Endosomes and Microtubles are Required for Productive Infection in Aquareovirus  

作　　者：Fuxian Zhang Hong Guo Qingxiu Chen Zheng Ruan Qin Fang 

机构地区：[1]State Key Laboratory of Virology,Wuhan Institute of Virology,Chinese Academy of Sciences.Wuhan 430071,China [2]Wuhan Center for Animal Diseases Prevention and Control,Wuhan 430071,China

出　　处：《Virologica Sinica》2020年第2期200-211,共12页中国病毒学（英文版）

基　　金：This work is supported in part by grants from the National Natural Science Foundation of China(31672693,31972838 and 31400139,31372565).

摘　　要：Grass carp reovirus(GCRV),the genus Aquareovirus in family Reoviridae,is viewed as the most pathogenic aquareovirus.To understand the molecular mechanism of how aquareovirus initiates productive infection,the roles of endosome and microtubule in cell entry of GCRV are investigated by using quantum dots(QDs)-tracking in combination with biochemical approaches.We found that GCRV infection and viral protein synthesis were significantly inhibited by pretreating host cells with endosome acidification inhibitors NH4Cl,chloroquine and bafilomycin A1(Bafi).Confocal images indicated that GCRV particles could colocalize with Rab5,Rab7 and lysosomes in host cells.Further ultrastructural examination validated that viral particle was found in late endosomes.Moreover,disruption of microtubules with nocodazole clearly blocked GCRV entry,while no inhibitory effects were observed with cytochalasin D treated cells in viral infection,hinting that intracellular transportation of endocytic uptake in GCRV infected cells is via microtubules but not actin filament.Notably,viral particles were observed to transport along microtubules by using QD-labeled GCRV.Altogether,our results suggest that GCRV can use endosomes and microtubules to initiate productive infection.

关 键 词：AQUAREOVIRUS Cell entry Quantum dot ENDOSOME MICROTUBULE 

分 类 号：S941.41[农业科学—水产养殖]