Literature DB >> 28784963

A Caenorhabditis elegans Nutritional-status Based Copper Aversion Assay.

Jason C Campbell1, Ian D Chin-Sang2, William G Bendena3.   

Abstract

To ensure survival, organisms must be capable of avoiding unfavorable habitats while ensuring a consistent food source. Caenorhabditis elegans alter their locomotory patterns upon detection of diverse environmental stimuli and can modulate their suite of behavioral responses in response to starvation conditions. Nematodes typically exhibit a decreased aversive response when removed from a food source for over 30 min. Observation of behavioral changes in response to a changing nutritional status can provide insight into the mechanisms that regulate the transition from a well-fed to starved state. We have developed an assay that measures a nematode's ability to cross an aversive barrier (i.e. copper) then reach a food source over a prolonged period of time. This protocol builds upon previous work by integrating multiple variables in a manner that allows for continued data collection as the organisms shift towards an increasingly starved condition. Moreover, this assay permits an increased sample size so that larger populations of nematodes can be simultaneously evaluated. Organisms defective for the ability to detect or respond to copper immediately cross the chemical barrier, while wild type nematodes are initially repelled. As wild type worms are increasingly starved, they begin to cross the barrier and reach the food source. We designed this assay to evaluate a mutant that is incapable of responding to diverse environmental cues, including food sensation or detection of aversive chemicals. When evaluated via this protocol, the defective organisms immediately crossed the barrier, but were also incapable of detecting a food source. Hence, these mutants repeatedly cross the chemical barrier despite temporarily reaching a food source. This assay can straightforwardly test populations of worms to evaluate potential pathway defects related to aversion and starvation.

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Year:  2017        PMID: 28784963      PMCID: PMC5612601          DOI: 10.3791/55939

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  31 in total

1.  Sensing of cadmium and copper ions by externally exposed ADL, ASE, and ASH neurons elicits avoidance response in Caenorhabditis elegans.

Authors:  Y Sambongi; T Nagae; Y Liu; T Yoshimizu; K Takeda; Y Wada; M Futai
Journal:  Neuroreport       Date:  1999-03-17       Impact factor: 1.837

2.  Dissecting a circuit for olfactory behaviour in Caenorhabditis elegans.

Authors:  Sreekanth H Chalasani; Nikos Chronis; Makoto Tsunozaki; Jesse M Gray; Daniel Ramot; Miriam B Goodman; Cornelia I Bargmann
Journal:  Nature       Date:  2007-11-01       Impact factor: 49.962

3.  Neocortical disconnectivity disrupts sensory integration in Alzheimer's disease.

Authors:  Elena K Festa; Rachel Z Insler; David P Salmon; Jessica Paxton; Joanne M Hamilton; William C Heindel
Journal:  Neuropsychology       Date:  2005-11       Impact factor: 3.295

4.  The burrowing behavior of the nematode Caenorhabditis elegans: a new assay for the study of neuromuscular disorders.

Authors:  C Beron; A G Vidal-Gadea; J Cohn; A Parikh; G Hwang; J T Pierce-Shimomura
Journal:  Genes Brain Behav       Date:  2015-04       Impact factor: 3.449

5.  Distinct signaling pathways mediate touch and osmosensory responses in a polymodal sensory neuron.

Authors:  A C Hart; J Kass; J E Shapiro; J M Kaplan
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

6.  Mechanosensory signalling in C. elegans mediated by the GLR-1 glutamate receptor.

Authors:  A V Maricq; E Peckol; M Driscoll; C I Bargmann
Journal:  Nature       Date:  1995-11-02       Impact factor: 49.962

7.  The genetics of Caenorhabditis elegans.

Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

8.  HEN-1, a secretory protein with an LDL receptor motif, regulates sensory integration and learning in Caenorhabditis elegans.

Authors:  Takeshi Ishihara; Yuichi Iino; Akiko Mohri; Ikue Mori; Keiko Gengyo-Ando; Shohei Mitani; Isao Katsura
Journal:  Cell       Date:  2002-05-31       Impact factor: 41.582

9.  C. elegans responds to chemical repellents by integrating sensory inputs from the head and the tail.

Authors:  Massimo A Hilliard; Cornelia I Bargmann; Paolo Bazzicalupo
Journal:  Curr Biol       Date:  2002-04-30       Impact factor: 10.834

10.  Sensory modulation disorders in childhood epilepsy.

Authors:  Jolien S van Campen; Floor E Jansen; Nienke J Kleinrensink; Marian Joëls; Kees Pj Braun; Hilgo Bruining
Journal:  J Neurodev Disord       Date:  2015-10-23       Impact factor: 4.025

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  1 in total

1.  Intestine-to-neuronal signaling alters risk-taking behaviors in food-deprived Caenorhabditis elegans.

Authors:  Molly A Matty; Hiu E Lau; Jessica A Haley; Anupama Singh; Ahana Chakraborty; Karina Kono; Kirthi C Reddy; Malene Hansen; Sreekanth H Chalasani
Journal:  PLoS Genet       Date:  2022-05-05       Impact factor: 6.020

  1 in total

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