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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1995 Aug;33(8):2145–2149. doi: 10.1128/jcm.33.8.2145-2149.1995

Production and characterization of monoclonal antibodies specific for lipooligosaccharide of Serpulina hyodysenteriae.

R B Westerman 1, R M Phillips 1, L A Joens 1
PMCID: PMC228352  PMID: 7559965

Abstract

Serpulina (Treponema) hyodysenteriae is the causative agent of swine dysentery, a contagious mucohemorrhagic disease of the colon. Diagnosis of swine dysentery is extremely difficult because of the presence of cross-reactive antibodies to the proteins of S. hyodysenteriae and Serpulina innocens, a nonpathogenic inhabitant of the porcine large intestine. Therefore, monoclonal antibodies (MAbs) against the serotype-specific lipooligosaccharide (LOS) antigens of S. hyodysenteriae were produced to rapidly differentiate S. hyodysenteriae from S. innocens. Whole-cell preparations of S. hyodysenteriae serotypes 1 through 7 were used as antigens. MAbs were characterized by an indirect enzyme-linked immunosorbent assay with whole-cell or LOS antigen and by Western blot (immunoblot) analysis with whole-cell lysates as antigen. A total of 12 LOS-specific MAbs which could identify and differentiate the seven original serotypes of S. hyodysenteriae were produced. The MAb serospecificities are as follows: MAb 9G8, serotype 1; MAb 31D9, serotype 2; MAb 7D3, serotypes 2 and 7; MAb 24B7, serotype 3; MAb 13C2, serotype 4; MAb 18E9, serotype 4; MAb 2B7, serotype 6; MAb 1D2, serotypes 2, 5, and 7; MAb 9C5, serotypes 2, 5, and 7; MAb 11C9, serotype 7; MAb 11E10, serotype 7; and MAb 6G11, serotype 7.

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Selected References

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  1. Alderton M. R., Smith S. C., Coloe P. J. Identification of a novel group of Serpulina hyodysenteriae isolates by using a lipopolysaccharide-specific monoclonal antibody. J Clin Microbiol. 1993 May;31(5):1326–1328. doi: 10.1128/jcm.31.5.1326-1328.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baum D. H., Joens L. A. Serotypes of beta-hemolytic Treponema hyodysenteriae. Infect Immun. 1979 Sep;25(3):792–796. doi: 10.1128/iai.25.3.792-796.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Combs B. G., Hampson D. J. Use of a whole chromosomal probe for identification of Treponema hyodysenteriae. Res Vet Sci. 1991 May;50(3):286–289. doi: 10.1016/0034-5288(91)90125-8. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. Halter M. R., Joens L. A. Lipooligosaccharides from Treponema hyodysenteriae and Treponema innocens. Infect Immun. 1988 Dec;56(12):3152–3156. doi: 10.1128/iai.56.12.3152-3156.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hudson M. J., Alexander T. J., Lysons R. J. Diagnosis of swine dysentery: spirochaetes which may be confused with Treponema hyodysenteriae. Vet Rec. 1976 Dec 18;99(25-26):498–500. doi: 10.1136/vr.99.25-26.498. [DOI] [PubMed] [Google Scholar]
  7. Hunter D., Saunders C. N. Diagnosis of swine dysentery using an absorbed fluorescent antiserum. Vet Rec. 1977 Oct 8;101(15):303–304. doi: 10.1136/vr.101.15.303. [DOI] [PubMed] [Google Scholar]
  8. Jensen N. S., Casey T. A., Stanton T. B. Detection and identification of Treponema hyodysenteriae by using oligodeoxynucleotide probes complementary to 16S rRNA. J Clin Microbiol. 1990 Dec;28(12):2717–2721. doi: 10.1128/jcm.28.12.2717-2721.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Joens L. A., Glock R. D. Experimental infection in mice with Treponema hyodysenteriae. Infect Immun. 1979 Aug;25(2):757–760. doi: 10.1128/iai.25.2.757-760.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 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]
  11. Joens L. A., Harris D. L., Kinyon J. M., Kaeberle M. L. Microtitration agglutination for detection of Treponema hyodysenteriae antibody. J Clin Microbiol. 1978 Sep;8(3):293–298. doi: 10.1128/jcm.8.3.293-298.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Joens L. A., Marquez M. R., Halter M. Comparison of outer-membrane fractions of Serpulina (Treponema) hyodysenteriae. Vet Microbiol. 1993 May;35(1-2):119–132. doi: 10.1016/0378-1135(93)90120-v. [DOI] [PubMed] [Google Scholar]
  13. Joens L. A., Marquez R. B. Molecular characterization of proteins from porcine spirochetes. Infect Immun. 1986 Dec;54(3):893–896. doi: 10.1128/iai.54.3.893-896.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Joens L. A., Nord N. A., Kinyon J. M., Egan I. T. Enzyme-linked immunosorbent assay for detection of antibody to Treponema hyodysenteriae antigens. J Clin Microbiol. 1982 Feb;15(2):249–252. doi: 10.1128/jcm.15.2.249-252.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kent K. A., Sellwood R., Lemcke R. M., Burrows M. R., Lysons R. J. Analysis of the axial filaments of Treponema hyodysenteriae by SDS-PAGE and immunoblotting. J Gen Microbiol. 1989 Jun;135(6):1625–1632. doi: 10.1099/00221287-135-6-1625. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. 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]
  18. Li Z. S., Bélanger M., Jacques M. Serotyping of Canadian isolates of Treponema hyodysenteriae and description of two new serotypes. J Clin Microbiol. 1991 Dec;29(12):2794–2797. doi: 10.1128/jcm.29.12.2794-2797.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Li Z., Jensen N. S., Bélanger M., L'Espérance M. C., Jacques M. Molecular characterization of Serpulina (Treponema) hyodysenteriae isolates representing serotypes 8 and 9. J Clin Microbiol. 1992 Nov;30(11):2941–2947. doi: 10.1128/jcm.30.11.2941-2947.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. 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]
  21. Taylor D. J., Lysons R. J., Bew J., Stevenson R., Lemcke R. M. Survival of Treponema hyodysenteriae in samples of dysenteric pig faeces sent by post and stored at room temperature. Vet Rec. 1985 Jan 12;116(2):48–49. doi: 10.1136/vr.116.2.48. [DOI] [PubMed] [Google Scholar]
  22. Westerman R. B., Fortner G. W., Mills K. W., Phillips R. M., Greenwood J. M. Use of monoclonal antibodies specific for the a determinant of K88 pili for detection of enterotoxigenic Escherichia coli in pigs. J Clin Microbiol. 1993 Feb;31(2):311–314. doi: 10.1128/jcm.31.2.311-314.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Westerman R. B., Mills K. W., Phillips R. M., Fortner G. W., Greenwood J. M. Predominance of the ac variant in K88-positive Escherichia coli isolates from swine. J Clin Microbiol. 1988 Jan;26(1):149–150. doi: 10.1128/jcm.26.1.149-150.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. de StGroth S. F., Scheidegger D. Production of monoclonal antibodies: strategy and tactics. J Immunol Methods. 1980;35(1-2):1–21. doi: 10.1016/0022-1759(80)90146-5. [DOI] [PubMed] [Google Scholar]

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