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    題名: Halitosis vaccines targeting FomA, a biofilm-bridging protein of fusobacteria nucleatum
    作者: 黃俊銘;Liu, P.-F.;Huang, I.-F.;Shu, C.-W.;Huang, C.-M.
    貢獻者: 生醫理工學院生醫科學與工程學系
    關鍵詞: Bacterial Outer Membrane Proteins - immunology;Bacterial Outer Membrane Proteins - metabolism;Bacterial Vaccines - immunology;Biofilms;Fusobacterium nucleatum;Fusobacterium nucleatum - immunology;Fusobacterium nucleatum - metabolism;Halitosis - microbiology;Halitosis - prevention & control;Humans;Mouth - microbiology;Porphyromonas gingivalis;Sulfur Compounds - metabolism
    日期: 2013-09-01
    上傳時間: 2026-04-23 11:16:14 (UTC+8)
    出版者: Bentham Science Publishers B.V.;Netherlands: Bentham Science Publishers Ltd
    摘要: 摘要: Halitosis (bad breath) is estimated to influence more than half of the world's population with varying degree of intensity. More than 85% of halitosis originates from oral bacterial infections. Foul-smelling breath mainly results from bacterial production of volatile sulfur compounds (VSCs) such as hydrogen sulfide and methyl mercaptan. To date, major treatments for elimination of oral malodor include periodontal therapy combined with antibiotics or antimicrobial agents, and mechanical approaches including tooth and tongue cleaning. These treatments may transiently reduce VSCs but carry risks of generating toxicity, increasing resistant strains and misbalancing the resident human flora. Therefore, there is a need to develop alternative therapeutic modalities for halitosis. Plaque biofilms are the principal source for generating VSCs which are originally metabolized from amino acids during co-aggregation of oral bacteria. Blocking the bacterial coaggregation, therefore, may prevent various biofilm-associated oral diseases such as periodontitis and halitosis. Fusobacterium nucleatum (F. nucleatum), a Gram-negative anaerobe oral bacterium, is a main bacterial strain related to halitosis. Aggregation of F. nucleatum with other bacteria to form plaque biofilms in oral cavity causes bad breath. FomA, the major outer membrane protein of F. nucleatum, recruits other oral pathogenic bacteria such as Porphyromonas gingivalis (P. gingivalis) in the periodontal pockets. A halitosis vaccine targeting F. bacterium FomA significantly abrogates the enhancement of bacterial co-aggregation, biofilms, production of VSCs, and gum inflammation mediated by an inter-species interaction of F. nucleatum with P. gingivalis, which suggests FomA of F. nucleatum to be a potential target for development of vaccines or drugs against bacterial biofilm formation and its associated pathogenicities.
    其他題名: CMM
    出版者: Netherlands: Bentham Science Publishers Ltd
    出版日期: 2013-09-01
    出處: Current Molecular Medicine, 2013-09, Vol.13 (8), p.1358-1367
    識別號: ISSN: 1566-5240
    識別號: ISSN: 1875-5666
    識別號: EISSN: 1875-5666
    識別號: DOI: 10.2174/15665240113139990063
    識別號: PMID: 23865430
    顯示於類別:[生醫科學與工程學系] 期刊論文

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