TY - JOUR
T1 - Multisystem screening reveals SARS-CoV-2 in neurons of the myenteric plexus and in megakaryocytes
AU - Gray-Rodriguez, Sandra
AU - Jensen, Melanie P.
AU - Otero-Jimenez, Maria
AU - Hanley, Brian
AU - Swann, Olivia C.
AU - Ward, Patrick A.
AU - Salguero, Francisco J.
AU - Querido, Nadira
AU - Farkas, Ildiko
AU - Velentza-Almpani, Elisavet
AU - Weir, Justin
AU - Barclay, Wendy S.
AU - Carroll, Miles W.
AU - Jaunmuktane, Zane
AU - Brandner, Sebastian
AU - Pohl, Ute
AU - Allinson, Kieren
AU - Thom, Maria
AU - Troakes, Claire
AU - Al-Sarraj, Safa
AU - Sastre, Magdalena
AU - Gveric, Djordje
AU - Gentleman, Steve
AU - Roufosse, Candice
AU - Osborn, Michael
AU - Alegre-Abarrategui, Javier
N1 - Funding Information:
The work was funded by the Community Jameel Imperial College Covid-19 Excellence Fund and the North West London Pathology Research Grant Commission. ICHTB is supported by the NIHR Biomedical Research Centre based at Imperial College Healthcare NHS Trust and Imperial College London. JAA has also received funding from the NIHR Imperial Biomedical Research Centre (BRC). MPJ is supported by an NIHR Academic Clinical Fellowship.
Funding Information:
The work was funded by the Community Jameel Imperial College Covid‐19 Excellence Fund and the North West London Pathology Research Grant Commission. ICHTB is supported by the NIHR Biomedical Research Centre based at Imperial College Healthcare NHS Trust and Imperial College London. JAA has also received funding from the NIHR Imperial Biomedical Research Centre (BRC). MPJ is supported by an NIHR Academic Clinical Fellowship.
Publisher Copyright:
© 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
PY - 2022/6
Y1 - 2022/6
N2 - 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.
AB - 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.
KW - COVID-19
KW - enteric nervous system
KW - gastrointestinal tract
KW - immunohistochemistry
KW - megakaryocytes
KW - myenteric plexus
KW - neurons
KW - Parkinson's Disease
KW - SARS-CoV-2
KW - tropism
UR - http://www.scopus.com/inward/record.url?scp=85127442166&partnerID=8YFLogxK
U2 - 10.1002/path.5878
DO - 10.1002/path.5878
M3 - Article
C2 - 35107828
AN - SCOPUS:85127442166
SN - 0022-3417
VL - 257
SP - 198
EP - 217
JO - Journal of Pathology
JF - Journal of Pathology
IS - 2
ER -