Life below the gum line:: Pathogenic mechanisms of Porphyromonas gingivalis

被引:795
作者
Lamont, RJ
Jenkinson, HF
机构
[1] Univ Washington, Dept Oral Biol, Seattle, WA 98195 USA
[2] Univ Bristol, Dept Oral & Dent Sci, Bristol BS1 2LY, Avon, England
关键词
D O I
10.1128/MMBR.62.4.1244-1263.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porphyromonas gingivalis, a gram-negative anaerobe, is a major etiological agent in the initiation and progression of severe forms of periodontal disease. All opportunistic pathogen, P. gingivalis can also exist in commensal harmony with the host, with disease episodes ensuing from a shift in the ecological balance within the complex periodontal microenvironment. Colonization of the subgingival region is facilitated by the ability to adhere to available substrates such as absorbed salivary molecules, matrix proteins, epithelial cells, and bacteria that are already established as a biofilm on tooth and epithelial surfaces. Binding to all of these substrates may be mediated by various regions of P. gingivalis fimbrillin, the structural subunit of the major fimbriae. P. gingivalis is an asaccharolytic organism with a requirement for hemin (as a source of iron) and peptides for growth. At least three hemagglutinins and five proteinases are produced to satisfy these requirements. The hemagglutinin and proteinase genes contain extensive regions of highly conserved sequences, with posttranslational processing of proteinase gene products contributing to the formation of multimeric surface protein-adhesin complexes. Many of the virulence properties of P. gingivalis appear to be consequent to its adaptations to obtain hemin and peptides. Thus, hemagglutinins participate in adherence interactions with host cells. while proteinases contribute to inactivation of the effector molecules of the immune response and to tissue destruction. In addition to direct assault on the periodontal tissues, ;P, gingivalis can modulate eucaryotic cell signal transduction pathways, directing its uptake by gingival epithelial cells. Within this privileged site, P. gingivalis can replicate and impinge upon components of the innate host defense Although a variety of surface molecules stimulate production of cytokines and other participants in the immune response, P. gingivalis may also undertake a stealth role whereby pivotal immune mediators are selectively inactivated. In keeping with its strict metabolic requirements, regulation of gene expression in P. gingivalis can he controlled at the transcriptional level. Finally, although periodontal disease is localized to the tissues surrounding the tooth, evidence is accumulating that infection with P. gingivalis may predispose to more serious systemic conditions such as cardiovascular disease and to delivery of preterm infants.
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页码:1244 / +
页数:21
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共 285 条
  • [1] Modification of cystatin C activity by bacterial proteinases and neutrophil elastase in periodontitis
    Abrahamson, M
    Wikström, M
    Potempa, J
    Renvert, S
    Hall, A
    [J]. JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 1997, 50 (06): : 291 - 297
  • [2] The Tla protein of Porphyromonas gingivalis W50: a homolog of the RI protease precursor (PrpRI) is an outer membrane receptor required for growth on low levels of hemin
    AduseOpoku, J
    Slaney, JM
    Rangarajan, M
    Muir, J
    Young, KA
    Curtis, MA
    [J]. JOURNAL OF BACTERIOLOGY, 1997, 179 (15) : 4778 - 4788
  • [3] CHARACTERIZATION, GENETIC-ANALYSIS, AND EXPRESSION OF A PROTEASE ANTIGEN (PRPRI) OF PORPHYROMONAS-GINGIVALIS W50
    ADUSEOPOKU, J
    MUIR, J
    SLANEY, JM
    RANGARAJAN, M
    CURTIS, MA
    [J]. INFECTION AND IMMUNITY, 1995, 63 (12) : 4744 - 4754
  • [4] Natural variation within the principal arginine-specific protease gene, prpR1, of Porphyromonas gingivalis
    Allaker, RP
    AduseOpoku, J
    Batten, JE
    Curtis, MA
    [J]. ORAL MICROBIOLOGY AND IMMUNOLOGY, 1997, 12 (05): : 298 - 302
  • [5] Structural domains of Porphyromonas gingivalis recombinant fimbrillin that mediate binding to salivary proline-rich protein and statherin
    Amano, A
    Sharma, A
    Lee, JY
    Sojar, HT
    Raj, PA
    Genco, RJ
    [J]. INFECTION AND IMMUNITY, 1996, 64 (05) : 1631 - 1637
  • [6] EFFECTS OF TEMPERATURE STRESS ON EXPRESSION OF FIMBRIAE AND SUPEROXIDE-DISMUTASE BY PORPHYROMONAS-GINGIVALIS
    AMANO, A
    SHARMA, A
    SOJAR, HT
    KURAMITSU, HK
    GENCO, RJ
    [J]. INFECTION AND IMMUNITY, 1994, 62 (10) : 4682 - 4685
  • [7] Binding sites of salivary statherin for Porphyromonas gingivalis recombinant fimbrillin
    Amano, A
    Kataoka, K
    Raj, PA
    Genco, RJ
    Shizukuishi, S
    [J]. INFECTION AND IMMUNITY, 1996, 64 (10) : 4249 - 4254
  • [8] CHARACTERIZATION OF SUPEROXIDE DISMUTASES PURIFIED FROM EITHER ANAEROBICALLY MAINTAINED OR AERATED BACTEROIDES-GINGIVALIS
    AMANO, A
    SHIZUKUISHI, S
    TAMAGAWA, H
    IWAKURA, K
    TSUNASAWA, S
    TSUNEMITSU, A
    [J]. JOURNAL OF BACTERIOLOGY, 1990, 172 (03) : 1457 - 1463
  • [9] Porphyromonas gingivalis fimbriae mediate coaggregation with Streptococcus oralis through specific domains
    Amano, A
    Fujiwara, T
    Nagata, H
    Kuboniwa, M
    Sharma, A
    Sojar, HT
    Genco, RJ
    Hamada, S
    Shizukuishi, S
    [J]. JOURNAL OF DENTAL RESEARCH, 1997, 76 (04) : 852 - 857
  • [10] THE PRIMARY STRUCTURE OF SUPEROXIDE-DISMUTASE PURIFIED FROM ANAEROBICALLY MAINTAINED BACTEROIDES-GINGIVALIS
    AMANO, A
    SHIZUKUISHI, S
    TSUNEMITSU, A
    MAEKAWA, K
    TSUNASAWA, S
    [J]. FEBS LETTERS, 1990, 272 (1-2) : 217 - 220