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. 1994 Jun;62(6):2244–2248. doi: 10.1128/iai.62.6.2244-2248.1994

Reduced virulence of Serpulina hyodysenteriae hemolysin-negative mutants in pigs and their potential to protect pigs against challenge with a virulent strain.

D R Hyatt 1, A A ter Huurne 1, B A van der Zeijst 1, L A Joens 1
PMCID: PMC186504  PMID: 8188345

Abstract

The role of the Serpulina hyodysenteriae hemolysin encoded by the tlyA gene in the pathogenesis of swine dysentery (SD) was studied. tlyA mutants of two S. hyodysenteriae strains (B204 and C5) were tested for virulence in pigs. None of the animals developed SD. However, after infection with wild-type strain B204 or C5, the incidence of SD was 100 or 60%, respectively. Thus, the tlyA-encoded hemolysin of S. hyodysenteriae is an important virulence factor in SD. The potential of these mutants to protect pigs against challenge with a virulent S. hyodysenteriae strain was also studied. After challenge with wild-type strain B204, 50% of pigs previously inoculated with the B204 tlyA mutant were protected, whereas all control pigs contracted SD. None of the pigs previously inoculated with the C5 tlyA mutant developed SD upon challenge with wild-type strain B204, whereas 40% of the control pigs developed SD in this experiment. Thus, previous colonization with S. hyodysenteriae tlyA mutants in pigs provides partial protection against challenge with a virulent S. hyodysenteriae strain.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Fisher L. F., Olander H. J. Shedding of Treponema hyodysenteriae, transmission of disease, and agglutinin response to pigs convalescent from swine dysentery. Am J Vet Res. 1981 Mar;42(3):450–455. [PubMed] [Google Scholar]
  2. Harris D. L., Glock R. D., Christensen C. R., Kinyon J. M. Inoculation of pigs with Treponema hyodysenteriae (new species) and reproduction f the disease. Vet Med Small Anim Clin. 1972 Jan;67(1):61–64. [PubMed] [Google Scholar]
  3. Joens L. A., Harris D. L., Baum D. H. Immunity to Swine dysentery in recovered pigs. Am J Vet Res. 1979 Oct;40(10):1352–1354. [PubMed] [Google Scholar]
  4. Kent K. A., Lemcke R. M., Lysons R. J. Production, purification and molecular weight determination of the haemolysin of Treponema hyodysenteriae. J Med Microbiol. 1988 Nov;27(3):215–224. doi: 10.1099/00222615-27-3-215. [DOI] [PubMed] [Google Scholar]
  5. Kinyon J. M., Harris D. L., Glock R. D. Enteropathogenicity of various isolates of Treponema hyodysenteriae. Infect Immun. 1977 Feb;15(2):638–646. doi: 10.1128/iai.15.2.638-646.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Knoop F. C. Investigation of a hemolysin produced by enteropathogenic Treponema hyodysenteriae. Infect Immun. 1981 Jan;31(1):193–198. doi: 10.1128/iai.31.1.193-198.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kunkle R. A., Kinyon J. M. Improved selective medium for the isolation of Treponema hyodysenteriae. J Clin Microbiol. 1988 Nov;26(11):2357–2360. doi: 10.1128/jcm.26.11.2357-2360.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lysons R. J., Kent K. A., Bland A. P., Sellwood R., Robinson W. F., Frost A. J. A cytotoxic haemolysin from Treponema hyodysenteriae--a probable virulence determinant in swine dysentery. J Med Microbiol. 1991 Feb;34(2):97–102. doi: 10.1099/00222615-34-2-97. [DOI] [PubMed] [Google Scholar]
  9. Mapother M. E., Joens L. A. New serotypes of Treponema hyodysenteriae. J Clin Microbiol. 1985 Aug;22(2):161–164. doi: 10.1128/jcm.22.2.161-164.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Muir S., Koopman M. B., Libby S. J., Joens L. A., Heffron F., Kusters J. G. Cloning and expression of a Serpula (Treponema) hyodysenteriae hemolysin gene. Infect Immun. 1992 Feb;60(2):529–535. doi: 10.1128/iai.60.2.529-535.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nuessen M. E., Joens L. A., Glock R. D. Involvement of lipopolysaccharide in the pathogenicity of Treponema hyodysenteriae. J Immunol. 1983 Aug;131(2):997–999. [PubMed] [Google Scholar]
  12. Stanton T. B., Cornell C. P. Erythrocytes as a source of essential lipids for Treponema hyodysenteriae. Infect Immun. 1987 Feb;55(2):304–308. doi: 10.1128/iai.55.2.304-308.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Taylor D. J., Alexander T. J. The production of dysentery in swine by feeding cultures containing a spirochaete. Br Vet J. 1971 Nov;127(11):58–61. doi: 10.1016/s0007-1935(17)37282-2. [DOI] [PubMed] [Google Scholar]
  14. ter Huurne A. A., van Houten M., Koopman M. B., van der Zeijst B. A., Gaastra W. Characterization of Dutch porcine Serpulina (Treponema) isolates by restriction endonuclease analysis and DNA hybridization. J Gen Microbiol. 1992 Sep;138(9):1929–1934. doi: 10.1099/00221287-138-9-1929. [DOI] [PubMed] [Google Scholar]
  15. ter Huurne A. A., van Houten M., Muir S., Kusters J. G., van der Zeijst B. A., Gaastra W. Inactivation of a Serpula (Treponema) hyodysenteriae hemolysin gene by homologous recombination: importance of this hemolysin in pathogenesis in mice. FEMS Microbiol Lett. 1992 Apr 1;71(1):109–113. doi: 10.1016/0378-1097(92)90550-8. [DOI] [PubMed] [Google Scholar]

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