CRISPR/Cas9-mediated viral interference in plants

被引:282
作者
Ali, Zahir
Abulfaraj, Aala
Idris, Ali
Ali, Shakila
Tashkandi, Manal
Mahfouz, Magdy M. [1 ]
机构
[1] 4700 King Abdullah Univ Sci & Technol, Lab Genome Engn, Ctr Desert Agr, Thuwal 239556900, Saudi Arabia
来源
GENOME BIOLOGY | 2015年 / 16卷
关键词
Plant genome engineering; CRISPR/Cas9; system; Synthetic site-specific nucleases; Viral-mediated genome editing; Virus resistance; Tomato yellow leaf curl virus; Tobacco rattle virus; LEAF-CURL-VIRUS; CRISPR INTERFERENCE; ADAPTIVE IMMUNITY; DNA-REPLICATION; TOMATO; RNA; GENE; GEMINIVIRUSES; TYLCV; ENDONUCLEASE;
D O I
10.1186/s13059-015-0799-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The CRISPR/Cas9 system provides bacteria and archaea with molecular immunity against invading phages and conjugative plasmids. Recently, CRISPR/Cas9 has been used for targeted genome editing in diverse eukaryotic species. Results: In this study, we investigate whether the CRISPR/Cas9 system could be used in plants to confer molecular immunity against DNA viruses. We deliver sgRNAs specific for coding and non-coding sequences of tomato yellow leaf curl virus (TYLCV) into Nicotiana benthamiana plants stably overexpressing the Cas9 endonuclease, and subsequently challenge these plants with TYLCV. Our data demonstrate that the CRISPR/Cas9 system targeted TYLCV for degradation and introduced mutations at the target sequences. All tested sgRNAs exhibit interference activity, but those targeting the stem-loop sequence within the TYLCV origin of replication in the intergenic region (IR) are the most effective. N. benthamiana plants expressing CRISPR/Cas9 exhibit delayed or reduced accumulation of viral DNA, abolishing or significantly attenuating symptoms of infection. Moreover, this system could simultaneously target multiple DNA viruses. Conclusions: These data establish the efficacy of the CRISPR/Cas9 system for viral interference in plants, thereby extending the utility of this technology and opening the possibility of producing plants resistant to multiple viral infections.
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页数:11
相关论文
共 43 条
[1]   Efficient Virus-Mediated Genome Editing in Plants Using the CRISPR/Cas9 System [J].
Ali, Zahir ;
Abul-faraj, Aala ;
Li, Lixin ;
Ghosh, Neha ;
Piatek, Marek ;
Mahjoub, Ali ;
Aouida, Mustapha ;
Piatek, Agnieszka ;
Baltes, Nicholas J. ;
Voytas, Daniel F. ;
Dinesh-Kumar, Savithramma ;
Mahfouz, Magdy M. .
MOLECULAR PLANT, 2015, 8 (08) :1288-1291
[2]   A Rapid and Efficient Method for Construction of an Infectious Clone of Tomato yellow leaf curl virus [J].
Bang, Bongjun ;
Lee, Jongyun ;
Kim, Sunyoung ;
Park, Jungwook ;
Thao Thi Nguyen ;
Seo, Young-Su .
PLANT PATHOLOGY JOURNAL, 2014, 30 (03) :310-315
[3]   CRISPR-Cas systems and RNA-guided interference [J].
Barrangou, Rodolphe .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2013, 4 (03) :267-278
[4]   CRISPR Interference Can Prevent Natural Transformation and Virulence Acquisition during In Vivo Bacterial Infection [J].
Bikard, David ;
Hatoum-Aslan, Asma ;
Mucida, Daniel ;
Marraffini, Luciano A. .
CELL HOST & MICROBE, 2012, 12 (02) :177-186
[5]   The core region of the coat protein gene is highly useful for establishing the provisional identification and classification of begomoviruses [J].
Brown, JK ;
Idris, AM ;
Torres-Jerez, I ;
Banks, GK ;
Wyatt, SD .
ARCHIVES OF VIROLOGY, 2001, 146 (08) :1581-1598
[6]   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
[7]   REPLICATION OF TOMATO YELLOW LEAF CURL VIRUS (TYLCV) DNA IN AGROINOCULATED LEAF-DISKS FROM SELECTED TOMATO GENOTYPES [J].
CZOSNEK, H ;
KHEYRPOUR, A ;
GRONENBORN, B ;
REMETZ, E ;
ZEIDAN, M ;
ALTMAN, A ;
RABINOWITCH, HD ;
VIDAVSKY, S ;
KEDAR, N ;
GAFNI, Y ;
ZAMIR, D .
PLANT MOLECULAR BIOLOGY, 1993, 22 (06) :995-1005
[8]   The new frontier of genome engineering with CRISPR-Cas9 [J].
Doudna, Jennifer A. ;
Charpentier, Emmanuelle .
SCIENCE, 2014, 346 (6213) :1077-+
[9]   Programmable plasmid interference by the CRISPR-Cas system in Thermococcus kodakarensis [J].
Elmore, Joshua R. ;
Yokooji, Yuusuke ;
Sato, Takaaki ;
Olson, Sara ;
Glover, Claiborne V. C., III ;
Graveley, Brenton R. ;
Atomi, Haruyuki ;
Terns, Rebecca M. ;
Terns, Michael P. .
RNA BIOLOGY, 2013, 10 (05) :828-840
[10]   Virus-Host and CRISPR Dynamics in Archaea-Dominated Hypersaline Lake Tyrrell, Victoria, Australia [J].
Emerson, Joanne B. ;
Andrade, Karen ;
Thomas, Brian C. ;
Norman, Anders ;
Allen, Eric E. ;
Heidelberg, Karla B. ;
Banfield, Jillian F. .
ARCHAEA-AN INTERNATIONAL MICROBIOLOGICAL JOURNAL, 2013, 2013