Abstract
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.
Original language | English |
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Article number | 1565043 |
Number of pages | 16 |
Journal | Journal of Oral Microbiology |
Volume | 11 |
Issue number | 1 |
Early online date | 24 Jan 2019 |
DOIs | |
Publication status | Published - Jan 2019 |
Keywords
- fusobacterium
- CEACAM1
- CEA
- Host-pathogen interaction
- adhesion
- binding
- trimeric autotransporter adhesin
- TAA
- Type V secretion
- Fusobacterium nucleatum
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Dive into the research topics of 'Fusobacterium spp. target human CEACAM1 via the trimeric autotransporter adhesin CbpF'. Together they form a unique fingerprint.Student theses
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Investigating Fusobacterium pathogenesis using molecular and genomic methods to inform vaccine design
Brewer, M. L. (Author), Hill, D. (Supervisor) & Brady, L. (Supervisor), 1 Oct 2019Student thesis: Doctoral Thesis › Doctor of Philosophy (PhD)
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Profiles
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Professor Darryl J Hill
- School of Cellular and Molecular Medicine - Professor of Infectious Diseases, Head of School
- Infection and Immunity
Person: Academic , Member, Professional and Administrative