Porphyromonas gingivalis in Alzheimer’s disease brains: Evidence for disease causation and treatment with small-molecule inhibitors

Author/s: 
Dominy, Stephen S., Lynch, Casey, Ermini, Florian, Benedyk, Malgorzata, Marczyk, Agata, Konradi, Andrei, Nguyen, Mai, Haditsch, Ursula, Raha, Debasish, Griffin, Christina, Holsinger, Leslie J., Arastu-Kapur, Shirin, Kaba, Samer, Lee, Alexander, Ryder, Mark I., Potempa, Barbara, Mydel, Piotr, Hellvard, Annelie, Adamowicz, Karina, Hasturk, Hatice, Walker, Glenn D., Reynolds, Eric C., Faull, Richard L., Curtis, Maurice A., Dragunow, Mike, Potempa, Jan
Date Added: 
January 25, 2019
Journal/Publication: 
Science Advances
Publisher: 
American Association for the Advancement of Science
Publication Date: 
January 22, 2019
Issue: 
1
Volume: 
5
Type: 
Clinical Research Results
Format: 
Article
DOI (1): 
10.1126/sciadv.aau3333

RPR Commentary

This relatively new theory regarding the etiology of Alzheimer’s Disease seemed worth posting.  If nothing else, it is a reminder of how important oral health is to general health.

Abstract

Porphyromonas gingivalis, the keystone pathogen in chronic periodontitis, was identified in the brain of Alzheimer’s disease patients. Toxic proteases from the bacterium called gingipains were also identified in the brain of Alzheimer’s patients, and levels correlated with tau and ubiquitin pathology. Oral P. gingivalisinfection in mice resulted in brain colonization and increased production of Aβ1–42, a component of amyloid plaques. Further, gingipains were neurotoxic in vivo and in vitro, exerting detrimental effects on tau, a protein needed for normal neuronal function. To block this neurotoxicity, we designed and synthesized small-molecule inhibitors targeting gingipains. Gingipain inhibition reduced the bacterial load of an established P. gingivalis brain infection, blocked Aβ1–42production, reduced neuroinflammation, and rescued neurons in the hippocampus. These data suggest that gingipain inhibitors could be valuable for treating P. gingivalis brain colonization and neurodegeneration in Alzheimer’s disease.

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