Cillo Fabrizio, Palukaitis Peter
Istituto di Virologia Vegetale, CNR, Bari, Italy.
Department of Horticultural Sciences, Seoul Women's University, Seoul, Republic of Korea.
Adv Virus Res. 2014;90:35-146. doi: 10.1016/B978-0-12-801246-8.00002-0.
Transgenic resistance to plant viruses is an important technology for control of plant virus infection, which has been demonstrated for many model systems, as well as for the most important plant viruses, in terms of the costs of crop losses to disease, and also for many other plant viruses infecting various fruits and vegetables. Different approaches have been used over the last 28 years to confer resistance, to ascertain whether particular genes or RNAs are more efficient at generating resistance, and to take advantage of advances in the biology of RNA interference to generate more efficient and environmentally safer, novel "resistance genes." The approaches used have been based on expression of various viral proteins (mostly capsid protein but also replicase proteins, movement proteins, and to a much lesser extent, other viral proteins), RNAs [sense RNAs (translatable or not), antisense RNAs, satellite RNAs, defective-interfering RNAs, hairpin RNAs, and artificial microRNAs], nonviral genes (nucleases, antiviral inhibitors, and plantibodies), and host-derived resistance genes (dominant resistance genes and recessive resistance genes), and various factors involved in host defense responses. This review examines the above range of approaches used, the viruses that were tested, and the host species that have been examined for resistance, in many cases describing differences in results that were obtained for various systems developed in the last 20 years. We hope this compilation of experiences will aid those who are seeking to use this technology to provide resistance in yet other crops, where nature has not provided such.
植物病毒转基因抗性是控制植物病毒感染的一项重要技术,就作物因病害造成的损失成本而言,该技术已在许多模式系统以及最重要的植物病毒中得到验证,对于许多感染各种水果和蔬菜的其他植物病毒也是如此。在过去28年里,人们采用了不同方法来赋予抗性,以确定特定基因或RNA在产生抗性方面是否更有效,并利用RNA干扰生物学的进展来产生更高效、对环境更安全的新型“抗性基因”。所采用的方法基于各种病毒蛋白(主要是衣壳蛋白,但也有复制酶蛋白、运动蛋白,以及程度较小的其他病毒蛋白)、RNA(正义RNA(可翻译或不可翻译)、反义RNA、卫星RNA、缺陷干扰RNA、发夹RNA和人工微小RNA)、非病毒基因(核酸酶、抗病毒抑制剂和植物抗体)以及宿主衍生的抗性基因(显性抗性基因和隐性抗性基因),以及宿主防御反应中涉及的各种因素。本综述考察了上述一系列所采用的方法、所测试的病毒以及为检测抗性而研究的宿主物种,在许多情况下描述了过去20年开发的各种系统所获得的结果差异。我们希望这一经验汇编能帮助那些试图利用这一技术在自然未赋予抗性的其他作物中提供抗性的人。