Time-resolved characterization of the innate immune response in the respiratory epithelium of human, porcine, and bovine during influenza virus infection

Viral cross-species transmission is recognized to be a major threat to both human and animal health, however detailed information on determinants underlying virus host tropism and susceptibility is missing. Influenza C and D viruses (ICV, IDV) are two respiratory viruses that share up to 50% genetic...

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Published inFrontiers in immunology Vol. 13; p. 970325
Main Authors Laloli, Laura, Licheri, Manon Flore, Probst, Lukas, Licheri, Matthias, Gultom, Mitra, Holwerda, Melle, V’kovski, Philip, Dijkman, Ronald
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LanguageEnglish
Published Frontiers Media S.A 19.08.2022
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Abstract Viral cross-species transmission is recognized to be a major threat to both human and animal health, however detailed information on determinants underlying virus host tropism and susceptibility is missing. Influenza C and D viruses (ICV, IDV) are two respiratory viruses that share up to 50% genetic similarity, and both employ 9-O-acetylated sialic acids to enter a host cell. While ICV infections are mainly restricted to humans, IDV possesses a much broader host tropism and has shown to have a zoonotic potential. This suggests that additional virus–host interactions play an important role in the distinct host spectrum of ICV and IDV. In this study, we aimed to characterize the innate immune response of the respiratory epithelium of biologically relevant host species during influenza virus infection to identify possible determinants involved in viral cross-species transmission. To this end, we performed a detailed characterization of ICV and IDV infection in primary airway epithelial cell (AEC) cultures from human, porcine, and bovine origin. We monitored virus replication kinetics, cellular and host tropism, as well as the host transcriptional response over time at distinct ambient temperatures. We observed that both ICV and IDV predominantly infect ciliated cells, independently from host and temperature. Interestingly, temperature had a profound influence on ICV replication in both porcine and bovine AEC cultures, while IDV replicated efficiently irrespective of temperature and host. Detailed time-resolved transcriptome analysis revealed both species-specific and species uniform host responses and highlighted 34 innate immune-related genes with clear virus-specific and temperature-dependent profiles. These data provide the first comprehensive insights into important common and species-specific virus-host dynamics underlying the distinct host tropism of ICV and IDV, as well as possible determinants involved in viral cross-species transmission.
AbstractList Viral cross-species transmission is recognized to be a major threat to both human and animal health, however detailed information on determinants underlying virus host tropism and susceptibility is missing. Influenza C and D viruses (ICV, IDV) are two respiratory viruses that share up to 50% genetic similarity, and both employ 9-O-acetylated sialic acids to enter a host cell. While ICV infections are mainly restricted to humans, IDV possesses a much broader host tropism and has shown to have a zoonotic potential. This suggests that additional virus–host interactions play an important role in the distinct host spectrum of ICV and IDV. In this study, we aimed to characterize the innate immune response of the respiratory epithelium of biologically relevant host species during influenza virus infection to identify possible determinants involved in viral cross-species transmission. To this end, we performed a detailed characterization of ICV and IDV infection in primary airway epithelial cell (AEC) cultures from human, porcine, and bovine origin. We monitored virus replication kinetics, cellular and host tropism, as well as the host transcriptional response over time at distinct ambient temperatures. We observed that both ICV and IDV predominantly infect ciliated cells, independently from host and temperature. Interestingly, temperature had a profound influence on ICV replication in both porcine and bovine AEC cultures, while IDV replicated efficiently irrespective of temperature and host. Detailed time-resolved transcriptome analysis revealed both species-specific and species uniform host responses and highlighted 34 innate immune-related genes with clear virus-specific and temperature-dependent profiles. These data provide the first comprehensive insights into important common and species-specific virus-host dynamics underlying the distinct host tropism of ICV and IDV, as well as possible determinants involved in viral cross-species transmission.
Author Dijkman, Ronald
Probst, Lukas
Laloli, Laura
Licheri, Manon Flore
Holwerda, Melle
Gultom, Mitra
V’kovski, Philip
Licheri, Matthias
AuthorAffiliation 4 Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern , Bern , Switzerland
3 Institute of Virology and Immunology (IVI) , Bern , Switzerland
2 Graduate School for Cellular and Biomedical Sciences, University of Bern , Bern , Switzerland
1 Institute for Infectious Diseases, University of Bern , Bern , Switzerland
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– name: 3 Institute of Virology and Immunology (IVI) , Bern , Switzerland
– name: 2 Graduate School for Cellular and Biomedical Sciences, University of Bern , Bern , Switzerland
– name: 4 Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern , Bern , Switzerland
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Edited by: Sarah Londrigan, The University of Melbourne, Australia
This article was submitted to Viral Immunology, a section of the journal Frontiers in Immunology
Reviewed by: Qin Zhao, Northwest A&F University, China; Fandan Meng, Harbin Veterinary Research Institute (CAAS), China
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Snippet Viral cross-species transmission is recognized to be a major threat to both human and animal health, however detailed information on determinants underlying...
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SubjectTerms cross-species transmission
Immunology
Influenza C virus
influenza D virus
innate immune response
respiratory epithelium
zoonoses
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Title Time-resolved characterization of the innate immune response in the respiratory epithelium of human, porcine, and bovine during influenza virus infection
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