Comparative analysis of nontoxigenic and neurotoxigenic Clostridium butyricum by molecular typing methods

X. Wang, T. Karasawa, T. Maegawa, S. Kozaki, Kentaro Tsukamoto, S. Nakamura

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Neurotoxigenic Clostridium butyricum has been identified as occurring in the natural environment. Nontoxigenic and neurotoxigenic C. butyricum strains were comparatively analyzed by PCR assay and Southern blot hybridization for the type E botulinum toxin gene (bont/E), random amplified polymorphic DNA (RAPD) assay, and pulsed-field gel electrophoresis (PFGE). With the PCR assay and Southern blot hybridization, the bont/E gene was detected in all seven strains of neurotoxigenic C. butyricum (BL 5262, BL 6340, LCL 155, LCL 063, LCL 095, KZ 1886, and KZ 1887), but not in nontoxigenic strains (MIYAIRI 588, MIYAIRI 595, MIYAIRI 630, SI 293-2, RU 063-3, GU-2, ATCC 19398, and IFO 3315), indicating that there were no partial bont/E gene fragments in the nontoxigenic C. butyricum strains. All strains were successfully analyzed by RAPD assay. In contrast to the RAPD assay, two strains of nontoxigenic C. butyricum could not be analyzed by PFGE, probably due to the DNase activity. Nontoxigenic strains SI 293-2 and GU-2 shared an identical RAPD or PFGE pattern. The other nontoxigenic strains showed unique RAPD and PFGE patterns, and these patterns differed from those of all neurotoxigenic C. butyricum strains. The present results are discussed in relation to the transfer of the bont/E gene.

Original languageEnglish
Pages (from-to)999-1004
Number of pages6
JournalJapanese Pharmacology and Therapeutics
Volume28
Issue number12
Publication statusPublished - 01-12-2000

Fingerprint

Clostridium butyricum
Molecular Typing
Pulsed Field Gel Electrophoresis
Botulinum Toxins
Genes
DNA
Southern Blotting
Polymerase Chain Reaction
Deoxyribonucleases

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Pharmacology (medical)

Cite this

Wang, X. ; Karasawa, T. ; Maegawa, T. ; Kozaki, S. ; Tsukamoto, Kentaro ; Nakamura, S. / Comparative analysis of nontoxigenic and neurotoxigenic Clostridium butyricum by molecular typing methods. In: Japanese Pharmacology and Therapeutics. 2000 ; Vol. 28, No. 12. pp. 999-1004.
@article{526cf281b1d94e1b961d30d6145f92d3,
title = "Comparative analysis of nontoxigenic and neurotoxigenic Clostridium butyricum by molecular typing methods",
abstract = "Neurotoxigenic Clostridium butyricum has been identified as occurring in the natural environment. Nontoxigenic and neurotoxigenic C. butyricum strains were comparatively analyzed by PCR assay and Southern blot hybridization for the type E botulinum toxin gene (bont/E), random amplified polymorphic DNA (RAPD) assay, and pulsed-field gel electrophoresis (PFGE). With the PCR assay and Southern blot hybridization, the bont/E gene was detected in all seven strains of neurotoxigenic C. butyricum (BL 5262, BL 6340, LCL 155, LCL 063, LCL 095, KZ 1886, and KZ 1887), but not in nontoxigenic strains (MIYAIRI 588, MIYAIRI 595, MIYAIRI 630, SI 293-2, RU 063-3, GU-2, ATCC 19398, and IFO 3315), indicating that there were no partial bont/E gene fragments in the nontoxigenic C. butyricum strains. All strains were successfully analyzed by RAPD assay. In contrast to the RAPD assay, two strains of nontoxigenic C. butyricum could not be analyzed by PFGE, probably due to the DNase activity. Nontoxigenic strains SI 293-2 and GU-2 shared an identical RAPD or PFGE pattern. The other nontoxigenic strains showed unique RAPD and PFGE patterns, and these patterns differed from those of all neurotoxigenic C. butyricum strains. The present results are discussed in relation to the transfer of the bont/E gene.",
author = "X. Wang and T. Karasawa and T. Maegawa and S. Kozaki and Kentaro Tsukamoto and S. Nakamura",
year = "2000",
month = "12",
day = "1",
language = "English",
volume = "28",
pages = "999--1004",
journal = "Japanese Pharmacology and Therapeutics",
issn = "0386-3603",
publisher = "Life Science Publishing Co. Ltd",
number = "12",

}

Comparative analysis of nontoxigenic and neurotoxigenic Clostridium butyricum by molecular typing methods. / Wang, X.; Karasawa, T.; Maegawa, T.; Kozaki, S.; Tsukamoto, Kentaro; Nakamura, S.

In: Japanese Pharmacology and Therapeutics, Vol. 28, No. 12, 01.12.2000, p. 999-1004.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Comparative analysis of nontoxigenic and neurotoxigenic Clostridium butyricum by molecular typing methods

AU - Wang, X.

AU - Karasawa, T.

AU - Maegawa, T.

AU - Kozaki, S.

AU - Tsukamoto, Kentaro

AU - Nakamura, S.

PY - 2000/12/1

Y1 - 2000/12/1

N2 - Neurotoxigenic Clostridium butyricum has been identified as occurring in the natural environment. Nontoxigenic and neurotoxigenic C. butyricum strains were comparatively analyzed by PCR assay and Southern blot hybridization for the type E botulinum toxin gene (bont/E), random amplified polymorphic DNA (RAPD) assay, and pulsed-field gel electrophoresis (PFGE). With the PCR assay and Southern blot hybridization, the bont/E gene was detected in all seven strains of neurotoxigenic C. butyricum (BL 5262, BL 6340, LCL 155, LCL 063, LCL 095, KZ 1886, and KZ 1887), but not in nontoxigenic strains (MIYAIRI 588, MIYAIRI 595, MIYAIRI 630, SI 293-2, RU 063-3, GU-2, ATCC 19398, and IFO 3315), indicating that there were no partial bont/E gene fragments in the nontoxigenic C. butyricum strains. All strains were successfully analyzed by RAPD assay. In contrast to the RAPD assay, two strains of nontoxigenic C. butyricum could not be analyzed by PFGE, probably due to the DNase activity. Nontoxigenic strains SI 293-2 and GU-2 shared an identical RAPD or PFGE pattern. The other nontoxigenic strains showed unique RAPD and PFGE patterns, and these patterns differed from those of all neurotoxigenic C. butyricum strains. The present results are discussed in relation to the transfer of the bont/E gene.

AB - Neurotoxigenic Clostridium butyricum has been identified as occurring in the natural environment. Nontoxigenic and neurotoxigenic C. butyricum strains were comparatively analyzed by PCR assay and Southern blot hybridization for the type E botulinum toxin gene (bont/E), random amplified polymorphic DNA (RAPD) assay, and pulsed-field gel electrophoresis (PFGE). With the PCR assay and Southern blot hybridization, the bont/E gene was detected in all seven strains of neurotoxigenic C. butyricum (BL 5262, BL 6340, LCL 155, LCL 063, LCL 095, KZ 1886, and KZ 1887), but not in nontoxigenic strains (MIYAIRI 588, MIYAIRI 595, MIYAIRI 630, SI 293-2, RU 063-3, GU-2, ATCC 19398, and IFO 3315), indicating that there were no partial bont/E gene fragments in the nontoxigenic C. butyricum strains. All strains were successfully analyzed by RAPD assay. In contrast to the RAPD assay, two strains of nontoxigenic C. butyricum could not be analyzed by PFGE, probably due to the DNase activity. Nontoxigenic strains SI 293-2 and GU-2 shared an identical RAPD or PFGE pattern. The other nontoxigenic strains showed unique RAPD and PFGE patterns, and these patterns differed from those of all neurotoxigenic C. butyricum strains. The present results are discussed in relation to the transfer of the bont/E gene.

UR - http://www.scopus.com/inward/record.url?scp=0034454862&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034454862&partnerID=8YFLogxK

M3 - Article

VL - 28

SP - 999

EP - 1004

JO - Japanese Pharmacology and Therapeutics

JF - Japanese Pharmacology and Therapeutics

SN - 0386-3603

IS - 12

ER -