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Response of Resistant Pepper Varieties to Viruses in the Genus Potyvirus.

机译:抗性辣椒品种对马铃薯痘病毒属中病毒的反应。

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摘要

Potyviruses are a persistent threat to bell pepper (Capsicum annuum L.) production worldwide. We have expended much effort to study the resistance response of pepper cultivars at cellular and whole plant levels. To evaluate the resistance response at the cellular level, mesophyll protoplasts are isolated and inoculated with viral RNA. An efficient isolation procedure was available but an inoculation procedure was needed that provided consistent and highly efficient inoculation. An electroporation inoculation procedure was developed by evaluation of key parameters that included voltage, number of pulses, time interval between pulses, viral RNA concentration and number of evaluated protoplasts. Consistent infection with the highest virus titer and protoplast viability resulted when 40 mug of virus RNA was used to inoculate 500,000 protoplasts using two 25-msec pulses of 200 volts each with a 10-sec time interval between pulses.;Two important sources of resistance were evaluated for their response to inoculation with four strains of Tobacco etch virus (TEV, genus Potyvirus). The resistant cultivars were CA4 and Dempsey which contain the pvr1 and pvr12 resistance genes, respectively. Both cultivars resisted infection by TEV strain NW; however, two CA4 plants inoculated with NW maintained in pepper became infected. When the infected CA4 plants were used as inoculum of additional CA4 plants, the newly inoculated plants developed systemic symptoms and accumulated virus in non-inoculated leaves more quickly than the originally infected CA4 plants. This new NW isolate, referred to as NW-CA4 was tested extensively and shown to overcome the resistances expressed by both CA4 and Dempsey. The potyviral VPg is believed to be the determinant for pvr1 and pvr12 resistance genes, both of which are eIF4E encoding genes. The VPg amino acid sequence for NW-CA4 was determined and compared with that of NW isolates; two substitutions were found within regions of the VPg that were shown to be associated with overcoming eIF4E related resistances by other potyviruses.
机译:杯状病毒对全世界的灯笼椒(Capsicum annuum L.)生产构成持续威胁。我们已经投入大量的努力来研究辣椒品种在细胞和整个植物水平上的抗性反应。为了在细胞水平上评估抗性反应,分离叶肉原生质体并用病毒RNA接种。可以使用有效的隔离程序,但是需要提供一致且高效的接种程序的接种程序。通过评估关键参数开发了电穿孔接种程序,这些关键参数包括电压,脉冲数,脉冲之间的时间间隔,病毒RNA浓度和评估的原生质体数。当使用40杯病毒RNA通过两个200伏的25毫秒脉冲,每个脉冲间隔10秒的时间间隔接种500,000原生质体时,产生了最高病毒滴度和原生质体活力的一致感染。两种重要的抗药性来源是评估了它们对接种四种烟草蚀刻病毒株(TEV,马铃薯病毒属)的反应。抗性品种是CA4和Dempsey,它们分别包含pvr1和pvr12抗性基因。两个品种都抵抗TEV NW菌株的感染。然而,用辣椒维持的两株接种了西北的CA4植物被感染。当将感染的CA4植物用作其他CA4植物的接种物时,新接种的植物比最初感染的CA4植物更快地出现系统症状,并且在未接种的叶片中积累病毒。已对这种新的NW分离株(称为NW-CA4)进行了广泛的测试,证明可以克服CA4和Dempsey均表现出的抗性。猪痘病毒VPg被认为是pvr1和pvr12抗性基因的决定因素,它们都是eIF4E编码基因。测定了NW-CA4的VPg氨基酸序列,并与NW分离株的VPg氨基酸序列进行了比较。在VPg区域内发现了两个取代,这些取代被证明与克服其他马铃薯病毒引起的eIF4E相关抗性有关。

著录项

  • 作者单位

    Auburn University.;

  • 授予单位 Auburn University.;
  • 学科 Agriculture Plant Pathology.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 88 p.
  • 总页数 88
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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