PCR-based specific detection of Ralstonia solanacearum race 4 strains

被引:40
作者
Horita M. [1 ]
Yano K. [2 ]
Tsuchiya K. [3 ]
机构
[1] Natl. Agric. Res. Ctr. Hokkaido Reg., Toyohira-ku, Sapporo 062-8555
[2] Kochi Agricultural Research Center, Kochi
[3] Natl. Inst. of Agro-Environ. Sci., Ibaraki
关键词
Bacterial wilt; PCR detection; Ralstonia solanacearum; rep-PCR; Zingiberaceae crop;
D O I
10.1007/s10327-004-0126-7
中图分类号
学科分类号
摘要
Two primer sets were designed based on the sequence of polymorphic bands that were derived from repetitive sequence-based polymerase chain reaction (repPCR) fingerprinting and specifically detected in Ralstonia solanacearum race 4 strains (ginger, mioga, and curcuma isolates). One primer set (AKIF-AKIR) amplified a single band (165 bp) from genomic DNA obtained from all mioga and curcuma and some ginger isolates; another set (21F-21R) amplified one band (125bp) from the other ginger isolates. These primer sets did not amplify the bands from genomic DNA of other R. solanacearum strains or of other related bacteria. PCR detection limit for the pathogen was 2 × 102cfu.
引用
收藏
页码:278 / 283
页数:5
相关论文
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