Pathogenic bacteria modulate pheromone response to promote mating.
Taihong WuMinghai GeMin WuFengyun DuanJingting LiangMaoting ChenXicotencatl GracidaHe LiuWenxing YangAbdul Rouf DarChengyin LiRebecca A ButcherArneet L SaltzmanYun ZhangPublished in: Nature (2023)
Pathogens generate ubiquitous selective pressures and host-pathogen interactions alter social behaviours in many animals 1-4 . 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 dispersal 5-13 . 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.
Keyphrases
- candida albicans
- poor prognosis
- pseudomonas aeruginosa
- spinal cord
- high glucose
- transcription factor
- healthcare
- mental health
- diabetic rats
- genetic diversity
- biofilm formation
- binding protein
- escherichia coli
- drug induced
- cystic fibrosis
- long non coding rna
- endothelial cells
- staphylococcus aureus
- young adults
- blood brain barrier
- drug resistant