Jaree Phattarunda, Boonchuen Pakpoom, Thawonsuwan Jumroensri, Kondo Hidehiro, Hirono Ikuo, Somboonwiwat Kunlaya
Center of Applied Shrimp Research and Innovation, Institute of Molecular Biosciences, Mahidol University, Salaya, Nakhon Pathom, Thailand.
School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
Fish Shellfish Immunol. 2022 Jan;120:31-44. doi: 10.1016/j.fsi.2021.11.006. Epub 2021 Nov 7.
The white spot syndrome virus (WSSV) has been considered a serious threat to shrimp aquaculture. Besides, the activation of cell metabolism as an immune reaction to the virus is now recognized as a piece of the pivotal puzzle of the antiviral responses. Hence, this study explores the relationship between metabolic gene expression and antiviral responses in shrimp using transcriptome analysis. The RNA-seq libraries of Fenneropenaeus merguensis hemocytes after WSSV challenge at early (6 hpi) and late (24 hpi) stages of infection were analyzed to identify differentially expressed genes (DEGs) that the WSSV subverted the expression. One-hundred-thirty-three DEGs that were expressed in response to WSSV infection at both stages were identified. Based on the GO annotation, they were related to innate immunity and metabolic pathway. The expression correlation between "full term" (NGS) and qRT-PCR of 16 representative DEGs is shown. Noticeably, the expression profiles of all the selected metabolic genes involved in glucose metabolism, lipid metabolism, amino acid metabolism, and nucleotide metabolism showed a specific correlation between NGS and qRT-PCR upon WSSV infection. Of these, we further characterized the function related to the WSSV response of glutamine: fructose-6-phosphate aminotransferase (FmGFAT), the rate-limiting enzyme of the hexosamine biosynthesis pathway, which was found to be up-regulated at the late stage of WSSV infection. Suppression of FmGFAT by RNA interference resulted in postponing the death of WSSV-infected shrimp and reduction of viral copy number. These results suggested that the FmGFAT is linked between metabolic change and WSSV responses in shrimp, where the virus-induced metabolic rewiring hijack biological compounds and/or energy sources to benefit the viral replication process.
白斑综合征病毒(WSSV)一直被认为是对虾类养殖的严重威胁。此外,细胞代谢的激活作为对病毒的免疫反应,如今被视为抗病毒反应关键谜题的一部分。因此,本研究利用转录组分析探索虾类中代谢基因表达与抗病毒反应之间的关系。分析了墨吉对虾血细胞在WSSV感染早期(感染后6小时)和晚期(感染后24小时)的RNA测序文库,以鉴定WSSV干扰表达的差异表达基因(DEG)。共鉴定出133个在两个阶段均对WSSV感染有反应而表达的DEG。基于基因本体(GO)注释,它们与先天免疫和代谢途径相关。展示了16个代表性DEG的“完整数据”(NGS)与定量逆转录聚合酶链反应(qRT-PCR)之间的表达相关性。值得注意的是,所有参与葡萄糖代谢、脂质代谢、氨基酸代谢和核苷酸代谢的选定代谢基因的表达谱在WSSV感染时,在NGS和qRT-PCR之间呈现出特定的相关性。其中,我们进一步表征了谷氨酰胺:果糖-6-磷酸氨基转移酶(FmGFAT)(己糖胺生物合成途径的限速酶)与WSSV反应相关的功能,发现其在WSSV感染后期上调。通过RNA干扰抑制FmGFAT导致WSSV感染的虾死亡延迟且病毒拷贝数减少。这些结果表明,FmGFAT在虾类的代谢变化与WSSV反应之间建立了联系,病毒诱导的代谢重编程劫持生物化合物和/或能量来源以利于病毒复制过程。