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Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome
Dysbiosis of the oral microbiome mediates chronic periodontal disease. Realignment of microbial dysbiosis towards health may prevent disease. Treatment with antibiotics and probiotics can modulate the microbial, immunological, and clinical landscape of periodontal disease with some success. Antibact...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174264/ https://www.ncbi.nlm.nih.gov/pubmed/35672331 http://dx.doi.org/10.1038/s41522-022-00307-x |
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author | Gao, Li Kuraji, Ryutaro Zhang, Martin Jinye Martinez, April Radaic, Allan Kamarajan, Pachiyappan Le, Charles Zhan, Ling Ye, Changchang Rangé, Hélène Sailani, M. Reza Kapila, Yvonne L. |
author_facet | Gao, Li Kuraji, Ryutaro Zhang, Martin Jinye Martinez, April Radaic, Allan Kamarajan, Pachiyappan Le, Charles Zhan, Ling Ye, Changchang Rangé, Hélène Sailani, M. Reza Kapila, Yvonne L. |
author_sort | Gao, Li |
collection | PubMed |
description | Dysbiosis of the oral microbiome mediates chronic periodontal disease. Realignment of microbial dysbiosis towards health may prevent disease. Treatment with antibiotics and probiotics can modulate the microbial, immunological, and clinical landscape of periodontal disease with some success. Antibacterial peptides or bacteriocins, such as nisin, and a nisin-producing probiotic, Lactococcus lactis, have not been examined in this context, yet warrant examination because of their biomedical benefits in eradicating biofilms and pathogenic bacteria, modulating immune mechanisms, and their safety profile in humans. This study’s goal was to examine the potential for nisin and a nisin-producing probiotic to abrogate periodontal bone loss, the host inflammatory response, and changes in oral microbiome composition in a polymicrobial mouse model of periodontal disease. Nisin and a nisin-producing Lactococcus lactis probiotic significantly decreased the levels of several periodontal pathogens, alveolar bone loss, and the oral and systemic inflammatory host response. Surprisingly, nisin and/or the nisin-producing L. lactis probiotic enhanced the population of fibroblasts and osteoblasts despite the polymicrobial infection. Nisin mediated human periodontal ligament cell proliferation dose-dependently by increasing the proliferation marker, Ki-67. Nisin and probiotic treatment significantly shifted the oral microbiome towards the healthy control state; health was associated with Proteobacteria, whereas 3 retroviruses were associated with disease. Disease-associated microbial species were correlated with IL-6 levels. Nisin or nisin-producing probiotic’s ability to shift the oral microbiome towards health, mitigate periodontal destruction and the host immune response, and promote a novel proliferative phenotype in reparative connective tissue cells, addresses key aspects of the pathogenesis of periodontal disease and reveals a new biomedical application for nisin in treatment of periodontitis and reparative medicine. |
format | Online Article Text |
id | pubmed-9174264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91742642022-06-09 Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome Gao, Li Kuraji, Ryutaro Zhang, Martin Jinye Martinez, April Radaic, Allan Kamarajan, Pachiyappan Le, Charles Zhan, Ling Ye, Changchang Rangé, Hélène Sailani, M. Reza Kapila, Yvonne L. NPJ Biofilms Microbiomes Article Dysbiosis of the oral microbiome mediates chronic periodontal disease. Realignment of microbial dysbiosis towards health may prevent disease. Treatment with antibiotics and probiotics can modulate the microbial, immunological, and clinical landscape of periodontal disease with some success. Antibacterial peptides or bacteriocins, such as nisin, and a nisin-producing probiotic, Lactococcus lactis, have not been examined in this context, yet warrant examination because of their biomedical benefits in eradicating biofilms and pathogenic bacteria, modulating immune mechanisms, and their safety profile in humans. This study’s goal was to examine the potential for nisin and a nisin-producing probiotic to abrogate periodontal bone loss, the host inflammatory response, and changes in oral microbiome composition in a polymicrobial mouse model of periodontal disease. Nisin and a nisin-producing Lactococcus lactis probiotic significantly decreased the levels of several periodontal pathogens, alveolar bone loss, and the oral and systemic inflammatory host response. Surprisingly, nisin and/or the nisin-producing L. lactis probiotic enhanced the population of fibroblasts and osteoblasts despite the polymicrobial infection. Nisin mediated human periodontal ligament cell proliferation dose-dependently by increasing the proliferation marker, Ki-67. Nisin and probiotic treatment significantly shifted the oral microbiome towards the healthy control state; health was associated with Proteobacteria, whereas 3 retroviruses were associated with disease. Disease-associated microbial species were correlated with IL-6 levels. Nisin or nisin-producing probiotic’s ability to shift the oral microbiome towards health, mitigate periodontal destruction and the host immune response, and promote a novel proliferative phenotype in reparative connective tissue cells, addresses key aspects of the pathogenesis of periodontal disease and reveals a new biomedical application for nisin in treatment of periodontitis and reparative medicine. Nature Publishing Group UK 2022-06-07 /pmc/articles/PMC9174264/ /pubmed/35672331 http://dx.doi.org/10.1038/s41522-022-00307-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gao, Li Kuraji, Ryutaro Zhang, Martin Jinye Martinez, April Radaic, Allan Kamarajan, Pachiyappan Le, Charles Zhan, Ling Ye, Changchang Rangé, Hélène Sailani, M. Reza Kapila, Yvonne L. Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title | Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title_full | Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title_fullStr | Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title_full_unstemmed | Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title_short | Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
title_sort | nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174264/ https://www.ncbi.nlm.nih.gov/pubmed/35672331 http://dx.doi.org/10.1038/s41522-022-00307-x |
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