Abstract
The sensorimotor transformation underlying Caenorhabditis elegans chemotaxis has been difficult to measure directly under normal assay conditions. Thus, key features of this transformation remain obscure, such as its time course and dependence on stimulus amplitude. Here, we present a comprehensive characterization of the transformation as obtained by inducing stepwise temporal changes in attractant concentration within the substrate as the worm crawls across it. We found that the step response is complex, with multiple phases and a nonlinear dependence on the sign and amplitude of the stimulus. Nevertheless, the step response could be reduced to a simple kinetic model that predicted the results of chemotaxis assays. Analysis of the model showed that chemotaxis results from the combined effects of approach and avoidance responses to concentration increases and decreases, respectively. Surprisingly, ablation of the ASE chemosensory neurons, known to be necessary for chemotaxis in chemical gradient assays, eliminated avoidance responses but left approach responses intact. These results indicate that the transformation can be dissected into components to which identified neurons can be assigned.
MeSH Terms
Animals
Animals, Genetically Modified
Behavior, Animal/drug effects,physiology
Caenorhabditis elegans/physiology
Caenorhabditis elegans Proteins/genetics
Chemoreceptor Cells/physiology
Chemotaxis/drug effects,physiology
Computer Simulation
Dose-Response Relationship, Drug
Drug Combinations
Estradiol/analogs & derivatives
Lasers/adverse effects
Models, Biological
Neurons/drug effects,physiology
Norethindrone
Probability
Sodium Chloride/pharmacology
Stimulation, Chemical
Testosterone/analogs & derivatives
Time Factors
Transcription Factors/genetics
Chemicals
CHE-1 protein, C elegans
Caenorhabditis elegans Proteins
Drug Combinations
Transcription Factors
estradiol, norethisterone, testosterone drug combination
Testosterone
Sodium Chloride
Estradiol
Norethindrone
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Miller Adam C
Institute of Neuroscience, University of Oregon, Eugene, Oregon 97403-1254, USA.
Thiele Tod R
Faumont Serge
Moravec Marin L
Lockery Shawn R
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