Literature DB >> 1864927

Identification of Clostridium botulinum, Clostridium argentinense, and related organisms by cellular fatty acid analysis.

F M Ghanem1, A C Ridpath, W E Moore, L V Moore.   

Abstract

On the basis of 686 analyses of 285 strains of Clostridium botulinum, Clostridium argentinense (formerly C. botulinum type G), and phenotypically related organisms, 14 cellular fatty acid (CFA) groups of toxic organisms and 6 CFA groups of nontoxic organisms were delineated. The CFA groups of toxic strains included two of type A, three of proteolytic strains of type B, two of proteolytic strains of type F, one each of nonproteolytic strains of types B, E, and F, and one each of types C alpha, C beta, and D and C. argentinense. The groups of phenotypically similar nontoxic strains included Clostridium sporogenes, Clostridium putrificum, nontoxic strains with phenotypic characteristics similar to those of nonproteolytic strains of C. botulinum types B, E, and F (BEF-like), two groups of nontoxigenic organisms with phenotypic characteristics similar to those of C. botulinum types C and D and Clostridium novyi (CDN-like), and Clostridium subterminale, which has phenotypic characteristics similar to those of C. argentinense. Within the toxin types, 89 to 100% of the strains were correctly identified by CFA analysis, and 74 to 100% of the analyses were correct. Of 36 strains of C. sporogenes, 30 (83%) were correctly identified; 17% of the strains of C. sporogenes were incorrectly identified as C. botulinum type A or B. All analyses of C. putrificum and C. subterminale were correctly identified. There was no significant level of similarity between strains of C. botulinum and phenotypically similar organisms and 85 other species of clostridia or 407 other taxa of gram-positive and gram-negative bacteria. Additionally, the one strain each of Clostridium baratii and Clostridium butyricum previously reported to produce C. botulinum toxin could be differentiated from C.botulinum types as well as from strains of C. baratii and C. butyricum that did not produce neurotoxin.

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Year:  1991        PMID: 1864927      PMCID: PMC269954          DOI: 10.1128/jcm.29.6.1114-1124.1991

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  10 in total

1.  Taxonomy of the Clostridia: ribosomal ribonucleic acid homologies among the species.

Authors:  J L Johnson; B S Francis
Journal:  J Gen Microbiol       Date:  1975-06

2.  Polyacrylamide slab gel electrophoresis of soluble proteins for studies of bacterial floras.

Authors:  W E Moore; D E Hash; L V Holdeman; E P Cato
Journal:  Appl Environ Microbiol       Date:  1980-04       Impact factor: 4.792

3.  Interspecies conversion of Clostridium botulinum type C to Clostridium novyi type A by bacteriophage.

Authors:  M W Eklund; F T Poysky; J A Meyers; G A Pelroy
Journal:  Science       Date:  1974-11-01       Impact factor: 47.728

4.  Phage-conversion of toxigenicity in Clostridium botulinum types C and D.

Authors:  H Iida; K Oguma; K Inoue
Journal:  Jpn J Med Sci Biol       Date:  1974-04

5.  The genetic relatedness of proteolytic Clostridium botulinum strains.

Authors:  W H Lee; H Riemann
Journal:  J Gen Microbiol       Date:  1970-11

6.  Correlation of toxic and non-toxic strains of Clostridium botulinum by DNA composition and homology.

Authors:  W H Lee; H Riemann
Journal:  J Gen Microbiol       Date:  1970-01

7.  Interconversion of type C and D strains of Clostridium botulinum by specific bacteriophages.

Authors:  M W Eklund; F T Poysky
Journal:  Appl Microbiol       Date:  1974-01

8.  Characterization of an organism that produces type E botulinal toxin but which resembles Clostridium butyricum from the feces of an infant with type E botulism.

Authors:  L M McCroskey; C L Hatheway; L Fenicia; B Pasolini; P Aureli
Journal:  J Clin Microbiol       Date:  1986-01       Impact factor: 5.948

9.  Isolation of an organism resembling Clostridium barati which produces type F botulinal toxin from an infant with botulism.

Authors:  J D Hall; L M McCroskey; B J Pincomb; C L Hatheway
Journal:  J Clin Microbiol       Date:  1985-04       Impact factor: 5.948

10.  Characterization of clostridia by gas chromatography. I. Differentiation of species by cellular fatty acids.

Authors:  C W Moss; V J Lewis
Journal:  Appl Microbiol       Date:  1967-03
  10 in total
  13 in total

1.  Osteosynthesis-associated bone infection caused by a nonproteolytic, nontoxigenic Clostridium botulinum-like strain.

Authors:  Jean-Philippe Carlier; Guylène K'ouas; Alain Lozniewski; François Sirveaux; Philippe Cailloux; Francine Mory
Journal:  J Clin Microbiol       Date:  2004-01       Impact factor: 5.948

2.  Identification of Clostridium species and DNA fingerprinting of Clostridium perfringens by amplified fragment length polymorphism analysis.

Authors:  Riikka Keto-Timonen; Annamari Heikinheimo; Erkki Eerola; Hannu Korkeala
Journal:  J Clin Microbiol       Date:  2006-09-13       Impact factor: 5.948

3.  Gas-liquid chromatographic analysis of cellular fatty acids for identification of gram-negative anaerobic bacilli.

Authors:  L Stoakes; T Kelly; B Schieven; D Harley; M Ramos; R Lannigan; D Groves; Z Hussain
Journal:  J Clin Microbiol       Date:  1991-11       Impact factor: 5.948

4.  Isolation of gram-positive rods that resemble but are clearly distinct from Actinomyces pyogenes from mixed wound infections.

Authors:  J Wüst; G M Lucchini; J Lüthy-Hottenstein; F Brun; M Altwegg
Journal:  J Clin Microbiol       Date:  1993-05       Impact factor: 5.948

5.  Investigation of the influences of puberty, genetics, and environment on the composition of subgingival periodontal floras.

Authors:  W E Moore; J A Burmeister; C N Brooks; R R Ranney; K H Hinkelmann; R M Schieken; L V Moore
Journal:  Infect Immun       Date:  1993-07       Impact factor: 3.441

6.  Actinomyces pyogenes-like bacteria.

Authors:  D Lindquist; J Wong
Journal:  J Clin Microbiol       Date:  1993-12       Impact factor: 5.948

7.  Cellular fatty acid composition, soluble-protein profile, and antimicrobial resistance pattern of Eubacterium lentum.

Authors:  A Mosca; P Summanen; S M Finegold; G De Michele; G Miragliotta
Journal:  J Clin Microbiol       Date:  1998-03       Impact factor: 5.948

8.  Cellular fatty acids in Fusobacterium species as a tool for identification.

Authors:  K Tunér; E J Baron; P Summanen; S M Finegold
Journal:  J Clin Microbiol       Date:  1992-12       Impact factor: 5.948

9.  Use of electrophoretic polymorphisms of esterases for differentiation of Clostridium argentinense strains.

Authors:  P N Bories; C Antoniotti; J L Pons; G Leluan
Journal:  J Clin Microbiol       Date:  1993-01       Impact factor: 5.948

10.  Gas-liquid chromatography of cellular fatty acids for identification of staphylococci.

Authors:  L Stoakes; M A John; R Lannigan; B C Schieven; M Ramos; D Harley; Z Hussain
Journal:  J Clin Microbiol       Date:  1994-08       Impact factor: 5.948

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