specific human hosts may eventually help us to develop new tools to reduce the spread of deadly mosquito-borne diseases.
How complicated behaviors arise from and are regulated by the brain is perhaps the greatest mystery in biology. Sexual behavior in the fly provides a reductionist and genetically malleable system for addressing this mystery. Drosophila melanogaster exhibit a particularly well-studied sexually dimorphic set of innate behaviors in their precopulatory courtship. In the classical view, male Drosophila initiate courtship and perform stereotyped behaviors in order to woo the female. The female, for her part, may respond by being receptive to copulation or avoiding it. We are interested in understanding how flies use courtship to make the decision whether, and with whom, to mate. The decision to mate is based first of all upon the drive to reproduce, and both the fly’s internal state and sensory information from the environment influence the choice. During courtship, flies gather information about potential mates via visual, auditory, tactile, and chemical cues. We want to understand how these cues are interpreted by the fly to decide whether or not to mate with a given individual. Previous analyses of courtship have largely focused on the behavior of the male, but given the equal importance of mating to females, we are working to understand the female’s role in the decision to mate.
Human body heat is a strong host-seeking cue to a female mosquito searching for a blood meal. In fact, female Aedes aegypti are attracted to warm inanimate objects, and probe at them as though they were a host. We have established quantitative assays to measure heat-seeking behavior in Aedes aegypti, as well as to test interactions between warmth and other host-seeking cues such as carbon dioxide. Using these assays, along with targeted mutagenesis, we are examining the molecular basis of thermosensation and heat-seeking behavior in the mosquito.
Host odor is a long-range, attractive cue that guides mosquitoes to their hosts. The mosquito perceives differences in host odor, both between and within species, to determine which host to feed upon. Until recently, the molecular mechanism by which mosquitoes translate host odor information into host-seeking behavior has only been inferred. To shed new light on mosquito olfaction and host-seeking behavior, we developed a technique for targeted mutagenesis in Aedes aegypti using zinc-finger nucleases. Using this technique, my co-authors and I demonstrated that orco, an olfactory co-receptor, enables host odor attraction, the preference of mosquitoes for human hosts, and DEET-driven repellency. In addition, the establishment of loss-of-function genetics in Aedes aegypti using zinc-finger nucleases has opened new paths of investigation in vector biology.
How volatile DEET drives repellency in insects is an unresolved controversy. We have identified Orco and the ORs as behaviorally relevant, olfactory receptors necessary for both Drosophila melanogaster and Aedes aegypti to avoid DEET. Experiments are underway to understand how DEET hijacks ORs to make attractive cues unappealing. We wonder whether DEET activates a specific neural circuit that drives repulsive behavior or whether DEET alters the perception of attractive odors.
We not only seek to understand how the mosquito responds to odor cues from the environment, but how the nutritional status of the mosquito regulates odor perception. The transmission of vector borne disease involves female mosquitoes making behavioral shifts from host-seeking to oviposition during each gonotrophic cycle. Understanding how these behavioral shifts are accomplished could open up new strategies for vector control. One of the advantages of Aedes aegypti is its clearly defined cyclical host-seeking behavior that is under humoral control. These behavioral changes have been correlated with alterations in antennal sensitivity to odors. To begin to address the genetic basis of these behavioral shifts, I initiated an in depth analysis of the neural and chemosensory response to blood-feeding using RNA-seq. We are in the process of identifying candidate genes that regulate the behavioral switch from host-seeking to oviposition.
My research aims to (1) identify the olfactory receptors that mediate human odor perception (2) understand the mechanism of action of DEET and (3) determine how host-seeking is regulated by changes in nutritional status during the gonotrophic cycle.
Using genetic labeling of olfactory sensory neurons expressing a given receptor, we generated a nearly complete map connecting odorant receptor expression to olfactory neuron convergence to antennal lobe glomeruli in adult Drosophila.
This work was supported in part by an individual F31 NRSA training grant from NIH/NIDCD to E.F. (5F31DC006795).
The etiology of compulsive feeding behaviors including bulimia nervosa and binge eating disorder in humans is poorly understood. We propose that studying these important clinical conditions in a simpler genetic model system, the larva of the fruit fly Drosophila melanogaster, may shed new light on this important health problem. Fruit flies go through four distinct life stages: embryo, larva, pupa, and adult. While adult flies regulate their feeding according to hunger status and the circadian clock just like normal humans, the larva resembles a binge eater because it feeds continuously for nearly 72 hrs, eating 3-5 times its own weight in food. About 24 hrs before puparation, the larva abruptly leaves the food medium and stops eating. This highly stereotyped behavior provides an attractive experimental model to explore the neuronal mechanisms that drive and sustain continuous (compulsive) feeding. We hypothesize that continuous feeding in the Drosophila larva is a behavior accessible to genetic and pharmacological modulation. We are carrying out microarray analysis to identify candidate genes subject to regulation during continuous feeding. Using a genome-wide RNA interference (RNAi) screen, we hope to identify genes that modulate food intake. We will complement the RNAi screen with a small molecule screen that will look for compounds that reduce food intake. Finally, we will study the neuronal circuits modulating continuous feeding. Our long-term goal is to identify genes and neuronal circuits mediating the continuous feeding behavior of larvae and to prove that this compulsive-like behavior can be decreased by specific pharmacological interventions. We hope to illuminate common principles underlying the regulation of feeding behavior that will be applicable to parallel processes occurring in human patients suffering from compulsive eating disorders.
Funded by a grant from the Klarman Family Foundation Grants Program in Eating Disorders Research
Rhythmic cellular functions, such as the heartbeat and the timing of daily rhythms of activity and sleep, are regulated by the activity of cellular pacemakers. We are using genetic approaches to study the role of the Drosophila hyperpolarization- and cyclic nucleotide-gated ion channel, DmIh, in these processes. This project was a collaboration with Dr. Gareth Tibbs at Columbia University and Dr. Michael Nitabach at Yale University.
According to the National Health and Nutrition Examination Survey, 14.1 million American citizens suffer from smell impairment and 3.6 million have completely lost their sense of smell, which is a condition named anosmia. Even though smell disorders can present insidiously, dramatic consequences on quality of life, mental well-being, and mortality occur. The management of these conditions urgently needs improvement. We explore the possibilities of addressing current limitations in smell tests to develop ground-breaking and innovative tools to measure a patient’s sense of smell. Although smells in nature are often composed of multiple molecules (e.g the smell of roses contains more than 200 molecules), current smell tests are based on single volatile molecules such as n-butanol or phenylethyl alcohol. This constitutes two large problems. First, due to large genetic variability in odorant receptor genes among the population, individuals have variable sensitivity and perception to a given molecule. Second, the results of currently used smell tests depend on a patient’s cultural background and previous experiences with these molecules. These two issues limit the generalizability and accuracy of these tests. We use complex mixtures of molecules to overcome these limitations and to develop an “olfactory resolution test.” The goal of this work is to develop high performance clinical tests to improve the management of smell disorders for clinicians from around the world.
Olfactory stimuli are not well understood. Olfactory psychophysics has traditionally relied on testing the perception of small groups of odors of special interest. It has been difficult to draw general conclusions about olfactory psychophysics from these vignettes. We therefore decided on an unbiased, high-throughput approach in which we test the perception of large numbers of olfactory stimuli. One current study addresses the connection between physical and chemical properties of odor molecules and their perceived odor quality. Our most recent study is designed to answer the question how many distinguishable odors there are.
As part of our overall mission to understand the genetic and neuronal basis of how odors guide behaviors, we are conducting psychophysical studies with human subjects to find correlations between genetic variability in odorant receptor genes and variability in cognitive and physiological responses to odors. In collaboration with Hiroaki Matsunami’s group at Duke University we have shown that variability in one odorant receptor gene, OR7D4, influences the perception of odorous steroids. Currently we are extending our studies to include more odors and more odorant receptor genes. We are also interested in how variability in OR genes influences perceived odor quality. To include subliminal and physiological responses to odors in this project, we also investigate the genetic basis of changes in salivary cortisol and mood induced by an odorous steroid.
Olfactory cues guide mosquitoes toward humans, from which the mosquitoes derive the blood they need to complete ovarian development. We are carrying out two conceptually related projects in mosquitoes.
In the yellow fever and dengue vector mosquito, Aedes aegypti, host-seeking is suppressed or inhibited for about 72 hours after the mosquito takes a blood meal. The molecular basis for how host-seeking behavior is regulated is unknown, but may be explained by a humoral control mechanism in which the sensitivity of the olfactory system is altered following blood-feeding. In this project, we are examining the hypothesis that regulation of specific olfactory and neurohumoral genes modifies the host-seeking behavior of female Aedes aegypti after blood-feeding.
Ancestral populations of the Dengue-Fever mosquito Aedes aegypti from sub-Saharan Africa are largely generalists. They are not particularly attracted to humans, they feed on a wide variety of animals, and they breed in tree holes in natural habitats.
Outside of Africa, however, recently evolved populations of Aedes aegypti specialize on humans. They are strongly attracted to human scent, they thrive on human blood, and they breed in artificial containers in human-disturbed habitats – often even in water stored inside people’s homes. Previous work has shown that these two ecologically divergent forms of the mosquito coexist in several villages along the coast of East Africa where they maintain their differences despite living in close proximity. This project aims to (1) identify the genetic basis of recently evolved preference for human odor and (2) to describe the evolutionary processes by which this trait arose and is maintained.
This work is funded in part by a grant to Richard Axel and L.B.V. from the Foundation for the National Institutes of Health through the Grand Challenges in Global Health Initiative
Carbon dioxide (CO2) exhaled in breath is a potent chemosensory cue that lures deadly mosquitoes towards humans to blood-feed. Aedes aegypti senses CO2 using a specialized class of olfactory sensory neuron on the maxillary palp that co-expresses three gustatory receptors (Gr1, Gr2 and Gr3) thought to mediate responses to this volatile gas. We are using genome-editing techniques, coupled with large-scale laboratory and semi-field based analyses of mosquito behavior to (i) dissect the molecular basis of CO2 reception in Aedes aegypti; (ii) determine the relative role of CO2 detection to mosquito host-seeking behavior; and (iii) identify sensory networks that ultimately drive mosquito attraction to humans.
Insects have exquisitely sensitive olfactory systems that are tuned to food odors and pheromonal cues emitted by members of the same species. We have been studying the molecular mechanisms by which insect olfactory neurons respond to and discriminate among the numerous possible odors in the environment. Several years ago, we and others identified a divergent family of seven transmembrane domain receptors now known to be the insect odorant receptors (ORs). One member of the odorant receptor gene family, Orco, has the unique property that it is expressed in nearly all olfactory neurons. Therefore, each olfactory neuron in the fly is likely to express a conventional odorant receptor along with the co-receptor Or83b. Our recent work has shown that the insect odorant receptor is a heteromeric complex of the OR83b co-receptor with a conventional ligand binding odorant receptor. Orco is necessary and sufficient to target this OR/Orco complex to the ciliated dendrite of the olfactory sensory neuron. Together with our collaborator Dr. Kazushige Touhara and colleagues at the University of Tokyo, we investigated whether Orco has additional signaling functions beyond its role in ciliary trafficking. Our recent work provides strong evidence that the OR/Orco complex forms an odor-gated non-selective cation channel that does not depend upon G protein signaling. We are carrying out a large-scale in vivo structure-function analysis of Orco and the conventional odorant receptors to further probe the biology of these unusual membrane receptors. The goal is to map those domains that are necessary for the heteromeric association of the OR/Orco complex, domains necessary for trafficking, and residues that are necessary for odor signal transduction. We are particularly interested in discovering which residues may contribute to forming the ion-conducting pore. Going beyond conventional genetics, are using chemical biology to probe for small molecules that interfere with heterodimerization, trafficking, or signaling of OR/Orco complexes. Some of these compounds may be useful elements in a chemical strategy to block olfactory host-seeking behaviors in mosquitoes and other pest insects. These compounds may act as insect repellents that could be useful to control insect vectors that transmit human infectious diseases.
This work was funded in part by a grant to Richard Axel and L.B.V. from the Foundation for the National Institutes of Health through the Grand Challenges in Global Health Initiative
The perception of hunger and satiety and the regulation of food intake are controlled in the nervous system by evaluating internal metabolic state and external chemosensory information. The proper function of this complex physiological system is essential for humans and other animals to balance nutrient intake, to maintain stable body weight, and to regulate metabolism. After fasting, the drive to eat increases, leading to enhanced foraging and food intake until the energy deficiency is compensated and metabolic homeostasis returns. When the balance between hunger and satiety is perturbed, food intake is misregulated, leading to excessive or insufficient eating. In humans, this abnormal nutrient consumption cause metabolic conditions, such as obesity, and eating disorders, such as anorexia nervosa, bulimia, and binge eating disorder. Similar to other animals and humans, feeding state in the fly (Drosophila melanogaster) regulates attractiveness to food odors and responsiveness to sugars. After fasting, flies increase their food intake to compensate for the energy deficiency incurred. In this project, we aim to discover novel genes that are essential for proper food intake in a model organism, Drosophila melanogaster, in which large behavioral genetic screens are feasible. Our long-term goal is to relate our results to the homologous mammalian genes with similar functions and thus to discover conserved pathways that regulate hunger and satiety. We are also developing technologies such as an automated instrument called EXPRESSO that measures real-time food consumption, which will greatly accelerate the feeding research in the fly.