In order to study the diversity and community of genus Mycobacterium in polluted soils, we tried to isolate mycobacteria from 11 soil samples collected from an illegal dumping site and 3 landfills in Japan. Using culture methods with or without Acanthamoeba culbertsoni, a total of 19 isolates of mycobacteria were obtained from 5 soil samples and 3 of them were isolated only by the co-culture method with the amoeba. Conventional biochemical tests and sequencing of the hsp65, rpoB, and 16S rRNA genes were performed for species identification of 17 of the 19 isolates. Among the 17 isolates, there was one isolate each of Mycobacterium vanbaalenii, Mycobacterium mageritense, Mycobacterium frederiksbergense, M. vanbaalenii or Mycobacterium austroafricanum, and Mycobacterium chubuense or Mycobacterium chlorophenolicum. The remaining 12 isolates could not be precisely identified at the species level. A phylogenic tree based on the hsp65 sequences indicated that 2 of the 12 isolates were novel species. In addition, 4 isolates were phylogenically close to species that degrade polycyclic aromatic hydrocarbons, which induce some cancers in humans. These results demonstrated that there were many hitherto-unreported mycobacteria in the polluted soils, and suggested that some mycobacteria might play roles in the natural attenuation and engineered bioremediation of contaminated sites with other microorganisms.Key words: Mycobacteria, Amoebal co-culture, hsp65, Landfills 513 Microbiol. Immunol., 50(7), [513][514][515][516][517][518][519][520][521][522][523][524] 2006 *Address correspondence to Dr. Hatsumi Taniguchi, Department of Microbiology, School of Medicine, University of Occupational and Environmental Health, Japan, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka 807-8555, Japan. Fax: ϩ81-93-602-4799. E-mail: hatsumi@med.uoeh-u.ac.jp Abbreviations: ARB, amoeba resistant bacteria; CFU, colony forming unit; DSMZ, the German National Resource Centre for Biological Material; hsp65, heat shock protein gene 65-kilodalton; MOI, multiplicity of infection; PAH, polycyclic aromatic hydrocarbons; PBS, phosphate buffered saline; PCDDS, polychlorinated dibenzo-p-dioxins; PCR, polymerase chain reaction; rpoB, RNA polymerase β-subunit gene; SDS, sodium dodecyl sulfate; Z-N, Ziehl-Neelsen staining; 16S rRNA, 16S ribosomal RNA.tion of contaminated sites with other microorganisms (5,10,17,19,22,41,44). Detailed analyses of the interaction between environmental conditions and mycobacteria are needed. However, purposeful isolation of mycobacteria from soil is difficult because of their relatively slow growth rate and susceptibility to overgrowth by faster-growing organisms on solid media. Therefore, an amoebal co-culture method was applied in this study.Generally, amoebae serve as a reservoir to protect internalized bacteria from environmental stress or toxicity (7,15,36). An amoebal co-culture procedure has also been reported to be useful to isolate amoeba resistant bacteria (ARB) and fastidious bacteria in water supplies and...