RT Journal Article SR Electronic(1) A1 Takewak, Syun-Ichi A1 Okuzumi, Katsuko A1 Manabe, Ichiro A1 Tanimura, Masako A1 Miyamura, Kikuko A1 Nakahara, Ken-Ichi A1 Yazaki, Yoshio A1 Ohkubo, Akiyuki A1 Nagai, RyozoYR 1994 T1 Nucleotide Sequence Comparison of the Mycobacterial dnaJ Gene and PCR-Restriction Fragment Length Polymorphism Analysis for Identification of Mycobacterial Species JF International Journal of Systematic and Evolutionary Microbiology, VO 44 IS 1 SP 159 OP 166 DO https://doi.org/10.1099/00207713-44-1-159 PB Microbiology Society, SN 1466-5034, AB Abstract We recently reported a genus-specific PCR for the mycobacterial dnaJ gene. In the present study, we have determined the nucleotide sequences of the dnaJ gene from 19 mycobacterial species (Mycobacterium tuberculosis, M. bovis, M. bovis BCG, M. africanum, M. microti, M. marinum, M. kansasii, M. gastri, M. simiae, M. scrofulaceum, M. szulgai, M. gordonae, M. avium, M. intracellulare, M. xenopi, M. fortuitum, M. chelonae, M. hemophilum, and M. paratuberculosis). On the basis of the amplified dnaJ gene nucleotide sequences, we constructed a phylogenetic tree of the mycobacterial species by using the neighbor-joining method and unweighted pairwise grouping method of arithmetic average. We found that the phylogenetic relationship inferred within the slowly growing species was in good agreement with the traditional classification, with three major branches corresponding to Runyon’s groups I, II, and III. An exception was M. simiae, which was phylogenetically closer to the cluster including members of Runyon’s group III than to that of Runyon’s group I. On the other hand, the rapid growers, such as M. fortuitum and M. chelonae, did not form a coherent line corresponding to Runyon’s group IV, indicating that our phylogenetic analysis based on the dnaJ gene reflects the phenotypic characteristics such as pigmentation but not the growth rate. Finally, we revealed the species-specific restriction sites within the amplified dnaJ gene to differentiate most of the mycobacterial DNA by a combination of PCR with restriction fragment length polymorphism analysis., UL https://www.microbiologyresearch.org/content/journal/ijsem/10.1099/00207713-44-1-159