4.6 Article

Influenza A(H1N1)pdm09 Virus but Not Respiratory Syncytial Virus Interferes with SARS-CoV-2 Replication during Sequential Infections in Human Nasal Epithelial Cells

Journal

VIRUSES-BASEL
Volume 14, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/v14020395

Keywords

viral interference; influenza virus; SARS-CoV-2; respiratory syncytial virus; human nasal epithelium; interferon

Categories

Funding

  1. Canadian Institutes of Health Research [148361]

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The interactions between SARS-CoV-2 and influenza A(H1N1)pdm09 or respiratory syncytial virus (RSV) were studied in this research. It was found that SARS-CoV-2 interferes with RSV-A2 replication during simultaneous infection but has no effect on A(H1N1)pdm09 replication. Prior infection with SARS-CoV-2 reduces the replication of both respiratory viruses, while prior infection with A(H1N1)pdm09 only reduces subsequent infection with SARS-CoV-2. The mechanism of viral interference between SARS-CoV-2 and A(H1N1)pdm09 is mediated by the production of interferon.
The types of interactions between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and other respiratory viruses are not well-characterized due to the low number of co-infection cases described since the onset of the pandemic. We have evaluated the interactions between SARS-CoV-2 (D614G mutant) and influenza A(H1N1)pdm09 or respiratory syncytial virus (RSV) in the nasal human airway epithelium (HAE) infected simultaneously or sequentially (24 h apart) with virus combinations. The replication kinetics of each virus were determined by RT-qPCR at different post-infection times. Our results showed that during simultaneous infection, SARS-CoV-2 interferes with RSV-A2 but not with A(H1N1)pdm09 replication. The prior infection of nasal HAE with SARS-CoV-2 reduces the replication kinetics of both respiratory viruses. SARS-CoV-2 replication is decreased by a prior infection with A(H1N1)pdm09 but not with RSV-A2. The pretreatment of nasal HAE with BX795, a TANK-binding kinase 1 inhibitor, partially alleviates the reduced replication of SARS-CoV-2 or influenza A(H1N1)pdm09 during sequential infection with both virus combinations. Thus, a prior infection of nasal HAE with SARS-CoV-2 interferes with the replication kinetics of A(H1N1)pdm09 and RSV-A2, whereas only A(H1N1)pdm09 reduces the subsequent infection with SARS-CoV-2. The mechanism involved in the viral interference between SARS-CoV-2 and A(H1N1)pdm09 is mediated by the production of interferon.

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