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Nisin lantibiotic prevents NAFLD liver steatosis and mitochondrial oxidative stress following periodontal disease by abrogating oral, gut and liver dysbiosis.
Kuraji, Ryutaro; Ye, Changchang; Zhao, Chuanjiang; Gao, Li; Martinez, April; Miyashita, Yukihiro; Radaic, Allan; Kamarajan, Pachiyappan; Le, Charles; Zhan, Ling; Range, Helene; Sunohara, Masataka; Numabe, Yukihiro; Kapila, Yvonne L.
Affiliation
  • Kuraji R; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Ye C; Department of Periodontology, The Nippon Dental University School of Life Dentistry at Tokyo, Tokyo, Japan.
  • Zhao C; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Gao L; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Periodontology, West China School of Stomatology, Sichuan University, Chengdu, China.
  • Martinez A; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Miyashita Y; Department of Periodontology, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
  • Radaic A; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Kamarajan P; Department of Periodontology, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
  • Le C; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Zhan L; Department of Periodontology, The Nippon Dental University School of Life Dentistry at Tokyo, Tokyo, Japan.
  • Range H; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Sunohara M; Sections of Biosystems and Function and Periodontics, School of Dentistry, University of California Los Angeles, Los Angeles, CA, USA.
  • Numabe Y; Orofacial Sciences Department, School of Dentistry, University of California, San Francisco, San Francisco, CA, USA.
  • Kapila YL; Sections of Biosystems and Function and Periodontics, School of Dentistry, University of California Los Angeles, Los Angeles, CA, USA.
NPJ Biofilms Microbiomes ; 10(1): 3, 2024 Jan 17.
Article in En | MEDLINE | ID: mdl-38233485
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Periodontal Diseases / Bacteriocins / Non-alcoholic Fatty Liver Disease / Nisin Limits: Animals / Humans Language: En Journal: NPJ Biofilms Microbiomes Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Periodontal Diseases / Bacteriocins / Non-alcoholic Fatty Liver Disease / Nisin Limits: Animals / Humans Language: En Journal: NPJ Biofilms Microbiomes Year: 2024 Document type: Article Affiliation country: Estados Unidos
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