IMR Press / FBL / Volume 12 / Issue 13 / DOI: 10.2741/2428

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Open Access Article

A role for gingipains in cellular responses and bacterial survival in Porphyromonas gingivalis-infected cells

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1 Department of Pharmacology, Graduate School of Dental Science, Kyushu University, Fukuoka, 812-8582, Japan
Academic Editor:George Hajishengallis
Front. Biosci. (Landmark Ed) 2007, 12(13), 4800–4809; https://doi.org/10.2741/2428
Published: 1 September 2007
Abstract

Porphyromonas gingivalis is one of the primary etiologic agents of adult periodontitis and is known to produce a unique class of cysteine proteinases, termed gingipains. They consist of Arg-gingipain (Rgp) and Lys-gingipain (Kgp) and exist in the cell-associated and secreted forms. In the current review, we summarize recent knowledge on the pathophysiological role of gingipains in the virulence of P. gingivalis including host cell responses to bacterial infection and its evasion from host defense mechanisms. Studies with various P. gingivalis mutants deficient in Rgp- and/or Kgp-encoding genes and proteinase inhibitors specific for each enzyme have demonstrated that both enzymes play a substantial role in disruption of host defense mechanisms by the bacterium and its survival in vivo. Gingipains are also important in the bacterium-mediated host cell responses and the subsequent intracellular signaling in the infected cells. P. gingivalis can evade the autophagic pathway and instead directly traffic to the endocytic pathway to lysosomes in the infected cells. In addition, gingipains play an important role in acquiring resistance against destruction of the bacterium in the lysosomal system. Furthermore, a major form of the cell-associated gingipain complex composed of the catalytic domains of both enzymes, their adhesin domains, phospholipids, and lipopolysaccharide has recently been isolated and shown to contribute the bacterial evasion of host defense mechanisms and the host tissue breakdown.

Keywords
Autophagy
Arg-Gingipain
Host Defense
Lipopolysaccharide
Lys-Gingipain
Periodontitis
Porphyromonas gingivalis
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