Back to Search
Start Over
Transcription of reference genes used for quantitative RT-PCR in Atlantic salmon is affected by viral infection
- Source :
- Veterinary Research, Vol 42, Iss 1, p 8 (2011), Veterinary Research
- Publication Year :
- 2011
- Publisher :
- Springer Science and Business Media LLC, 2011.
-
Abstract
- 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.
- Subjects :
- Ribosomal Proteins
Time Factors
VDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Genetikk og genomikk: 474
Salmo salar
Short Report
VDP::Landbruks- og Fiskerifag: 900::Fiskerifag: 920::Akvakultur: 922
Alphavirus
VDP::Mathematics and natural science: 400::Basic biosciences: 470::Genetics and genomics: 474
Fish Diseases
Transcription (biology)
Reference genes
RNA, Ribosomal, 18S
medicine
Animals
Alphavirus infection
Gene
VDP::Agriculture and fishery disciplines: 900::Fisheries science: 920::Aquaculture: 922
Life Cycle Stages
lcsh:Veterinary medicine
General Veterinary
biology
Alphavirus Infections
Reverse Transcriptase Polymerase Chain Reaction
Gene Expression Profiling
biology.organism_classification
medicine.disease
veterinary(all)
Virology
Actins
Gene expression profiling
Real-time polymerase chain reaction
lcsh:SF600-1100
Viral load
Subjects
Details
- ISSN :
- 12979716
- Volume :
- 42
- Database :
- OpenAIRE
- Journal :
- Veterinary Research
- Accession number :
- edsair.doi.dedup.....50696f1e09eef3f7295c973db2e61248
- Full Text :
- https://doi.org/10.1186/1297-9716-42-8