Topical application of <i>Porphyromonas gingivalis</i> into the gingival pocket in mice leads to chronic‑active infection, periodontitis and systemic inflammation
Sharon Kim, Yasuhiko Bando, Chungyu Chang, Jeonga Kwon, Berta Tarverti, Doo-Hyun Kim, Sung Lee, Hung Ton‐That, Reuben Kim, Peter L. Nara, No-Hee Park
Abstract
<em>Porphyromonas gingivalis</em> (<em>Pg</em>), one of the ‘red‑complex’ perio‑pathogens known to play a critical role in the development of periodontitis, has been used in various animal models to mimic human bacteria‑induced periodontitis. In order to achieve a more realistic animal model of human <em>Pg</em> infection, the present study investigated whether repeated small‑volume topical applications of <em>Pg</em> directly into the gingival pocket can induce local infection, including periodontitis and systemic vascular inflammation in wild‑type mice. Freshly cultured <em>Pg</em> was topically applied directly into the gingival pocket of the second molars for 5 weeks (3 times/week). After the final application, the mice were left in cages for 4 or 8 weeks and sacrificed. The status of <em>Pg</em> colony formation in the pocket, gingival inflammation, alveolar bone loss, the expression levels of pro‑inflammatory cytokines in the serum and aorta, the presence of anti‑<em>Pg</em> lipopolysaccharide (LPS) and gingipain (Kpg and RgpB) antibodies in the serum, as well as the accumulation of <em>Pg</em> LPS and gingipain aggregates in the gingiva and arterial wall were evaluated. The topical application of <em>Pg</em> into the gingival pocket induced the following local and systemic pathohistological changes in mice when examined at 4 or 8 weeks after the final topical <em>Pg</em> application: <em>Pg</em> colonization in the majority of gingival pockets; increased gingival pocket depths; gingival inflammation indicated by the increased expression of TNF‑α, IL‑6 and IL‑1β; significant loss of alveolar bone at the sites of topical <em>Pg</em> application; and increased levels of pro‑inflammatory cytokines, such as TNF‑α, IL‑1β, IL‑17, IL‑13, KC and IFN‑γ in the serum in comparison to those from mice receiving PBS. In addition, the <em>Pg</em> application/colonization model induced anti‑<em>Pg</em> LPS and gingipain antibodies in serum, as well as the accumulation of <em>Pg</em> LPS and gingipain aggregates in the gingivae and arterial walls. To the best of our knowledge, this mouse model represents the first example of creating a more sustained local infection in the gingival tissues of wild‑type mice and may prove to be useful for the investigation of the more natural and complete pathogenesis of the bacteria in the development of local oral and systemic diseases, such as atherosclerosis. It may also be useful for the determination of a treatment/prevention/efficacy model associated with <em>Pg</em>‑induced colonization periodontitis in mice.