Abstract |
Streptococcus agalactiae (group B Streptococcus, GBS) is the predominant cause of early-onset infectious disease in neonates and is responsible for life-threatening infections in elderly and immunocompromised individuals. Clinical manifestations of GBS infection include sepsis, pneumonia, and meningitis. Here, we describe BspA, a deviant antigen I/II family polypeptide that confers adhesive properties linked to pathogenesis in GBS. Heterologous expression of BspA on the surface of the non-adherent bacterium Lactococcus lactis confers adherence to scavenger receptor gp340, human vaginal epithelium, and to the fungus Candida albicans Complementary crystallographic and biophysical characterization of BspA reveal a novel β-sandwich adhesion domain and unique asparagine-dependent super-helical stalk. Collectively, these findings establish a new bacterial adhesin structure that has in effect been hijacked by a pathogenic Streptococcus species to provide competitive advantage in human mucosal infections.
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Authors | Sara Rego, Timothy J Heal, Grace R Pidwill, Marisa Till, Alice Robson, Richard J Lamont, Richard B Sessions, Howard F Jenkinson, Paul R Race, Angela H Nobbs |
Journal | The Journal of biological chemistry
(J Biol Chem)
Vol. 291
Issue 31
Pg. 15985-6000
(07 29 2016)
ISSN: 1083-351X [Electronic] United States |
PMID | 27311712
(Publication Type: Journal Article)
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Copyright | © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. |
Chemical References |
- Adhesins, Bacterial
- Bacterial Proteins
- BspA protein, bacteria
- Membrane Proteins
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Topics |
- Adhesins, Bacterial
(chemistry, genetics, metabolism)
- Bacterial Adhesion
(physiology)
- Bacterial Proteins
(chemistry, genetics, metabolism)
- Candida albicans
(genetics, metabolism)
- Cell Wall
(chemistry, genetics, metabolism)
- Female
- Humans
- Lactococcus lactis
(chemistry, genetics, metabolism)
- Membrane Proteins
(chemistry, genetics, metabolism)
- Protein Domains
- Protein Structure, Secondary
- Streptococcus agalactiae
(chemistry, genetics, metabolism)
- Structure-Activity Relationship
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