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Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model
Clinical evidence of vascular dysfunction and hypercoagulability as well as pulmonary vascular damage and microthrombosis are frequently reported in severe cases of human coronavirus disease 2019 (COVID-19). Syrian golden hamsters recapitulate histopathologic pulmonary vascular lesions reported in p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Investigative Pathology. Published by Elsevier Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998130/ https://www.ncbi.nlm.nih.gov/pubmed/36906263 http://dx.doi.org/10.1016/j.ajpath.2023.02.013 |
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author | Ball, Erin E. Weiss, Christopher M. Liu, Hongwei Jackson, Kenneth Keel, M. Kevin Miller, Christopher J. Van Rompay, Koen K.A. Coffey, Lark L. Pesavento, Patricia A. |
author_facet | Ball, Erin E. Weiss, Christopher M. Liu, Hongwei Jackson, Kenneth Keel, M. Kevin Miller, Christopher J. Van Rompay, Koen K.A. Coffey, Lark L. Pesavento, Patricia A. |
author_sort | Ball, Erin E. |
collection | PubMed |
description | Clinical evidence of vascular dysfunction and hypercoagulability as well as pulmonary vascular damage and microthrombosis are frequently reported in severe cases of human coronavirus disease 2019 (COVID-19). Syrian golden hamsters recapitulate histopathologic pulmonary vascular lesions reported in patients with COVID-19. Herein, special staining techniques and transmission electron microscopy further define vascular pathologies in a Syrian golden hamster model of human COVID-19. The results show that regions of active pulmonary inflammation in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are characterized by ultrastructural evidence of endothelial damage with platelet marginalization and both perivascular and subendothelial macrophage infiltration. SARS-CoV-2 antigen/RNA was not detectable within affected blood vessels. Taken together, these findings suggest that the prominent microscopic vascular lesions in SARS-CoV-2–inoculated hamsters likely occur due to endothelial damage followed by platelet and macrophage infiltration. |
format | Online Article Text |
id | pubmed-9998130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Investigative Pathology. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99981302023-03-10 Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model Ball, Erin E. Weiss, Christopher M. Liu, Hongwei Jackson, Kenneth Keel, M. Kevin Miller, Christopher J. Van Rompay, Koen K.A. Coffey, Lark L. Pesavento, Patricia A. Am J Pathol Regular Article Clinical evidence of vascular dysfunction and hypercoagulability as well as pulmonary vascular damage and microthrombosis are frequently reported in severe cases of human coronavirus disease 2019 (COVID-19). Syrian golden hamsters recapitulate histopathologic pulmonary vascular lesions reported in patients with COVID-19. Herein, special staining techniques and transmission electron microscopy further define vascular pathologies in a Syrian golden hamster model of human COVID-19. The results show that regions of active pulmonary inflammation in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are characterized by ultrastructural evidence of endothelial damage with platelet marginalization and both perivascular and subendothelial macrophage infiltration. SARS-CoV-2 antigen/RNA was not detectable within affected blood vessels. Taken together, these findings suggest that the prominent microscopic vascular lesions in SARS-CoV-2–inoculated hamsters likely occur due to endothelial damage followed by platelet and macrophage infiltration. American Society for Investigative Pathology. Published by Elsevier Inc. 2023-06 2023-03-10 /pmc/articles/PMC9998130/ /pubmed/36906263 http://dx.doi.org/10.1016/j.ajpath.2023.02.013 Text en © 2023 American Society for Investigative Pathology. Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Regular Article Ball, Erin E. Weiss, Christopher M. Liu, Hongwei Jackson, Kenneth Keel, M. Kevin Miller, Christopher J. Van Rompay, Koen K.A. Coffey, Lark L. Pesavento, Patricia A. Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title | Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title_full | Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title_fullStr | Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title_full_unstemmed | Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title_short | Severe Acute Respiratory Syndrome Coronavirus 2 Vasculopathy in a Syrian Golden Hamster Model |
title_sort | severe acute respiratory syndrome coronavirus 2 vasculopathy in a syrian golden hamster model |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998130/ https://www.ncbi.nlm.nih.gov/pubmed/36906263 http://dx.doi.org/10.1016/j.ajpath.2023.02.013 |
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