Efficient resistance to grass carp reovirus infection in JAM-A knockout cells using CRISPR/Cas9

被引:56
作者
Ma, Jie [1 ,2 ,3 ]
Fan, Yuding [1 ]
Zhou, Yong [1 ]
Liu, Wenzhi [1 ]
Jiang, Nan [1 ]
Zhang, Jieming [1 ]
Zeng, Lingbing [1 ]
机构
[1] Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Div Fish Dis, Wuhan 430223, Hubei, Peoples R China
[2] Univ Idaho, Coll Nat Resources, Dept Fish & Wildlife Sci, Moscow, ID 83844 USA
[3] Univ Idaho, Coll Nat Resources, Aquaculture Res Inst, Moscow, ID 83844 USA
基金
中国国家自然科学基金;
关键词
GCRV; JAM-A; CRISPR/Cas9; Knockout; Resistance;
D O I
10.1016/j.fsi.2018.02.039
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The hemorrhagic disease of grass carp (Ctenopharyngodon idellus) induced by grass carp reovirus (GCRV) leads to huge economic losses in China and currently, there are no effective methods available for prevention and treatment. The various GCRV genotypes may be one of the major obstacles in the pursuit of an effective antiviral treatment. In this study, we exploited CRISPR/Cas9 gene editing to specifically knockout the DNA sequence of the grass carp Junctional Adhesion Molecule-A (gcJAM-A) and evaluated in vitro resistance against various GCRV genotypes. Our results show that CRISPR/Cas9 effectively knocked out gcJAM-A and reduced GCRV infection for two different genotypes in permissive grass carp kidney cells (CIK), as evidenced by suppressed cytopathic effect (CPE) and GCRV progeny production in infected cells. In addition, with ectopic expression of gcJAM-A in cells, non-permissive cells derived from Chinese giant salamander (Andrias davidianus) muscle (GSM) could be highly infected by both GCRV-JX0901 and Hubei grass carp disease reovirus (HGDRV) strains that have different genotypes. Taken together, the results demonstrate that gcJAM-A is necessary for GCRV infection, implying a potential approach for viral control in aquaculture.
引用
收藏
页码:206 / 215
页数:10
相关论文
共 39 条
[1]  
[Anonymous], J FISH CHINA
[2]  
[Anonymous], 2019, STAT WORLD FISH AQ
[3]   Junctional Adhesion Molecule-A Is Required for Hematogenous Dissemination of Reovirus [J].
Antar, Annukka A. R. ;
Konopka, Jennifer L. ;
Campbell, Jacquelyn A. ;
Henry, Rachel A. ;
Perdigoto, Ana L. ;
Carter, Bruce D. ;
Pozzi, Ambra ;
Abel, Ty W. ;
Dermody, Terence S. .
CELL HOST & MICROBE, 2009, 5 (01) :59-71
[4]   Junction adhesion molecule is a receptor for reovirus [J].
Barton, ES ;
Forrest, JC ;
Connolly, JL ;
Chappell, JD ;
Liu, Y ;
Schnell, FJ ;
Nusrat, A ;
Parkos, CA ;
Dermody, TS .
CELL, 2001, 104 (03) :441-451
[5]   Junctional adhesion molecule a serves as a receptor for prototype and field-isolate strains of mammalian reovirus [J].
Campbell, JA ;
Schelling, P ;
Wetzel, JD ;
Johnson, EM ;
Forrest, JC ;
Wilson, GAR ;
Aurrand-Lions, M ;
Imhof, BA ;
Stehle, T ;
Dermody, TS .
JOURNAL OF VIROLOGY, 2005, 79 (13) :7967-7978
[6]   Increased DC trafficking to lymph nodes and contact hypersensitivity in junctional adhesion molecule-A-deficient mice [J].
Cera, MR ;
Del Prete, A ;
Vecchi, A ;
Corada, M ;
Martin-Padura, I ;
Motoike, T ;
Tonetti, P ;
Bazzoni, G ;
Vermi, W ;
Gentili, F ;
Bernasconi, S ;
Sato, TN ;
Mantovani, A ;
Dejana, E .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (05) :729-738
[7]   Identification of Type I IFN in Chinese giant salamander (Andrias davidianus) and the response to an iridovirus infection [J].
Chen, Qian ;
Ma, Jie ;
Fan, Yuding ;
Meng, Yan ;
Xu, Jin ;
Zhou, Yong ;
Liu, Wenzhi ;
Zeng, Xianhui ;
Zeng, Lingbing .
MOLECULAR IMMUNOLOGY, 2015, 65 (02) :350-359
[8]   Multiplex Genome Engineering Using CRISPR/Cas Systems [J].
Cong, Le ;
Ran, F. Ann ;
Cox, David ;
Lin, Shuailiang ;
Barretto, Robert ;
Habib, Naomi ;
Hsu, Patrick D. ;
Wu, Xuebing ;
Jiang, Wenyan ;
Marraffini, Luciano A. ;
Zhang, Feng .
SCIENCE, 2013, 339 (6121) :819-823
[9]   Establishment of a highly efficient virus-inducible CRISPR/Cas9 system in insect cells [J].
Dong, Zhan-Qi ;
Chen, Ting-Ting ;
Zhang, Jun ;
Hu, Nan ;
Cao, Ming-Ya ;
Dong, Fei-Fan ;
Jiang, Ya-Ming ;
Chen, Peng ;
Lu, Cheng ;
Pan, Min-Hui .
ANTIVIRAL RESEARCH, 2016, 130 :50-57
[10]   Cloning and preliminary functional studies of the JAM-A gene in grass carp (Ctenopharyngodon idellus) [J].
Du, Fukuan ;
Su, Jianguo ;
Huang, Rong ;
Liao, Lanjie ;
Zhu, Zuoyan ;
Wang, Yaping .
FISH & SHELLFISH IMMUNOLOGY, 2013, 34 (06) :1476-1484