How resistance-nodulation-division (RND) efflux pumps contribute to virulence

In Gram-negative bacteria, multi-subunit efflux pumps transport molecules across the inner membrane, periplasm, and outer membrane to the extracellular environment. These efflux pumps include the Resistance-Nodulation-Cell Division (RND) superfamily, which utilize the membrane proton motive force to export a wide range of substrates against a concentration gradient. RND efflux pumps have been extensively studied for their fundamental role in the export of antibiotics, but they also play multifaceted roles in bacterial physiology. Notably, they are required for pathogen survival in the mammalian host when antibiotics are absent, an emerging aspect of their biology that is not well understood. Here, we analyze the evidence supporting several intertwined mechanistic hypotheses regarding the requirement for RND efflux pumps during infection. To do this, we explore why host- and bacterial-derived substrates need to be exported during pathogenesis, and the effects of proton translocation from the periplasm to the cytosol. We close by highlighting knowledge gaps and directions for future work regarding the role of RND efflux pumps in bacterial virulence.

Authors

Publication Details

Journal
PLoS Pathogens
Published
2026-05-14
DOI
https://doi.org/10.1371/journal.ppat.1014228
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
0.00
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article

How resistance-nodulation-division (RND) efflux pumps contribute to virulence

Corrella S. Detweiler, Ilyas Alav
PLoS Pathogens
Bacterial Genetics and Biotechnology
article

How resistance-nodulation-division (RND) efflux pumps contribute to virulence

Corrella S. Detweiler, Ilyas Alav
article en

Abstract

In Gram-negative bacteria, multi-subunit efflux pumps transport molecules across the inner membrane, periplasm, and outer membrane to the extracellular environment. These efflux pumps include the Resistance-Nodulation-Cell Division (RND) superfamily, which utilize the membrane proton motive force to export a wide range of substrates against a concentration gradient. RND efflux pumps have been extensively studied for their fundamental role in the export of antibiotics, but they also play multifaceted roles in bacterial physiology. Notably, they are required for pathogen survival in the mammalian host when antibiotics are absent, an emerging aspect of their biology that is not well understood. Here, we analyze the evidence supporting several intertwined mechanistic hypotheses regarding the requirement for RND efflux pumps during infection. To do this, we explore why host- and bacterial-derived substrates need to be exported during pathogenesis, and the effects of proton translocation from the periplasm to the cytosol. We close by highlighting knowledge gaps and directions for future work regarding the role of RND efflux pumps in bacterial virulence.

PLoS PathogensVol. 22(5)
Openalex Percentile: Top 4%
Bacterial Genetics and Biotechnology
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