Specificity, the selective partnership between a host and particular microbial taxa, is a fundamental feature of microbial symbioses, yet the mechanisms that generate and maintain specificity can be difficult to disentangle across the evolutionary, ecological and molecular scales at which they operate. Binary symbioses, in which a single host and microbial species interact, offer powerful systems for investigating these mechanisms across biological scales. Here, current knowledge of the symbiosis between siphonfish in the genus Siphamia and their bioluminescent symbiont, Photobacterium mandapamensis, is synthesized to illustrate ways in which specificity operates across multiple scales in this vertebrate-bacteria association. At the evolutionary scale, P. mandapamensis is the exclusive symbiont across all Siphamia species throughout the Indo-Pacific examined to date, indicating specificity is a conserved feature of the association. At the ecological scale, host behavior may generate local symbiont pools that reinforce specificity across host generations, promoting fine-scale genetic divergence among symbiont populations. At the molecular scale, comparative genomics between P. mandapamensis and the closely related, yet incompatible P. leiognathi reveals candidate loci unique to P. mandapamensis that encode putative systems for exopolysaccharide biosynthesis, iron transport, host-specific attachment and surface recognition, and nitrogen assimilation. Together, these findings illustrate that specificity in this system is not the product of any single mechanism, but of multiple processes operating across these scales and feeding back to one another, positioning the Siphamia-P. mandapamensis symbiosis as a tractable model for investigating how partner fidelity is generated, maintained, and potentially disrupted in a changing world.
Alison L. Gould (Thu,) studied this question.