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

mBio

Toshihiro Aono¹  Jun-ichi Matsuoka¹  Katsuharu Saito²  Kengo Morohashi³  Keigo Kurumisawa³  Tetsuhiro Ogawa⁴  Fumiko Ishizuna⁴  Makoto Hidaka⁴  Tatsuhiro Ezawa⁵ 

[1] Biotechnology Research Center, The University of Tokyo, Tokyo, Japan;Faculty of Agriculture, Shinshu University, Matsumoto, Nagano, Japan;Faculty of Science and Technology, Tokyo University of Science, Tokyo, Japan;Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan;Graduate School of Agriculture, Hokkaido University, Sapporo, Hokkaido Prefecture, Japan;

关键词: R body;    legume;    pathogenesis;    reb gene;    rhizobia;    symbiosis;   

DOI  :  10.1128/mBio.00715-17

来源: DOAJ

【 摘 要 】

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.

【 授权许可】

Unknown