Direct sensing of host ferric iron by an archetype histidine kinase mediates virulence of an enteric pathogen.

Abstract

Two-component system (TCS) histidine kinases enable bacterial pathogens to sense environmental signals and regulate adaptive responses during infection. The EnvZ/OmpR TCS, known for its role in osmolarity/pH-dependent regulation of outer membrane porins across bacterial species, is also a central virulence regulator. However, the environmental cues that activate EnvZ/OmpR to trigger pathogenicity have remained unclear, limiting our understanding of host-pathogen interactions. Here, we demonstrate that in <i>Vibrio parahaemolyticus</i>, a major etiological agent of seafood-associated gastroenteritis, EnvZ functions as a direct ferric iron (Fe³⁺) sensor governing virulence programs. Fe³⁺-EnvZ interaction triggers kinase phosphorylation and activation, enabling transcriptional control of biofilm formation, swarming motility, and type 3/6 secretion systems. An iron-binding-deficient EnvZ mutant (EnvZ^Q103A) abrogated Fe³⁺ responsiveness and downstream signaling pathways. In an infant rabbit infection model, Fe³⁺ enhanced <i>V. parahaemolyticus</i> intestinal colonization and virulence through EnvZ/OmpR signaling. This study identifies Fe³⁺ as the physiological ligand activating the EnvZ/OmpR virulence regulon and provides insight into how enteric pathogens exploit host-derived iron cues to promote infection.