Your browser doesn't support javascript.
loading
Evolutionary remodelling of N-terminal domain loops fine-tunes SARS-CoV-2 spike.
Cantoni, Diego; Murray, Matthew J; Kalemera, Mphatso D; Dicken, Samuel J; Stejskal, Lenka; Brown, Georgina; Lytras, Spyros; Coey, Jonathon D; McKenna, James; Bridgett, Stephen; Simpson, David; Fairley, Derek; Thorne, Lucy G; Reuschl, Ann-Kathrin; Forrest, Calum; Ganeshalingham, Maaroothen; Muir, Luke; Palor, Machaela; Jarvis, Lisa; Willett, Brian; Power, Ultan F; McCoy, Laura E; Jolly, Clare; Towers, Greg J; Doores, Katie J; Robertson, David L; Shepherd, Adrian J; Reeves, Matthew B; Bamford, Connor G G; Grove, Joe.
Afiliação
  • Cantoni D; MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK.
  • Murray MJ; Division of Infection and Immunity, University College London, London, UK.
  • Kalemera MD; Division of Infection and Immunity, University College London, London, UK.
  • Dicken SJ; Division of Infection and Immunity, University College London, London, UK.
  • Stejskal L; Division of Evolution, Infection and Genomics, University of Manchester, Manchester, UK.
  • Brown G; Division of Infection and Immunity, University College London, London, UK.
  • Lytras S; MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK.
  • Coey JD; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
  • McKenna J; Belfast Health and Social Care Trust, Belfast, UK.
  • Bridgett S; Belfast Health and Social Care Trust, Belfast, UK.
  • Simpson D; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
  • Fairley D; Belfast Health and Social Care Trust, Belfast, UK.
  • Thorne LG; Division of Infection and Immunity, University College London, London, UK.
  • Reuschl AK; Division of Infection and Immunity, University College London, London, UK.
  • Forrest C; Division of Infection and Immunity, University College London, London, UK.
  • Ganeshalingham M; Division of Infection and Immunity, University College London, London, UK.
  • Muir L; Division of Infection and Immunity, University College London, London, UK.
  • Palor M; Division of Infection and Immunity, University College London, London, UK.
  • Jarvis L; Scottish National Blood Transfusion Service, Glasgow, UK.
  • Willett B; MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK.
  • Power UF; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
  • McCoy LE; Division of Infection and Immunity, University College London, London, UK.
  • Jolly C; Division of Infection and Immunity, University College London, London, UK.
  • Towers GJ; Division of Infection and Immunity, University College London, London, UK.
  • Doores KJ; Department of Infectious Diseases, King's College London, London, UK.
  • Robertson DL; MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK.
  • Shepherd AJ; Department of Biological Sciences, Birkbeck College London, London, UK.
  • Reeves MB; Division of Infection and Immunity, University College London, London, UK.
  • Bamford CGG; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
  • Grove J; MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK.
EMBO Rep ; 23(10): e54322, 2022 10 06.
Article em En | MEDLINE | ID: mdl-35999696
ABSTRACT
The emergence of SARS-CoV-2 variants has exacerbated the COVID-19 global health crisis. Thus far, all variants carry mutations in the spike glycoprotein, which is a critical determinant of viral transmission being responsible for attachment, receptor engagement and membrane fusion, and an important target of immunity. Variants frequently bear truncations of flexible loops in the N-terminal domain (NTD) of spike; the functional importance of these modifications has remained poorly characterised. We demonstrate that NTD deletions are important for efficient entry by the Alpha and Omicron variants and that this correlates with spike stability. Phylogenetic analysis reveals extensive NTD loop length polymorphisms across the sarbecoviruses, setting an evolutionary precedent for loop remodelling. Guided by these analyses, we demonstrate that variations in NTD loop length, alone, are sufficient to modulate virus entry. We propose that variations in NTD loop length act to fine-tune spike; this may provide a mechanism for SARS-CoV-2 to navigate a complex selection landscape encompassing optimisation of essential functionality, immune-driven antigenic variation and ongoing adaptation to a new host.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Limite: Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Limite: Humans Idioma: En Revista: EMBO Rep Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido