Low-Abundance Biofilm Species Orchestrates Inflammatory Periodontal Disease through the Commensal Microbiota and Complement

被引:854
作者
Hajishengallis, George [1 ,2 ]
Liang, Shuang [2 ]
Payne, Mark A. [3 ]
Hashim, Ahmed [3 ]
Jotwani, Ravi [2 ]
Eskan, Mehmet A. [1 ,2 ]
McIntosh, Megan L. [1 ,2 ]
Alsam, Asil [3 ]
Kirkwood, Keith L. [4 ]
Lambris, John D. [5 ]
Darveau, Richard P. [6 ]
Curtis, Michael A. [3 ]
机构
[1] Univ Louisville, Sch Med, Dept Microbiol & Immunol, Louisville, KY 40292 USA
[2] Univ Louisville, Sch Dent, Ctr Oral Hlth & Syst Dis, Louisville, KY 40292 USA
[3] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizzrd Inst, Ctr Immunol & Infect Dis, London E1 2AT, England
[4] Med Univ S Carolina, Coll Dent Med, Ctr Oral Hlth Res, Dept Craniofacial Biol, Charleston, SC 29425 USA
[5] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[6] Univ Washington, Sch Dent, Dept Periodont, Seattle, WA 98195 USA
基金
英国医学研究理事会;
关键词
ALVEOLAR BONE LOSS; PORPHYROMONAS-GINGIVALIS; INTESTINAL MICROBIOTA; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS; BACTEROIDES-GINGIVALIS; PREVOTELLA-INTERMEDIA; RECEPTOR CROSSTALK; IMMUNE-RESPONSE; HOMEOSTASIS; COLITIS;
D O I
10.1016/j.chom.2011.10.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porphyromonas gingivalis is a low-abundance oral anaerobic bacterium implicated in periodontitis, a polymicrobial inflammatory disease, and the associated systemic conditions. However, the mechanism by which P. gingivalis contributes to inflammation and disease has remained elusive. Here we show that P. gingivalis, at very low colonization levels, triggers changes to the amount and composition of the oral commensal microbiota leading to inflammatory periodontal bone loss. The commensal microbiota and complement were both required for P. gin givalis-induced bone loss, as germ-free mice or conventionally raised C3a and C5a receptor-deficient mice did not develop bone loss after inoculation with P. gingivalis. These findings demonstrate that a single, low-abundance species can disrupt host-microbial homeostasis to cause inflammatory disease. The identification and targeting of similar low-abundance pathogens with community-wide impact may be important for treating inflammatory diseases of polymicrobial etiology.
引用
收藏
页码:497 / 506
页数:10
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