4.3 Article

Ecology and Evolution of Soil Nematode Chemotaxis

Journal

JOURNAL OF CHEMICAL ECOLOGY
Volume 38, Issue 6, Pages 615-628

Publisher

SPRINGER
DOI: 10.1007/s10886-012-0118-6

Keywords

Carbon dioxide; Caenorhabditis elegans; Chemotaxis; Entomopathogenic nematodes; Functional phylogenetic; Nematode; Plant-parasitic nematodes; Sense organs; Soil chemical ecology

Funding

  1. Swiss National Science Foundation [PZ00P3_131956/1]
  2. Swiss National Science Foundation (SNF) [PZ00P3_131956] Funding Source: Swiss National Science Foundation (SNF)

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Plants influence the behavior of and modify community composition of soil-dwelling organisms through the exudation of organic molecules. Given the chemical complexity of the soil matrix, soil-dwelling organisms have evolved the ability to detect and respond to these cues for successful foraging. A key question is how specific these responses are and how they may evolve. Here, we review and discuss the ecology and evolution of chemotaxis of soil nematodes. Soil nematodes are a group of diverse functional and taxonomic types, which may reveal a variety of responses. We predicted that nematodes of different feeding guilds use host-specific cues for chemotaxis. However, the examination of a comprehensive nematode phylogeny revealed that distantly related nematodes, and nematodes from different feeding guilds, can exploit the same signals for positive orientation. Carbon dioxide (CO2), which is ubiquitous in soil and indicates biological activity, is widely used as such a cue. The use of the same signals by a variety of species and species groups suggests that parts of the chemo-sensory machinery have remained highly conserved during the radiation of nematodes. However, besides CO2, many other chemical compounds, belonging to different chemical classes, have been shown to induce chemotaxis in nematodes. Plants surrounded by a complex nematode community, including beneficial entomopathogenic nematodes, plant-parasitic nematodes, as well as microbial feeders, are thus under diffuse selection for producing specific molecules in the rhizosphere that maximize their fitness. However, it is largely unknown how selection may operate and how belowground signaling may evolve. Given the paucity of data for certain groups of nematodes, future work is needed to better understand the evolutionary mechanisms of communication between plant roots and soil biota.

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