Phylogenetic study and multiplex PCR-based detection of Burkholderia plantarii, Burkholderia glumae and Burkholderia gladioli using gyrB and rpoD sequences

被引:68
作者
Maeda, Yukiko
Shinohara, Hirosuke
Kiba, Akinori
Ohnishi, Kouhei
Furuya, Naruto
Kawamura, Yoshiaki
Ezaki, Takayuki
Vandamme, Peter
Tsushima, Seiya
Hikichi, Yasufumi
机构
[1] Kochi Univ, Lab Plant Pathol & Biotechnol, Kochi 7838502, Japan
[2] Kochi Univ, Res Inst Mol Genet, Kochi 7838502, Japan
[3] Natl Agr Res Ctr Tohoku Reg, Fukushima 9602156, Japan
[4] Kyushu Univ, Lab Plant Pathol, Fukuoka 8128581, Japan
[5] Gifu Univ, Grad Sch Med, Dept Microbiol, Gifu 5011194, Japan
[6] Univ Ghent, Microbiol Lab, B-9000 Ghent, Belgium
[7] Natl Inst Agroenvironm Sci, Tsukuba, Ibaraki 3058604, Japan
关键词
D O I
10.1099/ijs.0.64184-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In order to develop a detection method for the rice pathogens Burkholderia plantarii, Burkholderia glumae and Burkholderia gladioli, the phylogeny of six plant-pathogenic Burkholderia species was analysed using the combined nucleotide sequences of gyrB and rpoD. B. plantarii, B. glumae and B. gladioli formed tight monophyletic branches supported by high bootstrap probabilities. The high sequence similarity revealed a close phylogenetic relationship between B. glumae and B. plantarii. B. plantarii strains were divided into three subdusters comprising rice strains, whereas the single Vanda strain occupied a unique position in the phylogenetic tree. The gyrB and rpoD sequences of all B. glumae strains examined were highly conserved. In contrast, B. gladioli strains demonstrated a far greater sequence diversity, but this diversity did not correlate with pathovar, host plant or geographical origin of the strains. A multiplex-PCR protocol using specific primers from the gyrB sequences was designed that allowed the specific detection and identification of B, plantarii, B. glumae and B. gladioli in rice seeds infected with these pathogenic species.
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页码:1031 / 1038
页数:8
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