De-Novo Transcriptome Sequencing of a Normalized cDNA Pool from Influenza Infected Ferrets
Author(s) -
Jeremy V. Camp,
Thomas Svensson,
Alexis McBrayer,
Colleen B. Jonsson,
Peter Liljeström,
Carl E.G. Bruder
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0037104
Subject(s) - biology , transcriptome , complementary dna , gene , genbank , genetics , cdna library , de novo transcriptome assembly , innate immune system , gene expression profiling , dna sequencing , computational biology , gene expression , immune system
The ferret is commonly used as a model for studies of infectious diseases. The genomic sequence of this animal model is not yet characterized, and only a limited number of fully annotated cDNAs are currently available in GenBank. The majority of genes involved in innate or adaptive immune response are still lacking, restricting molecular genetic analysis of host response in the ferret model. To enable de novo identification of transcriptionally active ferret genes in response to infection, we performed de-novo transcriptome sequencing of animals infected with H1N1 A/California/07/2009. We also included splenocytes induced with bacterial lipopolysaccharide to allow for identification of transcripts specifically induced by Gram-negative bacteria. We pooled and normalized the cDNA library in order to delimit the risk of sequencing only highly expressed genes. While normalization of the cDNA library removes the possibility of assessing expression changes between individual animals, it has been shown to increase identification of low abundant transcripts. In this study, we identified more than 19000 partial ferret transcripts, including more than 1000 gene orthologs known to be involved in the innate and the adaptive immune response.
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