Chemosensory systems are crucial for insect survival, enabling host-seeking, food acquisition, and oviposition site selection. While insect-associated microbes are known to influence host development and immunity, their role in modulating chemosensory behavior remains poorly understood. Here, we show that mono-association with Escherichia coli alters sensory-driven behaviors in both larval and adult axenic Drosophila melanogaster. In larvae, E. coli mono-association altered phototaxis and mechanosensory responses across genotypes, while changes in tunneling and thermosensory behaviors were reduced or absent in ionotropic receptor (IR) co-receptor mutants. In adults, E. coli mono-association increased attraction to fermentation cues (apple cider vinegar, ethanol) and enhanced sucrose consumption in wild-type and Orco-deficient flies, whereas these effects were reduced or absent in IR co-receptor mutants (IR25a− and IR76b−). Together, these findings indicate that under defined gnotobiotic conditions, E. coli exposure alters sensory-driven behavioral outputs relative to axenic controls. Effects are reduced or absent in IR co-receptor mutants, consistent with a role for IR pathways in mediating these behavioral shifts. These findings support a role for microbial cues in shaping insect sensory-driven behaviors and highlight the importance of microbial status in interpreting behavioral phenotypes. This work provides a framework for future studies investigating how microbial signals interact with conserved sensory pathways.
Darwish et al. (Tue,) studied this question.