Literature DB >> 16558033

Pathogenesis of Clostridium botulinum Type A: Study of In Vivo Toxin Release by Implantation of Diffusion Chambers Containing Spores, Vegetative Cells, and Free Toxin.

J B Suzuki1, R Booth, A Benedik, N Grecz.   

Abstract

Millipore diffusion chambers (MDC) with 0.22-mum filters loaded with spores or vegetative cells of Clostridium botulinum were surgically implanted intraperitoneally (ip) into guinea pigs. MDC expose C. botulinum spores or vegetative cells to body fluids yet protect them from phagocytes. Guinea pigs receiving MDC containing 10(9) spores plus 10(8) polymorphonuclear (PMN) leukocytes and MDC with 10(9) vegetative cells died within 48 hr, indicating that toxin was released and diffused out. MDC with 10(9) spores alone allowed 90% of animals to survive for at least 96 hr. Microscopically, it was observed that vegetative cells in MDC were disintegrated and leukocytes plus spores were phagocytized and germinated; spores alone remained intact and phase bright. Chemotactic attraction of leukocytes to MDC walls was also observed. Apparently, body fluids do not attack spores; thus, PMN leukocyte engulfment is essential for germination and release of spore-bound toxin in this type of C. botulinum pathogenesis. However, vegetative cells appear to be attacked by bacteriolytic enzymes (e.g., lysozyme) in body fluids, and leukocyte engulfment is not essential for toxin release.

Entities:  

Year:  1971        PMID: 16558033      PMCID: PMC416213          DOI: 10.1128/iai.3.5.659-663.1971

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  17 in total

1.  The biochemical basis of phagocytosis. I. Metabolic changes during the ingestion of particles by polymorphonuclear leukocytes.

Authors:  A J SBARRA; M L KARNOVSKY
Journal:  J Biol Chem       Date:  1959-06       Impact factor: 5.157

2.  Antimicrobial factors of normal tissues and fluids.

Authors:  R C SKARNES; D W WATSON
Journal:  Bacteriol Rev       Date:  1957-12

3.  In vivo cell culture.

Authors:  G H ALGIRE
Journal:  Med Bull (Ann Arbor)       Date:  1956-11

4.  Growth of cells in vivo in diffusion chambers. I. Survival of homografts in immunized mice.

Authors:  G H ALGIRE; J M WEAVER; R T PREHN
Journal:  J Natl Cancer Inst       Date:  1954-12       Impact factor: 13.506

5.  Sequential use of Wright's and Ziehl-Neelsen's stains for demonstrating phagocytosis of bacterial spores.

Authors:  R Booth; J B Suzuki; N Grecz
Journal:  Stain Technol       Date:  1971-01

6.  Chemical composition of the cell walls of Clostridium botulinum type A.

Authors:  K Takumi; T Kawata
Journal:  Jpn J Microbiol       Date:  1970-01

7.  The nature of heat resistant toxin in spores of Clostridium botulinum.

Authors:  N Grecz; C A Lin; T Tang; W L So; L R Sehgal
Journal:  Jpn J Microbiol       Date:  1967-12

8.  Surveillance for botulism in the United States, 1968-1969.

Authors:  J A Donadio; E J Gangarosa
Journal:  J Infect Dis       Date:  1970 Jul-Aug       Impact factor: 5.226

9.  In vivo and in vitro release of Ca 45 from spores of clostridium botulinum type A as further evidence for spore germination.

Authors:  J B Suzuki; R Booth; N Grecz
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1971-01

10.  Pathogenesis of Clostridium botulinum type A: release of toxin from C. botulinum spores in vitro by leucocytes.

Authors:  J B Suzuki; R R Booth; N Grecz
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1970-09
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