RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions

Respiratory viral infections constitute a global public health concern. Among prevalent respiratory viruses, two pneumoviruses can be life-threatening in high-risk populations. In young children, they constitute the first cause of hospitalization due to severe lower respiratory tract diseases. A bet...

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Main Authors: Johan Geiser, Guy Boivin, Song Huang, Samuel Constant, Laurent Kaiser, Caroline Tapparel, Manel Essaidi-Laziosi
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/1/139
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author Johan Geiser
Guy Boivin
Song Huang
Samuel Constant
Laurent Kaiser
Caroline Tapparel
Manel Essaidi-Laziosi
author_facet Johan Geiser
Guy Boivin
Song Huang
Samuel Constant
Laurent Kaiser
Caroline Tapparel
Manel Essaidi-Laziosi
author_sort Johan Geiser
collection DOAJ
description Respiratory viral infections constitute a global public health concern. Among prevalent respiratory viruses, two pneumoviruses can be life-threatening in high-risk populations. In young children, they constitute the first cause of hospitalization due to severe lower respiratory tract diseases. A better understanding of their pathogenesis is still needed as there are no approved efficient anti-viral nor vaccine against pneumoviruses. We studied Respiratory Syncytial virus (RSV) and human Metapneumovirus (HMPV) in single and dual infections in three-dimensional cultures, a highly relevant model to study viral respiratory infections of the airway epithelium. Our investigation showed that HMPV is less pathogenic than RSV in this model. Compared to RSV, HMPV replicated less efficiently, induced a lower immune response, did not block cilia beating, and was more sensitive to IFNs. In dual infections, RSV-infected epithelia were less permissive to HMPV. By neutralizing IFNs in co-infection assays, we partially prevented HMPV inhibition by RSV and significantly increased the number of co-infected cells in the tissue. This suggests that interference in dual infection would be at least partly mediated by the host immune response. In summary, this work provides new insight regarding virus-host and virus-virus interactions of pneumoviruses in the airway epithelium. This could be helpful for the proper handling of at-risk patients.
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spelling doaj.art-c164687c1fdc43aba7390be48b56277a2023-12-03T13:52:45ZengMDPI AGViruses1999-49152021-01-0113113910.3390/v13010139RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus InteractionsJohan Geiser0Guy Boivin1Song Huang2Samuel Constant3Laurent Kaiser4Caroline Tapparel5Manel Essaidi-Laziosi6Department of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, 1211 Geneva, SwitzerlandResearch Center in Infectious Diseases, CHU of Quebec and Laval University, Quebec City, QC 47762, CanadaEpithelix Sàrl, 1228 Geneva, SwitzerlandEpithelix Sàrl, 1228 Geneva, SwitzerlandDepartment of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, 1211 Geneva, SwitzerlandDepartment of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, 1211 Geneva, SwitzerlandDepartment of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, 1211 Geneva, SwitzerlandRespiratory viral infections constitute a global public health concern. Among prevalent respiratory viruses, two pneumoviruses can be life-threatening in high-risk populations. In young children, they constitute the first cause of hospitalization due to severe lower respiratory tract diseases. A better understanding of their pathogenesis is still needed as there are no approved efficient anti-viral nor vaccine against pneumoviruses. We studied Respiratory Syncytial virus (RSV) and human Metapneumovirus (HMPV) in single and dual infections in three-dimensional cultures, a highly relevant model to study viral respiratory infections of the airway epithelium. Our investigation showed that HMPV is less pathogenic than RSV in this model. Compared to RSV, HMPV replicated less efficiently, induced a lower immune response, did not block cilia beating, and was more sensitive to IFNs. In dual infections, RSV-infected epithelia were less permissive to HMPV. By neutralizing IFNs in co-infection assays, we partially prevented HMPV inhibition by RSV and significantly increased the number of co-infected cells in the tissue. This suggests that interference in dual infection would be at least partly mediated by the host immune response. In summary, this work provides new insight regarding virus-host and virus-virus interactions of pneumoviruses in the airway epithelium. This could be helpful for the proper handling of at-risk patients.https://www.mdpi.com/1999-4915/13/1/139HMPVRSVairway epitheliasingle and dual infectionsinnate immunity and IFN response
spellingShingle Johan Geiser
Guy Boivin
Song Huang
Samuel Constant
Laurent Kaiser
Caroline Tapparel
Manel Essaidi-Laziosi
RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
Viruses
HMPV
RSV
airway epithelia
single and dual infections
innate immunity and IFN response
title RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
title_full RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
title_fullStr RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
title_full_unstemmed RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
title_short RSV and HMPV Infections in 3D Tissue Cultures: Mechanisms Involved in Virus-Host and Virus-Virus Interactions
title_sort rsv and hmpv infections in 3d tissue cultures mechanisms involved in virus host and virus virus interactions
topic HMPV
RSV
airway epithelia
single and dual infections
innate immunity and IFN response
url https://www.mdpi.com/1999-4915/13/1/139
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