Abstract
The pathogenic mechanisms responsible for the development of lesions in swine and mice after infection with Treponema hyodysenteriae have not been fully characterized. The release of inflammatory mediators from mast cells has been postulated to play a role in lesion development during swine dysentery. Therefore, C3H/HeN mice were infected with T. hyodysenteriae, and mucosal mast cell (MMC) numbers were examined in cecal sections. An initial increase in MMC numbers from 13 to 22 per 50 crypt villus units was observed, but at 20 days postinfection the numbers significantly decreased (P less than 0.05) to 5 MMC per 50 crypt villus units. Immunohistochemical analysis performed on cecal sections failed to show a significant change in lamina proprial T-lymphocyte subsets. Numbers of T. hyodysenteriae CFU recovered from the cecum were stable throughout the experimental time period. Mast cell-deficient W/Wv mice and their mast cell-sufficient littermates were also infected to determine whether MMCs were necessary for the occurrence of T. hyodysenteriae-induced lesions. W/Wv mice were as susceptible to infection as their normal littermates and developed similar macroscopic and microscopic lesions. These results indicate that changes in MMC numbers can be detected after an infection with T. hyodysenteriae; however, on the basis of observations of infected W/Wv mice, mast cells are not required for lesion development in the murine model.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Albassam M. A., Olander H. J., Thacker H. L., Turek J. J. Ultrastructural characterization of colonic lesions in pigs inoculated with Treponema hyodysenteriae. Can J Comp Med. 1985 Oct;49(4):384–390. [PMC free article] [PubMed] [Google Scholar]
- Beer D. J., Matloff S. M., Rocklin R. E. The influence of histamine on immune and inflammatory responses. Adv Immunol. 1984;35:209–268. doi: 10.1016/s0065-2776(08)60577-5. [DOI] [PubMed] [Google Scholar]
- Crowle P. K. Mucosal mast cell reconstitution and Nippostrongylus brasiliensis rejection by W/Wv mice. J Parasitol. 1983 Feb;69(1):66–69. [PubMed] [Google Scholar]
- Crowle P. K., Reed N. D. Rejection of the intestinal parasite Nippostrongylus brasiliensis by mast cell-deficient W/Wv anemic mice. Infect Immun. 1981 Jul;33(1):54–58. doi: 10.1128/iai.33.1.54-58.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glock R. D., Harris D. L. Swine dysentery. II. Characterization of lesions in pigs inoculated with Treponema hyodysenteriae in pure and mixed culture. Vet Med Small Anim Clin. 1972 Jan;67(1):65–68. [PubMed] [Google Scholar]
- Ha T. Y., Reed N. D., Crowle P. K. Delayed expulsion of adult Trichinella spiralis by mast cell-deficient W/Wv mice. Infect Immun. 1983 Jul;41(1):445–447. doi: 10.1128/iai.41.1.445-447.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ha T. Y., Reed N. D., Crowle P. K. Immune response potential of mast cell-deficient W/Wv mice. Int Arch Allergy Appl Immunol. 1986;80(1):85–94. doi: 10.1159/000234031. [DOI] [PubMed] [Google Scholar]
- 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]
- Harris D. L., Kinyon J. M., Mullin M. T., Glock R. D. Isolation and propagation of spirochetes from the colon of swine dysentery affected pigs. Can J Comp Med. 1972 Jan;36(1):74–76. [PMC free article] [PubMed] [Google Scholar]
- Hughes R., Olander H. J., Williams C. B. Swine dysentery: pathogenicity of Treponema hyodysenteriae. Am J Vet Res. 1975 Jul;36(7):971–977. [PubMed] [Google Scholar]
- Joens L. A., Glock R. D., Kinyon J. M. Differentiation of Treponema hyodysenteriae from T innocens by enteropathogenicity testing in the CF1 mouse. Vet Rec. 1980 Dec 6;107(23):527–529. [PubMed] [Google Scholar]
- 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]
- Kamiya M., Oku Y., Itayama H., Ohbayashi M. Prolonged expulsion of adult Trichinella spiralis and eosinophil infiltration in mast cell-deficient W/Wv mice. J Helminthol. 1985 Sep;59(3):233–239. doi: 10.1017/s0022149x00008002. [DOI] [PubMed] [Google Scholar]
- Kennedy M. J., Rosnick D. K., Ulrich R. G., Yancey R. J., Jr Association of Treponema hyodysenteriae with porcine intestinal mucosa. J Gen Microbiol. 1988 Jun;134(6):1565–1576. doi: 10.1099/00221287-134-6-1565. [DOI] [PubMed] [Google Scholar]
- Kitamura Y., Go S., Hatanaka K. Decrease of mast cells in W/Wv mice and their increase by bone marrow transplantation. Blood. 1978 Aug;52(2):447–452. [PubMed] [Google Scholar]
- 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]
- Lemcke R. M., Burrows M. R. Studies on a haemolysin produced by Treponema hyodysenteriae. J Med Microbiol. 1982 May;15(2):205–214. doi: 10.1099/00222615-15-2-205. [DOI] [PubMed] [Google Scholar]
- Levy D. A., Wefald A. Gut mucosal mast cells and goblet cells during acute graft-versus-host disease in rats. Ann Inst Pasteur Immunol. 1986 Sep-Oct;137D(2):281–288. [PubMed] [Google Scholar]
- MacDonald T. T., Spencer J. Evidence that activated mucosal T cells play a role in the pathogenesis of enteropathy in human small intestine. J Exp Med. 1988 Apr 1;167(4):1341–1349. doi: 10.1084/jem.167.4.1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nabel G., Galli S. J., Dvorak A. M., Dvorak H. F., Cantor H. Inducer T lymphocytes synthesize a factor that stimulates proliferation of cloned mast cells. Nature. 1981 May 28;291(5813):332–334. doi: 10.1038/291332a0. [DOI] [PubMed] [Google Scholar]
- Norrby K. Evidence of mast-cell histamine being mitogenic in intact tissue. Agents Actions. 1985 Apr;16(3-4):287–290. doi: 10.1007/BF01983162. [DOI] [PubMed] [Google Scholar]
- Nuessen M. E., Birmingham J. R., Joens L. A. Biological activity of a lipopolysaccharide extracted from Treponema hyodysenteriae. Infect Immun. 1982 Jul;37(1):138–142. doi: 10.1128/iai.37.1.138-142.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Oku Y., Itayama H., Kamiya M. Expulsion of Trichinella spiralis from the intestine of W/Wv mice reconstituted with haematopoietic and lymphopoietic cells and origin of mucosal mast cells. Immunology. 1984 Oct;53(2):337–344. [PMC free article] [PubMed] [Google Scholar]
- Saheb S. A., Massicotte L., Picard B. Purification and characterization of Treponema hyodysenteriae hemolysin. Biochimie. 1980;62(11-12):779–785. doi: 10.1016/s0300-9084(80)80133-7. [DOI] [PubMed] [Google Scholar]
- Wannemuehler M. J., Hubbard R. D., Greer J. M. Characterization of the major outer membrane antigens of Treponema hyodysenteriae. Infect Immun. 1988 Dec;56(12):3032–3039. doi: 10.1128/iai.56.12.3032-3039.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilcock B. P., Olander H. J. Studies on the pathogenesis of swine dysentery. I. Characterization of the lesions in colons and colonic segments inoculated with pure cultures or colonic content containing Treponema hyodysenteriae. Vet Pathol. 1979 Jul;16(4):450–465. doi: 10.1177/030098587901600409. [DOI] [PubMed] [Google Scholar]
- Woodbury R. G., Miller H. R., Huntley J. F., Newlands G. F., Palliser A. C., Wakelin D. Mucosal mast cells are functionally active during spontaneous expulsion of intestinal nematode infections in rat. 1984 Nov 29-Dec 5Nature. 312(5993):450–452. doi: 10.1038/312450a0. [DOI] [PubMed] [Google Scholar]