Abstract

Fish under intensive rearing conditions experience various stressors which have negative impacts on survival, growth, reproduction and fillet quality. Identifying and characterizing the molecular mechanisms underlying stress responses will facilitate the development of strategies that aim to improve animal welfare and aquaculture production efficiency. In this study, we used RNA-seq to identify transcripts which are differentially expressed in the rainbow trout liver in response to handling and confinement stress. These stressors were selected due to their relevance in aquaculture production. Total RNA was extracted from the livers of individual fish in five tanks having eight fish each, including three tanks of fish subjected to a 3 hour handling and confinement stress and two control tanks. Equal amount of total RNA of six individual fish was pooled by tank to create five RNA-seq libraries which were sequenced in one lane of Illumina HiSeq 2000. Three sequencing runs were conducted to obtain a total of 491,570,566 reads which were mapped onto the previously generated stress reference transcriptome to identify 316 differentially expressed transcripts (DETs). Twenty one DETs were selected for qPCR to validate the RNA-seq approach. The fold changes in gene expression identified by RNA-seq and qPCR were highly correlated (R2 = 0.88). Several gene ontology terms including transcription factor activity and biological process such as glucose metabolic process were enriched among these DETs. Pathways involved in response to handling and confinement stress were implicated by mapping the DETs to reference pathways in the KEGG database.Accession NumbersRaw RNA-seq reads have been submitted to the NCBI Short Read Archive under accession number SRP022881.Customized Perl ScriptsAll customized scripts described in this paper are available from Dr. Guangtu Gao or the corresponding author.

Highlights

  • Aquaculture is the fastest-growing animal food producing sector of agriculture

  • As the mapping results were in great agreement among runs (Fig. S1), we used the combined mapping results to identify differentially expressed transcripts (DETs) in response to handling and confinement stress

  • 74 DETs were downregulated with a range of fold change from 21.6 to 212.9; the remaining 242 DETs were up-regulated with a range of fold change from 1.6 to 22.4

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Summary

Introduction

Aquaculture is the fastest-growing animal food producing sector of agriculture. Rainbow trout (Oncorhynchus mykiss) is an important aquaculture species; it is a primary research model for fish [1]. Stress has been shown to have negative impacts on survival, growth, reproduction and fillet quality [2,3,4,5,6,7,8,9], to improve production efficiency it is crucial to understand stress responses at the physiological and molecular levels. To this end stress responses have been extensively studied in fishes [4,10,11,12]. Detection is limited to the probes included in the microarray design, the detection range is limited by background signal and signal saturation, and differences in expression between paralogous genes is complicated by cross-hybridization, which is a particular problem for species such as the rainbow trout where more than half of the genes are thought to be duplicated due to a relatively recent whole genome duplication [17,18]

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