co-incubation enhances virulence and increases migration of infected human oral keratinocytes.

J Oral Microbiol

Cellular Communication Laboratory, Center for Studies on Exercise, Metabolism and Cancer (CEMC), Advanced Center for Chronic Diseases (Accdis), Faculty of Medicine, Universidad de Chile, Santiago, Chile.

Published: August 2022

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

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

Results: Pre-incubation of with enhanced biofilm formation, bacterial internalization into OKs and hemagglutination. Infection with pre-incubated 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 no longer stimulated OK migration.

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

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377229PMC
http://dx.doi.org/10.1080/20002297.2022.2107691DOI Listing

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