Multisystem screening reveals SARS-CoV-2 in neurons of the myenteric plexus and in megakaryocytes.
Sandra Gray-RodriguezMelanie P JensenMaria Otero-JimenezBrian HanleyOlivia C SwannPatrick A WardFrancisco J SalgueroNadira QueridoIldiko FarkasElisavet Velentza-AlmpaniJustin WeirWendy S BarclayMiles W CarrollZane JaunmuktaneSebastian BrandnerUte PohlKieren AllinsonMaria ThomClaire TroakesSafa Al-SarrajMagdalena SastreDjordje GvericSteve GentlemanCandice RoufosseMichael OsbornJavier Alegre-AbarrateguiPublished in: The Journal of pathology (2022)
SARS-CoV-2, the causative agent of COVID-19, typically manifests as a respiratory illness, although extrapulmonary involvement, such as in the gastrointestinal tract and nervous system, as well as frequent thrombotic events, are increasingly recognised. How this maps onto SARS-CoV-2 organ tropism at the histological level, however, remains unclear. Here, we perform a comprehensive validation of a monoclonal antibody against the SARS-CoV-2 nucleocapsid protein (NP) followed by systematic multisystem organ immunohistochemistry analysis of the viral cellular tropism in tissue from 36 patients, 16 postmortem cases and 16 biopsies with polymerase chain reaction (PCR)-confirmed SARS-CoV-2 status from the peaks of the pandemic in 2020 and four pre-COVID postmortem controls. SARS-CoV-2 anti-NP staining in the postmortem cases revealed broad multiorgan involvement of the respiratory, digestive, haematopoietic, genitourinary and nervous systems, with a typical pattern of staining characterised by punctate paranuclear and apical cytoplasmic labelling. The average time from symptom onset to time of death was shorter in positively versus negatively stained postmortem cases (mean = 10.3 days versus mean = 20.3 days, p = 0.0416, with no cases showing definitive staining if the interval exceeded 15 days). One striking finding was the widespread presence of SARS-CoV-2 NP in neurons of the myenteric plexus, a site of high ACE2 expression, the entry receptor for SARS-CoV-2, and one of the earliest affected cells in Parkinson's disease. In the bone marrow, we observed viral SARS-CoV-2 NP within megakaryocytes, key cells in platelet production and thrombus formation. In 15 tracheal biopsies performed in patients requiring ventilation, there was a near complete concordance between immunohistochemistry and PCR swab results. Going forward, our findings have relevance to correlating clinical symptoms with the organ tropism of SARS-CoV-2 in contemporary cases as well as providing insights into potential long-term complications of COVID-19. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- end stage renal disease
- bone marrow
- induced apoptosis
- ejection fraction
- coronavirus disease
- chronic kidney disease
- newly diagnosed
- monoclonal antibody
- cell cycle arrest
- prognostic factors
- risk factors
- radiation therapy
- intensive care unit
- signaling pathway
- poor prognosis
- cell proliferation
- oxidative stress
- acute respiratory distress syndrome
- physical activity
- mesenchymal stem cells
- systematic review
- patient reported outcomes
- climate change
- mechanical ventilation
- angiotensin ii
- rectal cancer
- clinical evaluation