Fusobacterium spp. target human CEACAM1 via the trimeric autotransporter adhesin CbpF

被引:36
作者
Brewer, Matthew L. [1 ]
Dymock, David [2 ]
Brady, R. Leo [1 ]
Singer, Bernhard B. [3 ]
Virji, Mumtaz [4 ]
Hill, Darryl J. [4 ]
机构
[1] Univ Bristol, Sch Biochem, Bristol, Avon, England
[2] Univ Bristol, Sch Oral & Dent Sci, Bristol, Avon, England
[3] Univ Klinikum Essen, Inst Anat, Essen, Germany
[4] Univ Bristol, Sch Cellular & Mol Med, Bristol, Avon, England
来源
JOURNAL OF ORAL MICROBIOLOGY | 2019年 / 11卷 / 01期
基金
英国生物技术与生命科学研究理事会;
关键词
Fusobacterium; CEACAM1; CEA; host-pathogen interaction; adhesion; binding; trimeric autotransporter adhesin; TAA; Type V secretion; Fusobacterium nucleatum; OUTER-MEMBRANE PROTEIN; CARCINOEMBRYONIC ANTIGEN FAMILY; MORAXELLA-CATARRHALIS; NEISSERIA-GONORRHOEAE; EPITHELIAL-CELLS; N-DOMAIN; CRITICAL DETERMINANTS; OPA PROTEINS; CEA; NUCLEATUM;
D O I
10.1080/20002297.2018.1565043
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Neisseria meningitidis, Haemophilus influenzae, and Moraxella catarrhalis are pathogenic bacteria adapted to reside on human respiratory mucosal epithelia. One common feature of these species is their ability to target members of the carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family, especially CEACAM1, which is achieved via structurally distinct ligands expressed by each species. Beside respiratory epithelial cells, cells at the dentogingival junction express high levels of CEACAM1. It is possible that bacterial species resident within the oral cavity also utilise CEACAM1 for colonisation and invasion of gingival tissues. From a screen of 59 isolates from the human oral cavity representing 49 bacterial species, we identified strains from Fusobacterium bound to CEACAM1. Of the Fusobacterium species tested, the CEACAM1-binding property was exhibited by F. nucleatum (Fn) and F. vincentii (Fv) but not F. polymorphum (Fp) or F. animalis (Fa) strains tested. These studies identified that CEACAM adhesion was mediated using a trimeric autotransporter adhesin (TAA) for which no function has thus far been defined. We therefore propose the name CEACAM binding protein of Fusobacterium (CbpF). CbpF was identified to be present in the majority of unspeciated Fusobacterium isolates confirming a subset of Fusobacterium spp. are able to target human CEACAM1.
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页数:16
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