Abstract
In this study, we describe the development of an efficient transpositional mutagenesis system for Porphyromonas gingivalis using the Bacteroides fragilis transposon Tn4351. Using this system, we have isolated and characterized a Tn4351-generated mutant of P. gingivalis A7436, designated MSM-1, which exhibits enhanced resistance to polymorphonuclear leukocyte (PMN) phagocytosis and killing. P. gingivalis MSM-1 was initially selected based on its colony morphology; MSM-1 appeared as a mucoid, beige-pigmented colony. Analysis of P. gingivalis MSM-1 by electron microscopy and staining with ruthenium red revealed the presence of a thick ruthenium red-staining layer that was twice the thickness of this layer observed in the parent strain. P. gingivalis MSM-1 was found to be more hydrophilic than strain A7436 by hydrocarbon partitioning. Analysis of phenol-water extracts prepared from P. gingivalis A7436 and MSM-1 by Western (immunoblot) analysis and immunodiffusion with hyperimmune sera raised against A7436 and MSM-1 revealed the loss of a high-molecular-weight anionic polysaccharide component in extracts prepared from MSM-1. P. gingivalis MSM-1 was also found to be more resistant to PMN phagocytosis and intracellular killing than the parent strain, as assessed in a fluorochrome phagocytosis microassay. These differences were statistically significant (P < 0.05) when comparing PMN phagocytosis in nonimmune serum and intracellular killing in nonimmune and immune sera. P. gingivalis MSM-1 was also more resistant to killing by crude granule extracts from PMNs than was P. gingivalis A7436. These results indicate that the increased evasion of PMN phagocytosis and killing exhibited by P. gingivalis MSM-1 may result from alterations in polysaccharide-containing antigens.
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- Absolom D. R. The role of bacterial hydrophobicity in infection: bacterial adhesion and phagocytic ingestion. Can J Microbiol. 1988 Mar;34(3):287–298. doi: 10.1139/m88-054. [DOI] [PubMed] [Google Scholar]
- Altman L. C., Page R. C., Ebersole J. L., Vandesteen E. G. Assessment of host defenses and serum antibodies to suspected periodontal pathogens in patients with various types of periodontitis. J Periodontal Res. 1982 Sep;17(5):495–497. doi: 10.1111/j.1600-0765.1982.tb02037.x. [DOI] [PubMed] [Google Scholar]
- Anderson K. L., Salyers A. A. Genetic evidence that outer membrane binding of starch is required for starch utilization by Bacteroides thetaiotaomicron. J Bacteriol. 1989 Jun;171(6):3199–3204. doi: 10.1128/jb.171.6.3199-3204.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Collings S., Love D. N. Further studies on some physical and biochemical characteristics of asaccharolytic pigmented Bacteroides of feline origin. J Appl Bacteriol. 1992 Jun;72(6):529–535. doi: 10.1111/j.1365-2672.1992.tb01871.x. [DOI] [PubMed] [Google Scholar]
- Cutler C. W., Arnold R. R., Schenkein H. A. Inhibition of C3 and IgG proteolysis enhances phagocytosis of Porphyromonas gingivalis. J Immunol. 1993 Dec 15;151(12):7016–7029. [PubMed] [Google Scholar]
- Cutler C. W., Kalmar J. R., Arnold R. R. Antibody-dependent alternate pathway of complement activation in opsonophagocytosis of Porphyromonas gingivalis. Infect Immun. 1991 Jun;59(6):2105–2109. doi: 10.1128/iai.59.6.2105-2109.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cutler C. W., Kalmar J. R., Arnold R. R. Phagocytosis of virulent Porphyromonas gingivalis by human polymorphonuclear leukocytes requires specific immunoglobulin G. Infect Immun. 1991 Jun;59(6):2097–2104. doi: 10.1128/iai.59.6.2097-2104.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dyer D. W., Bilalis G., Michel J. H., Malek R. Conjugal transfer of plasmid and transposon DNA from Escherichia coli into Porphyromonas gingivalis. Biochem Biophys Res Commun. 1992 Jul 31;186(2):1012–1019. doi: 10.1016/0006-291x(92)90847-e. [DOI] [PubMed] [Google Scholar]
- Edwards M. S., Nicholson-Weller A., Baker C. J., Kasper D. L. The role of specific antibody in alternative complement pathway-mediated opsonophagocytosis of type III, group B Streptococcus. J Exp Med. 1980 May 1;151(5):1275–1287. doi: 10.1084/jem.151.5.1275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Edwards M. S., Wessels M. R., Baker C. J. Capsular polysaccharide regulates neutrophil complement receptor interactions with type III group B streptococci. Infect Immun. 1993 Jul;61(7):2866–2871. doi: 10.1128/iai.61.7.2866-2871.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Engels W., Endert J., Kamps M. A., van Boven C. P. Role of lipopolysaccharide in opsonization and phagocytosis of Pseudomonas aeruginosa. Infect Immun. 1985 Jul;49(1):182–189. doi: 10.1128/iai.49.1.182-189.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Genco C. A., Cutler C. W., Kapczynski D., Maloney K., Arnold R. R. A novel mouse model to study the virulence of and host response to Porphyromonas (Bacteroides) gingivalis. Infect Immun. 1991 Apr;59(4):1255–1263. doi: 10.1128/iai.59.4.1255-1263.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goldman R. C., Joiner K., Leive L. Serum-resistant mutants of Escherichia coli O111 contain increased lipopolysaccharide, lack an O antigen-containing capsule, and cover more of their lipid A core with O antigen. J Bacteriol. 1984 Sep;159(3):877–882. doi: 10.1128/jb.159.3.877-882.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gray P. W., Flaggs G., Leong S. R., Gumina R. J., Weiss J., Ooi C. E., Elsbach P. Cloning of the cDNA of a human neutrophil bactericidal protein. Structural and functional correlations. J Biol Chem. 1989 Jun 5;264(16):9505–9509. [PubMed] [Google Scholar]
- Guthrie E. P., Salyers A. A. Use of targeted insertional mutagenesis to determine whether chondroitin lyase II is essential for chondroitin sulfate utilization by Bacteroides thetaiotaomicron. J Bacteriol. 1986 Jun;166(3):966–971. doi: 10.1128/jb.166.3.966-971.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haapasalo M., Kerosuo E., Lounatmaa K. Hydrophobicities of human polymorphonuclear leukocytes and oral Bacteroides and Porphyromonas spp., Wolinella recta, and Eubacterium yurii with special reference to bacterial surface structures. Scand J Dent Res. 1990 Dec;98(6):472–481. doi: 10.1111/j.1600-0722.1990.tb01001.x. [DOI] [PubMed] [Google Scholar]
- Hoover C. I., Abarbarchuk E., Ng C. Y., Felton J. R. Transposition of Tn4351 in Porphyromonas gingivalis. Plasmid. 1992 May;27(3):246–250. doi: 10.1016/0147-619x(92)90028-9. [DOI] [PubMed] [Google Scholar]
- Horwitz M. A. Phagocytosis of microorganisms. Rev Infect Dis. 1982 Jan-Feb;4(1):104–123. doi: 10.1093/clinids/4.1.104. [DOI] [PubMed] [Google Scholar]
- Hwa V., Shoemaker N. B., Salyers A. A. Direct repeats flanking the Bacteroides transposon Tn4351 are insertion sequence elements. J Bacteriol. 1988 Jan;170(1):449–451. doi: 10.1128/jb.170.1.449-451.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Joiner K. A., Schmetz M. A., Goldman R. C., Leive L., Frank M. M. Mechanism of bacterial resistance to complement-mediated killing: inserted C5b-9 correlates with killing for Escherichia coli O111B4 varying in O-antigen capsule and O-polysaccharide coverage of lipid A core oligosaccharide. Infect Immun. 1984 Jul;45(1):113–117. doi: 10.1128/iai.45.1.113-117.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kalmar J. R., Arnold R. R., van Dyke T. E. Direct interaction of Actinobacillus actinomycetemcomitans with normal and defective (LJP) neutrophils. J Periodontal Res. 1987 May;22(3):179–181. doi: 10.1111/j.1600-0765.1987.tb01561.x. [DOI] [PubMed] [Google Scholar]
- 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]
- Mayrand D., Holt S. C. Biology of asaccharolytic black-pigmented Bacteroides species. Microbiol Rev. 1988 Mar;52(1):134–152. doi: 10.1128/mr.52.1.134-152.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Min H., Cowman M. K. Combined alcian blue and silver staining of glycosaminoglycans in polyacrylamide gels: application to electrophoretic analysis of molecular weight distribution. Anal Biochem. 1986 Jun;155(2):275–285. doi: 10.1016/0003-2697(86)90437-9. [DOI] [PubMed] [Google Scholar]
- Miyasaki K. T., Bodeau A. L. In vitro killing of oral Capnocytophaga by granule fractions of human neutrophils is associated with cathepsin G activity. J Clin Invest. 1991 May;87(5):1585–1593. doi: 10.1172/JCI115172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moore W. E. Microbiology of periodontal disease. J Periodontal Res. 1987 Sep;22(5):335–341. doi: 10.1111/j.1600-0765.1987.tb01595.x. [DOI] [PubMed] [Google Scholar]
- Odelson D. A., Rasmussen J. L., Smith C. J., Macrina F. L. Extrachromosomal systems and gene transmission in anaerobic bacteria. Plasmid. 1987 Mar;17(2):87–109. doi: 10.1016/0147-619x(87)90016-3. [DOI] [PubMed] [Google Scholar]
- Ooi C. E., Weiss J., Doerfler M. E., Elsbach P. Endotoxin-neutralizing properties of the 25 kD N-terminal fragment and a newly isolated 30 kD C-terminal fragment of the 55-60 kD bactericidal/permeability-increasing protein of human neutrophils. J Exp Med. 1991 Sep 1;174(3):649–655. doi: 10.1084/jem.174.3.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pantosti A., Tzianabos A. O., Reinap B. G., Onderdonk A. B., Kasper D. L. Bacteroides fragilis strains express multiple capsular polysaccharides. J Clin Microbiol. 1993 Jul;31(7):1850–1855. doi: 10.1128/jcm.31.7.1850-1855.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Podschun R., Penner I., Ullmann U. Interaction of Klebsiella capsule type 7 with human polymorphonuclear leucocytes. Microb Pathog. 1992 Nov;13(5):371–379. doi: 10.1016/0882-4010(92)90080-8. [DOI] [PubMed] [Google Scholar]
- Progulske-Fox A., Oberste A., Drummond C., McArthur W. P. Transfer of plasmid pE5-2 from Escherichia coli to Bacteroides gingivalis and B. intermedius. Oral Microbiol Immunol. 1989 Sep;4(3):132–134. doi: 10.1111/j.1399-302x.1989.tb00239.x. [DOI] [PubMed] [Google Scholar]
- Rubens C. E., Heggen L. M., Haft R. F., Wessels M. R. Identification of cpsD, a gene essential for type III capsule expression in group B streptococci. Mol Microbiol. 1993 May;8(5):843–855. doi: 10.1111/j.1365-2958.1993.tb01631.x. [DOI] [PubMed] [Google Scholar]
- Salyers A. A., Pajeau M. Competitiveness of different polysaccharide utilization mutants of Bacteroides thetaiotaomicron in the intestinal tracts of germfree mice. Appl Environ Microbiol. 1989 Oct;55(10):2572–2578. doi: 10.1128/aem.55.10.2572-2578.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salyers A. A., Pajeau M., McCarthy R. E. Importance of mucopolysaccharides as substrates for Bacteroides thetaiotaomicron growing in intestinal tracts of exgermfree mice. Appl Environ Microbiol. 1988 Aug;54(8):1970–1976. doi: 10.1128/aem.54.8.1970-1976.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salyers A. A., Shoemaker N. B., Guthrie E. P. Recent advances in Bacteroides genetics. Crit Rev Microbiol. 1987;14(1):49–71. doi: 10.3109/10408418709104435. [DOI] [PubMed] [Google Scholar]
- Sansano M., Jr, Reynard A. M., Cunningham R. K. Inhibition of serum bactericidal reaction by lipopolysaccharide. Infect Immun. 1985 Jun;48(3):759–762. doi: 10.1128/iai.48.3.759-762.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schenkein H. A. Failure of Bacteroides gingivalis W83 to accumulate bound C3 following opsonization with serum. J Periodontal Res. 1989 Jan;24(1):20–27. doi: 10.1111/j.1600-0765.1989.tb00853.x. [DOI] [PubMed] [Google Scholar]
- Schenkein H. A. The effect of periodontal proteolytic Bacteroides species on proteins of the human complement system. J Periodontal Res. 1988 May;23(3):187–192. doi: 10.1111/j.1600-0765.1988.tb01356.x. [DOI] [PubMed] [Google Scholar]
- Schifferle R. E., Reddy M. S., Zambon J. J., Genco R. J., Levine M. J. Characterization of a polysaccharide antigen from Bacteroides gingivalis. J Immunol. 1989 Nov 1;143(9):3035–3042. [PubMed] [Google Scholar]
- Schifferle R. E., Wilson M. E., Levine M. J., Genco R. J. Activation of serum complement by polysaccharide-containing antigens of Porphyromonas gingivalis. J Periodontal Res. 1993 Jul;28(4):248–254. doi: 10.1111/j.1600-0765.1993.tb02091.x. [DOI] [PubMed] [Google Scholar]
- Scribner D. J., Fahrney D. Neutrophil receptors for IgG and complement: their roles in the attachment and ingestion phases of phagocytosis. J Immunol. 1976 Apr;116(4):892–897. [PubMed] [Google Scholar]
- Shoemaker N. B., Getty C., Gardner J. F., Salyers A. A. Tn4351 transposes in Bacteroides spp. and mediates the integration of plasmid R751 into the Bacteroides chromosome. J Bacteriol. 1986 Mar;165(3):929–936. doi: 10.1128/jb.165.3.929-936.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Slots J., Genco R. J. Black-pigmented Bacteroides species, Capnocytophaga species, and Actinobacillus actinomycetemcomitans in human periodontal disease: virulence factors in colonization, survival, and tissue destruction. J Dent Res. 1984 Mar;63(3):412–421. doi: 10.1177/00220345840630031101. [DOI] [PubMed] [Google Scholar]
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
- Steadman R., Knowlden J., Lichodziejewska M., Williams J. The influence of net surface charge on the interaction of uropathogenic Escherichia coli with human neutrophils. Biochim Biophys Acta. 1990 Jun 12;1053(1):37–42. doi: 10.1016/0167-4889(90)90023-7. [DOI] [PubMed] [Google Scholar]
- Sundqvist G., Bloom G. D., Enberg K., Johansson E. Phagocytosis of Bacteroides melaninogenicus and Bacteroides gingivalis in vitro by human neutrophils. J Periodontal Res. 1982 Mar;17(2):113–121. doi: 10.1111/j.1600-0765.1982.tb01137.x. [DOI] [PubMed] [Google Scholar]
- Sundqvist G., Figdor D., Hänström L., Sörlin S., Sandström G. Phagocytosis and virulence of different strains of Porphyromonas gingivalis. Scand J Dent Res. 1991 Apr;99(2):117–129. doi: 10.1111/j.1600-0722.1991.tb01874.x. [DOI] [PubMed] [Google Scholar]
- Tabeta H., Kohno N., Kamei K., Honda A., Unno H., Nagao K., Yamaguchi T., Miyaji M. [The defensive role of human pulmonary alveolar macrophages and polymorphonuclear leukocytes against a strongly or weakly virulent strains of Cryptococcus neoformans]. Nihon Kyobu Shikkan Gakkai Zasshi. 1991 Sep;29(9):1174–1179. [PubMed] [Google Scholar]
- Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsai C. M., Frasch C. E. A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem. 1982 Jan 1;119(1):115–119. doi: 10.1016/0003-2697(82)90673-x. [DOI] [PubMed] [Google Scholar]
- Tzianabos A. O., Onderdonk A. B., Rosner B., Cisneros R. L., Kasper D. L. Structural features of polysaccharides that induce intra-abdominal abscesses. Science. 1993 Oct 15;262(5132):416–419. doi: 10.1126/science.8211161. [DOI] [PubMed] [Google Scholar]
- Van Dyke T. E., Horoszewicz H. U., Cianciola L. J., Genco R. J. Neutrophil chemotaxis dysfunction in human periodontitis. Infect Immun. 1980 Jan;27(1):124–132. doi: 10.1128/iai.27.1.124-132.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van Steenbergen T. J., Delemarre F. G., Namavar F., De Graaff J. Differences in virulence within the species Bacteroides gingivalis. Antonie Van Leeuwenhoek. 1987;53(4):233–244. doi: 10.1007/BF00393930. [DOI] [PubMed] [Google Scholar]
- Wilkinson B. J., Sisson S. P., Kim Y., Peterson P. K. Localization of the third component of complement on the cell wall of encapsulated Staphylococcus aureus M: implications for the mechanism of resistance to phagocytosis. Infect Immun. 1979 Dec;26(3):1159–1163. doi: 10.1128/iai.26.3.1159-1163.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Oss C. J., Absolom D. R., Neumann A. W. Interaction of phagocytes with other blood cells and with pathogenic and nonpathogenic microbes. Ann N Y Acad Sci. 1983;416:332–350. doi: 10.1111/j.1749-6632.1983.tb35197.x. [DOI] [PubMed] [Google Scholar]
- van Oss C. J. Phagocytosis as a surface phenomenon. Annu Rev Microbiol. 1978;32:19–39. doi: 10.1146/annurev.mi.32.100178.000315. [DOI] [PubMed] [Google Scholar]
- van Winkelhoff A. J., Appelmelk B. J., Kippuw N., de Graaff J. K-antigens in Porphyromonas gingivalis are associated with virulence. Oral Microbiol Immunol. 1993 Oct;8(5):259–265. doi: 10.1111/j.1399-302x.1993.tb00571.x. [DOI] [PubMed] [Google Scholar]