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首页> 外文期刊>Science China Life Sciences >Rice yellow stunt virus activates polyamine biosynthesis to promote viral propagation in insect vectors by disrupting ornithine decarboxylase antienzyme function
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Rice yellow stunt virus activates polyamine biosynthesis to promote viral propagation in insect vectors by disrupting ornithine decarboxylase antienzyme function

机译:米黄色特技病毒激活多胺生物合成,通过破坏鸟氨酸脱羧酶抗舟液佐功能来促进昆虫载体中的病毒繁殖

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Intracellular polyamines (putrescine, spermidine, and spermine) have emerged as important molecules for viral infection; however, how viruses activate polyamines biosynthesis to promote viral infection remains unclear. Ornithine decarboxylase 1 (ODC1) and its antienzyme 1 (OAZ1) are major regulators of polyamine biosynthesis in animal cells. Here, we report that rice yellow stunt virus (RYSV), a plant rhabdovirus, could activate putrescine biosynthesis in leafhoppers to promote viral propagation by inhibiting OAZ1 expression. We observed that the reduction of putrescine biosynthesis by treatment with difluormethylornithine (DFMO), a specific nontoxic inhibitor of ODC1, or with in vitro synthesized dsRNAs targeting ODC1 mRNA could inhibit viral infection. In contrast, the supplement of putrescine or the increase of putrescine biosynthesis by treatment with dsRNAs targeting OAZ1 mRNA could facilitate viral infection. We further determined that both RYSV matrix protein M and ODC1 directly bind to the ODC-binding domain at the C-terminus of OAZ1. Thus, viral propagation in leafhoppers would decrease the ability of OAZ1 to target and mediate the degradation of ODC1, which finally activates putrescine production to benefit viral propagation. This work reveals that polyamine-metabolizing enzymes are directly exploited by a vector-borne virus to increase polyamine production, thereby facilitating viral infection in insect vectors.
机译:细胞内多胺(Putrescine,Fepermidine和Flemermine)出现为病毒感染的重要分子;然而,病毒如何激活多胺生物合成以促进病毒感染仍然不清楚。鸟氨酸脱羧酶1(ODC1)及其抗胶质表1(OAZ1)是动物细胞中多胺生物合成的主要调节因子。在这里,我们举报了米黄色特技病毒(Rysv),植物rhabdovirus,可以通过抑制OAZ1表达来激活叶蝉中的Putrescine生物合成,以促进病毒繁殖。我们观察到通过用二氟甲醇(DFMO),ODC1的特异性无毒抑制剂或靶向ODC1 mRNA的体外合成的DSRNA治疗来减少Putrescine生物合成,或者靶向ODC1 mRNA的体外的DSRNA可以抑制病毒感染。相比之下,通过用靶向OAZ1 mRNA的DSRNA治疗来补充Putrescine或Putrescine生物合成的增加可以促进病毒感染。我们进一步确定Rysv基质蛋白M和ODC1两种术语均直接与OAZ1的C-末端的ODC结合结构域结合。因此,叶蝉中的病毒繁殖会降低OAZ1对靶向的能力,并介导ODC1的降解,最终激活腐败的产生以益处病毒繁殖。该工作表明,多胺代谢酶被载体传播病毒直接利用,以增加多胺产生,从而促进昆虫载体中的病毒感染。

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