Transcriptome analyses of amoebic gill disease-affected Atlantic salmon (Salmo salar) tissues reveal localized host gene suppression

• Published in: Marine Biotechnology
• Main Authors: Wynne, James, O'Sullivan, Maree, Cook, Mathew, Stone, Glenn, Nowak, Barbara, Lovell, David, Elliott, Nicholas
• Format: Article in Journal/Newspaper
• Language: unknown
• Published: Springer New York 2008
• Subjects: AGD; Ameliorate; Amoeba; Amoebic gill disease (AGD); Amoebida; Animals; Atlantic salmon; DNA; DNA microarray; Disease control; Fish Diseases; Genetic engineering; Gills; Host response; Marine biology; Microarray; Oligonucleotide Array Sequence Analysis; Parasite infection; QPCR analysis; Real time control; Reproducibility of Results; Salmo salar; Salmonid; Salmonidae; Salmonids; Sarcomastigophora Infections; Tissue engineering; Transcription; animal; animal disease; article; fish disease; gene expression; gene expression profiling; gene expression regulation; genetics; gill; kidney; liver; metabolism; parasite infestation; parasitic disease; parasitism; parasitology; pathology; physiology; polymerase chain reaction; reproducibility; sarcomastigophora infection
• Online Access: https://eprints.qut.edu.au/79856/

The transcriptome response of Atlantic salmon (Salmo salar) displaying advanced stages of amoebic gill disease (AGD) was investigated. Naïve smolt were challenged with AGD for 19 days, at which time all fish were euthanized and their severity of infection quantified through histopathological scoring. Gene expression profiles were compared between heavily infected and naïve individuals using a 17 K Atlantic salmon cDNA microarray with real-time quantitative RT-PCR (qPCR) verification. Expression profiles were examined in the gill, anterior kidney, and liver. Twenty-seven transcripts were significantly differentially expressed within the gill; 20 of these transcripts were down-regulated in the AGD-affected individuals compared with naïve individuals. In contrast, only nine transcripts were significantly differentially expressed within the anterior kidney and five within the liver. Again the majority of these transcripts were down-regulated within the diseased individuals. A down-regulation of transcripts involved in apoptosis (procathepsin L, cathepsin H precursor, and cystatin B) was observed in AGD-affected Atlantic salmon. Four transcripts encoding genes with antioxidant properties also were down-regulated in AGD-affected gill tissue according to qPCR analysis. The most up-regulated transcript within the gill was an unknown expressed sequence tag (EST) whose expression was 218-fold (± SE 66) higher within the AGD affected gill tissue. Our results suggest that Atlantic salmon experiencing advanced stages of AGD demonstrate general down-regulation of gene expression, which is most pronounced within the gill. We propose that this general gene suppression is parasite-mediated, thus allowing the parasite to withstand or ameliorate the host response. © 2008 Springer Science+Business Media, LLC.