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Ultrastructural insight into SARS-CoV-2 entry and budding in human airway epithelium.
Pinto, Andreia L; Rai, Ranjit K; Brown, Jonathan C; Griffin, Paul; Edgar, James R; Shah, Anand; Singanayagam, Aran; Hogg, Claire; Barclay, Wendy S; Futter, Clare E; Burgoyne, Thomas.
  • Pinto AL; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SW3 6NP, UK.
  • Rai RK; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SW3 6NP, UK.
  • Brown JC; Department of Infectious Disease, Imperial College London, London, W2 1PG, UK.
  • Griffin P; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SW3 6NP, UK.
  • Edgar JR; Department of Pathology, University of Cambridge, Cambridge, CB2 1QP, UK.
  • Shah A; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SW3 6NP, UK.
  • Singanayagam A; MRC Centre of Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London, W2 1PG, UK.
  • Hogg C; Department of Infectious Disease, Imperial College London, London, W2 1PG, UK.
  • Barclay WS; Centre for Molecular Bacteriology and Infection, Imperial College London, London, SW7 2DD, UK.
  • Futter CE; Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SW3 6NP, UK.
  • Burgoyne T; Academic Health Sciences Centre, Imperial College, London, London, SW3 6LY, UK.
Nat Commun ; 13(1): 1609, 2022 03 25.
Article in English | MEDLINE | ID: covidwho-1764179
ABSTRACT
Ultrastructural studies of SARS-CoV-2 infected cells are crucial to better understand the mechanisms of viral entry and budding within host cells. Here, we examined human airway epithelium infected with three different isolates of SARS-CoV-2 including the B.1.1.7 variant by transmission electron microscopy and tomography. For all isolates, the virus infected ciliated but not goblet epithelial cells. Key SARS-CoV-2 entry molecules, ACE2 and TMPRSS2, were found to be localised to the plasma membrane including microvilli but excluded from cilia. Consistently, extracellular virions were seen associated with microvilli and the apical plasma membrane but rarely with ciliary membranes. Profiles indicative of viral fusion where tomography showed that the viral membrane was continuous with the apical plasma membrane and the nucleocapsids diluted, compared with unfused virus, demonstrate that the plasma membrane is one site of entry where direct fusion releasing the nucleoprotein-encapsidated genome occurs. Intact intracellular virions were found within ciliated cells in compartments with a single membrane bearing S glycoprotein. Tomography showed concentration of nucleocapsids round the periphery of profiles strongly suggestive of viral budding into these compartments and this may explain how virions gain their S glycoprotein containing envelope.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-29255-y

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-29255-y