Affiliation:
1. Division of Microbiology, Food and Drug Administration, Washington, D.C. 20204
Abstract
Pure spore antigens for the immunization of rabbits were prepared by enzymic digestion of vegetative components and separation of the cleaned spores in polyethylene glycol. Spore antisera were prepared to strains representative of toxigenic
Clostridium botulinum
type E; nontoxigenic boticin E-producing variants; nontoxigenic nonproducers of boticin E; nontoxigenic “atypical” strains, which differ somewhat from
C. botulinum
type E in their physiology;
C. botulinum
types A and B; and
C. bifermentans
. They were tested against these and additional strains representative of the above groups, other types of
C. botulinum
, and other
Clostridium
species. There was no evidence of agglutination of flagellar or somatic antigens of vegetative cells by these antisera. Agglutination and agglutinin absorption tests showed common antigens among toxigenic type E strains and nontoxigenic variants, both producers and nonproducers of boticin E. Some nontoxigenic “atypical” strains varied in their ability to be agglutinated by type E antisera, and others did not agglutinate at all. Of those atypical strains that were not agglutinated, one was agglutinated by
C. bifermentans
antiserum. Antisera prepared against
C. botulinum
types A and B and
C. bifermentans
did not agglutinate the spores of type E or its variants nor share antigens common to each other. Similarly, antisera to type E, its nontoxigenic variants, and nontoxigenic atypical strains did not agglutinate other
C. botulinum
types or any other
Clostridium
species investigated.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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