Section for immunoprophylaxis, National Veterinary Institute, P,O, Box 750 Sentrum, 0106 Oslo, Norway.
Vet Res. 2011 Jan 18;42(1):8. doi: 10.1186/1297-9716-42-8.
Relative quantification using RT-qPCR is a widely used method for transcription profiling. Transcript levels of target genes in fish after experimental infection is often reported without documentation of stably transcribed reference genes. We present results demonstrating that transcription of typically used reference genes in Atlantic salmon is not stable during experimental infection with salmon pancreas disease virus (SPDV). Transcript levels 0 to 6 weeks after challenge revealed statistically significant changes between time-points that corresponded with a peak in viral load 3 weeks after challenge. The results emphasize the need for thorough method validation prior to transcriptional studies during viral infections.
相对定量 RT-qPCR 是一种广泛用于转录谱分析的方法。在实验感染后,鱼类靶基因的转录本水平通常在没有稳定转录参考基因记录的情况下报告。我们提供的结果表明,在感染三文鱼胰腺坏死病病毒(SPDV)的实验中,通常用于大西洋三文鱼的参考基因的转录并不稳定。在挑战后 0 到 6 周的转录本水平显示出统计学上显著的时间点变化,与挑战后 3 周病毒载量峰值相对应。这些结果强调了在病毒感染期间进行转录研究之前需要进行彻底的方法验证。