Porphyromonas gingivalis-Helicobacter pylori co-incubation enhances Porphyromonas gingivalis virulence and increases migration of infected human oral keratinocytes

J Oral Microbiol. 2022 Aug 12;14(1):2107691. doi: 10.1080/20002297.2022.2107691. eCollection 2022.

Abstract

Background: Porphyromonas gingivalis is part of the subgingival biofilm and a keystone species in the development of periodontitis. Interactions between P.gingivalis and other bacteria in biofilms have been shown to affect bacterial virulence. Helicobacter pylori also inhabits the subgingival biofilm, but the consequences of interactions there with P.gingivalis remain unknown. Here, we investigated how the pre-incubation of P.gingivalis with H.pylori affects P.gingivalis virulence.

Methods: We assayed P.gingivalis internalization by oral keratinocytes (OKs), hemagglutination and biofilm formation to identify alterations in virulence after pre-incubation with H. pylori. Also, we evaluated viability and migration of OKs infected with P. gingivalis, as well as the role of toll-like receptor 4 (TLR4). In addition, we quantified the mRNA of genes associated with P.gingivalis virulence.

Results: Pre-incubation of P.gingivalis with H.pylori enhanced P.gingivalis biofilm formation, bacterial internalization into OKs and hemagglutination. Infection with pre-incubated P.gingivalis increased OK migration in a manner dependent on the O-antigen and linked to increased expression of the gingipain RgpB. Also, OK TLR4 participates in these events, because upon TLR4 knock-down, pre-incubated P.gingivalis no longer stimulated OK migration.

Discussion: We provide here for the first time insight to the consequences of direct interaction between P.gingivalis and H.pylori. In doing so, we shed light on the mechanism by which H. pylori presence in the oral cavity increases the severity or progression of periodontitis.

Keywords: Helicobacter pylori; O-antigen ligase; Porphyromonas gingivalis; gingipains; hemagglutinins; oral keratinocytes migration; toll-like receptor 4.

Grants and funding

This work was supported by Fondo de Investigación Avanzada en Áreas Prioritarias (FONDAP) Grant [15130011 (AFGQ, DB)], Fondo de investigación en Ciencia y Tecnología (FONDECYT) Grant [1170925, 1210644 (AFGQ) and 1200877 (DB)] and Fondo para la Investigación en Odontología (FIOUCh) Grant [17/020 (DB)] and (ANID) fellowships for PhD students (CS) [2016-21160942]; Agencia Nacional de Investigación y Desarrollo.