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Nisin probiotic prevents inflammatory bone loss while promoting reparative proliferation and a healthy microbiome

乳酸链球菌素 益生菌 乳酸乳球菌 失调 微生物学 微生物群 生物 免疫学 免疫系统 背景(考古学) 抗菌剂 肠道菌群 细菌 生物信息学 乳酸 古生物学 遗传学
作者
Li Gao,Ryutaro Kuraji,Martin Jinye Zhang,April Martínez,Allan Radaic,Pachiyappan Kamarajan,Charles Le,Ling Zhan,Changchang Ye,Hélène Rangé,M. Reza Sailani,Yvonne L. Kapila
出处
期刊:npj biofilms and microbiomes [Nature Portfolio]
卷期号:8 (1) 被引量:24
标识
DOI:10.1038/s41522-022-00307-x
摘要

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.
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