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. 1976 Sep;14(3):597-602.
doi: 10.1128/iai.14.3.597-602.1976.

Phage conversion to hemagglutinin production in Clostridium botulinum types C and D

Phage conversion to hemagglutinin production in Clostridium botulinum types C and D

K Oguma et al. Infect Immun. 1976 Sep.

Abstract

Five toxigenic strains of Clostridium botulinum types C and D were incubated at 37 degrees C for 7 days in 15 ml of the following media: LYG medium, cooked-meat medium, egg meat medium, and N-Z-amine medium. The supernatants of these cultures were tested for hemagglutinin production with 1% erythrocytes obtained from mice, guinea pigs, chickens, sheep, monkeys, and humans. Four toxigenic strains produced hemagglutinin. The highest hemagglutinin titer was obtained with a combination of human erythrocytes and cultures incubated in LYG medium. When the same experiment was carried out with many nontoxigenic strains, hemagglutination was observed in only one strain, C-N71. Strains producing hemagglutinin also produced phages. The phages obtained from toxin- and hemagglutinin-producing strains converted nontoxigenic indicator strains to produce both toxin and hemagglutinin. The phage obtained from a toxin-positive hemagglutinin-negative strain could only induce cultures to produce toxin, and the phage from a toxin-negative hemagglutinin-positive strain could only induce production of hemagglutinin. These studies suggest that the production of hemagglutinin by C. botulinum types C and D is governed by bacteriophages and that hemagglutinin production can be transmitted separately or concomitantly with toxin production.

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References

    1. Science. 1954 Apr 2;119(3092):440-1 - PubMed
    1. Am J Hyg. 1953 Jan;57(1):46-59 - PubMed
    1. Nat New Biol. 1972 Jan 5;235(53):16-7 - PubMed
    1. Jpn J Vet Res. 1972 Jun;20(1):19-30 - PubMed
    1. Immunology. 1973 Nov;25(5):773-82 - PubMed

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