Nonstructural Protein 1 (NS1)-Mediated Inhibition of c-Abl Results in Acute Lung Injury and Priming for Bacterial Co-infections: Insights Into 1918 H1N1 Pandemic?

作者：Hrincius Eike R; Liedmann Swantje; Finkelstein David; Vogel Peter; Gansebom Shane; Ehrhardt Christina; Ludwig Stephan; Hains David S; Webby Richard; McCullers Jonathan A^*

来源：Journal of Infectious Diseases, 2015, 211(9): 1418-1428.

DOI：10.1093/infdis/jiu609

• Influenza A virus
• NS1 protein
• c-Abl
• acute lung injury
• bacterial coinfections

Background. Nonstructural protein 1 (NS1) proteins from avian influenza viruses like the 1918 pandemic NS1 are capable of inhibiting the key signaling integrator c-Abl (Abl1), resulting in massive cytopathic cell alterations.
Methods. In the current study, we addressed the consequences of NS1-mediated alteration of c-Abl on acute lung injury and pathogenicity in an in vivo mouse model.
Results. Comparing isogenic strains that differ only in their ability to inhibit c-Abl, we observed elevated pathogenicity for the c-Abl-inhibiting virus. NS1-mediated blockade of c-Abl resulted in severe lung pathology and massive edema formation and facilitated secondary bacterial pneumonia. This phenotype was independent of differences in replication and immune responses, defining it as an NS1 virulence mechanism distinct from its canonical functions. Microarray analysis revealed extensive downregulation of genes involved in cell integrity and vascular endothelial regulation.
Conclusions. NS1 protein-mediated blockade of c-Abl signaling drives acute lung injury and primes for bacterial coinfections revealing potential insights into the pathogenicity of the 1918 pandemic virus.

• 出版日期2015-5-1