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Broad sialic acid usage amongst species D human adenovirus.
Mundy, Rosie M; Baker, Alexander T; Bates, Emily A; Cunliffe, Tabitha G; Teijeira-Crespo, Alicia; Moses, Elise; Rizkallah, Pierre J; Parker, Alan L.
Afiliação
  • Mundy RM; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Baker AT; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Bates EA; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Cunliffe TG; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Teijeira-Crespo A; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Moses E; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Rizkallah PJ; Division of Infection & Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
  • Parker AL; Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.
Npj Viruses ; 1(1): 1, 2023.
Article em En | MEDLINE | ID: mdl-38665237
ABSTRACT
Human 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article