Toxin Production in Clostridium botulinum as Demonstrated by Electron Microscopy

Author:

Duda John J.1,Slack John M.1

Affiliation:

1. Department of Microbiology, Medical Center, West Virginia University, Morgantown, West Virginia 26506

Abstract

Spheroplasts of Clostridium botulinum 62A were prepared with the use of lysozyme. These spheroplasts were then exposed to ferritin-labeled type A antitoxin. Ultrathin sections of these specimens revealed the ferritin-labeled antibody symmetrically arranged around the outer spore coats but not within the spore cortex. The ferritin-labeled antibody was also observed in the bacterial cytoplasm. Here it was arranged in aggregates and strands, although it was not associated with any identifiable cell structure. Controls included sections of C. botulinum spheroplasts treated with a 1.5% solution of ferritin as well as spheroplasts of C. roseum and Bacillus subtilis treated with conjugated type A antitoxin or a 1.5% solution of ferritin. No intracellular or extracellular ferritin was demonstrable in these specimens.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference14 articles.

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2. Determination of serum proteins by means of the biuret reaction;Gornall A. G.;J. Biol. Chem.,1949

3. Function and structure in microorganisms;Halvorson H.;Symp. Soc. Gen. Microbiol.,1965

4. Electron microscopic study of DNA containing plasms;Kellenberger E.;J. Biophys. Biochem. Cytol.,1958

5. Ferritin labeled antibody as an electron dense stain for phage protein;Lee S.;Exptl. Cell Res.,1960

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