NYMC Faculty Publications

EmrA1 Membrane Fusion Protein of Francisella Tularensis LVS is Required for Resistance to Oxidative Stress, Intramacrophage Survival and Virulence in Mice

Author Type(s)

Faculty

DOI

10.1111/mmi.12509

Journal Title

Molecular Microbiology

First Page

976

Last Page

995

Document Type

Article

Publication Date

3-1-2014

Department

Pathology, Microbiology and Immunology

Keywords

Amino Acid Sequence, Animals, Anti-Bacterial Agents, Antioxidants, Bacterial Proteins, Bacterial Secretion Systems, Drug Resistance, Bacterial, Francisella tularensis, Genome, Bacterial, Humans, Hydrogen Peroxide, Macrophages, Membrane Fusion, Membrane Glycoproteins, Mice, Mice, Inbred C57BL, Microbial Viability, Molecular Sequence Data, Mutation, NADPH Oxidase 2, NADPH Oxidases, Oxidative Stress, Tularemia, Virulence

Disciplines

Medicine and Health Sciences

Abstract

Francisella tularensis is a category A biodefence agent that causes a fatal human disease known as tularaemia. The pathogenicity of F. tularensis depends on its ability to persist inside host immune cells primarily by resisting an attack from host-generated reactive oxygen and nitrogen species (ROS/RNS). Based on the ability of F. tularensis to resist high ROS/RNS levels, we have hypothesized that additional unknown factors act in conjunction with known antioxidant defences to render ROS resistance. By screening a transposon insertion library of F. tularensis LVS in the presence of hydrogen peroxide, we have identified an oxidant-sensitive mutant in putative EmrA1 (FTL_0687) secretion protein. The results demonstrate that the emrA1 mutant is highly sensitive to oxidants and several antimicrobial agents, and exhibits diminished intramacrophage growth that can be restored to wild-type F. tularensis LVS levels by either transcomplementation, inhibition of ROS generation or infection in NADPH oxidase deficient (gp91Phox(-/-)) macrophages. The emrA1 mutant is attenuated for virulence, which is restored by infection in gp91Phox(-/-) mice. Further, EmrA1 contributes to oxidative stress resistance by affecting secretion of Francisella antioxidant enzymes SodB and KatG. This study exposes unique links between transporter activity and the antioxidant defence mechanisms of F. tularensis.

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