Behavioral Motifs and Neural Pathways Coordinating O2 Responses and Aggregation in C. elegans

BACKGROUND Simple stimuli can evoke complex behavioral responses coordinated by multiple neural circuits. O(2) is an important environmental variable for most animals. The nematode C. elegans avoids high O(2), and O(2) levels regulate its foraging and aggregation. RESULTS Here, we dissect aggregation and responses to O(2) gradients into behavioral motifs and show how O(2) responses can promote aggregation. To remain in a group, C. elegans continually modify their movement. Animals whose heads emerge from a group will reverse or turn, thereby returning to the group. Re-entry inhibits further reversal, aiding retention in the group. If an animal's tail exits a group during a reversal, it switches to forward movement, returning to the group. Aggregating C. elegans locally deplete O(2). The rise in O(2) levels experienced by animals leaving a group induces both reversal and turning. Conversely, the fall in O(2) encountered when entering a clump suppresses reversal, turning, and high locomotory activity. The soluble guanylate cyclases GCY-35 and GCY-36, which are expressed in head and tail neurons, promote reversal and turning when O(2) rises. Avoidance of high O(2) is also promoted by the TRP-related channel subunits OCR-2 and OSM-9, and the transmembrane protein ODR-4, acting in the nociceptive neurons ASH and ADL. Both O(2) responsiveness and aggregation can be modified by starvation, but this is regulated by natural variation in the npr-1 neuropeptide receptor. CONCLUSIONS Our work provides insights into how a complex behavior emerges from simpler behavioral motifs coordinated by a distributed circuit.

[1]  Cori Bargmann,et al.  Social feeding in Caenorhabditis elegans is induced by neurons that detect aversive stimuli , 2002, Nature.

[2]  Rajesh Ranganathan,et al.  C. elegans Locomotory Rate Is Modulated by the Environment through a Dopaminergic Pathway and by Experience through a Serotonergic Pathway , 2000, Neuron.

[3]  Mario de Bono,et al.  Experience-Dependent Modulation of C. elegans Behavior by Ambient Oxygen , 2005, Current Biology.

[4]  S. Brenner,et al.  The structure of the nervous system of the nematode Caenorhabditis elegans. , 1986, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[5]  V. Ambros,et al.  Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences. , 1991, The EMBO journal.

[6]  PRELIMINARY EXPERIMENTS ON THE CONTROL OF MYCOPHAGOUS EELWORMS IN MUSHROOM BEDS, WITH A NOTE ON THEIR SWARMING , 1966 .

[7]  W. Wood The Nematode Caenorhabditis elegans , 1988 .

[8]  M. de Bono,et al.  Neuronal substrates of complex behaviors in C. elegans. , 2005, Annual review of neuroscience.

[9]  J. N. Thomson,et al.  Mutant sensory cilia in the nematode Caenorhabditis elegans. , 1986, Developmental biology.

[10]  Cori Bargmann,et al.  Divergent seven transmembrane receptors are candidate chemosensory receptors in C. elegans , 1995, Cell.

[11]  S. Lahiri Oxygen sensing: molecule to man , 1999 .

[12]  M. Denny,et al.  Air and water : the biology and physics of life's media , 1993 .

[13]  Marie-Anne Félix,et al.  High Local Genetic Diversity and Low Outcrossing Rate in Caenorhabditis elegans Natural Populations , 2005, Current Biology.

[14]  Thomas M. Morse,et al.  The Fundamental Role of Pirouettes in Caenorhabditis elegans Chemotaxis , 1999, The Journal of Neuroscience.

[15]  M. Drew SOIL AERATION AND PLANT ROOT METABOLISM , 1992 .

[16]  Mario de Bono,et al.  Antagonistic pathways in neurons exposed to body fluid regulate social feeding in Caenorhabditis elegans , 2002, Nature.

[17]  Cornelia I. Bargmann,et al.  Oxygen sensation and social feeding mediated by a C. elegans guanylate cyclase homologue , 2004, Nature.

[18]  Cori Bargmann,et al.  Natural Variation in a Neuropeptide Y Receptor Homolog Modifies Social Behavior and Food Response in C. elegans , 1998, Cell.

[19]  Mario de Bono,et al.  Inhibition of Caenorhabditis elegans social feeding by FMRFamide-related peptide activation of NPR-1 , 2003, Nature Neuroscience.

[20]  M. D. Bono,et al.  Soluble Guanylate Cyclases Act in Neurons Exposed to the Body Fluid to Promote C. elegans Aggregation Behavior , 2004, Current Biology.

[21]  K. Nishikawa,et al.  Exclusive expression of C. elegans osm-3 kinesin gene in chemosensory neurons open to the external environment. , 1995, Journal of Molecular Biology.

[22]  S. Ward,et al.  Broad oxygen tolerance in the nematode Caenorhabditis elegans. , 2000, The Journal of experimental biology.

[23]  P. Grewal,et al.  Migration of Caenorhabditis elegans (Nematoda : Rhabditidae) larvae towards bacteria and the nature of the bacterial stimulus , 1992 .

[24]  D. Zinkler,et al.  Local PO2 measurements in the environment of submerged soil microarthropods , 1994 .

[25]  P. Grewal,et al.  Effects of Caenorhabditis elegans (Nematoda: Rhabditidae) on yield and quality of the cultivated mushroom Agaricus bisporus , 1991 .

[26]  J. Hodgkin,et al.  Natural variation and copulatory plug formation in Caenorhabditis elegans. , 1997, Genetics.

[27]  K. Groschner,et al.  Evidence for a role of Trp proteins in the oxidative stress-induced membrane conductances of porcine aortic endothelial cells. , 1999, Cardiovascular research.

[28]  Cori Bargmann,et al.  Polarized Dendritic Transport and the AP-1 μ1 Clathrin Adaptor UNC-101 Localize Odorant Receptors to Olfactory Cilia , 2001, Neuron.

[29]  J. P. Hollis Nature of Swarming in Nematodes , 1962, Nature.

[30]  J. López-Barneo,et al.  Cellular mechanism of oxygen sensing. , 2001, Annual review of physiology.

[31]  Phenomenon of Swarming in Nematodes , 1966, Nature.

[32]  M. Vidal,et al.  GATEWAY recombinational cloning: application to the cloning of large numbers of open reading frames or ORFeomes. , 2000, Methods in enzymology.