Analysis of IAV Replication and Co-infection Dynamics by a Versatile RNA Viral Genome Labeling Method

Cell Rep. 2017 Jul 5;20(1):251-263. doi: 10.1016/j.celrep.2017.06.021.

Abstract

Genome delivery to the proper cellular compartment for transcription and replication is a primary goal of viruses. However, methods for analyzing viral genome localization and differentiating genomes with high identity are lacking, making it difficult to investigate entry-related processes and co-examine heterogeneous RNA viral populations. Here, we present an RNA labeling approach for single-cell analysis of RNA viral replication and co-infection dynamics in situ, which uses the versatility of padlock probes. We applied this method to identify influenza A virus (IAV) infections in cells and lung tissue with single-nucleotide specificity and to classify entry and replication stages by gene segment localization. Extending the classification strategy to co-infections of IAVs with single-nucleotide variations, we found that the dependence on intracellular trafficking places a time restriction on secondary co-infections necessary for genome reassortment. Altogether, these data demonstrate how RNA viral genome labeling can help dissect entry and co-infections.

Keywords: IAV cell co-infections; IAV entry; IAV replication cycle; RNA labeling; RNA viruses; influenza A virus; single-cell IAV genome trafficking; single-nucleotide specificity; vRNAs; viral genome labeling and localization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dogs
  • Epithelial Cells / virology
  • Genome, Viral*
  • HEK293 Cells
  • Humans
  • Influenza A virus / genetics
  • Influenza A virus / physiology*
  • Madin Darby Canine Kidney Cells
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • RNA, Viral / metabolism*
  • Single-Cell Analysis / methods*
  • Staining and Labeling / methods*
  • Viral Proteins / metabolism
  • Virus Replication*

Substances

  • RNA, Viral
  • Viral Proteins