Simultaneous detection of Bacteroides fragilis group species by leuB-directed PCR

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  • Miki Tsuyoshi
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Kuwahara Tomomi
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Nakayama Haruyuki
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Okada Natsumi
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Kataoka Keiko
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Arimochi Hideki
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School
  • Ohnishi Yoshinari
    Department of Molecular Bacteriology, Institute of Health Biosciences, The University of Tokushima Graduate School

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Bacteroides species, saccharolytic Gram-negative obligate anaerobes, are frequently isolated from human infections such as peritonitis, abscesses and bacteremia. Among the species in the genus Bacteroides, the species called “B. fragilis group” are particularly involved in human infections and are medically important because they account for a major part of anaerobic isolates from clinical specimens. The purpose of this study was to develop PCR primers that specifically and simultaneously amplify the β-isopropylmalate dehydrogenase gene leuB in B. fragilis group species. We determined partial nucleotide sequences of leuB genes and compared them in seventeen strains of nine B. fragilis group species, and the regions that are conserved among Bacteroides strains but different from other species were used as a B. fragilis group-specific PCR primer set, BacLBF-BacLBR. Specificity tests of the primer set using 52 phenotypically characterized strains and 75 isolates from rat feces showed only one case each of false-positive and false-negative. The detection limit of the leuB-directed PCR using BacLBF and BacLBR was 3.9×103 colony-forming units. These results indicate that leuB amplification using BacLBF and BacLBR is a useful tool for rapid diagnosis of Bacteriodes infection and for rapid differential diagnosis of anaerobic infections. J. Med. Invest. 52: 101-108, February, 2005

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