Abstract

Oral microbiome dysbiosis mediates chronic periodontal disease, gut microbial dysbiosis, and mucosal barrier disfunction that leads to steatohepatitis via the enterohepatic circulation. Improving this dysbiosis towards health may improve liver disease. Treatment with antibiotics and probiotics have been used to modulate the microbial, immunological, and clinical landscape of periodontal disease with some success. The aim of the present investigation was to evaluate the potential for nisin, an antimicrobial peptide produced by Lactococcus lactis, to counteract the periodontitis-associated gut dysbiosis and to modulate the glycolipid-metabolism and inflammation in the liver. Periodontal pathogens, namely Porphyromonas gingivalis, Treponema denticola, Tannerella forsythia and Fusobacterium nucleatum, were administrated topically onto the oral cavity to establish polymicrobial periodontal disease in mice. In the context of disease, nisin treatment significantly shifted the microbiome towards a new composition, commensurate with health while preventing the harmful inflammation in the small intestine concomitant with decreased villi structural integrity, and heightened hepatic exposure to bacteria and lipid and malondialdehyde accumulation in the liver. Validation with RNA Seq analyses, confirmed the significant infection-related alteration of several genes involved in mitochondrial dysregulation, oxidative phosphorylation, and metal/iron binding and their restitution following nisin treatment. In support of these in vivo findings indicating that periodontopathogens induce gastrointestinal and liver distant organ lesions, human autopsy specimens demonstrated a correlation between tooth loss and severity of liver disease. Nisin’s ability to shift the gut and liver microbiome towards a new state commensurate with health while mitigating enteritis, represents a novel approach to treating NAFLD-steatohepatitis-associated periodontal disease.

Details

Title
Nisin lantibiotic prevents NAFLD liver steatosis and mitochondrial oxidative stress following periodontal disease by abrogating oral, gut and liver dysbiosis
Author
Kuraji, Ryutaro 1   VIAFID ORCID Logo  ; Ye, Changchang 2   VIAFID ORCID Logo  ; Zhao, Chuanjiang 3 ; Gao, Li 3   VIAFID ORCID Logo  ; Martinez, April 4   VIAFID ORCID Logo  ; Miyashita, Yukihiro 5   VIAFID ORCID Logo  ; Radaic, Allan 6   VIAFID ORCID Logo  ; Kamarajan, Pachiyappan 6 ; Le, Charles 4 ; Zhan, Ling 4 ; Range, Helene 7 ; Sunohara, Masataka 8   VIAFID ORCID Logo  ; Numabe, Yukihiro 5   VIAFID ORCID Logo  ; Kapila, Yvonne L. 6   VIAFID ORCID Logo 

 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); The Nippon Dental University School of Life Dentistry at Tokyo, Department of Periodontology, Tokyo, Japan (GRID:grid.412196.9) (ISNI:0000 0001 2293 6406) 
 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); National Clinical Research Center for Oral Diseases, Department of Periodontology, West China School of Stomatology, Sichuan University, State Key Laboratory of Oral Diseases, Chengdu, China (GRID:grid.13291.38) (ISNI:0000 0001 0807 1581) 
 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Department of Periodontology, Guangzhou, China (GRID:grid.12981.33) (ISNI:0000 0001 2360 039X) 
 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811) 
 The Nippon Dental University School of Life Dentistry at Tokyo, Department of Periodontology, Tokyo, Japan (GRID:grid.412196.9) (ISNI:0000 0001 2293 6406) 
 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); School of Dentistry, University of California Los Angeles, Sections of Biosystems and Function and Periodontics, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0001 2167 8097) 
 School of Dentistry, University of California, San Francisco, Orofacial Sciences Department, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); University of Rennes, UFR of Odontology; Service d’Odontologie, CHU de Rennes, Department of Periodontology, Rennes, France (GRID:grid.411154.4) (ISNI:0000 0001 2175 0984); INSERM CHU Rennes, Institut NUMECAN (Nutrition Metabolisms and Cancer); CIC 1414, Rennes, France (GRID:grid.411154.4) 
 The Nippon Dental University School of Life Dentistry at Tokyo, Department of Anatomy, Tokyo, Japan (GRID:grid.412196.9) (ISNI:0000 0001 2293 6406) 
Pages
3
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20555008
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2915818800
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.