Transcriptome profiling and histology changes in juvenile blunt snout bream (Megalobrama amblycephala) liver tissue in response to acute thermal stress

To understand the precise mechanism and the pathways activated by thermal stress in fish, we sampled livers from juvenile Megalobrama amblycephala exposed to control (25 °C) and test (35 °C) conditions, and performed short read (100 bp) next-generation RNA sequencing (RNA-seq). Using reads from diff...

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Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 2019-05, Vol.111 (3), p.242-250
Hauptverfasser: Li, Bing, Sun, Shengming, Zhu, Jian, Yanli, Su, Wuxiao, Zhang, Ge, Xianping
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Sprache:eng
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Zusammenfassung:To understand the precise mechanism and the pathways activated by thermal stress in fish, we sampled livers from juvenile Megalobrama amblycephala exposed to control (25 °C) and test (35 °C) conditions, and performed short read (100 bp) next-generation RNA sequencing (RNA-seq). Using reads from different temperature, expression analysis identified a total of 440 differentially-expressed genes. These genes were related to oxidative stress, apoptosis, immune responses and so on. We used quantitative real-time reverse transcriptase PCR to assess the differential mRNA expression of selected genes that encode antioxidant enzymes and heat shock proteins in response to thermal stress. Fish exposed to thermal stress also showed liver damage associated with serum biochemical parameter changes. The set of genes identified showed regulatory modulation at different temperatures, and therefore could be further studied to determine how thermal stress damages M. amblycephala livers and the possible roles of reactive oxygen species in this process. •Under thermal stress, genes linked to oxidative stress and immune responses were up-regulated.•These genes could be used as biomarkers of thermal stress.•Thermal stress also changed the histology of hepatocytes.•Heat-damaged mitochondria could increase production of reactive oxygen species and cause oxidative stress.
ISSN:0888-7543
1089-8646
DOI:10.1016/j.ygeno.2018.11.011