A comparison of experience-dependent locomotory behaviors and biogenic amine neurons in nematode relatives of Caenorhabditis elegans
- Laura Rivard†1,
- Jagan Srinivasan†2,
- Allison Stone1,
- Stacy Ochoa1,
- Paul W Sternberg2Email author and
- Curtis M Loer1Email author
© Rivard et al; licensee BioMed Central Ltd. 2010
Received: 19 August 2009
Accepted: 19 February 2010
Published: 19 February 2010
Survival of an animal depends on its ability to match its responses to environmental conditions. To generate an optimal behavioral output, the nervous system must process sensory information and generate a directed motor output in response to stimuli. The nervous system should also store information about experiences to use in the future. The diverse group of free-living nematodes provides an excellent system to study macro- and microevolution of molecular, morphological and behavioral character states associated with such nervous system function. We asked whether an adaptive behavior would vary among bacterivorous nematodes and whether differences in the neurotransmitter systems known to regulate the behavior in one species would reflect differences seen in the adaptive behavior among those species. Caenorhabditis elegans worms slow in the presence of food; this 'basal' slowing is triggered by dopaminergic mechanosensory neurons that detect bacteria. Starved worms slow more dramatically; this 'enhanced' slowing is regulated by serotonin.
We examined seven nematode species with known phylogenetic relationship to C. elegans for locomotory behaviors modulated by food (E. coli), and by the worm's recent history of feeding (being well-fed or starved). We found that locomotory behavior in some species was modulated by food and recent feeding experience in a manner similar to C. elegans, but not all the species tested exhibited these food-modulated behaviors. We also found that some worms had different responses to bacteria other than E. coli. Using histochemical and immunological staining, we found that dopaminergic neurons were very similar among all species. For instance, we saw likely homologs of four bilateral pairs of dopaminergic cephalic and deirid neurons known from C. elegans in all seven species examined. In contrast, there was greater variation in the patterns of serotonergic neurons. The presence of presumptive homologs of dopaminergic and serotonergic neurons in a given species did not correlate with the observed differences in locomotory behaviors.
This study demonstrates that behaviors can differ significantly between species that appear morphologically very similar, and therefore it is important to consider factors, such as ecology of a species in the wild, when formulating hypotheses about the adaptive significance of a behavior. Our results suggest that evolutionary changes in locomotory behaviors are less likely to be caused by changes in neurotransmitter expression of neurons. Such changes could be caused either by subtle changes in neural circuitry or in the function of the signal transduction pathways mediating these behaviors.
Animals use their nervous systems to sense and respond dynamically to changing environments. Nematodes constitute one of the most diverse and populous phyla in the animal kingdom, with estimates of up to 1 million extant species . Although all nematodes share a similar basic body plan, they have distinct morphological adaptations and can differ in length by four orders of magnitude. They have a wide geographical distribution, exploit diverse ecological niches, and can survive extreme environments like the Antarctic . Nematodes are both parasitic and free-living and can obtain nutrients from a wide variety of materials. Additionally, nematodes have evolved several different reproductive strategies, exhibiting gonochorism (male-female), hermaphroditism, heterogony, and parthenogenesis . The phylum Nematoda also exhibits genomic diversity. An analysis of expressed-sequence tags from 30 different species revealed that 30-50% of the sequences studied were unique to individual species [4, 5].
The detailed molecular genetic and neuronal bases of many nematode behaviors such as egg laying [6, 7], mechanosensation , pharyngeal-pumping , and male-mating  have been described in detail from C. elegans. Intraspecific variation in behaviors has also been examined in C. elegans and other nematode species, as well as differences between related species. For example, some wild isolates of C. elegans aggregate and feed socially whereas other strains disperse and forage independently . Species from two clades of entomopathogenic nematodes, Steinernematidae and Heterorhabditidae, exhibit different behaviors associated with infection of host insects . Four closely related species of Pristionchus have unique chemoattraction profiles to 11 compounds classified as insect pheromones or plant volatiles . Finally, males of two gonochoristic Caenorhabditis species, C. remanei and C. brenneri, are more efficient at spicule insertion during mating than males of the hermaphroditic species C. briggsae and C. elegans .
Few studies, however, have attempted to address the neural control of behavior across different species of nematodes [15, 16]. Such a study first requires the identification of a behavior that is at least partially conserved in multiple species. Then, the neural circuitry of the selected species can be examined.
We undertook an interspecific comparison of a locomotory behavior modulated by feeding. Sawin and colleagues  showed that the presence or absence of food (bacteria) as well as feeding status (well-fed or starved) affects the rate of locomotion of C. elegans. Well-fed C. elegans worms have the fastest rate of locomotion in the absence of food, and their locomotion slows when food is present. This behavior is known as the "basal slowing response" (BSR). Worms recently deprived of food move even more slowly in food, exhibiting a behavior known as the "enhanced slowing response" (ESR). The neural circuits that control the basal and enhanced slowing responses are distinct . The BSR is mediated by the dopaminergic CEP, ADE, and PDE neurons, which have sensory endings in the cuticle and likely detect the presence of bacteria by a mechanical stimulus. The ESR is mediated by serotonin. Mutant strains lacking serotonin have a defective ESR that can be rescued by the addition of exogenous serotonin . Fluoxetine, a selective serotonin reuptake inhibitor, potentiates the ESR, while serotonin antagonists prevent the behavior . Ablation experiments have failed, however, to unambiguously identify the serotonergic neurons required for the ESR .
We scored several species of nematodes whose phylogenetic relationships to C. elegans are known for the presence of the basal and enhanced slowing responses. We examined the patterns of dopamine-containing neurons in these species, and then also investigated whether the ESR was modulated by serotonin and what serotonergic neurons are present. We found that only some of the species examined had slowing responses under the conditions tested, and there was no stereotypical array of serotonergic neurons present that might be required for the ESR. Dopamine-containing neurons were highly conserved although the BSR under the conditions tested was not. We propose the evolutionary source of the slowing behaviors based on a nematode phylogeny.
Phylogenetic relationships of the nematode species tested for food-modulated behaviors
Some nematode species do not exhibit basal and enhanced slowing responses
Dopaminergic neurons are similar across nematode species
We observed that all seven species had FIF-positive somata that are plausible homologs of the bilaterally symmetric head cephalic sensory neuron CEPs, the anterior deirid neuron ADEs and postdeirid PDEs (Figure 4E-J). In all the species examined, presumptive ventral CEPs (CEPV) were slightly more anterior than dorsal CEPs (CEPD), just as in C. elegans. The putative CEP neurons were more strongly and reliably stained by FIF; in some species, we saw putative ADE neurons less often and PDE neurons infrequently. This may partly be due to the very high background fluorescence in the body, especially from the intestine. There is typically much less background in the head and tail. Putative ADEs were located in the posterior head around the posterior bulb of the pharynx, although in some species these cells were further anterior than typically found in C. elegans. Along the dorsoventral axis, ADE somata were located laterally to sublaterally. Putative PDE homologs were located subdorsally, and mid-posterior along the anteroposterior axis of the body.
For the species examined, we saw that FIF staining worked better in larvae than adults. We consistently observed 3 pairs of cell bodies in the head of the larvae, indicating little or no change in DA cells postembryonically other than the appearance of the PDE. The PDE neurons are born postembryonically in mid-late L2 stage in both C. elegans and Panagrellus redivivus [28, 29], and hence are seen only in older larvae and adults. In a few species, we occasionally found an additional FIF-positive cell in adults in the head and/or body, but these were less reliable. In Pristionchus, we saw what appeared to be a ventral unpaired neuron in few adult heads; in O. myriophila we saw a few worms with a pair of FIF-positive cells in the tail.
In our studies we found that FIF stained neuronal cell bodies, but only rarely processes. To obtain a better picture of the neuronal processes, we used serotonin antibody staining after treating worms with 5-hydroxytryptophan (5HTP), the immediate precursor to serotonin. 5HTP is taken up by both serotonergic and dopaminergic neurons and converted into serotonin by their shared AADC enzyme [30, 31]. Therefore, dopaminergic neurons are stained among a background of known serotonergic neurons. With this technique, neuronal processes are often well-stained, revealing the morphology of the neurons. In stained worms where we had previously seen FIF-positive somata, we observed serotonin immunoreactive cells that were not seen without 5HTP treatment. [5HTP-stained cells must be matched with FIF-positive cells since 5HTP can also strengthen staining in weakly or variably staining serotonergic cells.] Deirid neurons (ADEs and PDEs), which are relatively isolated from other neurons (including other known serotonergic neurons), were well-stained by this technique, showing bipolar cell bodies with sensory dendrites extending toward the outer surface of the worm. The morphology of putative ADE and PDE neurons in every species was very similar to that known from C. elegans, with minor differences in some species (Figure 4, Columns 2 and 4 '+5HTP'). For example, the putative PDE homolog in Pristionchus pacificus had a longer dendrite that extended anteriorly rather than dorsally.
The heads in 5HTP-treated worms were more difficult to assess, especially in species that have numerous serotonergic neurons in the same region of the head as putative CEP neurons (see descriptions of serotonergic head neurons below). Nevertheless, we were frequently able to see 4 additional somata in the same location of FIF positive cells in the head. We also often saw 4 additional processes extending anteriorly into the 'nose' of the worms, consistent with the morphology known for C. elegans CEP neurons. Overall, the patterns of dopaminergic neurons in all the species we examined were nearly identical, suggesting strong conservation of this portion of the nervous system.
Serotonergic neurons in the head differ dramatically across nematode species
To explore which neurons might be associated with the ESR, we examined serotonin immunoreactivity in the heads of the seven nematode species used in our behavioral studies. Neurons required for the ESR may be conserved in species that also exhibit the behavior. We observed clearly identifiable NSMs with cell bodies located ventrally in the anterior bulb of the pharynx in all species studied (Figure 5A-H arrows). The NSMs had bifurcating neurites projecting through the isthmus just to the posterior bulb of the pharynx, as observed in C. elegans. All the species tested in our analysis showed strong serotonin immunoreactivity in putative NSM neurons. [The presence of putative NSM homologs in these species has been described previously (Loer & Rivard, 2007).] We also examined other serotonin-IR head neurons compared to those found in C. elegans. We observed ADF-like neurons in all species except R. axei (Figure 5B-H, F and 5H insets). These neurons were categorized as ADF-like based on the position of their somata and occasionally a visible projection that is likely part of the amphid (Figure 5C, D, F and 5H insets closed arrowheads). Again, there was no correlation between the presence of an ADF-like neuron and the ESR. Some species contained possible AIM and RIH homologs, however, such identification would be highly tentative based on soma position alone in the absence of stained projections. Other serotonin-IR neurons that can be identified as likely homologs across species include a faintly staining bilaterally symmetric pair located within the pharynx just anterior to the NSMs, seen in Oscheius myriophila, Pristionchus pacificus, and Panagrellus redivivus (Figure 5D, F, H). These cells are not seen in C. elegans, and, as before, there was no correlation between the presence of these neurons and the ESR.
The number of serotonin-IR head neurons varied dramatically in the species examined. O. myriophila had up to thirteen serotonin-IR head neurons (Figure 5D), which was the most observed; Caenorhabditis sp. 3 and R. axei had the fewest, with four each (Figure 5C, E). It is possible, however, that the cells in Caenorhabditis sp. 3 match those of C. elegans and C. briggsae. We noted that the axons of the NSMs in Caenorhabditis sp. 3 have numerous brightly staining varicosities, which could be obscuring a faint second pair of serotonin-IR neurons. Caenorhabditis sp. 3 also rarely appear to have a faint unpaired cell. Among all the species, the number of serotonin-IR neurons in the head does not appear to correlate with the presence of the ESR. Caenorhabditis sp. 3 and R. axei both have only four serotonin-IR head neurons (Figure 5C, D) but Caenorhabditis sp. 3 exhibited an ESR, and R. axei did not. The staining patterns of Pristionchus pacificus and Panagrellus redivivus appear very similar to that of C. elegans, with the addition of the faintly staining pair of neurons anterior to the NSMs (Figure 5A, F and 5H); C. elegans exhibits an ESR whereas Pristionchus pacificus and Panagrellus redivivus does not. Finally, there was no correlation between the number of serotonin-IR head neurons and the overall rate of locomotion under well-fed or starved conditions. Overall, we conclude that the pattern of serotonin-IR neurons in the species studied cannot be used as an indicator of locomotory behavior.
The enhanced slowing response is blocked by a serotonin antagonist in some, but not all species
In contrast, mianserin had a very different effect in Caenorhabditis sp. 3 (Figure 6C). Mianserin significantly reduced the locomotory rate both off and on bacteria (with a BSR still apparent in the presence of mianserin, P < 0.001, comparison not shown on graph), but had no effect on the locomotion of food-deprived worms on bacteria (Figure 6C, food-deprived worms on bacteria, untreated or treated with mianserin, P > 0.05). In the presence of mianserin, an ESR is also still apparent (Figure 6C, well-fed worms on bacteria vs. food-deprived worms on bacteria, both mianserin-treated, P < 0.05). One possibility is that mianserin in C. sp. 3 is acting more like a 5HT agonist than an antagonist, reducing the rate of locomotion overall; this could make it more difficult to detect an effect on the ESR. Clearly the effect of mianserin is altered in Caenorhabditis sp. 3 relative to the other species tested, and the expression patterns or specificity of 5HT receptors in Caenorhabditis sp. 3 seems likely to be quite different. Whatever the change, the same results were obtained in locomotory assays of Caenorhabditis sp. 3 preincubated in 44 μM methiothepin mesylate (data not shown); methiothepin is a serotonin antagonist that in C. elegans has broader specificity and also inhibits MOD-1 . These preliminary pharmacology experiments are suggestive of a similar function of serotonin in mediating the ESR in C. briggsae and O. myriophila, although they must be viewed with caution given our currently limited information about drug responses and specificity in these other species.
Basal and enhanced slowing responses in the Eurhabditids vs. outgroups
We should note that a purely mechanosensory effect of bacteria on modulating locomotion in well-fed worms - the model proposed by Sawin and colleages  - is called into question by our observations of locomotory rates on various bacteria in C. elegans. Although both E. coli strains elicited slowing, the other bacterial species either had no effect, or caused worms to speed up. All these bacteria are of similar size and shape, and it is difficult to imagine that their mechanical properties are more different from E. coli than similar-sized Sephadex beads (which can elicit a BSR ). Therefore it seems likely that bacteria elicit more than just a mechanosensory effect, even in well-fed worms. Perhaps in C. elegans and other species, chemosensation can override mechanosensory input to prevent slowing in less desirable or unfamiliar food sources.
For the enhanced slowing response, we must ask, how long a period of food-deprivation is sufficient to 'motivate' worms to slow in food? Perhaps we would see a BSR and ESR in the presence of a desirable edible microbe, and an ESR given an adequate period of starvation. What about the normal ecology of the species examined? The laboratory environment may not sufficiently mimic the natural ecology of some species to induce slowing behaviors. In general, the ecology of free-living nematodes and how their natural history influences their behavior is poorly understood (see Kiontke and Sudhaus, 2006 for review ). Other environmental conditions that are known to strongly affect behavior include oxygen concentration; thick bacterial lawns can have significantly lower levels of oxygen . The use of very thin lawns in our experiments should reduce the possibility of such a separate influence of bacteria on behavior. But a different oxygen concentration environment, for example, might reveal a BSR and ESR in the other species. Some or all of these worms likely prefer lower oxygen levels; C. elegans seems to prefer ~5-12% O2 .
Our studies suggest that particular forms of BSR and ESR are present in the species in question, and are missing in the others. Therefore, the available molecular phylogeny  can suggest that the BSR and ESR we observed may have evolved in the Eurhabditis clade and were perhaps lost in R. axei (Figure 7). Perhaps some aspect of behavioral and/or trophic ecology of R. axei is different from the other Eurhaditids - despite R. axei having been isolated from compost like many of the other species. Worm species lacking a BSR or ESR might have evolved alternate behaviors, such as increased pharyngeal pumping, that optimize foraging without slowing locomotion. We must also consider whether laboratory strains may have lost behaviors that are found in the wild, due to genetic drift and selection in laboratory culture. While considering such a possibility we note that the C. elegans laboratory wildtype strain N2 - which has the BSR and ESR - has been raised in the laboratory much longer than any of the other strains we tested, being isolated from the wild in 1956 [41, 42].
It is interesting to note that distinct, non-overlapping circuits mediate the BSR and ESR in C. elegans. This is seen most strikingly in C. elegans mutants lacking dopamine: although there is a complete loss of the BSR, after food-deprivation, the ESR is undiminished . Therefore, under conditions evoking an ESR, there is no contribution in slowing by a BSR. A plausible explanation for this observation is that the separation in the pathways mediating basal slowing versus enhanced slowing behaviors might have evolved at different times. Given such a justification, however, it is interesting to note that among the species we examined, either both responses are seen or neither is seen.
Evolution of biogenic amine neurons mediating slowing responses in Rhabditids
The basal slowing response in C. elegans, presumably present to slow worms in food to increase feeding, is triggered by the mechanical sensation of bacteria by sensory neurons that release dopamine. These four bilaterally paired ciliated neurons appear to be highly conserved in nematodes. Cephalic sensilla were likely present in the nematode stem species, deirids in the stem species of Secernentea and Plectida; postdeirids perhaps only in the stem species of Secernentea (K. Kiontke, personal communication), which includes all the species we examined. Expression of dopamine in likely homologs may also be highly conserved. Trichinella spiralis, traditionally considered a 'basal' nematode, has four catecholamine-positive cells with neurites in the cephalic sensilla . The distantly-related plant parasitic nematode Xiphinema americanum, also has four FIF-positive cephalic sensilla neurons and 2 possible deirid neurons in locations very similar to those described here . A similar pattern of dopamine-containing neurons to what we report here, but via dopamine immunoreactivity, has also previously been described for Panagrellus redivivus .
In our study, the presumptive CEP, ADE and PDE homologs all appear to contain dopamine as they do in C. elegans (Figure 7). The positions of FIF-positive somata in the head and body were very similar in all worms, and the morphology of processes seen by 5HTP-induced serotonin immunoreactivity was also mostly like that seen in C. elegans DA neurons. The most parsimonious explanation is that these are all homologous neurons. The alternative explanation - that different, non-homologous neurons express dopamine in some of the species we examined - requires two events: loss of expression in one cell type, and new expression in another.
It seems likely that the mechanosensory function of cephalic and deirid sensilla neurons is also conserved, despite the lack of conservation of the BSR in all the species we examined. As suggested above, perhaps the type of microbe matters: the mechanical properties of some bacteria (such as E. coli) could be insufficient to activate the cells appropriately in some species. Or, the neural circuitry could be different - either by altered connections, or distribution and number of receptors - so that the role of dopamine is changed. In C. elegans, dopamine actually plays a complex (and extrasynaptic) role in regulating the BSR: whereas knockout of the dop-3 dopamine receptor causes loss of the BSR, in a double knockout mutant for both dop-1 and dop-3 dopamine receptors, the BSR is partially restored . This indicates that dopamine also inhibits the BSR (promotes locomotion), and that a balance of these antagonistic influences likely fine-tunes the locomotory rate. Therefore, it is easy to imagine the system being biased toward a different effect of dopamine release. Such a shift in the balance of positive and negative influences of dopamine could underlie the increased locomotion of Pristionchus on bacteria. In addition, other environmental conditions or the behavioral state of the worm that affects dopamine or its receptors could mean that a BSR will not be seen under the conditions we tested.
The role of serotonin and specific serotonergic neurons in experience-dependent modulation of locomotion in C. elegans is less clear-cut than the role of dopamine. Loss of serotonin causes partial loss of the ESR, and ablation of the NSMs only slightly reduces the ESR. Ablation of many other serotonergic neurons along with NSMs does not reduce the ESR more than NSM ablation alone . The clearest effect of serotonin in the ESR is demonstrated by the role of the inhibitory MOD-1 serotonin receptor . It is likely that both serotonin and the neurons that use serotonin have both positive and negative effects on regulation of locomotion, similar to what is seen with dopamine. Serotonin has been demonstrated to both promote and inhibit egg laying in C. elegans [46, 47]. It is possible that the ESR in C. elegans is primarily triggered by serotonin (and perhaps other neurotransmitters) released from the NSM. As with our examination of BSR and dopaminergic neurons, the presence of a given neuron in other species does not correlate with the presence of the behavior. NSMs are clearly recognizable, and highly conserved among these nematodes (and many other free-living species, as reported elsewhere ). It is certainly possible that the serotonergic NSMs are required, but not sufficient, for generating an ESR in the species in which we observed it. Other neurons are less well conserved, and difficult to identify definitively as homologous neurons. Although likely ADF homologs are found in many of the species in question, their presence does not correlate with the ESR, and evidence in C. elegans suggests they do not play a role in the ESR .
Our experiments with the serotonin antagonist mianserin suggest that the ESR, like in C. elegans, is serotonin-dependent in Oschieus myriophila, although this is less clear in C. briggsae. It should be noted, however, that we do not know the specificity of this antagonist with all the biogenic amine receptors in C. elegans, let alone in the other species. Furthermore, more recent experiments have shown that mianserin can also affect identified tyramine receptors in C. elegans [49, 50], although there is no evidence of tyramine or octopamine involvement in slowing behaviors . The role of serotonin in regulating locomotion may have changed in Caenorhabditis sp. 3 - the serotonin antagonists mianserin and methiothepin depress the rate of locomotion with or without bacteria, and do not appear to block the ESR. If these agents still work as antagonists (another possibility is that the pharmacology of the receptors has changed so that both these agents act more like agonists), the balance has shifted in Caenorhabditis sp. 3 wherein serotonin's normal predominant role may be to increase rather than inhibit locomotion. We may also conclude that evolutionary changes in behavior are less likely to be caused by obvious, gross changes in neurotransmitter expression of neurons, but by more subtle changes in neural circuitry or changes in gene expression in the different species. It has been shown that in certain conserved behaviors, the sensory architecture mediating these behaviors shows marked flexibility during nematode evolution [15, 52].
Therefore, in conclusion the changes we observe in our modulated locomotion studies suggest that some of these changes could occur at the level of the neural circuitry mediating these behaviors. Further understanding of the neural circuitry and the signaling pathways mediating these behaviors could shed light onto how these behaviors evolved.
We cultured free-living nematode strains using standard methods for C. elegans . Worms were raised at 20°C on NGM plates seeded with the OP50 or HB101 E. coli strain (see below). Nomenclature used here conforms to the conventions for C. elegans genetics set forth by R. Horvitz and others (1979). Conventions for naming wild-type non-C. elegans nematode strains are similar, with each unique isolate receiving a unique strain designation.
We used the following worm strains: Caenorhabditis elegans (N2) , Caenorhabditis briggsae (AF16) , Caenorhabditis sp. 3 (PS1010), Oscheius myriophila (DF5020), Pellioditis typica (DF5025), Rhabditella axei (DF5006) (NYU Rhabditid collection), Pristionchus pacificus (PS312) , and Panagrellus redivivus (PS2298; PS1163) . For Panagrellus redivivus, PS1163 was used for studies of dopamine-containing neurons, but PS2298 was used in all locomotory behavior assays. There are no apparent differences in neurons of the two strains . For testing locomotory behavior on other bacterial strains, we chose E. coli HB101, Bacillus subtilis, Pseudomonas aeruginosa (PA15) and Serratia marcescens. All the bacterial strains tested are gram negative except for B. subtilis, which is gram positive. Both Pseudomonas aeruginosa and Serratia marcescens strains are pathogenic for C. elegans [56, 57]
Manual counting of body bends
10-12 L4 hermaphrodites or females were picked onto 6 cm NGM plates seeded with HB101 E. coli and stored in an incubator at 20°C 16-20 hours prior to the assay; these worms had been continuously cultured on HB101 . Ring plates were also prepared 16-20 hours prior to the assay by spreading 80 μl of HB101 bacteria on 6 cm NGM plates, leaving a circle approximately 1.5 cm in diameter in the center and the edge of the agar unseeded. The plates were incubated overnight at 37°C. For the assay, worms were removed from their overnight cultures using M9. They were rinsed and briefly centrifuged at 6000 rpm to facilitate the transfer of the worms to an assay plate. For 'normal/baseline locomotion', worms were transferred to unseeded 6 cm NGM plates. To test the basal slowing response, worms were transferred to seeded 6 cm ring plates. For 'enhanced slowing', the worms that were used for the 'normal/baseline locomotion' assay were allowed to remain on the unseeded plate for 30 minutes before they were transferred to a ring plate. Worms were allowed to acclimate to the assay plates for 5 minutes, and then the number of body bends/20 seconds was determined for each worm.
Automated worm tracking and data extraction
Worms tested by automated tracking were continuously cultured on E. coli OP50, and tested on OP50. For assaying 'normal/baseline locomotion', 10 cm non-seeded NGM plates were used. To test the 'basal slowing' response, worms were placed on assay plates with a thin lawn of an overnight culture of E. coli OP50 . For 'enhanced slowing' studies, worms grown overnight at 20°C on seeded plates with food, were placed on a standard 10 cm NGM plate without food for 30 minutes as described in Sawin et al. . Care was taken to avoid transferring any food from the seeded plates to the assay plates. After 30 minutes, each individual worm was tested for 5 minutes on assay plates containing food.
As previously described , 10 cm NGM plates used for recordings were equilibrated to 20°C for 18-20 hours. Approximately one hour before beginning recordings, 600 μl of fresh OP50 overnight culture was spread on each plate to achieve a thin, featureless lawn of food across the entire surface. Excess solution was drawn from the edge with a Pipetman. Food was allowed to dry on the agar surface of a tissue-covered plate until the surface exhibited a matte finish (about 45 minutes), at which time, tissues were replaced by Petri dish lids and plates were ready for use. L4 hermaphrodites or females of each species were picked to fresh seeded plates 16-20 hours prior to recording. Individual worms were transferred to assay plates and the plate placed in a holder on the microscope stage. After two minutes recovery, the worm was located and recording begun using an automated worm tracker and image recorder specially designed for studying worm locomotion [7, 58]. Each worm was recorded for five minutes. Data extraction, processing and analysis was done using image processing and analysis software as previously described [7, 58]. From each video recording of 5 minutes, we used the middle 4 minutes, and used the software to derive values for frequency of undulations. All incubations and recordings were done in a constant temperature room at 20°C.
For all behavioral studies, we performed 1-factor ANOVA followed by planned pairwise comparisons made with Scheffè's F-test ; all statistical analyses were performed using Excel.
Serotonin antagonist studies
Behavioral studies were performed as described with the following modification. Approximately 1 hour prior to the assay, mianserin hydrochloride or methiothepin mesylate was added to unseeded and seeded 60 mm NGM plates for a final concentration of 20 μM mianserin hydrochloride or 44 μM methiothepin mesylate (both from Sigma-Aldrich). Worms were transferred to the plates and incubated for 30 minutes at 20°C prior to the start of the behavioral assays.
Formaldehyde induced fluorescence (FIF)
A simplified version of the FIF technique has been described ( and R. Lints, personal communication). A small number of worms were picked directly into a 5 μl drop of 4% paraformaldehyde (PFA) in 0.1 M sodium/potassium phosphate buffer (pH 7.2) on a microscope slide. The PFA solution was wicked away with filter paper leaving dry worms by 5 min of exposure; the slide was then heated to 98°C for 10 min on a metal block. The slide was briefly cooled to room temp, a drop of 100% glycerol added to the worms, and a coverslip was placed over the prep. Worms were viewed with a Chroma 11003v2 Blue/Violet filter set; DA fluorescence had a characteristic blue-green color whereas most background fluorescence was more yellow-green. In all species, the best staining was in young larvae; older larvae and adults more rarely had good FIF staining, and had higher background. For reliable FIF in Panagrellus, worms had to be cut open in the 4% PFA solution, suggesting that access in larger intact worms is the key problem.
Worms were incubated at 20°C for 8-12 hr on 60 mm NGM agar plates containing 5 mM 5-hydroxytryptophan (5HTP, Sigma-Aldrich) and seeded with bacteria. Worms were removed from the plate by washing with M9 buffer, and subsequently processed with the standard anti-serotonin protocol (below). Overall background staining was typically increased in 5HTP-treated preparations.
Rabbit anti-serotonin antibody (antigen: serotonin paraformaldehyde-conjugated to bovine serum albumin) was purchased from Sigma (St. Louis, MO; catalog S4454, lot 091K4831). We have previously tested the specificity of staining with this antiserum in 14 different species of free-living nematode, including all those tested here . Staining is blocked by the antigen, and partially by free serotonin, but not other agents. We have similarly shown no staining in controls with secondary antibody alone . A previously described fixation and staining procedure was used , with some modification . Briefly, worms in a mixed-stage population were washed from 60-mm culture plates with M9 buffer, rinsed three times to remove bacteria, and then fixed overnight (ON) at 4°C in 4% PFA in PBS. The worms were rinsed in 0.5% Triton X-100/PBS (TPBS), incubated ON at 37°C in 5% 2-mercaptoethanol/1% TX-100/0.1 M Tris (pH 7.4), rinsed in TPBS, and then incubated for 30 minutes to 4 hours at 37°C in 2000 U/ml collagenase type IV (Sigma) in 1 mM CaCl2/1% TX-100/0.1 M Tris, pH 7.4. Following TPBS rinses, the worms were "blocked" for ≥ 1 hour in 1% BSA/TPBS at RT, then incubated ON at RT in 1:100 antiserotonin serum in 1% BSA/TPBS. The worms were rinsed 2× in TPBS, then for 1 hour in 0.1% BSA/TPBS, incubated for 2-4 hours at 37°C with 1:100 TRITC- conjugated goat anti-rabbit IgG, and rinsed briefly several times in 0.1% BSA/TPBS. About 5-10 μl worms from the final preparation were pipetted onto an agarose pad, coverslipped, and viewed with epifluorescence. Worms were also often stained with DAPI to mark nuclei. In some cases this was necessary to determine whether a stained structure was a neuronal cell body (with a DAPI-stained nucleus) or not.
We thank David Fitch for strains and advice, and Karin Kiontke for discussions about nematode sensilla evolution. Some strains were obtained from the Caenorhabditis Genetics Center, an NIH Research Resource. We thank Kris Carter and Jason Kehrer (USD) who also contributed to the project. CL is supported by an endowment from the Fletcher Jones Foundation; some of this work was also supported by NIGMS Grant R15GM60203 (to CL). We also thank Christopher Cronin for assistance in worm locomotion scripts and members of the Sternberg lab for comments and discussions on the manuscript. JS is an Associate and PWS is an Investigator of the Howard Hughes Medical Institute, which supported this research.
- Lambshead P: Recent developments in marine benthic biodiversity research. Oceanis. 1993, 19: 5-24.Google Scholar
- Wharton DA: The environmental physiology of Antarctic terrestrial nematodes: a review. J Comp Physiol [B]. 2003, 173 (8): 621-628.View ArticleGoogle Scholar
- Kiontke K, Fitch DH: The phylogenetic relationships of Caenorhabditis and other rhabditids. WormBook. 2005, 1-11.Google Scholar
- Parkinson J, Mitreva M, Hall N, Blaxter M, McCarter JP: 400000 nematode ESTs on the Net. Trends Parasitol. 2003, 19 (7): 283-286. 10.1016/S1471-4922(03)00132-6.View ArticlePubMedGoogle Scholar
- Parkinson J, Mitreva M, Whitton C, Thomson M, Daub J, Martin J, Schmid R, Hall N, Barrell B, Waterston RH, et al.: A transcriptomic analysis of the phylum Nematoda. Nat Genet. 2004, 36 (12): 1259-1267. 10.1038/ng1472.View ArticlePubMedGoogle Scholar
- Schafer WR: Egg-laying. WormBook. 2005, 1-7.Google Scholar
- Cronin CJ, Feng Z, Schafer WR: Automated imaging of C. elegans behavior. Methods Mol Biol. 2006, 351: 241-251.PubMedGoogle Scholar
- Goodman MB: Mechanosensation. WormBook. 2006, 1-14.Google Scholar
- Chase DL, Koelle MR: Biogenic amine neurotransmitters in C. elegans. WormBook. 2007, 1-15.Google Scholar
- Barr MM, Garcia LR: Male mating behavior. WormBook. 2006, 1-11.Google Scholar
- de Bono M, Bargmann CI: Natural variation in a neuropeptide Y receptor homolog modifies social behavior and food response in C. elegans. Cell. 1998, 94 (5): 679-689. 10.1016/S0092-8674(00)81609-8.View ArticlePubMedGoogle Scholar
- Campbell JF, Lewis EE, Stock SP, Nadler S, Kaya HK: Evolution of host search strategies in entomopathogenic nematodes. J Nematol. 2003, 35 (2): 142-145.PubMed CentralPubMedGoogle Scholar
- Hong RL, Sommer RJ: Chemoattraction in Pristionchus nematodes and implications for insect recognition. Curr Biol. 2006, 16 (23): 2359-2365. 10.1016/j.cub.2006.10.031.View ArticlePubMedGoogle Scholar
- Garcia LR, LeBoeuf B, Koo P: Diversity in mating behavior of hermaphroditic and male-female Caenorhabditis nematodes. Genetics. 2007, 175 (4): 1761-1771. 10.1534/genetics.106.068304.PubMed CentralView ArticlePubMedGoogle Scholar
- Srinivasan J, Durak O, Sternberg PW: Evolution of a polymodal sensory response network. BMC Biol. 2008, 6: 52-10.1186/1741-7007-6-52.PubMed CentralView ArticlePubMedGoogle Scholar
- Chiang JT, Steciuk M, Shtonda B, Avery L: Evolution of pharyngeal behaviors and neuronal functions in free-living soil nematodes. J Exp Biol. 2006, 209 (Pt 10): 1859-1873. 10.1242/jeb.02165.View ArticlePubMedGoogle Scholar
- Sawin ER, Ranganathan R, Horvitz HR: C. elegans locomotory rate is modulated by the environment through a dopaminergic pathway and by experience through a serotonergic pathway. Neuron. 2000, 26 (3): 619-631. 10.1016/S0896-6273(00)81199-X.View ArticlePubMedGoogle Scholar
- Blaxter ML, De Ley P, Garey JR, Liu LX, Scheldeman P, Vierstraete A, Vanfleteren JR, Mackey LY, Dorris M, Frisse LM, et al.: A molecular evolutionary framework for the phylum Nematoda. Nature. 1998, 392 (6671): 71-75. 10.1038/32160.View ArticlePubMedGoogle Scholar
- Kiontke K, Sudhaus W: Ecology of Caenorhabditis species. WormBook. 2006, 1-14.Google Scholar
- Sommer RJ, Carta LK, Kim SY, Sternberg PW: Morphological, genetic and molecular description of Pristionchus pacificus sp. n. (Nematoda: Neodiplogastridae. Fundamental and Applied Nematology. 1996, 19 (6): 511-521.Google Scholar
- Dieterich C, Clifton SW, Schuster LN, Chinwalla A, Delehaunty K, Dinkelacker I, Fulton L, Fulton R, Godfrey J, Minx P, et al.: The Pristionchus pacificus genome provides a unique perspective on nematode lifestyle and parasitism. Nat Genet. 2008, 40 (10): 1193-1198. 10.1038/ng.227.View ArticlePubMedGoogle Scholar
- Herrmann M, Mayer WE, Sommer RJ: Nematodes of the genus Pristionchus are closely associated with scarab beetles and the Colorado potato beetle in Western Europe. Zoology (Jena). 2006, 109 (2): 96-108.View ArticleGoogle Scholar
- Goodey T: Soil and freshwater nematodes. 1963, London: Methuen, SecondGoogle Scholar
- Sanyal S, Wintle RF, Kindt KS, Nuttley WM, Arvan R, Fitzmaurice P, Bigras E, Merz DC, Hebert TE, Kooy van der D, et al.: Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans. EMBO J. 2004, 23 (2): 473-482. 10.1038/sj.emboj.7600057.PubMed CentralView ArticlePubMedGoogle Scholar
- Sulston J, Dew M, Brenner S: Dopaminergic neurons in the nematode Caenorhabditis elegans. J Comp Neurol. 1975, 163 (2): 215-226. 10.1002/cne.901630207.View ArticlePubMedGoogle Scholar
- Chase DL, Pepper JS, Koelle MR: Mechanism of extrasynaptic dopamine signaling in Caenorhabditis elegans. Nat Neurosci. 2004, 7 (10): 1096-1103. 10.1038/nn1316.View ArticlePubMedGoogle Scholar
- Ward S: Chemotaxis by the nematode Caenorhabditis elegans : identification of attractants and analysis of the response by use of mutants. Proc Natl Acad Sci USA. 1973, 70 (3): 817-821. 10.1073/pnas.70.3.817.PubMed CentralView ArticlePubMedGoogle Scholar
- Sternberg PW, Horvitz HR: Postembryonic nongonadal cell lineages of the nematode Panagrellus redivivus : description and comparison with those of Caenorhabditis elegans. Dev Biol. 1982, 93 (1): 181-205. 10.1016/0012-1606(82)90251-2.View ArticlePubMedGoogle Scholar
- Sulston JE, Horvitz HR: Post-embryonic cell lineages of the nematode, Caenorhabditis elegans. Dev Biol. 1977, 56 (1): 110-156. 10.1016/0012-1606(77)90158-0.View ArticlePubMedGoogle Scholar
- Hare EE, Loer CM: Function and evolution of the serotonin-synthetic bas-1 gene and other aromatic amino acid decarboxylase genes in Caenorhabditis. BMC Evol Biol. 2004, 4: 24-10.1186/1471-2148-4-24.PubMed CentralView ArticlePubMedGoogle Scholar
- Loer CM, Kenyon CJ: Serotonin-deficient mutants and male mating behavior in the nematode Caenorhabditis elegans. J Neurosci. 1993, 13 (12): 5407-5417.PubMedGoogle Scholar
- Zhang Y, Lu H, Bargmann CI: Pathogenic bacteria induce aversive olfactory learning in Caenorhabditis elegans. Nature. 2005, 438 (7065): 179-184. 10.1038/nature04216.View ArticlePubMedGoogle Scholar
- Ranganathan R, Cannon SC, Horvitz HR: MOD-1 is a serotonin-gated chloride channel that modulates locomotory behaviour in C. elegans. Nature. 2000, 408 (6811): 470-475. 10.1038/35044083.View ArticlePubMedGoogle Scholar
- Horvitz HR, Chalfie M, Trent C, Sulston JE, Evans PD: Serotonin and octopamine in the nematode Caenorhabditis elegans. Science. 1982, 216 (4549): 1012-1014. 10.1126/science.6805073.View ArticlePubMedGoogle Scholar
- Albertson DG, Thomson JN: The pharynx of Caenorhabditis elegans. Philos Trans R Soc Lond B Biol Sci. 1976, 275 (938): 299-325. 10.1098/rstb.1976.0085.View ArticlePubMedGoogle Scholar
- Axang C, Rauthan M, Hall DH, Pilon M: Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR. BMC Dev Biol. 2008, 8: 38-10.1186/1471-213X-8-38.PubMed CentralView ArticlePubMedGoogle Scholar
- White JG: The structure of the nervous system of the nematode Caenorhabditis elegans. Philos Trans R Soc Lond B Biol Sci. 1986, 314 (1165): 1-340. 10.1098/rstb.1986.0056.View ArticlePubMedGoogle Scholar
- Glennon RA: Central serotonin receptors as targets for drug research. J Med Chem. 1987, 30 (1): 1-12. 10.1021/jm00384a001.View ArticlePubMedGoogle Scholar
- Carre-Pierrat M, Baillie D, Johnsen R, Hyde R, Hart A, Granger L, Segalat L: Characterization of the Caenorhabditis elegans G protein-coupled serotonin receptors. Invert Neurosci. 2006, 6 (4): 189-205. 10.1007/s10158-006-0033-z.View ArticlePubMedGoogle Scholar
- Gray JM, Karow DS, Lu H, Chang AJ, Chang JS, Ellis RE, Marletta MA, Bargmann CI: Oxygen sensation and social feeding mediated by a C. elegans guanylate cyclase homologue. Nature. 2004, 430 (6997): 317-322. 10.1038/nature02714.View ArticlePubMedGoogle Scholar
- Hansen LE, Yarwood EA, Nicholas WL, Francis WS: Differential Nutritional Requirements for Reproduction of Two Strains of Caenorhabditis elegans in Axenic Culture. Nematologica. 1960, 5 (1): 27-31.View ArticleGoogle Scholar
- McGrath PT, Rockman MV, Zimmer M, Jang H, Macosko EZ, Kruglyak L, Bargmann CI: Quantitative mapping of a digenic behavioral trait implicates globin variation in C. elegans sensory behaviors. Neuron. 2009, 61 (5): 692-699. 10.1016/j.neuron.2009.02.012.PubMed CentralView ArticlePubMedGoogle Scholar
- Lee DL, Ko RC: Catecholaminergic neurons in Trichinella spiralis (Nematoda). Parasitol Res. 1991, 77 (3): 269-270. 10.1007/BF00930871.View ArticlePubMedGoogle Scholar
- Hogger C, Estey RH, Croll NA: Xiphinema americanum : cholinesterase and biogenic amines in the nervous system. Exp Parasitol. 1978, 45 (1): 139-149. 10.1016/0014-4894(78)90053-X.View ArticlePubMedGoogle Scholar
- Stewart GR, Perry RN, Wright DJ: Occurrence of dopamine in Panagrellus redivivus and Meloidogyne incognita. Nematology. 2001, 3 (8): 843-848. 10.1163/156854101753625335.View ArticleGoogle Scholar
- Carnell L, Illi J, Hong SW, McIntire SL: The G-protein-coupled serotonin receptor SER-1 regulates egg laying and male mating behaviors in Caenorhabditis elegans. J Neurosci. 2005, 25 (46): 10671-10681. 10.1523/JNEUROSCI.3399-05.2005.View ArticlePubMedGoogle Scholar
- Shyn SI, Kerr R, Schafer WR: Serotonin and Go modulate functional states of neurons and muscles controlling C. elegans egg-laying behavior. Curr Biol. 2003, 13 (21): 1910-1915. 10.1016/j.cub.2003.10.025.View ArticlePubMedGoogle Scholar
- Loer CM, Rivard L: Evolution of neuronal patterning in free-living rhabditid nematodes I: Sex-specific serotonin-containing neurons. J Comp Neurol. 2007, 502 (5): 736-767. 10.1002/cne.21288.View ArticlePubMedGoogle Scholar
- Rex E, Hapiak V, Hobson R, Smith K, Xiao H, Komuniecki R: TYRA-2 (F01E11.5): a Caenorhabditis elegans tyramine receptor expressed in the MC and NSM pharyngeal neurons. J Neurochem. 2005, 94 (1): 181-191. 10.1111/j.1471-4159.2005.03180.x.View ArticlePubMedGoogle Scholar
- Rex E, Komuniecki RW: Characterization of a tyramine receptor from Caenorhabditis elegans. J Neurochem. 2002, 82 (6): 1352-1359. 10.1046/j.1471-4159.2002.01065.x.View ArticlePubMedGoogle Scholar
- Alkema MJ, Hunter-Ensor M, Ringstad N, Horvitz HR: Tyramine Functions independently of octopamine in the Caenorhabditis elegans nervous system. Neuron. 2005, 46 (2): 247-260. 10.1016/j.neuron.2005.02.024.View ArticlePubMedGoogle Scholar
- Shtonda BB, Avery L: Dietary choice behavior in Caenorhabditis elegans. J Exp Biol. 2006, 209 (Pt 1): 89-102. 10.1242/jeb.01955.PubMed CentralView ArticlePubMedGoogle Scholar
- Brenner S: The genetics of Caenorhabditis elegans. Genetics. 1974, 77 (1): 71-94.PubMed CentralPubMedGoogle Scholar
- Fodor A, Riddle DL, Kenneth Nelson F, Golden JW: Comparison of a new wild-type Caenorhabditis briggsae with laboratory strains of C. briggsae and C. elegans. Nematologica. 1983, 29: 203-217.View ArticleGoogle Scholar
- Sternberg PW, Horvitz HR: Gonadal cell lineages of the nematode Panagrellus redivivus and implications for evolution by the modification of cell lineage. Dev Biol. 1981, 88 (1): 147-166. 10.1016/0012-1606(81)90226-8.View ArticlePubMedGoogle Scholar
- Pujol N, Link EM, Liu LX, Kurz CL, Alloing G, Tan MW, Ray KP, Solari R, Johnson CD, Ewbank JJ: A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans. Curr Biol. 2001, 11 (11): 809-821. 10.1016/S0960-9822(01)00241-X.View ArticlePubMedGoogle Scholar
- Tan MW, Rahme LG, Sternberg JA, Tompkins RG, Ausubel FM: Pseudomonas aeruginosa killing of Caenorhabditis elegans used to identify P. aeruginosa virulence factors. Proc Natl Acad Sci USA. 1999, 96 (5): 2408-2413. 10.1073/pnas.96.5.2408.PubMed CentralView ArticlePubMedGoogle Scholar
- Cronin CJ, Mendel JE, Mukhtar S, Kim YM, Stirbl RC, Bruck J, Sternberg PW: An automated system for measuring parameters of nematode sinusoidal movement. BMC Genet. 2005, 6 (1): 5-10.1186/1471-2156-6-5.PubMed CentralView ArticlePubMedGoogle Scholar
- Sokal RR, Rohlf FJ: Biometry: the principles and practice of statistics in biological research. 1981, San Francisco: W H Freeman, 2Google Scholar
- Lints R, Jia L, Kim K, Li C, Emmons SW: Axial patterning of C. elegans male sensilla identities by selector genes. Dev Biol. 2004, 269 (1): 137-151. 10.1016/j.ydbio.2004.01.021.View ArticlePubMedGoogle Scholar
- Desai C, Garriga G, McIntire SL, Horvitz HR: A genetic pathway for the development of the Caenorhabditis elegans HSN motor neurons. Nature. 1988, 336 (6200): 638-646. 10.1038/336638a0.View ArticlePubMedGoogle Scholar
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