Xu Jingxiang, Ruan Lingwei, Shi Hong
School of Life Science, Xiamen University, Xiamen 361005, PR China; State Key Laboratory Breeding Base of Marine Genetic Resources, Xiamen 361005, PR China.
State Key Laboratory Breeding Base of Marine Genetic Resources, Xiamen 361005, PR China; Key Laboratory of Marine Genetic Resources, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, PR China; Key Laboratory of Marine Genetic Resources, Fujian Province, Xiamen 361005, PR China.
Fish Shellfish Immunol. 2014 Oct;40(2):609-15. doi: 10.1016/j.fsi.2014.08.016. Epub 2014 Aug 20.
The alpha subunit of Eukaryotic Initiation Factor 2 (eIF2α) is a key translation regulator that plays an important role in cellular stress responses, which including virus infection. To investigate whether WSSV infection can activate the PERK-eIF2α pathway, the eIF2α in shrimp Litopenaeus vannamei, designed as LveIF2α, was analyzed. The LveIF2α, a 332-amino acid polypeptide, shares a high degree of similarity with eIF2α from other species, having two eIF2α protein signatures at the 13-88 aa and 192-243 aa. The WSSV challenge experiment showed that the protein level of the total LveIF2α was decreased after infection, while the phosphorylation of LveIF2α has no significant change, which indicated that the phosphorylation ratio of LveIF2α was increased after infection. Furthermore, inhibitor treatment led to a significant decrease of WSSV loads. Moreover, the Binding immunoglobulin protein (BiP), an endoplasmic reticulum (ER) stress sensor, and PERK were also investigated during virus infection and it was shown that they were both up-regulated. Taken together, these results suggested that WSSV infection can induce ER stress and activated the unfolded protein response (UPR), and the PERK-eIF2α pathway is important for innate immune during WSSV infection in shrimp.
真核起始因子2(eIF2α)的α亚基是一种关键的翻译调节因子,在包括病毒感染在内的细胞应激反应中发挥重要作用。为了研究白斑综合征病毒(WSSV)感染是否能激活PERK-eIF2α途径,对凡纳滨对虾中的eIF2α(命名为LveIF2α)进行了分析。LveIF2α是一种由332个氨基酸组成的多肽,与其他物种的eIF2α具有高度相似性,在第13 - 88位氨基酸和第192 - 243位氨基酸处有两个eIF2α蛋白特征序列。WSSV攻毒实验表明,感染后LveIF2α的总蛋白水平下降,而LveIF2α的磷酸化水平无显著变化,这表明感染后LveIF2α的磷酸化比例增加。此外,抑制剂处理导致WSSV载量显著降低。此外,还研究了病毒感染过程中内质网应激传感器结合免疫球蛋白蛋白(BiP)和PERK,结果表明它们均上调。综上所述,这些结果表明WSSV感染可诱导内质网应激并激活未折叠蛋白反应(UPR),且PERK-eIF2α途径在对虾WSSV感染期间的先天免疫中起重要作用。