Appearance of mouse-lethal toxin in liquid cultures of Bordetella pertussis
- PMID: 4300172
- PMCID: PMC547663
- DOI: 10.1128/am.16.9.1400-1405.1968
Appearance of mouse-lethal toxin in liquid cultures of Bordetella pertussis
Abstract
The mouse-lethal toxin present in liquid cultures of most smooth strains of Bordetella pertussis is known to originate in the cytoplasm of the organism but to be most lethal for mice when released into the supernatant fluid. It is also recognized that cell degeneration and lysis occur in liquid cultures during the stationary and decline phases of growth. For these reasons, it is generally believed that most of the toxicity demonstrable in liquid cultures at the time of harvest is released during the later stages of cultivation, when high alkalinity and aging of cells favor lysis. However, the results reported here have indicated that high levels of mouse-lethal toxicity arise during very early log phase and that the peak of toxicity is reached before the end of the log phase. No further increase in toxicity was observed during stationary and decline phases. The very early appearance of toxicity could not be explained by the presence in the inoculum of a proportion of dead and degenerating cells, and it is concluded that the toxin is produced mainly by actively growing cells. This was confirmed by tests on organisms growing in continuous culture. Electron-microscopic examination of cells from a very early log-phase culture revealed the presence of large numbers of small vesicles on the cell walls of about 5% of the population. It is suggested that these vesicles may be associated with the releases of toxin from living cells. It is concluded that no useful reduction in the toxicity of cultures would result from harvesting before the end of the log phase of growth.
Similar articles
-
Detoxification of liquid cultures of Bordetella pertussis by forced aeration at high pH.Appl Microbiol. 1968 Aug;16(8):1211-4. doi: 10.1128/am.16.8.1211-1214.1968. Appl Microbiol. 1968. PMID: 4300091 Free PMC article.
-
Use of glutamic acid to supplement fluid medium for cultivation of Bordetella pertussis.Appl Microbiol. 1970 Mar;19(3):512-20. doi: 10.1128/am.19.3.512-520.1970. Appl Microbiol. 1970. PMID: 4314842 Free PMC article.
-
Effect of relevant culture parameters on Pertussis Toxin expression by Bordetella pertussis.Biologicals. 2006 Sep;34(3):213-20. doi: 10.1016/j.biologicals.2005.11.002. Epub 2006 Feb 21. Biologicals. 2006. PMID: 16497513
-
[Cell components of Bordetella pertussis and their biological activities].Tanpakushitsu Kakusan Koso. 1972;17(2):139-49. Tanpakushitsu Kakusan Koso. 1972. PMID: 4337077 Review. Japanese. No abstract available.
-
Molecular aspects of Bordetella pertussis pathogenesis.Int Microbiol. 1999 Sep;2(3):137-44. Int Microbiol. 1999. PMID: 10943406 Review.
Cited by
-
Extracytoplasmic adenylate cyclase of Bordetella pertussis.Proc Natl Acad Sci U S A. 1976 Jun;73(6):1926-30. doi: 10.1073/pnas.73.6.1926. Proc Natl Acad Sci U S A. 1976. PMID: 180529 Free PMC article.
-
Intracellular localization of the dermonecrotic toxin of Bordetella pertussis.Infect Immun. 1979 Sep;25(3):896-901. doi: 10.1128/iai.25.3.896-901.1979. Infect Immun. 1979. PMID: 227787 Free PMC article.
-
Studies on the ultrastructure of Bordetella pertussis. I. Morphology, origin, and biological activity of structures present in the extracellular fluid of liquid cultures of Bordetella pertussis.J Exp Med. 1970 Jun 1;131(6):1342-57. doi: 10.1084/jem.131.6.1342. J Exp Med. 1970. PMID: 4315895 Free PMC article.
-
Induction of a novel morphological response in Chinese hamster ovary cells by pertussis toxin.Infect Immun. 1983 Jun;40(3):1198-203. doi: 10.1128/iai.40.3.1198-1203.1983. Infect Immun. 1983. PMID: 6682833 Free PMC article.
-
Morphology of cells and hemagglutinogens of Bordetella species: resolution of substructural units in fimbriae of Bordetella pertussis.Infect Immun. 1983 Oct;42(1):308-17. doi: 10.1128/iai.42.1.308-317.1983. Infect Immun. 1983. PMID: 6137457 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources