Stringent Expression Control of Pathogenic R-body Production in Legume Symbiont Azorhizobium caulinodans

Author:

Matsuoka Jun-ichi1,Ishizuna Fumiko2,Kurumisawa Keigo3,Morohashi Kengo3,Ogawa Tetsuhiro2,Hidaka Makoto2,Saito Katsuharu4,Ezawa Tatsuhiro5,Aono Toshihiro1ORCID

Affiliation:

1. Biotechnology Research Center, The University of Tokyo, Tokyo, Japan

2. Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan

3. Faculty of Science and Technology, Tokyo University of Science, Tokyo, Japan

4. Faculty of Agriculture, Shinshu University, Matsumoto, Nagano, Japan

5. Graduate School of Agriculture, Hokkaido University, Sapporo, Hokkaido Prefecture, Japan

Abstract

ABSTRACT R bodies are insoluble large polymers consisting of small proteins encoded by reb genes and are coiled into cylindrical structures in bacterial cells. They were first discovered in Caedibacter species, which are obligate endosymbionts of paramecia. Caedibacter confers a killer trait on the host paramecia. R-body-producing symbionts are released from their host paramecia and kill symbiont-free paramecia after ingestion. The roles of R bodies have not been explained in bacteria other than Caedibacter . Azorhizobium caulinodans ORS571, a microsymbiont of the legume Sesbania rostrata , carries a reb operon containing four reb genes that are regulated by the repressor PraR. Herein, deletion of the praR gene resulted in R-body formation and death of host plant cells. The rebR gene in the reb operon encodes an activator. Three PraR binding sites and a RebR binding site are present in the promoter region of the reb operon. Expression analyses using strains with mutations within the PraR binding site and/or the RebR binding site revealed that PraR and RebR directly control the expression of the reb operon and that PraR dominantly represses reb expression. Furthermore, we found that the reb operon is highly expressed at low temperatures and that 2-oxoglutarate induces the expression of the reb operon by inhibiting PraR binding to the reb promoter. We conclude that R bodies are toxic not only in paramecium symbiosis but also in relationships between other bacteria and eukaryotic cells and that R-body formation is controlled by environmental factors. IMPORTANCE Caedibacter species, which are obligate endosymbiotic bacteria of paramecia, produce R bodies, and R-body-producing endosymbionts that are released from their hosts are pathogenic to symbiont-free paramecia. Besides Caedibacter species, R bodies have also been observed in a few free-living bacteria, but the significance of R-body production in these bacteria is still unknown. Recent advances in genome sequencing technologies revealed that many Gram-negative bacteria possess reb genes encoding R-body components, and interestingly, many of them are animal and plant pathogens. Azorhizobium caulinodans , a microsymbiont of the tropical legume Sesbania rostrata , also possesses reb genes. In this study, we demonstrate that A. caulinodans has ability to kill the host plant cells by producing R bodies, suggesting that pathogenicity conferred by an R body might be universal in bacteria possessing reb genes. Furthermore, we provide the first insight into the molecular mechanism underlying the expression of R-body production in response to environmental factors, such as temperature and 2-oxoglutarate.

Funder

MEXT | Japan Society for the Promotion of Science

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Reference35 articles.

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4. A Mutation in the R Body-Coding Sequence Destroys Expression of the Killer Trait in P. tetraurelia

5. Characterization of genetic determinants for R body synthesis and assembly in Caedibacter taeniospiralis 47 and 116

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