Science and Research

Cardiac glycosides decrease influenza virus replication by inhibiting cell protein translational machinery

Cardiac glycosides (CGs) are used primarily for cardiac failure and have been reported to have other effects, including inhibition of viral replication. Here we set out to study mechanisms by which CGs as inhibitors of the Na-K-ATPase decrease influenza A virus (IAV) replication in the lungs. We found that CGs inhibit influenza virus replication in alveolar epithelial cells by decreasing intracellular potassium, which in turn inhibits protein translation, independently of viral entry, mRNA transcription, and protein degradation. These effects were independent of the Src signaling pathway and intracellular calcium concentration changes. We found that short-term treatment with ouabain prevented IAV replication without cytotoxicity. Rodents express a Na-K-ATPase-alpha1 resistant to CGs. Thus we utilized Na-K-ATPase-alpha1-sensitive mice, infected them with high doses of influenza virus, and observed a modest survival benefit when treated with ouabain. In summary, we provide evidence that the inhibition of the Na-K-ATPase by CGs decreases influenza A viral replication by modulating the cell protein translational machinery and results in a modest survival benefit in mice.

  • Amarelle, L.
  • Katzen, J.
  • Shigemura, M.
  • Welch, L. C.
  • Cajigas, H.
  • Peteranderl, C.
  • Celli, D.
  • Herold, S.
  • Lecuona, E.
  • Sznajder, J. I.

Keywords

  • A549 Cells
  • Alveolar Epithelial Cells/virology
  • Animals
  • Antiviral Agents/pharmacology
  • Cardiac Glycosides/*pharmacology
  • Cell Line, Tumor
  • Dogs
  • Enzyme Inhibitors/*pharmacology
  • Female
  • Humans
  • Influenza A virus
  • Influenza, Human/*drug therapy
  • Lung/virology
  • Madin Darby Canine Kidney Cells
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Ouabain/pharmacology
  • Potassium/metabolism
  • Protein Biosynthesis/*physiology
  • Sodium-Potassium-Exchanging ATPase/*antagonists & inhibitors
  • Virus Replication/*physiology
  • *Na-K-ATPase
  • *antiviral treatment
  • *intracellular potassium
Publication details
DOI: 10.1152/ajplung.00173.2018
Journal: American journal of physiology. Lung cellular and molecular physiology
Pages: L1094-L1106 
Number: 6
Work Type: Original
Location: UGMLC
Disease Area: PALI
Partner / Member: JLU
Access-Number: 30892074
See publication on PubMed

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