Limited Role for Iron Regulation in Coxiella burnetii Pathogenesis

Author:

Briggs Heather L.1,Pul Nicolein1,Seshadri Rekha2,Wilson Mary J.1,Tersteeg Claudia1,Russell-Lodrigue Kasi E.1,Andoh Masako1,Bäumler Andreas J.3,Samuel James E.1

Affiliation:

1. TAMUS Health Science Center, Department of Microbial and Molecular Pathogenesis, College Station, Texas

2. The Institute of Genomic Research, Rockville, Maryland

3. University of California, Department of Medical Microbiology and Immunology, Davis, California

Abstract

ABSTRACT In gram-negative bacteria, iron acquisition proteins are commonly regulated by Fur ( f erric u ptake r egulator), which binds iron-regulated promoters (the Fur box). We hypothesized that Coxiella burnetii requires iron and employs an iron-regulatory system and used various approaches to define a Fur regulon. Cloned C. burnetii fur complemented an Escherichia coli fur deletion mutant. A ferrous iron transporter gene (CBU1766), a putative iron binding protein-encoding gene (CBU0970), and a cation efflux pump gene (CBU1362) were identified by genome annotation and using a Fur titration assay. Bioinformatically predicted Fur box-containing promoters were tested for transcriptional control by iron. Five genes demonstrated at least a twofold induction with minimal iron. Putatively regulated genes were evaluated in a two-plasmid regulator/promoter heterologous expression system. These data suggested a very limited Fur-regulated system in C. burnetii . In an in vitro tissue culture model, a significant increase in bacterial growth was observed with infected cells treated with deferoxamine in comparison to growth under iron-replete conditions. In an iron-overloaded animal model in vivo, the level of bacterial growth detected in the iron-injected animals was significantly decreased in comparison to growth in control animals. In a low-iron-diet animal model, a significant increase in splenomegaly was observed, but no significant change in bacterial growth was identified. The small number of predicted iron acquisition systems, few Fur-regulated genes, and enhanced replication under a decreased iron level predict a requirement of a low level of iron for survival, perhaps to avoid creation of additional reactive oxygen radicals.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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