
doi: 10.2139/ssrn.6161570
Grass carp is the most produced freshwater aquaculture species in China. However, high-density farming is often accompanied by severe disease outbreaks, causing significant economic losses to the industry. To support disease research and control, we developed an immersion challenge model in which fish were exposed to type II grass carp reovirus (4.23 × 103 copies/μL) for 30 min under controlled conditions (28 ℃, dissolved oxygen > 6 mg/L). This method resulted in an infection mortality rate of 86% and induced typical symptoms of grass carp hemorrhagic disease, including hemorrhage at the fin base and body surface, hemosiderin deposition in the spleen, and intestinal damage. Transcriptome sequencing of spleen collected at 0, 12, 36, 72, and 120 hours post-infection (hpi) yielded high-quality data from 15 samples. Compared to the 0 hpi group, 7182, 3856, 5770, and 5123 differentially expressed genes (DEGs) were identified at 12, 36, 72, and 120 hpi, respectively. These DEGs were significantly enriched in pathways related to innate and adaptive immunity, such as inflammatory responses, immunoglobulin receptor binding, and Toll-like receptor signaling pathway. Further analysis revealed significant upregulation of key immune gene families, including TLRs, RLRs, IFNs, IRFs, SOCS, antigen-presenting molecules, and immunoglobulins. In conclusion, the immersion challenge method established in this study effectively activates both the innate and adaptive immune system in grass carp, providing a reliable experimental model and theoretical foundation for elucidating the pathogenic mechanisms of grass carp hemorrhagic disease, advancing vaccine development, and disease-resistant breeding.
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