Rescue of a plant cytorhabdovirus as versatile expression platforms for planthopper and cereal genomic studies

被引:93
作者
Gao, Qiang [1 ,2 ]
Xu, Wen-Ya [1 ,2 ]
Yan, Teng [1 ,2 ]
Fang, Xiao-Dong [1 ,2 ]
Cao, Qing [1 ,2 ]
Zhang, Zhen-Jia [1 ,2 ]
Ding, Zhi-Hang [1 ,2 ]
Wang, Ying [3 ]
Wang, Xian-Bing [1 ,2 ]
机构
[1] China Agr Univ, Coll Biol Sci, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
[2] China Agr Univ, Coll Biol Sci, Minist Agr, Key Lab Soil Microbiol, Beijing 100193, Peoples R China
[3] China Agr Univ, Coll Plant Protect, Beijing 100193, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Barley yellow striate mosaic virus; cereals; genomic studies; plant rhabdovirus; planthopper; STRIATE-MOSAIC-VIRUS; MOLECULAR-CLONING; REVERSE GENETICS; SILENCING VECTOR; FOREIGN GENES; WILD-TYPE; WHEAT; SUPPRESSION; MULTIPLICATION; TRANSMISSION;
D O I
10.1111/nph.15889
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plant viruses have been used as rapid and cost-effective expression vectors for heterologous protein expression in genomic studies. However, delivering large or multiple foreign proteins in monocots and insect pests is challenging. Here, we recovered a recombinant plant cytorhabdovirus, Barley yellow striate mosaic virus (BYSMV), for use as a versatile expression platform in cereals and the small brown planthopper (SBPH, Laodelphax striatellus) insect vector. We engineered BYSMV vectors to provide versatile expression platforms for simultaneous expression of three foreign proteins in barley plants and SBPHs. Moreover, BYSMV vectors could express the c. 600-amino-acid beta-glucuronidase (GUS) protein and a red fluorescent protein stably in systemically infected leaves and roots of cereals, including wheat, barley, foxtail millet, and maize plants. Moreover, we have demonstrated that BYSMV vectors can be used in barley to analyze biological functions of gibberellic acid (GA) biosynthesis genes. In a major technical advance, BYSMV vectors were developed for simultaneous delivery of CRISPR/Cas9 nuclease and single guide RNAs for genomic editing in Nicotiana benthamiana leaves. Taken together, our results provide considerable potential for rapid screening of functional proteins in cereals and planthoppers, and an efficient approach for developing other insect-transmitted negative-strand RNA viruses.
引用
收藏
页码:2120 / 2133
页数:14
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