Pathogenic bacteria modulate pheromone response to promote mating

Nature. 2023 Jan;613(7943):324-331. doi: 10.1038/s41586-022-05561-9. Epub 2023 Jan 4.

Abstract

Pathogens generate ubiquitous selective pressures and host-pathogen interactions alter social behaviours in many animals1-4. However, very little is known about the neuronal mechanisms underlying pathogen-induced changes in social behaviour. Here we show that in adult Caenorhabditis elegans hermaphrodites, exposure to a bacterial pathogen (Pseudomonas aeruginosa) modulates sensory responses to pheromones by inducing the expression of the chemoreceptor STR-44 to promote mating. Under standard conditions, C. elegans hermaphrodites avoid a mixture of ascaroside pheromones to facilitate dispersal5-13. We find that exposure to the pathogenic Pseudomonas bacteria enables pheromone responses in AWA sensory neurons, which mediate attractive chemotaxis, to suppress the avoidance. Pathogen exposure induces str-44 expression in AWA neurons, a process regulated by a transcription factor zip-5 that also displays a pathogen-induced increase in expression in AWA. STR-44 acts as a pheromone receptor and its function in AWA neurons is required for pathogen-induced AWA pheromone response and suppression of pheromone avoidance. Furthermore, we show that C. elegans hermaphrodites, which reproduce mainly through self-fertilization, increase the rate of mating with males after pathogen exposure and that this increase requires str-44 in AWA neurons. Thus, our results uncover a causal mechanism for pathogen-induced social behaviour plasticity, which can promote genetic diversity and facilitate adaptation of the host animals.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans Proteins / metabolism
  • Caenorhabditis elegans* / metabolism
  • Caenorhabditis elegans* / microbiology
  • Caenorhabditis elegans* / physiology
  • Female
  • Glycolipids / metabolism
  • Hermaphroditic Organisms / physiology
  • Male
  • Pheromones* / metabolism
  • Pseudomonas aeruginosa* / pathogenicity
  • Pseudomonas aeruginosa* / physiology
  • Receptors, Pheromone / metabolism
  • Reproduction* / physiology
  • Sensory Receptor Cells / metabolism
  • Sexual Behavior, Animal*

Substances

  • Caenorhabditis elegans Proteins
  • Glycolipids
  • Pheromones
  • Receptors, Pheromone
  • STR-44 protein, C elegans