[
MicroPubl Biol,
2022]
C. elegans' experiences and microbiome have been shown to shape its responses to certain stimuli; a recent study found that C. elegans grown on Providencia alcalifaciens JUb39 exhibited increased attraction to that same growth bacteria while also lowered replusion to the odor 1-octanol (O'Donnell et al. 2020). This prompted us to ask whether other strains of bacteria could likewise alter C. elegans' responses to bacterial food and volatile chemicals. So, to expand upon current knowledge, we cultured wild-type C. elegans (N2) on an unidentified Escherichia coli ( E. coli sp?), Pseudomonas mendocina (MSPm1), Pseudomonas lurida (MYb11), Stenotrophomonas maltophilia (JUb19), or Proteus mirabilis strain ( P. mirabilis sp?). After several generations, we examined how their choice of bacterial food was affected. In addition, we looked at their response to the olfactory stimuli 2-butanone; 2,3-butanedione; 2,3-pentanedione; and 2-nonanone, as well as their response to the gustatory stimulus sodium chloride. Interestingly, we found that growth on any of these bacterial strains led to their bacterial preferences and behavioral responses to 2-butanone; 2,3-pentanedione; diacetyl; and sodium chloride remaining unchanged. However, we also saw that C. elegans showed a preference for MSPm1 and P. mirabilis sp? to HB101, and HB101 to MYb11. Furthermore, worms that are grown on MSPm1 showed stronger attraction to a 1:10 dilution of 2-nonanone (AWB-sensed odorant) as compared to worms grown on the other bacterial strains.
[
Neuron,
2000]
Animals in complex environments must discriminate between salient and uninformative sensory cues. Caenorhabditis elegans uses one pair of olfactory neurons called AWC to sense many different odorants, yet the animal can distinguish each odorant from the others in discrimination assays. We demonstrate that the transmembrane guanylyl cyclase ODR-1 is essential for responses to all AWC-sensed odorants. ODR-1 appears to be a shared signaling component downstream of odorant receptors. Overexpression of ODR-1 protein indicates that ODR-1 can influence odor discrimination and adaptation as well as olfaction. Adaptation to one odorant, butanone, is disrupted by ODR-1 overexpression. Olfactory discrimination is also disrupted by ODR-1 overexpression, probably by overproduction of the shared second messenger cGMP. We propose that AWC odorant signaling pathways are insulated to permit odor discrimination.AD - Howard Hughes Medical Institute, Department of Anatomy, University of California, San Francisco 94143, USA.FAU - L'Etoile, N DAU - L'Etoile NDFAU - Bargmann, C IAU - Bargmann CILA - engSI - GENBANK/AF235027PT - Journal ArticleCY - UNITED STATESTA - NeuronJID - 8809320RN - 0 (Benzaldehydes)RN - 0 (Butanones)RN - 0 (Galpha protein ODR-3)RN - 0 (Pentanols)RN - 0 (Receptors, Odorant)RN - 123-51-3 (isopentyl alcohol)RN - EC 3.6.1.- (Heterotrimeric GTP-Binding Proteins)RN - EC 4.6.1.2 (Guanylate Cyclase)SB - IM
[
J Vis Exp,
2012]
During sustained stimulation most sensory neurons will adapt their response by decreasing their sensitivity to the signal. The adaptation response helps shape attention and also protects cells from over-stimulation. Adaptation within the olfactory circuit of C. elegans was first described by Colbert and Bargmann(1,2). Here, the authors defined parameters of the olfactory adaptation paradigm, which they used to design a genetic screen to isolate mutants defective in their ability to adapt to volatile odors sensed by the Amphid Wing cells type C (AWC) sensory neurons. When wildtype C. elegans animals are exposed to an attractive AWC-sensed odor(3) for 30 min they will adapt their responsiveness to the odor and will then ignore the adapting odor in a chemotaxis behavioral assay for ~1 hr. When wildtype C. elegans animals are exposed to an attractive AWC-sensed odor for ~1 hr they will then ignore the adapting odor in a chemotaxis behavioral assay for ~3 hr. These two phases of olfactory adaptation in C. elegans were described as short-term olfactory adaptation (induced after 30 min odor exposure), and long-term olfactory adaptation (induced after 60 min odor exposure). Later work from L'Etoile et al.,(4) uncovered a Protein Kinase G (PKG) called EGL-4 that is required for both the short-term and long-term olfactory adaptation in AWC neurons. The EGL-4 protein contains a nuclear localization sequence that is necessary for long-term olfactory adaptation responses but dispensable for short-term olfactory adaptation responses in the AWC(4). By tagging EGL-4 with a green fluorescent protein, it was possible to visualize the localization of EGL-4 in the AWC during prolonged odor exposure. Using this fully functional GFP-tagged EGL-4 (GFP::EGL-4) molecule we have been able to develop a molecular readout of long-term olfactory adaptation in the AWC(5). Using this molecular readout of olfactory adaptation we have been able to perform both forward and reverse genetic screens to identify mutant animals that exhibit defective subcellular localization patterns of GFP::EGL-4 in the AWC(6,7). Here we describe: 1) the construction of GFP::EGL-4 expressing animals; 2) the protocol for cultivation of animals for long-term odor-induced nuclear translocation assays; and 3) the scoring of the long-term odor-induced nuclear translocation event and recovery (re-sensitization) from the nuclear GFP::EGL-4 state.