Zebrafish as a new model to study effects of periodontal pathogens on cardiovascular diseases

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作者
Magdalena Widziolek
Tomasz K. Prajsnar
Simon Tazzyman
Graham P. Stafford
Jan Potempa
Craig Murdoch
机构
[1] Faculty of Biochemistry,Department of Microbiology
[2] Biophysics and Biotechnology,Department of Molecular Biology and Microbiology
[3] Jagiellonian University,Department of Infection
[4] The Batson Centre,Department of Oral Immunology and Infectious Diseases
[5] University of Sheffield,undefined
[6] The Krebs Institute,undefined
[7] University of Sheffield,undefined
[8] Immunity and Cardiovascular Disease,undefined
[9] University of Sheffield,undefined
[10] School of Clinical Dentistry,undefined
[11] University of Sheffield,undefined
[12] University of Louisville School of Dentistry,undefined
来源
Scientific Reports | / 6卷
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摘要
Porphyromonas gingivalis (Pg) is a keystone pathogen in the aetiology of chronic periodontitis. However, recent evidence suggests that the bacterium is also able to enter the bloodstream, interact with host cells and tissues, and ultimately contribute to the pathogenesis of cardiovascular disease (CVD). Here we established a novel zebrafish larvae systemic infection model showing that Pg rapidly adheres to and penetrates the zebrafish vascular endothelium causing a dose- and time-dependent mortality with associated development of pericardial oedemas and cardiac damage. The in vivo model was then used to probe the role of Pg expressed gingipain proteases using systemically delivered gingipain-deficient Pg mutants, which displayed significantly reduced zebrafish morbidity and mortality compared to wild-type bacteria. In addition, we used the zebrafish model to show efficacy of a gingipain inhibitor (KYT) on Pg-mediated systemic disease, suggesting its potential use therapeutically. Our data reveal the first real-time in vivo evidence of intracellular Pg within the endothelium of an infection model and establishes that gingipains are crucially linked to systemic disease and potentially contribute to CVD.
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