Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1997 Jun;63(6):2318–2323. doi: 10.1128/aem.63.6.2318-2323.1997

Isolation and characterization of fimbriae from a sparsely fimbriated strain of Porphyromonas gingivalis.

H T Sojar 1, N Hamada 1, R J Genco 1
PMCID: PMC168524  PMID: 9172351

Abstract

Porphyromonas gingivalis W50 (ATCC 53978) possesses the gene for fimbriae; however, the surface-expressed fimbriae are sparse and have not been previously isolated and characterized. We purified fimbriae from strain W50 to homogeneity by ammonium sulfate precipitation and reverse-phase high-performance liquid chromatography [H. T. Sojar, N. Hamada, and R. J. Genco, Protein Expr. Purif. 9(1):49-52, 1997]. Negative staining of purified fimbriae viewed by electron microscopy revealed that the fimbriae were identical in diameter to fimbriae of other P. gingivalis strains, such as 2561, but were shorter in length. On sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis, the apparent molecular weight of isolated fimbrillin from strain W50 was found to be identical to that of the fimbrillin molecule of strain 2561. Unlike 2561 fimbriae, W50 fimbriae, under reducing condition, exhibited a monomeric structure on SDS-PAGE at room temperature. However, under nonreduced conditions, even at 100 degrees C, no monomer was observed. In immunoblot analysis as well as immunogold labeling of isolated fimbriae, polyclonal antibodies against 2561 fimbriae, as well as antibodies against peptide I (V-V-M-A-N-T-G-A-M-E-V-G-K-T-L-A-E-V-K-Cys) and peptide J (A-L-T-T-E-L-T-A-E-N-Q-E-A-A-G-L-I-M-T-A-E-P-Cys), reacted. However, antifimbrial antibodies against strain 2561 reacted very weakly compared to anti-peptide I and anti-peptide J. Negative staining of whole W50 cells, as well as immunogold electron microscopy with anti-peptide I and anti-peptide J, showed fimbriae shorter in length and very few in number compared to those of strain 2561. Purified fimbriae showed no hemagglutinating activity. Amino acid composition was very similar to that of previously reported fimbriae of the 2561 strain.

Full Text

The Full Text of this article is available as a PDF (684.6 KB).

Selected References

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

  1. De Nardin A. M., Sojar H. T., Grossi S. G., Christersson L. A., Genco R. J. Humoral immunity of older adults with periodontal disease to Porphyromonas gingivalis. Infect Immun. 1991 Dec;59(12):4363–4370. doi: 10.1128/iai.59.12.4363-4370.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Evans R. T., Klausen B., Sojar H. T., Bedi G. S., Sfintescu C., Ramamurthy N. S., Golub L. M., Genco R. J. Immunization with Porphyromonas (Bacteroides) gingivalis fimbriae protects against periodontal destruction. Infect Immun. 1992 Jul;60(7):2926–2935. doi: 10.1128/iai.60.7.2926-2935.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fujiwara T., Morishima S., Takahashi I., Hamada S. Molecular cloning and sequencing of the fimbrilin gene of Porphyromonas gingivalis strains and characterization of recombinant proteins. Biochem Biophys Res Commun. 1993 Nov 30;197(1):241–247. doi: 10.1006/bbrc.1993.2467. [DOI] [PubMed] [Google Scholar]
  4. Fujiwara T., Nakagawa I., Morishima S., Takahashi I., Hamada S. Inconsistency between the fimbrilin gene and the antigenicity of lipopolysaccharides in selected strains of Porphyromonas gingivalis. FEMS Microbiol Lett. 1994 Dec 15;124(3):333–341. doi: 10.1111/j.1574-6968.1994.tb07305.x. [DOI] [PubMed] [Google Scholar]
  5. Goulbourne P. A., Ellen R. P. Evidence that Porphyromonas (Bacteroides) gingivalis fimbriae function in adhesion to Actinomyces viscosus. J Bacteriol. 1991 Sep;173(17):5266–5274. doi: 10.1128/jb.173.17.5266-5274.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Haffajee A. D., Socransky S. S., Dzink J. L., Taubman M. A., Ebersole J. L., Smith D. J. Clinical, microbiological and immunological features of subjects with destructive periodontal diseases. J Clin Periodontol. 1988 Apr;15(4):240–246. doi: 10.1111/j.1600-051x.1988.tb01577.x. [DOI] [PubMed] [Google Scholar]
  7. Hanazawa S., Hirose K., Ohmori Y., Amano S., Kitano S. Bacteroides gingivalis fimbriae stimulate production of thymocyte-activating factor by human gingival fibroblasts. Infect Immun. 1988 Jan;56(1):272–274. doi: 10.1128/iai.56.1.272-274.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hanazawa S., Murakami Y., Hirose K., Amano S., Ohmori Y., Higuchi H., Kitano S. Bacteroides (Porphyromonas) gingivalis fimbriae activate mouse peritoneal macrophages and induce gene expression and production of interleukin-1. Infect Immun. 1991 Jun;59(6):1972–1977. doi: 10.1128/iai.59.6.1972-1977.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hanazawa S., Murakami Y., Takeshita A., Kitami H., Ohta K., Amano S., Kitano S. Porphyromonas gingivalis fimbriae induce expression of the neutrophil chemotactic factor KC gene of mouse peritoneal macrophages: role of protein kinase C. Infect Immun. 1992 Apr;60(4):1544–1549. doi: 10.1128/iai.60.4.1544-1549.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Handley P. S., Tipler L. S. An electron microscope survey of the surface structures and hydrophobicity of oral and non-oral species of the bacterial genus Bacteroides. Arch Oral Biol. 1986;31(5):325–335. doi: 10.1016/0003-9969(86)90047-6. [DOI] [PubMed] [Google Scholar]
  11. Isogai H., Isogai E., Yoshimura F., Suzuki T., Kagota W., Takano K. Specific inhibition of adherence of an oral strain of Bacteroides gingivalis 381 to epithelial cells by monoclonal antibodies against the bacterial fimbriae. Arch Oral Biol. 1988;33(7):479–485. doi: 10.1016/0003-9969(88)90028-3. [DOI] [PubMed] [Google Scholar]
  12. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  13. Lee J. Y., Sojar H. T., Amano A., Genco R. J. Purification of major fimbrial proteins of Porphyromonas gingivalis. Protein Expr Purif. 1995 Aug;6(4):496–500. doi: 10.1006/prep.1995.1066. [DOI] [PubMed] [Google Scholar]
  14. Lee J. Y., Sojar H. T., Bedi G. S., Genco R. J. Porphyromonas (Bacteroides) gingivalis fimbrillin: size, amino-terminal sequence, and antigenic heterogeneity. Infect Immun. 1991 Jan;59(1):383–389. doi: 10.1128/iai.59.1.383-389.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lee J. Y., Sojar H. T., Bedi G. S., Genco R. J. Synthetic peptides analogous to the fimbrillin sequence inhibit adherence of Porphyromonas gingivalis. Infect Immun. 1992 Apr;60(4):1662–1670. doi: 10.1128/iai.60.4.1662-1670.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Malek R., Fisher J. G., Caleca A., Stinson M., van Oss C. J., Lee J. Y., Cho M. I., Genco R. J., Evans R. T., Dyer D. W. Inactivation of the Porphyromonas gingivalis fimA gene blocks periodontal damage in gnotobiotic rats. J Bacteriol. 1994 Feb;176(4):1052–1059. doi: 10.1128/jb.176.4.1052-1059.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Morris J. A., Stevens A. E., Sojka W. J. Preliminary characterization of cell-free K99 antigen isolated from Escherichia coli B41. J Gen Microbiol. 1977 Apr;99(2):353–357. doi: 10.1099/00221287-99-2-353. [DOI] [PubMed] [Google Scholar]
  18. Ogawa T., Ogo H., Hamada S. Chemotaxis of human monocytes by synthetic peptides that mimic segments of Porphyromonas gingivalis fimbrial protein. Oral Microbiol Immunol. 1994 Oct;9(5):257–261. doi: 10.1111/j.1399-302x.1994.tb00068.x. [DOI] [PubMed] [Google Scholar]
  19. Ogawa T., Shimauchi H., Hamada S. Mucosal and systemic immune responses in BALB/c mice to Bacteroides gingivalis fimbriae administered orally. Infect Immun. 1989 Nov;57(11):3466–3471. doi: 10.1128/iai.57.11.3466-3471.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ogawa T., Uchida H., Hamada S. Porphyromonas gingivalis fimbriae and their synthetic peptides induce proinflammatory cytokines in human peripheral blood monocyte cultures. FEMS Microbiol Lett. 1994 Feb 15;116(2):237–242. doi: 10.1111/j.1574-6968.1994.tb06707.x. [DOI] [PubMed] [Google Scholar]
  21. Ogawa T., Uchida H., Yasuda K. Mapping of murine Th1 and Th2 helper T-cell epitopes on fimbriae from Porphyromonas gingivalis. J Med Microbiol. 1995 Mar;42(3):165–170. doi: 10.1099/00222615-42-3-165. [DOI] [PubMed] [Google Scholar]
  22. Okuda K., Yamamoto A., Naito Y., Takazoe I., Slots J., Genco R. J. Purification and properties of hemagglutinin from culture supernatant of Bacteroides gingivalis. Infect Immun. 1986 Dec;54(3):659–665. doi: 10.1128/iai.54.3.659-665.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Slots J. Subgingival microflora and periodontal disease. J Clin Periodontol. 1979 Oct;6(5):351–382. doi: 10.1111/j.1600-051x.1979.tb01935.x. [DOI] [PubMed] [Google Scholar]
  24. Sojar H. T., Hamada N., Genco R. J. High-performance liquid chromatographic separation of Porphyromonas gingivalis fimbriae. Protein Expr Purif. 1997 Feb;9(1):49–52. doi: 10.1006/prep.1996.0662. [DOI] [PubMed] [Google Scholar]
  25. Sojar H. T., Lee J. Y., Bedi G. S., Cho M. I., Genco R. J. Purification, characterization and immunolocalization of fimbrial protein from Porphyromonas (bacteroides) gingivalis. Biochem Biophys Res Commun. 1991 Mar 15;175(2):713–719. doi: 10.1016/0006-291x(91)91624-l. [DOI] [PubMed] [Google Scholar]
  26. Suzuki Y., Yoshimura F., Takahashi K., Tani H., Suzuki T. Detection of fimbriae and fimbrial antigens on the oral anaerobe Bacteroides gingivalis by negative staining and serological methods. J Gen Microbiol. 1988 Oct;134(10):2713–2720. doi: 10.1099/00221287-134-10-2713. [DOI] [PubMed] [Google Scholar]
  27. Suzuki Y., Yoshimura F., Tani H., Suzuki T. Fimbriae from the oral anaerobe Bacteroides gingivalis: a screening of clinical isolates from various places. Adv Dent Res. 1988 Nov;2(2):301–303. doi: 10.1177/08959374880020021601. [DOI] [PubMed] [Google Scholar]
  28. Takahashi Y., Yoshimura F., Kawanami M., Kato H. Detection of fimbrilin gene (fimA) in Porphyromonas (Bacteroides) gingivalis by Southern blot analysis. J Periodontal Res. 1992 Nov;27(6):599–603. doi: 10.1111/j.1600-0765.1992.tb01742.x. [DOI] [PubMed] [Google Scholar]
  29. Tanner A. C., Haffer C., Bratthall G. T., Visconti R. A., Socransky S. S. A study of the bacteria associated with advancing periodontitis in man. J Clin Periodontol. 1979 Oct;6(5):278–307. doi: 10.1111/j.1600-051x.1979.tb01931.x. [DOI] [PubMed] [Google Scholar]
  30. Yamamoto A., Takahashi M., Takamori K., Sasaki T. Ultrastructure of the outer membrane surface of black-pigmented Bacteroides isolated from human oral cavity. Bull Tokyo Dent Coll. 1982 Feb;23(1):47–60. [PubMed] [Google Scholar]
  31. Yoshimura F., Takahashi K., Nodasaka Y., Suzuki T. Purification and characterization of a novel type of fimbriae from the oral anaerobe Bacteroides gingivalis. J Bacteriol. 1984 Dec;160(3):949–957. doi: 10.1128/jb.160.3.949-957.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Yoshimura F., Takahashi Y., Hibi E., Takasawa T., Kato H., Dickinson D. P. Proteins with molecular masses of 50 and 80 kilodaltons encoded by genes downstream from the fimbrilin gene (fimA) are components associated with fimbriae in the oral anaerobe Porphyromonas gingivalis. Infect Immun. 1993 Dec;61(12):5181–5189. doi: 10.1128/iai.61.12.5181-5189.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. van Steenbergen T. J., Kastelein P., Touw J. J., de Graaff J. Virulence of black-pigmented Bacteroides strains from periodontal pockets and other sites in experimentally induced skin lesions in mice. J Periodontal Res. 1982 Jan;17(1):41–49. doi: 10.1111/j.1600-0765.1982.tb01129.x. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES