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抗菌药物诱导的口腔菌群失调会加重自然发生的牙槽骨丧失。

Antimicrobial-induced oral dysbiosis exacerbates naturally occurring alveolar bone loss.

机构信息

Department of Oral Health Sciences, College of Dental Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

Department of Stomatology-Division of Periodontics, College of Dental Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

出版信息

FASEB J. 2021 Nov;35(11):e22015. doi: 10.1096/fj.202101169R.

Abstract

Periodontitis-mediated alveolar bone loss is caused by dysbiotic shifts in the commensal oral microbiota that upregulate proinflammatory osteoimmune responses. The study purpose was to determine whether antimicrobial-induced disruption of the commensal microbiota has deleterious effects on alveolar bone. We administered an antibiotic cocktail, minocycline, or vehicle-control to sex-matched C57BL/6T mice from age 6- to 12 weeks. Antibiotic cocktail and minocycline had catabolic effects on alveolar bone in specific-pathogen-free (SPF) mice. We then administered minocycline or vehicle-control to male mice reared under SPF and germ-free conditions, and we subjected minocycline-treated SPF mice to chlorhexidine oral antiseptic rinses. Alveolar bone loss was greater in vehicle-treated SPF versus germ-free mice, demonstrating that the commensal microbiota drives naturally occurring alveolar bone loss. Minocycline- versus vehicle-treated germ-free mice had similar alveolar bone loss outcomes, implying that antimicrobial-driven alveolar bone loss is microbiota dependent. Minocycline induced phylum-level shifts in the oral bacteriome and exacerbated naturally occurring alveolar bone loss in SPF mice. Chlorhexidine further disrupted the oral bacteriome and worsened alveolar bone loss in minocycline-treated SPF mice, validating that antimicrobial-induced oral dysbiosis has deleterious effects on alveolar bone. Minocycline enhanced osteoclast size and interface with alveolar bone in SPF mice. Neutrophils and plasmacytoid dendritic cells were upregulated in cervical lymph nodes of minocycline-treated SPF mice. Paralleling the upregulated proinflammatory innate immune cells, minocycline therapy increased T 1 and T 17 cells that have known pro-osteoclastic actions in the alveolar bone. This report reveals that antimicrobial perturbation of the commensal microbiota induces a proinflammatory oral dysbiotic state that exacerbates naturally occurring alveolar bone loss.

摘要

牙周炎介导的牙槽骨丧失是由共生口腔微生物群落的失调引起的,这种失调会上调促炎的骨免疫反应。本研究旨在确定抗微生物药物引起的共生微生物群落的破坏是否对牙槽骨有不良影响。我们从 6 到 12 周龄开始,给雌雄匹配的 C57BL/6T 小鼠使用抗生素鸡尾酒、米诺环素或载体对照药物。抗生素鸡尾酒和米诺环素对无特定病原体(SPF)小鼠的牙槽骨有分解代谢作用。然后,我们给在 SPF 和无菌条件下饲养的雄性小鼠使用米诺环素或载体对照药物,并对接受米诺环素处理的 SPF 小鼠进行洗必泰口腔抗菌漱口水冲洗。与无菌小鼠相比,载体处理的 SPF 小鼠的牙槽骨丢失更多,表明共生微生物群驱动自然发生的牙槽骨丢失。米诺环素处理的无菌小鼠与载体处理的无菌小鼠的牙槽骨丢失结果相似,这意味着抗微生物驱动的牙槽骨丢失依赖于微生物群。米诺环素诱导口腔细菌群落的门水平转移,并加剧 SPF 小鼠自然发生的牙槽骨丢失。洗必泰进一步破坏了口腔细菌群落,并使接受米诺环素处理的 SPF 小鼠的牙槽骨丢失恶化,验证了抗微生物诱导的口腔失调对牙槽骨有不良影响。米诺环素增强了 SPF 小鼠破骨细胞的大小和与牙槽骨的界面。中性粒细胞和浆细胞样树突状细胞在接受米诺环素处理的 SPF 小鼠的颈淋巴结中上调。与上调的促炎先天免疫细胞平行的是,米诺环素治疗增加了 T1 和 T17 细胞,这些细胞在牙槽骨中具有已知的促破骨细胞作用。本报告揭示了抗微生物药物对共生微生物群落的干扰会诱导促炎的口腔失调状态,从而加剧自然发生的牙槽骨丧失。

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