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SARS-CoV-2 Viral Replication Persists in the Human Lung for Several Weeks after Symptom Onset

  • Michele Tomasicchio
  • , Shameem Jaumdally
  • , Lindsay Wilson
  • , Andrea Kotze
  • , Lynn Semple
  • , Stuart Meier
  • , Anil Pooran
  • , Aliasgar Esmail
  • , Komala Pillay
  • , Riyaadh Roberts
  • , Raymond Kriel
  • , Richard Meldau
  • , Suzette Oelofse
  • , Carley Mandviwala
  • , Jessica Burns
  • , Rolanda Londt
  • , Malika Davids
  • , Charnay van der Merwe
  • , Aqeedah Roomaney
  • , Louie Kuhn
  • Tahlia Perumal, Alex J. Scott, Martin J. Hale, Vicky Baillie, Sana Mahtab, Carolyn Williamson, Rageema Joseph, Alex Sigal, Ivan Joubert, Jenna Piercy, David Thomson, David L. Fredericks, Malcolm G.A. Miller, Marta C. Nunes, Shabir A. Madhi, Keertan Dheda*
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Rationale: In the upper respiratory tract, replicating (culturable) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is recoverable for 4–8 days after symptom onset, but there is a paucity of data about the frequency and duration of replicating virus in the lower respiratory tract (i.e., the human lung). Objectives: We undertook lung tissue sampling (needle biopsy) shortly after death in 42 mechanically ventilated decedents during the Beta and Delta waves. An independent group of 18 ambulatory patients served as a control group. Methods: Lung biopsy cores from decedents underwent viral culture, histopathological analysis, electron microscopy, transcriptomic profiling, and immunohistochemistry. Measurements and Main Results: Thirty-eight percent (16 of 42) of mechanically ventilated decedents had culturable virus in the lung for a median of 15 days (persisting for up to 4 wk) after symptom onset. Lung viral culture positivity was not associated with comorbidities or steroid use. Delta but not Beta variant lung culture positivity was associated with accelerated death and secondary bacterial infection (P, 0.05). Nasopharyngeal culture was negative in 23.1% (6 of 26) of decedents despite lung culture positivity. This hitherto undescribed biophenotype of lung-specific persisting viral replication was associated with an enhanced transcriptomic pulmonary proinflammatory response but with concurrent viral culture positivity. Conclusions: Concurrent rather than sequential active viral replication continues to drive a heightened proinflammatory response in the human lung beyond the second week of illness and was associated with variant-specific increased mortality and morbidity. These findings have potential implications for the design of interventional strategies and clinical management of patients with severe coronavirus disease (COVID-19).

Original languageEnglish
Pages (from-to)840-851
Number of pages12
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume209
Issue number7
DOIs
StatePublished - 1 Apr 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2024 by the American Thoracic Society.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • COVID-19
  • SARS-CoV-2
  • mechanically ventilated patients
  • upper respiratory tract
  • virus replication

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