ABSTRACTFor over 20 years, bacterial multidrug resistance (MDR) efflux pumps have been studied because of their impact on resistance to antimicrobials. However, critical questions remain, including why produce efflux pumps under non-antimicrobial treatment conditions, and why have multiple pumps if their only purpose is antimicrobial efflux?Salmonellaspp. possess five efflux pump families, including the resistance-nodulation-division (RND) efflux pumps. Notably, the RND efflux pump AcrD has a unique substrate profile, distinct from otherSalmonellaefflux pumps. Here we show that inactivation ofacrDresults in a profoundly altered transcriptome and modulation of pathways integral toSalmonellabiology. The most significant transcriptome changes were central metabolism related, with additional changes observed in pathogenicity, environmental sensing, and stress response pathway expression. The extent of tricarboxylic acid cycle and fumarate metabolism expression changes led us to hypothesize thatacrDinactivation may result in motility defects due to perturbation of metabolite concentrations, such as fumarate, for which a role in motility has been established. Despite minimal detectable changes in flagellar gene expression, we found that anacrDmutantSalmonella entericaserovar Typhimurium isolate was significantly impaired for swarming motility, which was restored by addition of fumarate. TheacrDmutant outcompeted the wild type in fitness experiments. The results of these diverse experiments provide strong evidence that the AcrD efflux pump is not simply a redundant system providing response resilience, but also has distinct physiological functions. Together, these data indicate that the AcrD efflux pump has a significant and previously underappreciated impact on bacterial biology, despite only minor perturbations of antibiotic resistance profiles.IMPORTANCEEfflux pumps in Gram-negative bacteria are studied because of their important contributions to antimicrobial resistance. However, the role of these pumps in bacterial biology has remained surprisingly elusive. Here, we provide evidence that loss of the AcrD efflux pump significantly impacts the physiology ofSalmonella entericaserovar Typhimurium. Inactivation ofacrDled to changes in the expression of 403 genes involved in fundamental processes, including basic metabolism, virulence, and stress responses. Pathways such as these allowSalmonellato grow, survive in the environment, and cause disease. Indeed, our data show that theacrDmutant is more fit than wild-typeSalmonellaunder standard lab conditions. We hypothesized that inactivation ofacrDwould alter levels of bacterial metabolites, impacting traits such as swarming motility. We demonstrated this by exogenous addition of the metabolite fumarate, which partially restored theacrDmutant’s swarming defect. This work extends our understanding of the role of bacterial efflux pumps.
Study of the role of efflux pump in ciprofloxacin resistance in Salmonella enterica serotype Typhi
