Liu Hongsheng, Li Ying, Huang Xinxiang, Kawamura Yoshiaki, Ezaki Takayuki
Microbiology-Bioinformatics, Regeneration and Advanced Medical Science, Gifu University Graduate School of Medicine, Japan.
Microbiol Immunol. 2003;47(11):859-69. doi: 10.1111/j.1348-0421.2003.tb03452.x.
We sequenced about 930 bp of the dnaJ gene from 15 Legionella pneumophila serogroups and some other members of the genus Legionella. As L. pneumophila 16S rDNA sequences could not discriminate between all subspecies and serogroups, we assessed the use of dnaJ gene sequences to differentiate between Legionella subspecies as well as between L. pneumophila serogroups. A phylogenetic analysis revealed that dnaJ gene sequences were more variable between the L. pneumophila serogroups than mip gene and 16S rDNA sequences. By studying 61 strains from 41 species of the genus Legionella, as well as other genera, we established a PCR method that could amplify 285 bp of dnaJ gene from all L. pneumophila serogroups. This primer set was more sensitive than mip gene primers and was able to detect 0.25 ng of purified DNA. We also describe the 16S rDNA primers that were used to detect most Legionella genus members.
我们对15个嗜肺军团菌血清群以及军团菌属的其他一些成员的dnaJ基因约930 bp进行了测序。由于嗜肺军团菌16S rDNA序列无法区分所有亚种和血清群,我们评估了使用dnaJ基因序列来区分军团菌亚种以及嗜肺军团菌血清群。系统发育分析表明,嗜肺军团菌血清群之间的dnaJ基因序列比mip基因和16S rDNA序列更具变异性。通过研究军团菌属41个物种以及其他属的61株菌株,我们建立了一种PCR方法,该方法可以从所有嗜肺军团菌血清群中扩增出285 bp的dnaJ基因。该引物组比mip基因引物更灵敏,能够检测到0.25 ng的纯化DNA。我们还描述了用于检测大多数军团菌属成员的16S rDNA引物。