Salivary glands are a target for SARS-CoV-2: a source for saliva contamination.


Journal

The Journal of pathology
ISSN: 1096-9896
Titre abrégé: J Pathol
Pays: England
ID NLM: 0204634

Informations de publication

Date de publication:
07 2021
Historique:
revised: 12 03 2021
received: 14 10 2020
accepted: 06 04 2021
pubmed: 10 4 2021
medline: 22 6 2021
entrez: 9 4 2021
Statut: ppublish

Résumé

The ability of the new coronavirus SARS-CoV-2 to spread and contaminate is one of the determinants of the COVID-19 pandemic status. SARS-CoV-2 has been detected in saliva consistently, with similar sensitivity to that observed in nasopharyngeal swabs. We conducted ultrasound-guided postmortem biopsies in COVID-19 fatal cases. Samples of salivary glands (SGs; parotid, submandibular, and minor) were obtained. We analyzed samples using RT-qPCR, immunohistochemistry, electron microscopy, and histopathological analysis to identify SARS-CoV-2 and elucidate qualitative and quantitative viral profiles in salivary glands. The study included 13 female and 11 male patients, with a mean age of 53.12 years (range 8-83 years). RT-qPCR for SARS-CoV-2 was positive in 30 SG samples from 18 patients (60% of total SG samples and 75% of all cases). Ultrastructural analyses showed spherical 70-100 nm viral particles, consistent in size and shape with the Coronaviridae family, in the ductal lining cell cytoplasm, acinar cells, and ductal lumen of SGs. There was also degeneration of organelles in infected cells and the presence of a cluster of nucleocapsids, which suggests viral replication in SG cells. Qualitative histopathological analysis showed morphologic alterations in the duct lining epithelium characterized by cytoplasmic and nuclear vacuolization, as well as nuclear pleomorphism. Acinar cells showed degenerative changes of the zymogen granules and enlarged nuclei. Ductal epithelium and serous acinar cells showed intense expression of ACE2 and TMPRSS receptors. An anti-SARS-CoV-2 antibody was positive in 8 (53%) of the 15 tested cases in duct lining epithelial cells and acinar cells of major SGs. Only two minor salivary glands were positive for SARS-CoV-2 by immunohistochemistry. Salivary glands are a reservoir for SARS-CoV-2 and provide a pathophysiological background for studies that indicate the use of saliva as a diagnostic method for COVID-19 and highlight this biological fluid's role in spreading the disease. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Identifiants

pubmed: 33834497
doi: 10.1002/path.5679
pmc: PMC8250228
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

239-243

Subventions

Organisme : Bill and Melinda Gates Foundation
ID : 10.13039/100000865
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 401825/2020-5
Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : 10.13039/501100001807

Informations de copyright

© 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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Auteurs

Bruno Fernandes Matuck (BF)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Marisa Dolhnikoff (M)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Amaro Nunes Duarte-Neto (AN)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.
Adolfo Lutz Institute, Division of Pathology, São Paulo, Brazil.

Gilvan Maia (G)

Department of Otorhinolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Sara Costa Gomes (SC)

Department of Otorhinolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Daniel Isaac Sendyk (DI)

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

Amanda Zarpellon (A)

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

Nathalia Paiva de Andrade (NP)

Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.

Renata Aparecida Monteiro (RA)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

João Renato Rebello Pinho (JRR)

Department of Gastroenterology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Michele Soares Gomes-Gouvêa (MS)

Department of Gastroenterology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Suzana Com Souza (SC)

Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

Cristina Kanamura (C)

Adolfo Lutz Institute, Division of Pathology, São Paulo, Brazil.

Thais Mauad (T)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Paulo Hilário Nascimento Saldiva (PHN)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Paulo H Braz-Silva (PH)

Department of Otorhinolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.
Institute of Tropical Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.

Elia Garcia Caldini (EG)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Luiz Fernando Ferraz da Silva (LFF)

Department of Pathology, School of Medicine, University of São Paulo, São Paulo, Brazil.
São Paulo Autopsy Service, University of São Paulo, São Paulo, Brazil.

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