Viral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
J Pathol. 2013 Mar;229(4):535-45. doi: 10.1002/path.4145.
Most biopsy and autopsy tissues are formalin-fixed and paraffin-embedded (FFPE), but this process leads to RNA degradation that limits gene expression analysis. The RNA genome of the 1918 pandemic influenza virus was previously determined in a 9-year effort by overlapping RT-PCR from post-mortem samples. Here, the full genome of the 1918 virus at 3000× coverage was determined in one high-throughput sequencing run of a library derived from total RNA of a 1918 FFPE sample after duplex-specific nuclease treatments. Bacterial sequences associated with secondary bacterial pneumonias were also detected. Host transcripts were well represented in the library. Compared to a 2009 pandemic influenza virus FFPE post-mortem library, the 1918 sample showed significant enrichment for host defence and cell death response genes, concordant with prior animal studies. This methodological approach should assist in the analysis of FFPE tissue samples isolated over the past century from a variety of diseases.
大多数活检和尸检组织都经过福尔马林固定和石蜡包埋(FFPE)处理,但该过程会导致 RNA 降解,限制基因表达分析。1918 年大流感病毒的 RNA 基因组此前通过对死后样本进行重叠 RT-PCR 分析,历经 9 年的努力才得以确定。在这里,从 1918 年 FFPE 样本的总 RNA 衍生的文库中进行一次高通量测序运行,即可确定具有 3000×覆盖度的 1918 病毒的全基因组。还检测到与继发性细菌性肺炎相关的细菌序列。文库中很好地代表了宿主转录物。与 2009 年大流感病毒 FFPE 尸检文库相比,1918 年样本中宿主防御和细胞死亡反应基因明显富集,与之前的动物研究一致。这种方法应该有助于分析过去一个世纪以来从各种疾病中分离出来的 FFPE 组织样本。