C. elegans avoids toxin-producing Streptomyces using a seven transmembrane domain chemosensory receptor

Author:

Tran Alan1,Tang Angelina1,O'Loughlin Colleen T2,Balistreri Anthony3,Chang Eric1,Coto Villa Doris1,Li Joy1,Varshney Aruna1,Jimenez Vanessa1,Pyle Jacqueline1,Tsujimoto Bryan1,Wellbrook Christopher1,Vargas Christopher1,Duong Alex1,Ali Nebat1,Matthews Sarah Y3,Levinson Samantha3,Woldemariam Sarah4,Khuri Sami5,Bremer Martina6,Eggers Daryl K3,L'Etoile Noelle4,Miller Conrad Laura C3,VanHoven Miri K1ORCID

Affiliation:

1. Department of Biological Sciences, San Jose State University, California, United States

2. Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, United States

3. Department of Chemistry, San Jose State University, California, United States

4. Department of Cell & Tissue Biology, University of California San Francisco, San Francisco, United States

5. Department of Computer Science, San Jose State University, California, United States

6. Department of Mathematics and Statistics, San Jose State University, California, United States

Abstract

Predators and prey co-evolve, each maximizing their own fitness, but the effects of predator–prey interactions on cellular and molecular machinery are poorly understood. Here, we study this process using the predator Caenorhabditis elegans and the bacterial prey Streptomyces, which have evolved a powerful defense: the production of nematicides. We demonstrate that upon exposure to Streptomyces at their head or tail, nematodes display an escape response that is mediated by bacterially produced cues. Avoidance requires a predicted G-protein-coupled receptor, SRB-6, which is expressed in five types of amphid and phasmid chemosensory neurons. We establish that species of Streptomyces secrete dodecanoic acid, which is sensed by SRB-6. This behavioral adaptation represents an important strategy for the nematode, which utilizes specialized sensory organs and a chemoreceptor that is tuned to recognize the bacteria. These findings provide a window into the molecules and organs used in the coevolutionary arms race between predator and potential prey.

Funder

National Science Foundation

NIH MARC Fellowship

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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