Open Access
How to translate text using browser tools
1 September 2002 Differentiated Response to Sugars among Labellar Chemosensilla in Drosophila
Makoto Hiroi, Frédéric Marion-Poll, Teiichi Tanimura
Author Affiliations +

Recent findings have indicated that the Gr genes for putative gustatory receptors of Drosophila melanogaster are expressed in a spatially restricted pattern among chemosensilla on the labellum. However, evidence for a functional segregation among the chemosensilla is lacking. In this work, labellar chemosensilla were classified and numbered into three groups, L-, I- and S-type, based on their morphology. Electrophysiological responses to sugars and salt were recorded from all the accessible labellar chemosensilla by the tip-recording method. All the L-type sensilla gave good responses to sugars in terms of action potential firing rates, while the probability for successful recordings from the I-type and S-type sensilla was lower. No differences were found in the responses to sugars between chemosensilla belonging to the same type; however, dose-response curves for several different sugars varied among the sensilla types. The L-type sensilla gave the highest frequency of nerve responses to all the sugars. The I-type sensilla also responded to all the sugars but with a lower magnitude of firing rate than the L-type sensilla. The S-type sensilla gave a good response to sucrose, and lower responses to the other sugars. These results suggest that there might be variations in the expression level or pattern of multiple receptors for sugars among the three types of chemosensilla. The expression pattern of six Gr genes was examined using the Gal4/UAS-GFP system, and sensilla were identified according to the innervation pattern of each GFP-expressing taste cell. None of the spatial expression patterns of the six Gr genes corresponded to the sugar sensitivity differences we observed.


Chemoreception is essential for all living organisms to perceive chemical information in their environment. Remarkable progress has been made toward the molecular identification of olfactory receptors in some vertebrates and in Drosophila. Olfactory receptors have been identified as G-protein coupled transmembrane receptors (GPCRs) (for review, see Firestein, 2001). In relation to gustation, only a few GPCRs have been identified as functional gustatory receptors in mammals (for review, see Lewcock and Reed, 2001) and Drosophila (Ishimoto et al., 2000; Ueno et al., 2001; Dahanukar et al., 2001).

In Drosophila, gustatory neurons are housed in a hair-like structure, called a sensillum, on the labellum and tarsi. A typical sensillum houses one mechanoreceptor and four gustatory neurons, each of which responds to either water (W cell), sugar (S cell), low salt concentration (L1 cell) or high salt concentration (L2 cell) (Dethier, 1976; Rodrigues and Siddiqi, 1978; Fujishiro et al., 1984; Wieczorek and Wolff, 1989). The response properties of several sensilla on the prothoracic tarsi have been reported and it was shown that contrasting responses existed between sensilla (Meunier et al., 2000). On a labellum of Drosophila, 62 chemosensilla are present which can be grouped by their length into three types - long, short and intermediate types (L-, S- and I-) (Shanbhag et al., 2001). All previous electrophysiological recordings on the labellar sensilla were made on L-type sensilla which were considered as functionally equivalent each other. This is in sharp contrast with the multiplicity of putative gustatory receptor (Gr) genes recently found in the Drosophila genome using a computer algorithm to probe a database of the Drosophila genome (Clyne et al., 2000; Scott et al., 2001; Dunipace et al., 2001). Since some of these genes show an expression that is restricted to a limited number of sensilla, the probability exists that the taste responsiveness might differ among the labellar sensilla.

Here we recorded, using the tip-recording method, nerve responses to several different sugars from all the three types of labellar chemosensilla. We classified sensilla according to their responsiveness of each sensillum to a range of sugars and salts. In order to test if the functional types found by this method matched Gr gene segregation, we examined the green fluorescent protein (GFP) expression pattern of six of the 65 Gr genes. This study thus provides us with a basic understanding of the physiology of the gustatory sense in Drosophila.


Fly stocks

Strains of Drosophila melanogaster were maintained on a standard cornmeal-glucose agar medium at 25°C. Canton-S was used as wild type. One-day-old flies were fed on a fresh medium for one day before experiments. Gr promoter-Gal4 strains were provided by H. Amrein and R. Axel. The UAS-Gal4 strain, P{w+mC=UASGFP.S65T}, was from the Bloomington Drosophila Stock Center. The nomenclature of the Gr genes described in Flybase ( was used.

Scanning electron microscopy

Flies were fixed, dehydrated in acetone, and dried. Mounted flies were sputter-coated with platinum and observed by a JEOL JSM-5600 LV scanning electron microscope.

Visualizing GAL4 expression patterns by GFP

To visualize the expression pattern of Gr genes, the Gr promoter-Gal4 strains were crossed to the strains carrying a UAS-GFP transgene on the second chromosome. Homozygous strains for both transgenes were established. Proboscises were dissected from 2 day-old flies, fixed in 4% formaldehyde (MERCK, Haar, Germany) in phosphate buffered saline (PBS), washed with PBS, and mounted in Antifade (SlowFade-Light, Molecular Probes, Inc., Eugene, USA). GFP images of a half-labellar lobe were captured at 2 μm intervals across a 30–40 μm thick section by a confocal laser-scanning microscope (LSM510, Carl Zeiss, Inc., Germany).


KCl, NaCl and sucrose were purchased from Wako Pure Chemical Industries, Ltd (Tokyo, Japan). Trehalose, glucose and fructose were from Sigma-Aldrich Corp. (St. Louis, USA). All compounds were dissolved in a 1 mM KCl solution prepared using distilled water, and were stored at −20°C. Solutions for stimulation were stored at 4°C for less than one week.

Tip-recording method

The proboscis was fixed at the base of a labellum using lanolin (Wako Pure Chemical Industries, Ltd., Tokyo, Japan). A glass capillary filled with Drosophila Ringer solution was inserted from the abdomen through to the head and served as an indifferent electrode. Nerve responses from labellar chemosensilla of female flies were recorded by the tip-recording method (Hodgson et al., 1955). Chemosensilla on the labellum were stimulated by a recording electrode with a 20 μm tip diameter. Sugar solutions for stimulation contain 1 mM KCl as electric substance. 1 mM KCl dose not elicit salt spikes but only water spikes. The recording electrode was connected to a preamplifier (TastePROBE, Marion-Poll and Van der Pers, 1996), and electric signals were further amplified and filtered by a second amplifier (CyberAmp 320, Axon Instrument, Inc., USA, gain = 100, 8th order Bessel pass-band filter = 1 Hz - 2800 Hz). The recorded signals were digitized (DT2821, Data Translation, USA, sampling rate = 10 kHz, 12 bits), stored on computer and analyzed using a custom software, Awave (Marion-Poll, 1995, 1996) software. Action potentials were detected by a visually-adjusted threshold set across the digitally filtered signal. The action potentials were filtered by a running median algorithm spanning a 6 ms window (Fiore et al., 1996) and sorted on the basis of their amplitudes and shapes with the aid of interactive software procedures.


Arrangement of chemosensilla on the labellar surface

In Drosophila, 31 chemosensilla are consistently found on each side of the labellum. They are organized in four rows oriented in the anterior-posterior axis (Fig.1A). The 31 chemosensilla can be classified into three types; long (L), intermediate (I) and short (S) types, according to their length (Fig. 1B–D) (Shanbhag et al., 2001). Labellar chemosensilla generally house four gustatory neurons and one mechanosensory neuron. The I-type sensilla, however, have just two gustatory neurons and one mechanosensory neuron (Falk et al., 1976; Nayak and Singh, 1983; Ray et al., 1993; Shanbhag et al., 2001). We numbered the chemosensilla in each class from the anterior to the posterior side of the labellum (Fig. 2B) and found no variation in the total number of the L-type sensilla among females of the Canton-S strain. There were small variations in the total number of the S-type and I-type sensilla (S: 12–13, I: 9–10).

Fig. 1

Morphology of the labellar chemosensilla in Drosophila. Three types of sensillum, L-, I- and S-type, are visible on the label-lum (Shanbhag et al., 2001). (A) Lateral view of the left lobe of a labellum. Anterior is top and dorsal to the right. Chemosensilla are arranged in four rows oriented in the anterior-posterior axis (Falk et al., 1976; Ray et al., 1993). The S-type sensilla are in the most ventral area and the I-type sensilla are located in the most dorsal area. Enlarged images of L-type (B), I-type (C) and S-type sensilla (D). B–C are shown in the same scale. Scale bars represent 40 μm (A) and 10 μm (C and D).


Fig. 2

Classification and numbering of chemosensilla on the labellum. Anterior is top and dorsal to the right. (A) Surface image of a left label-lar lobe. Scale bar represents 30 μm. (B) Schematic diagram of sensilla arrangement modified from Shanbhag et al. (2001). Squares, triangles and open circles indicate, L-type, I-type and S-type sensilla, respectively. S5, S7, S11 and I6 sensilla are reported to have variable neuronal composition (Nayak and Singh, 1983; Ray et al., 1993; Shanbhag et al., 2001).


Expression pattern of several Gr promoter-Gal4 strains

Over 60 Gr genes have been proposed to be candidate taste receptor genes in Drosophila. The expression of a number of Gr genes in chemosensory organs was confirmed by in situ hybridization and reverse transcription polymerase chain reaction (RT-PCR) (Scott et al., 2001; Dunipace et al., 2001). These authors have independently generated 23 transgenic strains in total expressing GAL4 under the control of a Gr promoter, for which 20 Gr genes were covered. In 12 out of 23 lines, which covered 10 Gr genes, expression of the transgene was reported. We obtained these Gr promoter-Gal4 strains and re-examined their expression pattern. Six homozygous lines were established that contained both Gr promoter-Gal4 (Gr22c, Gr22e, Gr22f, Gr32a, Gr59b and Gr66a) and UAS-GFP transgenes. Fig. 3A-F shows the location of GFP-expressing cells in the six lines.

Fig. 3

Expression of Gr genes monitored by Gr promoter-Gal4/UAS-GFP. Images captured at 2 μm intervals for a 30–40 μm-thick section of a labellum were overlaid. (A–F) Each Gr promoter-Gal4 line shows a different expression pattern. In all lines, two levels of GFP expression were observed. A–F and G-I are each shown in the same scale. (G–I) Overlaid images of fluorescent and Nomarski images. Arrowheads show the identified sensilla. Scale bar in A is 40 μm and in G is 10 μm.


It was possible to identify the sensillum innervated by a particular sensory cell expressing GFP by tracing the pathway of a dendrite extending from a single cell (Fig. 3G-I). GFP expression was always observed in a subset of labellar chemosensilla (Table 1). For most Gr promoter-Gal4 strains, the expression seemed to be in a single cell of the S-type sensilla. For Gr22c, Gr22f and Gr59b, expression was observed in the L-type sensilla, but not in all of them. For Gr22c, the GFP expression was observed in sensory cells associated with only three L-type sensilla (L4, L5 and L6). For Gr22e and Gr66a, GFP was expressed both in the S-type and I-type sensilla. In Gr22f and Gr59b, expression was observed in both S-type and L-type sensilla, while for Gr32a, GFP was expressed only in the S-type sensilla. In all lines we noticed two different levels of GFP expression (shown in Table 1 as ‘++’ or ‘+’). All Gr genes except Gr22c showed strong expression only in the S-type sensilla (‘++’ in Table 1). The numbers of GFP-positive sensilla showing strong expression roughly agree with previous observations using the UAS-lacZ reporter gene (Scott et al., 2001; Dunipace et al., 2001).

Table 1

Expression profiles of Gr promoter-Gal4


Nerve response characteristics of three types of chemosensilla

In the present study, recordings were made from all labellar chemosensilla that were accessible by microelectrode. In this way, all the L- and I-type sensilla were accessible, while for the S-type sensilla, only two of them, S2 and S6, could be accessed. The remaining S-type sensilla could not be touched with an electrode because the tips of these sensilla are bent and located very close to each other on the margin of the labellar lobes.

A typical sensillum has four gustatory neurons, each of which responds to sugar (S cell), water (W cell) and salts (L1 and L2 cells). Fig. 4A shows a typical example in which a 1 mM KCl solution in the electrode elicited W spikes, while low concentrations of sugar (e.g. 30 mM sucrose) elicited spikes from both the S cell and W cell (Fig. 4D). Because the activity of the W cell is inhibited by stimulating solutions of increased osmolarity, higher concentrations of sugars elicited almost solely S spikes (Fig. 4E). Low concentrations of NaCl elicited L1 spikes (Fig. 4F), while high NaCl concentrations (e.g. 400 mM) elicited not only L1 spikes but also L2 spikes (Fig. 4G).

Fig. 4

Typical recordings from labellar chemosensilla. Traces show impulses during the first 500 ms after stimulation. Scale bar represents 3 mV. (A), (B) Stimulations with 1 mM KCl in L- (A) and I-type (B) sensilla. In the L-type sensilla W spikes can be seen. (C) Stimulation of an I-type sensillum (I7) with 50 mM sucrose. Only S spikes are observed. (D) Stimulation of an L-type sensillum (L3) with 30 mM sucrose. Open diamonds show W spikes, gray squares show S spikes. (E) Stimulation of an L-type sensillum (L3) with 100 mM sucrose. Most spikes are from the S cell. (F) Stimulation of an L-type sensillum (L7) with 50 mM NaCl. The spikes arise mainly from the L1 cell. (G) Stimulation of an L-type sensillum (L7) with 400 mM NaCl. With a high concentration of salt, spikes from the L2 cell are observed (shown as closed triangles).


The responses of W, L1, L2 and S cells were assessed using 1 mM KCl, 400 mM NaCl and four kinds of sugars (sucrose, trehalose, glucose and fructose) as stimulating solutions. Results shown in Table 2 are based on 6-10 recordings from each sensillum using 45 flies. The L-type sensilla responded to all compounds examined, while S-type sensilla showed W, L1, L2 and S cell activity. Trehalose and glucose gave noisy signals in S-type sensilla, and accordingly we could not confirm the responses of this sensillum-type to these two compounds. The I-type sensilla responded to 400 mM NaCl but not to 1 mM KCl (Fig. 4B). Stimulation of these sensilla with sugar elicited only S spikes (Fig. 4C).

Table 2

Response profile of labellar chemosensilla to water, sugars and salt


We occasionally failed to record any responses from some sensilla. Even in such cases where we obtained no response to sugars, we are certain that an electrical contact was established. Non-responsive sensilla were more frequently observed for I- and S-type sensilla than for L-type sensilla where more than 85% of recordings were successful (Fig. 5). In I-type sensilla, the percentage differed depending on their location, with low success rates (<35%) for sensilla from I1 to I3.

Fig. 5

Variation of successful recordings among sensilla. Mean values are shown, each from 15-22 recordings using 33 flies for stimulation with 100 mM sucrose.


Dose response curves for sugars

We recorded responses from sensilla L1-L9, I1-I10 and S2 and S6 (Fig. 2B), to four kinds of sugars (sucrose, trehalose, glucose and fructose) at five different concentrations ranging from 10 mM to 1000 mM. 5–13 recordings were obtained from each sensillum in response to stimulation by five concentration of sucrose. Similarly 5–10 recordings were made for each concentration of fructose, 5–9 recordings for glucose and 4–9 recordings for trehalose. Each sensillum belonging to the same type gave a similar dose-response curve, so results are shown as the average number of spikes per second of data obtained for each type of chemosensilla. The L-type sensilla responded to all sugars with a higher frequency than the other sensilla (Fig. 6). The I-type sensilla gave responses to all the sugars, but with a lower frequency. The S-type sensilla gave a good response to sucrose which was comparable to that of the L-type sensilla, but their responses to other sugars were weak. However, when recordings in response to stimulation by glucose and trehalose were obtained in the S-type sensilla, spike trains were noisy and spike identification was not possible. These results indicate that sugar response among the three types of chemosensilla differs and that responses of S-type sensilla to sugars are more difficult to obtain than are sugar-stimulated responses from the other types.

Fig. 6

Dose-response curves of the L-, S- and I-type sensilla to sucrose (A), glucose (B), fructose (C) and trehalose (D). Vertical bars represent standard errors. Responses of the L-, I- and S-type sensilla are shown as closed squares, open circles and open triangles, respectively. Each point was calculated from 40-52 recordings from L-type sensilla, 35-45 recordings from I-type sensilla and 10-21 recordings from S-type sensilla using 44 flies.



Variation of responsiveness among chemosensilla

In previous reports of electrophysiological recordings made on Drosophila taste sensilla, only L-type sensilla were examined (Tanimura and Shimada, 1981; Rodrigues and Siddiqi, 1981; Fujishiro et al., 1984; Wieczorek and Wolff, 1989). We presented here data on the basic electrophysio-logical responses of all the labellar chemosensilla. First we examined the rate of successful recordings from all sensilla. Results indicated that the I- and S-type sensilla gave a low response rate, with three sensilla of the I-type in particular having much lower success rates than the others on the labellum. These results explain why the previous studies used mainly the L-type marginal sensilla for recordings. The reason why some sensilla tend to fail to give responses to stimulants is not known. We occasionally observed that a sensillum gave responses to salt, but not to sugars, and vice versa. This may be caused by mechanical damage to a particular cell. However, in most cases a non-responding sensillum did not respond to any stimulus at all. We used only newly emerged flies and believe that mechanical damage and aging were unlikely to be the cause of the non-responsiveness. It has long been known that the nerve response of chemosensillum of flies is fairly variable, and depends on the fly being used and on each sensillum (Den Otter et al., 1972; Uehara and Morita, 1972). We have no sound explanation as to why particular groups of sensilla might give a poor response. One possible explanation for no responses is a contact failure, which can be caused by changes in conductivity at the tip of the chemosensilla (Maes and Den Otter, 1976). The involved structures are the viscous substance (Stürckow, 1967a), the pore in the dendrite-containing lumen and the opening mechanism in the dendrite-free lumen of the chemosensilla (Stürckow et al., 1967b, 1973).

The I-type sensilla lack water receptor cells

Typical chemosensilla have one mechanoreceptor and four gustatory neurons, each of which responds to water, sugar, and low or high concentrations of salt. An anatomical study by electron microscopy showed that only two gusta-tory neurons innervated the I-type sensilla (Falk et al., 1976; Shanbhag et al., 2001). In our experiments, W spikes were never observed in I-type sensilla when 1 mM KCl was used as the stimulus (which usually elicits only W spikes). The I-type sensilla responded to sugars and salts, apparently via two different cell types (Hiroi et al., in preparation) for which the developmental process to produce these two kinds of taste cells is probably different from that in the L- and S-type sensilla.

Differences in dose-response kinetics of sugars between the L-, I- and S-type sensilla

We found that the response to sugars differed among the three types of sensilla. The L-type sensilla showed the highest response to all sugars examined. The S-type sensilla responded to sucrose in a similar manner to that seen in the L-type sensilla, but responded to fructose with a firing rate of lower magnitude. The L-type and I-type sensilla both responded to the four sugars tested, whereas S-type sensilla did not produce good response for glucose and trehalose. The different sensilla types also differed in their maximal firing frequency, with the I-type sensilla firing at about one-third of the rate observed in the L-type sensilla. Such sensitivity differences to a sugar among different types of sensilla were also reported in blowfly (Liscia et al., 1998).

Our previous studies suggested the presence of at least three separate receptor sites, F, G and T, for fructose, glucose and trehalose, respectively, in the labellar sensilla (Tanimura and Shimada, 1981; Tanimura et al., 1982). If we consider the differences of excitability between the three sensilla types, it is possible that similar receptor proteins are expressed in cells of the L-type and I-type sensilla but that their expression level is lower in the I-type sensilla. Another possible explanation is that the signal transduction pathway may differ between the sensilla types. The S-type sensilla gave a good response to sucrose, but did not respond well to glucose and trehalose. If we assume the three receptor sites hypothesis, receptors for glucose and trehalose may not be properly expressed in the S-type sensilla. Previously, we postulated that the G site binds sucrose as well as glucose. The presence of cells exhibiting a good response to sucrose but a lower response to glucose suggests that separate receptor sites exist for these two sugars. Most of the S-type sensilla were not accessible with electrodes as described, but further studies are required to confirm these differentiated responses to sugars among sensilla types.

Possible functions of Gr genes

The 65 Gr genes belong to a large family of seven-transmembrane G-protein coupled receptors (Clyne et al., 2000; Dunipace et al., 2001; Scott et al., 2001; Robertson, personal communication to Flybase, 2001). Gr genes might code receptors for sugars, pheromones, bitter compounds, etc., if they function as taste receptors. So far only one Gr gene has been reported as a functional receptor (Ueno et al., 2001; Dahanukar et al., 2001). In our study we could not find any relationship between the pattern of Gr expression and variations of sugar sensitivities. Our data, obtained with six Gr promoter-Gal4 lines, suggest that these six genes are expressed mainly in the S-type sensilla. A limited number of L-type sensilla expressed Gr22c and Gr22f. To the present time we have not found that these particular sensilla show any unique sensitivity to sugars. There still remains a possibility that these sensilla respond to compounds other than sugars. Preliminary recordings using amino acid mixtures did not reveal any differences either. Most of the Gr genes examined in this study were originally chosen for their expression as confirmed by in situ hybridization on labella (Scott et al., 2001; Dunipace et al., 2001). We cannot exclude the possibility that other Gr genes, not examined in our study, with low levels of expression that cannot be monitored by promoter-Gal4 may function as taste receptors.

In the olfactory system of Drosophila, a single olfactory receptor gene is expressed in one sensory neuron in antennae (Vosshall et al., 2000). Each sensory neuron projects to a specific glomerulus in the antennal lobe. In this manner, chemical information of odors will be represented in the brain. In order to discriminate between thousands of chemicals, olfactory receptor number might have increased as a result of an evolutionary process. In the gustatory system, however, it might not be an essential prerequisite to be able to discriminate between different sugar molecules. All the sugars stimulate sugar receptor cells and the information about a chemical identity may not be particularly important for flies. These considerations do not, however, coincide with the view that multiple Gr genes are expressed in a spatially restricted manner and each receptor binds to a specific ligand (Scott et al., 2001; Dunipace et al., 2001).

The electrophysiological and histological study presented here reveals that the labellar chemosensilla are differentiated in their response to sugars. Further physiological and molecular studies are required to elucidate the molecular mechanism of taste in Drosophila.


We thank H. Amrein, R. Axel and the Bloomington Drosophila Stock Center for fly strains. We acknowledge F. Yokohari of Fukuoka University for use of the confocal microscope. We are grateful to T. Inoshita for establishing the Gr-Gal4/UAS-GFP strains and N. Meunier for helpful suggestions and discussions and T. Take-noshita and M. Haruta for technical support. This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas from the Ministry of Education, Culture, Sports, Science and Technology of Japan.



P. J. Clyne, C. G. Warr, and J. R. Carlson . 2000. Candidate taste receptors in Drosophila. Science 287:1830–1834. Google Scholar


A. Dahanukar, K. Foster, W. Van Naters, and J. R. Carlson . 2001. A Gr receptor is required for response to the sugar trehalose in taste neurons of Drosophila. Nat Neurosci 4:1182–1186. Google Scholar


C. J. Den Otter 1972. Differential sensitivity of insect chemoreceptors to alkali cations. J Insect Physiol 18:109–131. Google Scholar


V. G. Dethier and N. Goldrichrachman . 1976. Anesthetic stimulation of insect water receptors. Proc Natl Acad Sci USA 73:3315–3319. Google Scholar


L. Dunipace, S. Meister, C. McNealy, and H. Amrein . 2001. Spatially restricted expression of candidate taste receptors in the Drosophila gustatory system. Curr Biol 11:822–835. Google Scholar


R. Falk, N. Bleiseravivi, and J. Atidia . 1976. Labellar taste organs of Drosophila melanogaster. J Morphol 150:327–341. Google Scholar


L. Fiore, G. Corsini, and L. Geppetti . 1996. Application of non-linear filters based on the median filter to experimental and simulated multi-unit neural recordings. J Neurosci Methods 70:177–184. Google Scholar


S. Firestein 2001. How the olfactory system makes sense of scents. Nature 413:211–218. Google Scholar


N. Fujishiro, H. Kijima, and H. Morita . 1984. Impulse frequency and action-potential amplitude in labellar chemosensory neurons of Drosophila melanogaster. J Insect Physiol 30:317–325. Google Scholar


E. S. Hodgson, J. Y. Lettvin, and K. D. Roeder . 1955. Physiology of a primary chemoreceptor unit. Science 122:417–418. Google Scholar


H. Ishimoto, A. Matsumoto, and T. Tanimura . 2000. Molecular identification of a taste receptor gene for trehalose in Drosophila. Science 289:116–119. Google Scholar


J. W. Lewcock and R. R. Reed . 2001. Sweet successes. Neuron 31:515–517. Google Scholar


A. Liscia, R. Majone, P. Solari, I. T. Barbarossa, and R. Crnjar . 1998. Sugar response differences related to sensillum type and location on the labella of Protophormia terraenovae: a contribution to spatial representation of the stimulus. J Insect Physiol 44:471–481. Google Scholar


F. W. Maes and C. J. Den Otter . 1976. Relationship between taste cell responses and arrangement of labellar taste setae in the blow-fly Calliphora vicina. J Insect Physiol 22:377–384. Google Scholar


F. Marion-Poll 1995. Object-oriented approach to fast display of electrophysiological data under MS-Windows. J Neurosci Methods 63:197–204. Google Scholar


F. Marion-Poll 1996. Display and analysis of electrophysiological data under WindowsTM. Entomol Exp Appl 80:116–119. Google Scholar


F. Marion-Poll and J. Van der Pers . 1996. Un-filtered recordings from insect taste sensilla. Entomol Exp Appl 80:113–115. Google Scholar


N. Meunier, J. F. Ferveur, and F. Marion-Poll . 2000. Sex-specific non-pheromonal taste receptors in Drosophila. Curr Biol 10:1583–1586. Google Scholar


S. V. Nayak and R. N. Singh . 1983. Sensilla on the tarsal segments and mouthparts of adult Drosophila melanogaster Meigen (Diptera, Drosophilidae). Int J Insect Morphol Embryol 12:273–291. Google Scholar


K. Ray, V. Hartenstein, and V. Rodrigues . 1993. Development of the taste bristles on the labellum of Drosophila melanogaster. Dev Biol 155:26–37. Google Scholar


V. Rodrigues and O. Siddiqi . 1978. Genetic analysis of chemosensory pathway. Proc Indian Acad Sci Section B 87:147–160. Google Scholar


V. Rodrigues and O. Siddiqi . 1981. A gustatory mutant of Drosophila defective in pyranose receptors. Mol Gen Genet 181:406–408. Google Scholar


K. Scott, R. Brady, A. Cravchik, P. Morozov, A. Rzhetsky, C. Zuker, and R. Axel . 2001. A chemosensory gene family encoding candidate gustatory and olfactory receptors in Drosophila. Cell 104:661–673. Google Scholar


S. R. Shanbhag, S. K. Park, C. W. Pikielny, and R. A. Steinbrecht . 2001. Gusta-tory organs of Drosophila melanogaster: fine structure and expression of the putative odorant-binding protein PBPRP2. Cell Tissue Res 304:423–437. Google Scholar


B. Stürckow, J. R. Adams, and T. A. Wilcox . 1967a. The neurons in the labellar nerve of the blowfly. Z vergl Physiol 54:268–289. Google Scholar


B. Stürckow, P. E. Hokbert, J. R. Adams, and R. J. Anstead . 1973. Fine structure of the tip of the labellar taste hair of the blow flies Phormia regina (Mg.) and Calliphora vicina R.-D. (Diptera, Calliphoridae). Z Morph Tiere 75:87–109. Google Scholar


B. Stürckow, P. E. Holbert, and J. R. Adams . 1967b. Fine structure of the tip of chemosensitive hairs in two blow flies and the stable fly. Experientia 23:780–782. Google Scholar


T. Tanimura, K. Isono, T. Takamura, and I. Shimada . 1982. Genetic dimorphism in the taste sensitivity to trehalose in Drosophila melanogaster. J Comp Physiol A 147:433–437. Google Scholar


T. Tanimura and I. Shimada . 1981. Multiple receptor proteins for sweet taste in Drosophila discriminated by papain treatment. J Comp Physiol A 141:265–269. Google Scholar


S. Uehara and H. Morita . 1972. Effects of temperature on labellar chemoreceptors of blowfly. J Gen Physiol 59:213–226. Google Scholar


K. Ueno, M. Ohta, H. Morita, Y. Mikuni, S. Nakajima, K. Yamamoto, and K. Isono . 2001. Trehalose sensitivity in Drosophila correlates with mutations in and expression of the gustatory receptor gene Gr5a. Curr Biol 11:1451–1455. Google Scholar


L. B. Vosshall, A. M. Wong, and R. Axel . 2000. An olfactory sensory map in the fly brain. Cell 102:147–159. Google Scholar


H. Wieczorek and G. Wolff . 1989. The labellar sugar receptor of Drosophila. J Comp Physiol A 164:825–834. Google Scholar
Makoto Hiroi, Frédéric Marion-Poll, and Teiichi Tanimura "Differentiated Response to Sugars among Labellar Chemosensilla in Drosophila," Zoological Science 19(9), 1009-1018, (1 September 2002).
Received: 5 June 2002; Accepted: 1 July 2002; Published: 1 September 2002
Back to Top