Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication

Summary: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019. Few studies have compared replication dynamics and host responses to SARS-CoV-2 in cell lines from different tissues and species. Therefore, we investigated the role of tissue ty...

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Main Authors: Elizabeth Geerling, Amanda N. Pinski, Taylor E. Stone, Richard J. DiPaolo, Michael Z. Zulu, Kevin J. Maroney, James D. Brien, Ilhem Messaoudi, Amelia K. Pinto
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004221015236
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author Elizabeth Geerling
Amanda N. Pinski
Taylor E. Stone
Richard J. DiPaolo
Michael Z. Zulu
Kevin J. Maroney
James D. Brien
Ilhem Messaoudi
Amelia K. Pinto
author_facet Elizabeth Geerling
Amanda N. Pinski
Taylor E. Stone
Richard J. DiPaolo
Michael Z. Zulu
Kevin J. Maroney
James D. Brien
Ilhem Messaoudi
Amelia K. Pinto
author_sort Elizabeth Geerling
collection DOAJ
description Summary: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019. Few studies have compared replication dynamics and host responses to SARS-CoV-2 in cell lines from different tissues and species. Therefore, we investigated the role of tissue type and antiviral genes during SARS-CoV-2 infection in nonhuman primate (kidney) and human (liver, respiratory epithelial, gastric) cell lines. We report different viral growth kinetics and release among the cell lines despite comparable ACE2 expression. Transcriptomics revealed that absence of STAT1 in nonhuman primate cells appeared to enhance inflammatory responses without effecting infectious viral titer. Deletion of RL-6 in respiratory epithelial cells increased viral replication. Impaired infectious virus release was detected in Huh7 but not Huh7.5 cells, suggesting a role for RIG1. Gastric cells MKN45 exhibited robust antiviral gene expression and supported viral replication. Data here provide insight into molecular pathogenesis of and alternative cell lines for studying SARS-CoV-2 infection.
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spelling doaj.art-6706e14fa6744fd3962e3f683aaae4922022-12-22T04:10:17ZengElsevieriScience2589-00422022-01-01251103553Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replicationElizabeth Geerling0Amanda N. Pinski1Taylor E. Stone2Richard J. DiPaolo3Michael Z. Zulu4Kevin J. Maroney5James D. Brien6Ilhem Messaoudi7Amelia K. Pinto8Department of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO 63103, USADepartment of Molecular Biology and Biochemistry, University of California-Irvine, Irvine, CA 92697, USADepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO 63103, USADepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO 63103, USADepartment of Molecular Biology and Biochemistry, University of California-Irvine, Irvine, CA 92697, USADepartment of Molecular Biology and Biochemistry, University of California-Irvine, Irvine, CA 92697, USADepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO 63103, USADepartment of Molecular Biology and Biochemistry, University of California-Irvine, Irvine, CA 92697, USA; Corresponding authorDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO 63103, USA; Corresponding authorSummary: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019. Few studies have compared replication dynamics and host responses to SARS-CoV-2 in cell lines from different tissues and species. Therefore, we investigated the role of tissue type and antiviral genes during SARS-CoV-2 infection in nonhuman primate (kidney) and human (liver, respiratory epithelial, gastric) cell lines. We report different viral growth kinetics and release among the cell lines despite comparable ACE2 expression. Transcriptomics revealed that absence of STAT1 in nonhuman primate cells appeared to enhance inflammatory responses without effecting infectious viral titer. Deletion of RL-6 in respiratory epithelial cells increased viral replication. Impaired infectious virus release was detected in Huh7 but not Huh7.5 cells, suggesting a role for RIG1. Gastric cells MKN45 exhibited robust antiviral gene expression and supported viral replication. Data here provide insight into molecular pathogenesis of and alternative cell lines for studying SARS-CoV-2 infection.http://www.sciencedirect.com/science/article/pii/S2589004221015236ImmunologyMicrobiologyVirology
spellingShingle Elizabeth Geerling
Amanda N. Pinski
Taylor E. Stone
Richard J. DiPaolo
Michael Z. Zulu
Kevin J. Maroney
James D. Brien
Ilhem Messaoudi
Amelia K. Pinto
Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
iScience
Immunology
Microbiology
Virology
title Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
title_full Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
title_fullStr Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
title_full_unstemmed Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
title_short Roles of antiviral sensing and type I interferon signaling in the restriction of SARS-CoV-2 replication
title_sort roles of antiviral sensing and type i interferon signaling in the restriction of sars cov 2 replication
topic Immunology
Microbiology
Virology
url http://www.sciencedirect.com/science/article/pii/S2589004221015236
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