Author:
Mundy Rosie M.,Baker Alexander T.,Bates Emily A.,Cunliffe Tabitha G.,Teijeira-Crespo Alicia,Moses Elise,Rizkallah Pierre J.,Parker Alan L.
Abstract
AbstractHuman adenoviruses (HAdV) are widespread pathogens causing usually mild infections. The Species D (HAdV-D) cause gastrointestinal tract infections and epidemic keratoconjunctivitis (EKC). Despite being significant pathogens, knowledge around HAdV-D mechanism of cell infection is lacking. Sialic acid (SA) usage has been proposed as a cell infection mechanism for EKC causing HAdV-D. Here we highlight an important role for SA engagement by many HAdV-D. We provide apo state crystal structures of 7 previously undetermined HAdV-D fiber-knob proteins, and structures of HAdV-D25, D29, D30 and D53 fiber-knob proteins in complex with SA. Biologically, we demonstrate that removal of cell surface SA reduced infectivity of HAdV-C5 vectors pseudotyped with HAdV-D fiber-knob proteins, whilst engagement of the classical HAdV receptor CAR was variable. Our data indicates variable usage of SA and CAR across HAdV-D. Better defining these interactions will enable improved development of antivirals and engineering of the viruses into refined therapeutic vectors.
Funder
Medical Research Council
Tenovus
Cancer Research UK
Wellcome Trust
Knowledge Economy Skills Scholarships
Cancer Research Wales
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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