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J Bacteriol. 1965 October; 90(4): 1082-1095
Copyright © 1965 American Society for Microbiology. All Rights Reserved.

Structure and Composition of the Bacillus anthracis Capsule

A. A. Avakyan, L. N. Katz, K. N. Levina and I. B. Pavlova

Laboratory of Morphology of Microorganisms and Electron Microscopy, Gamaleya Institute of Epidemiology and Microbiology, Academy of Medical Sciences, Moscow, USSR

ABSTRACT

AVAKYAN, A. A. (Academy of Medical Sciences, Moscow, USSR), L. N. KATZ, K. N. LEVINA, AND I. B. PAVLOVA. Structure and composition of the Bacillus anthracis capsule. J. Bacteriol. 90:1082–1095. 1965.—Observations by various methods of light microscopy (phase contrast, dark-field, and fluorescence) revealed the complex structure of the Bacillus anthracis capsule, which changes regularly during the growth cycle of the culture. Special cytological methods of staining the capsule made it possible to study its fine structure, which is not revealed by negative staining with India ink. For example, the capsule shows a membranelike outline, fine transverse lines, and interruptions and transverse septa traversing the entire capsule. By using cytochemical methods, it was found that the capsule has a stratified structure and that the various layers of the capsule differ as to the value of the isoelectric point, metachromatic ability, sensitivity to various enzymes, and, consequently, chemical composition. It was thus shown that the membranelike outline of the capsule consists of peptides and neutral mucopolysaccharides. The middle part of the capsule consists of a complex of substances of both polysaccharide and protein nature, and the inner part consists of acid mucopolysaccharides. Observation of the capsular forms of B. anthracis by means of an electron microscope revealed differences in the osmiophilia and submicroscopic structure of the membranelike outline and the middle and inner parts of the capsule. Immunochemical studies conducted by the fluorescent-antibody method revealed localization of antigens in different parts of the capsule, and made it possible to differentiate the capsular antigens according to their serum-staining ability and according of their relations to enzymes, i.e., their chemical composition. This paper concerns the possibility of studying the fine structure of bacterial capsules in fixed preparations, and the differences and similarities of the antigens of the capsule and cell wall of B. anthracis and of the related species, B. megaterium.


J Bacteriol. 1965 October; 90(4): 1082-1095
Copyright © 1965 American Society for Microbiology. All Rights Reserved.




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