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Ultrastructure of cell trafficking pathways and coronavirus: how to recognise the wolf amongst the sheep.
Neil, Desley; Moran, Linda; Horsfield, Catherine; Curtis, Elizabeth; Swann, Olivia; Barclay, Wendy; Hanley, Brian; Hollinshead, Michael; Roufosse, Candice.
Afiliação
  • Neil D; Department of Cellular Pathology, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Moran L; School of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
  • Horsfield C; North West London Pathology, Imperial College Healthcare NHS Trust, London, UK.
  • Curtis E; Department of Immunology and Inflammation, Centre for Inflammatory Diseases, Faculty of Medicine, Imperial College London, London, UK.
  • Swann O; Department of Histopathology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Barclay W; Department of Cellular Pathology, Queen Elizabeth Hospital Birmingham, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Hanley B; Department of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Hollinshead M; Department of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Roufosse C; North West London Pathology, Imperial College Healthcare NHS Trust, London, UK.
J Pathol ; 252(4): 346-357, 2020 12.
Article em En | MEDLINE | ID: mdl-32918747
ABSTRACT
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has resulted in an urgent need to understand the pathophysiology of SARS-CoV-2 infection, to assist in the identification of treatment strategies. Viral tissue tropism is an active area of investigation, one approach to which is identification of virus within tissues by electron microscopy of post-mortem and surgical specimens. Most diagnostic histopathologists have limited understanding of the ultrastructural features of normal cell trafficking pathways, which can resemble intra- and extracellular coronavirus; in addition, viral replication pathways make use of these trafficking pathways. Herein, we review these pathways and their ultrastructural appearances, with emphasis on structures which may be confused with coronavirus. In particular, we draw attention to the fact that, when using routine fixation and processing, the typical 'crown' that characterises a coronavirus is not readily identified on intracellular virions, which are located in membrane-bound vacuoles. In addition, the viral nucleocapsid is seen as black dots within the virion and is more discriminatory in differentiating virions from other cellular structures. The identification of the viral replication organelle, a collection of membranous structures (convoluted membranes) seen at a relatively low scanning power, may help to draw attention to infected cells, which can be sparse. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Limite: Animals / Humans Idioma: En Revista: J Pathol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: SARS-CoV-2 / COVID-19 Limite: Animals / Humans Idioma: En Revista: J Pathol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido