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  1. Article ; Online: Evidence of SARS-CoV-2 infection in postmortem lung, kidney, and liver samples, revealing cellular targets involved in COVID-19 pathogenesis.

    Falcón-Cama, Viviana / Montero-González, Teresita / Acosta-Medina, Emilio F / Guillen-Nieto, Gerardo / Berlanga-Acosta, Jorge / Fernández-Ortega, Celia / Alfonso-Falcón, Anabel / Gilva-Rodríguez, Nathalie / López-Nocedo, Lilianne / Cremata-García, Daina / Matos-Terrero, Mariuska / Pentón-Rol, Giselle / Valdés, Iris / Oramas-Díaz, Leonardo / Suarez-Batista, Anamarys / Noa-Romero, Enrique / Cruz-Sui, Otto / Sánchez, Daisy / Borrego-Díaz, Amanda I /
    Valdés-Carreras, Juan E / Vizcaino, Ananayla / Suárez-Alba, José / Valdés-Véliz, Rodolfo / Bergado, Gretchen / González, Miguel A / Hernandez, Tays / Alvarez-Arzola, Rydell / Ramírez-Suárez, Anna C / Casillas-Casanova, Dionne / Lemos-Pérez, Gilda / Blanco-Águila, Omar R / Díaz, Angelina / González, Yorexis / Bequet-Romero, Mónica / Marín-Prida, Javier / Hernández-Perera, Julio C / Del Rosario-Cruz, Leticia / Marin-Díaz, Alina P / González-Bravo, Maritza / Borrajero, Israel / Acosta-Rivero, Nelson

    Archives of virology

    2023  Volume 168, Issue 3, Page(s) 96

    Abstract: There is an urgent need to understand severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-host interactions involved in virus spread and pathogenesis, which might contribute to the identification of new therapeutic targets. In this study, we ... ...

    Abstract There is an urgent need to understand severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-host interactions involved in virus spread and pathogenesis, which might contribute to the identification of new therapeutic targets. In this study, we investigated the presence of SARS-CoV-2 in postmortem lung, kidney, and liver samples of patients who died with coronavirus disease (COVID-19) and its relationship with host factors involved in virus spread and pathogenesis, using microscopy-based methods. The cases analyzed showed advanced stages of diffuse acute alveolar damage and fibrosis. We identified the SARS-CoV-2 nucleocapsid (NC) in a variety of cells, colocalizing with mitochondrial proteins, lipid droplets (LDs), and key host proteins that have been implicated in inflammation, tissue repair, and the SARS-CoV-2 life cycle (vimentin, NLRP3, fibronectin, LC3B, DDX3X, and PPARγ), pointing to vimentin and LDs as platforms involved not only in the viral life cycle but also in inflammation and pathogenesis. SARS-CoV-2 isolated from a patient´s nasal swab was grown in cell culture and used to infect hamsters. Target cells identified in human tissue samples included lung epithelial and endothelial cells; lipogenic fibroblast-like cells (FLCs) showing features of lipofibroblasts such as activated PPARγ signaling and LDs; lung FLCs expressing fibronectin and vimentin and macrophages, both with evidence of NLRP3- and IL1β-induced responses; regulatory cells expressing immune-checkpoint proteins involved in lung repair responses and contributing to inflammatory responses in the lung; CD34
    MeSH term(s) Humans ; COVID-19/pathology ; Fibronectins ; Vimentin ; SARS-CoV-2 ; Endothelial Cells ; NLR Family, Pyrin Domain-Containing 3 Protein ; PPAR gamma ; Lung ; Inflammation/pathology ; Kidney ; Liver
    Chemical Substances Fibronectins ; Vimentin ; NLR Family, Pyrin Domain-Containing 3 Protein ; PPAR gamma
    Language English
    Publishing date 2023-02-26
    Publishing country Austria
    Document type Journal Article
    ZDB-ID 7491-3
    ISSN 1432-8798 ; 0304-8608
    ISSN (online) 1432-8798
    ISSN 0304-8608
    DOI 10.1007/s00705-023-05711-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Evidence of SARS-CoV-2 infection in postmortem lung, kidney, and liver samples, revealing cellular targets involved in COVID-19 pathogenesis

    Falcón-Cama, Viviana / Montero-González, Teresita / Acosta-Medina, Emilio F. / Guillen-Nieto, Gerardo / Berlanga-Acosta, Jorge / Fernández-Ortega, Celia / Alfonso-Falcón, Anabel / Gilva-Rodríguez, Nathalie / López-Nocedo, Lilianne / Cremata-García, Daina / Matos-Terrero, Mariuska / Penton-Rol, Giselle / Valdés, Iris / Oramas-Díaz, Leonardo / Suarez-Batista, Anamarys / Noa-Romero, Enrique / Cruz-Sui, Otto / Sánchez, Daisy / Borrego-Díaz, Amanda I. /
    Valdés-Carreras, Juan E. / Vizcaino, Ananayla / Suárez-Alba, José / Valdés-Véliz, Rodolfo / Bergado, Gretchen / González, Miguel A. / Hernandez, Tays / Alvarez-Arzola, Rydell / Ramírez-Suárez, Anna C. / Casillas-Casanova, Dionne / Lemos-Pérez, Gilda / Blanco-Águila, Omar R. / Díaz, Angelina / González, Yorexis / Bequet-Romero, Mónica / Marín-Prida, Javier / Hernández-Perera, Julio C. / del Rosario-Cruz, Leticia / Marin-Díaz, Alina P. / González-Bravo, Maritza / Borrajero, Israel / Acosta-Rivero, Nelson

    Arch Virol. 2023 Mar., v. 168, no. 3 p.96-96

    2023  

    Abstract: There is an urgent need to understand severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-host interactions involved in virus spread and pathogenesis, which might contribute to the identification of new therapeutic targets. In this study, we ... ...

    Abstract There is an urgent need to understand severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-host interactions involved in virus spread and pathogenesis, which might contribute to the identification of new therapeutic targets. In this study, we investigated the presence of SARS-CoV-2 in postmortem lung, kidney, and liver samples of patients who died with coronavirus disease (COVID-19) and its relationship with host factors involved in virus spread and pathogenesis, using microscopy-based methods. The cases analyzed showed advanced stages of diffuse acute alveolar damage and fibrosis. We identified the SARS-CoV-2 nucleocapsid (NC) in a variety of cells, colocalizing with mitochondrial proteins, lipid droplets (LDs), and key host proteins that have been implicated in inflammation, tissue repair, and the SARS-CoV-2 life cycle (vimentin, NLRP3, fibronectin, LC3B, DDX3X, and PPARγ), pointing to vimentin and LDs as platforms involved not only in the viral life cycle but also in inflammation and pathogenesis. SARS-CoV-2 isolated from a patient´s nasal swab was grown in cell culture and used to infect hamsters. Target cells identified in human tissue samples included lung epithelial and endothelial cells; lipogenic fibroblast-like cells (FLCs) showing features of lipofibroblasts such as activated PPARγ signaling and LDs; lung FLCs expressing fibronectin and vimentin and macrophages, both with evidence of NLRP3- and IL1β-induced responses; regulatory cells expressing immune-checkpoint proteins involved in lung repair responses and contributing to inflammatory responses in the lung; CD34⁺ liver endothelial cells and hepatocytes expressing vimentin; renal interstitial cells; and the juxtaglomerular apparatus. This suggests that SARS-CoV-2 may directly interfere with critical lung, renal, and liver functions involved in COVID-19-pathogenesis.
    Keywords COVID-19 infection ; Severe acute respiratory syndrome coronavirus 2 ; cell culture ; epithelium ; fibronectins ; fibrosis ; hepatocytes ; humans ; inflammation ; kidneys ; lipids ; liver ; lungs ; macrophages ; mitochondria ; nose ; nucleocapsid ; pathogenesis ; patients ; therapeutics ; tissue repair ; vimentin ; viruses
    Language English
    Dates of publication 2023-03
    Size p. 96.
    Publishing place Springer Vienna
    Document type Article ; Online
    ZDB-ID 7491-3
    ISSN 1432-8798 ; 0304-8608
    ISSN (online) 1432-8798
    ISSN 0304-8608
    DOI 10.1007/s00705-023-05711-y
    Database NAL-Catalogue (AGRICOLA)

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