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Connaught Medical Research Laboratories, University of Toronto, Toronto, Ontario, Canada
ABSTRACT
SUMMARY: A simple, chemically defined medium is described consisting of sodium glutamate, proline, cystine, salts, and growth factors, which is suitable for the large-scale production of phase I Bordetella pertussis. More than 30 x 109 organisms/ml. were produced in 48 to 72 h. growth in shake flasks and fermentors. The cultures were detoxified by the addition of 0.14% formalin to yield vaccines which were non-toxic to mice and guinea pigs and had good mouse-protective antigen levels. The antigenic stability was satisfactory after storage of the final vaccines at elevated temperatures.
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T. M. Finn and D. F. Amsbaugh Vag8, a Bordetella pertussis bvg-Regulated Protein Infect. Immun., August 1, 1998; 66(8): 3985 - 3989. [Abstract] [Full Text] [PDF] |
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G. Martinez de Tejada, P. A. Cotter, U. Heininger, A. Camilli, B. J. Akerley, J. J. Mekalanos, and J. F. Miller Neither the Bvg- Phase nor the vrg6 Locus of Bordetella pertussis Is Required for Respiratory Infection in Mice Infect. Immun., June 1, 1998; 66(6): 2762 - 2768. [Abstract] [Full Text] [PDF] |
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F. C. Beaumont, H. Y. Kang, T. J. Brickman, and S. K. Armstrong Identification and Characterization of alcR, a Gene Encoding an AraC-Like Regulator of Alcaligin Siderophore Biosynthesis and Transport in Bordetella pertussis and Bordetella bronchiseptica J. Bacteriol., February 15, 1998; 180(4): 862 - 870. [Abstract] [Full Text] |
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E. Pradel, N. Guiso, and C. Locht Identification of AlcR, an AraC-Type Regulator of Alcaligin Siderophore Synthesis in Bordetella bronchiseptica and Bordetella pertussis J. Bacteriol., February 15, 1998; 180(4): 871 - 880. [Abstract] [Full Text] |
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