A CRISPR Activation Screen Identifies a Pan-avian Influenza Virus Inhibitory Host Factor

Cell Rep. 2017 Aug 15;20(7):1503-1512. doi: 10.1016/j.celrep.2017.07.060.

Abstract

Influenza A virus (IAV) is a pathogen that poses significant risks to human health. It is therefore critical to develop strategies to prevent influenza disease. Many loss-of-function screens have been performed to identify the host proteins required for viral infection. However, there has been no systematic screen to identify the host factors that, when overexpressed, are sufficient to prevent infection. In this study, we used CRISPR/dCas9 activation technology to perform a genome-wide overexpression screen to identify IAV restriction factors. The major hit from our screen, B4GALNT2, showed inhibitory activity against influenza viruses with an α2,3-linked sialic acid receptor preference. B4GALNT2 overexpression prevented the infection of every avian influenza virus strain tested, including the H5, H9, and H7 subtypes, which have previously caused disease in humans. Thus, we have used CRISPR/dCas9 activation technology to identify a factor that can abolish infection by avian influenza viruses.

Keywords: B4GALNT2; CRISPR activation screen; avian influenza virus; glycotransferase; influenza A virus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Animals
  • CRISPR-Cas Systems*
  • Carbohydrate Sequence
  • Dogs
  • Gene Expression
  • Genes, Reporter
  • Genetic Engineering
  • Genome, Human
  • HEK293 Cells
  • High-Throughput Screening Assays
  • Host-Parasite Interactions / immunology*
  • Humans
  • Influenza A virus / classification
  • Influenza A virus / genetics
  • Influenza A virus / immunology*
  • Luciferases / genetics
  • Luciferases / metabolism
  • Madin Darby Canine Kidney Cells
  • N-Acetylgalactosaminyltransferases / chemistry
  • N-Acetylgalactosaminyltransferases / genetics
  • N-Acetylgalactosaminyltransferases / immunology*
  • Polysaccharides / chemistry
  • Polysaccharides / immunology
  • Polysaccharides / metabolism
  • Receptors, Virus / chemistry
  • Receptors, Virus / genetics
  • Receptors, Virus / immunology*
  • Sialic Acids / chemistry
  • Sialic Acids / immunology*
  • Sialic Acids / metabolism

Substances

  • Polysaccharides
  • Receptors, Virus
  • Sialic Acids
  • Luciferases
  • N-Acetylgalactosaminyltransferases
  • beta-1,4-N-acetyl-galactosaminyl transferase 2