Evidence map›Paper›PMID 39082483›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2024

Hepatic endotheliitis in Golden Syrian hamsters (Mesocricetus auratus) experimentally infected with SARS-CoV-2.

Alex Junior Souza de Souza, Antônio Francisco de Souza Filho, Cristina Kraemer Zimpel, Marina Caçador Ayupe, Marcelo Valdemir de Araújo, Rafael Rahal Guaragna Machado, Erika Salles, Caio Loureiro Salgado, Mariana Silva Tavares, Taiana Tainá Silva-Pereira and 7 more

Abstract read
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Alex Junior Souza de SouzaUniversidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Patologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-6201-2777
Antônio Francisco de Souza FilhoUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-4728-1228
Cristina Kraemer ZimpelUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.
Marina Caçador AyupeUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-6070-7871
Marcelo Valdemir de AraújoUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-9695-3225
Rafael Rahal Guaragna MachadoUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-6974-5092
Erika SallesUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-9294-2382
Caio Loureiro SalgadoUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-4423-6723
Mariana Silva TavaresUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.
Taiana Tainá Silva-PereiraUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-9313-0151
Paula Carolina de SouzaUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, São Paulo, Brazil.
Edison Luiz DurigonUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-4898-6553
Marcos Bryan HeinemannUniversidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Medicina Veterinária Preventiva e Saúde Animal, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-6444-9788
Paulo Eduardo BrandãoUniversidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Medicina Veterinária Preventiva e Saúde Animal, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-0213-7839
Denise Morais da FonsecaUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-8310-0186
Ana Marcia de Sá GuimarãesUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-8261-5863
Lilian Rose Marques de SáUniversidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Patologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-1909-1550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic injuries in COVID-19 are not yet fully understood and indirect pathways (without viral replication in the liver) have been associated with the activation of vascular mechanisms of liver injury in humans infected with SARS-CoV-2. Golden Syrian hamsters are an effective model for experimental reproduction of moderate and self-limiting lung disease during SARS-CoV-2 infection. As observed in humans, this experimental model reproduces lesions of bronchointerstitial pneumonia and pulmonary vascular lesions, including endotheliitis (attachment of lymphoid cells to the luminal surface of endothelium). Extrapulmonary vascular lesions are well documented in COVID-19, but such extrapulmonary vascular lesions have not yet been described in the Golden Syrian hamster model of SARS-CoV-2 infection. The study aimed to evaluate microscopic liver lesions in Golden Syrian hamsters experimentally infected with SARS-CoV-2. In total, 38 conventional Golden Syrian hamsters, divided into infected group (n=24) and mock-infected group (n=14), were euthanized at 2-, 3-, 4-, 5-, 7-, 14-, and 15-days post infection with SARS-CoV-2. Liver fragments were evaluated by histopathology and immunohistochemical detection of SARS-CoV-2 Spike S2 antigens. The frequencies of portal vein endotheliitis, lobular activity, hepatocellular degeneration, and lobular vascular changes were higher among SARS-CoV-2-infected animals. Spike S2 antigen was not detected in liver. The main results indicate that SARS-CoV-2 infection exacerbated vascular and inflammatory lesions in the liver of hamsters with pre-existing hepatitis of unknown origin. A potential application of this animal model in studies of the pathogenesis and evolution of liver lesions associated with SARS-CoV-2 infection still needs further evaluation.

Indexed as

COVID-19Disease Models, AnimalLiverMesocricetusSARS-CoV-2AnimalsCricetinaeMale

Identifiers

PMID39082483
PMCPMC11295288

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.