Open AccessPhylogeny and distribution of extra‐slow‐growing Bradyrhizobium japonicum harboring high copy numbers of RSα, RSβ and IS 1631
Author(s) -
Sameshima Reiko,
Isawa Tsuyoshi,
Sadowsky Michael J.,
Hamada Tohru,
Kasai Hiroaki,
Shutsrirung Arawan,
Mitsui Hisayuki,
Minamisawa Kiwamu
Publication year - 2003
Publication title -
fems microbiology ecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.377
H-Index - 155
eISSN - 1574-6941
pISSN - 0168-6496
DOI - 10.1016/s0168-6496(03)00009-6
Subject(s) - biology , copy number variation , phylogenetic tree , bradyrhizobium japonicum , bradyrhizobium , phylogenetics , 16s ribosomal rna , strain (injury) , doubling time , genetics , gene , genome , bacteria , rhizobiaceae , rhizobium , symbiosis , anatomy , in vitro
We previously reported that extra‐slow‐growing Bradyrhizobium japonicum isolates obtained from three field sites in Japan, designated as HRS (highly reiterated sequence‐possessing) strains, have high copy numbers of the insertion sequences RSα and RSβ. When strain collections in the USA, Japan, Korea, Thailand and China were examined by Southern hybridization using RSα, RSβ and IS 1631 as probes, HRS strains were found in the Japanese, Chinese, and American collections, but not in the Korean and Thai ones. Copy number analyses of RSα and RSβ, calibrated with the copy number of rrs (16S rRNA gene), indicated that the HRS stains can be divided into two major groups. Group A is comprised of members with a high copy number of RSα (mean±S.D., 139±27), a low number of RSβ (mean±S.D., 30±13) sequences, and extremely slow growth rates (mean doubling time±S.D., 27±9 h). In contrast, group B is comprised of strains with a high copy number of RSβ (mean±S.D., 93±6) and a lower number of RSα. These groupings of HRS strains were well correlated with phylogenetic clusters based on rrs , gyrB and serogroups (110/122 and 123/135). Growth rate of B. japonicum strains was also correlated exclusively with RSα copy number. The ecological, evolutionary and biotechnological implications of the findings are discussed.