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Detection of long SARS-CoV-2 nucleocapsid sequences in peripheral blood monocytes collected soon after hospital admission
Nathan Pagano; Maudry Laurent-Rolle; Jack Chunchieh Hsu; - Yale IMPACT Research Team; Chantal BF Vogels; Nathan D Grubaugh; Laura Manuelidis.
Affiliation
  • Nathan Pagano; Yale Medical School
  • Maudry Laurent-Rolle; Yale Medical School
  • Jack Chunchieh Hsu; Yale Medical School
  • - Yale IMPACT Research Team; -
  • Chantal BF Vogels; Yale Medical School
  • Nathan D Grubaugh; Yale School of Public Health
  • Laura Manuelidis; Yale Medical School
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-423113
ABSTRACT
Many viruses infect circulating mononuclear cells thereby facilitating infection of diverse organs. Blood monocytes (PBMC) are being intensively studied as immunologic and pathologic responders to the new SARS-CoV-2 virus (CoV19) but direct evidence showing CoV19 in monocytes is lacking. Circulating myeloid cells that take up residence in various organs can harbor viral genomes for many years in lymphatic tissues and brain, and act as a source for re-infection and/or post-viral organ pathology. Because nucleocapsid (NC) proteins protect the viral genome we tested PBMC from acutely ill patients for the diagnostic 72bp NC RNA plus adjacent longer (301bp) transcripts. In 2/11 patient PBMC, but no uninfected controls, long NCs were positive as early as 2-6 days after hospital admission as validated by sequencing. Pathogenic viral fragments, or the infectious virus, are probably disseminated by rare myeloid migratory cells that incorporate CoV19 by several pathways. Predictably, these cells carried CoV19 to heart and brain educing the late post-viral pathologies now evident.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Prognostic_studies Language: En Year: 2020 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Prognostic_studies Language: En Year: 2020 Document type: Preprint