Isolating Viral and Host RNA Sequences from Archival Material and Production of cDNA Libraries for High-Throughput DNA Sequencing

Curr Protoc Microbiol. 2015 May 1:37:1E.8.1-16. doi: 10.1002/9780471729259.mc01e08s37.

Abstract

The vast majority of surgical biopsy and post-mortem tissue samples are formalin-fixed and paraffin-embedded (FFPE), but this process leads to RNA degradation that limits gene expression analysis. As an example, the viral RNA genome of the 1918 pandemic influenza A virus was previously determined in a 9-year effort by overlapping RT-PCR from post-mortem samples. Using the protocols described here, the full genome of the 1918 virus was determined at high coverage in one high-throughput sequencing run of a cDNA library derived from total RNA of a 1918 FFPE sample after duplex-specific nuclease treatments. This basic methodological approach should assist in the analysis of FFPE tissue samples isolated over the past century from a variety of infectious diseases.

Keywords: RNA; cDNA; high-throughput sequencing; influenza; library; polymerase chain reaction.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Gene Library*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Influenza A Virus, H1N1 Subtype / genetics*
  • Influenza A Virus, H1N1 Subtype / isolation & purification
  • Influenza Pandemic, 1918-1919
  • Pathology, Molecular / methods*
  • RNA, Viral / genetics
  • RNA, Viral / isolation & purification*

Substances

  • RNA, Viral