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Biological and molecular properties of potyviruses isolated from sweet potato.

机译:从甘薯中分离出的杯状病毒的生物学和分子特性。

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摘要

Ten potyvirus isolates from sweet potato (Ipomoea batatas) cv. Beauregard showing russet crack symptoms and three other isolates associated with internal cork and feathery mottle symptoms were obtained from commercial fields in the United States. The biological properties of these isolates and those of a mechanically transmitted virus obtained from I. purpurea were compared with a previously characterized sweet potato feathery mottle virus strain (SPFMV-C) from North Carolina. The symptoms induced in a range of hosts indicated that two of the isolates were associated with russet crack symptoms in the cultivar Jersey; however, none of them could be associated with russet-crack in 'Beauregard'.;Reverse transcription polymerase chain reaction (RT-PCR) based protocols were tested in order to evaluate their applicability for sweet potato virus detection. Results suggested that RT-PCR is an efficient method for molecular characterization of sweet potato viruses without the need for virus purification. However, it was inconsistent for routine diagnosis. Using a combination of primers (Pot1-Pot2 and Pot2-P89), conserved regions of 14 isolates were amplified, except the virus obtained from I. purpurea. The RT-PCR product from three isolates including SPFMV-C were cloned and sequenced. Comparison of the 5;Restriction fragment length polymorphism and single strand conformational polymorphism analysis of the cDNA of selected isolates did not reveal genomic differences that could be linked to different biological properties. Enzyme-linked immunosorbent assay tests using monoclonal antibodies specific for potyviruses detected the presence of potyviruses in symptomatic plants.
机译:从甘薯(Ipomoea batatas)cv中分离出十种马铃薯病毒。表现出红褐色裂纹症状的博勒格德和与内部软木塞和羽毛斑驳症状有关的其他三种分离株是从美国的商业领域获得的。将这些分离物的生物学特性和从紫菜中获得的机械传播病毒的生物学特性与北卡罗来纳州先前鉴定的甘薯羽状斑驳病毒株(SPFMV-C)进行了比较。在一系列宿主中诱发的症状表明其中两个分离株与泽西品种的赤褐色裂纹症状有关。然而,它们均与“ Beauregard”中的赤褐色裂纹没有关系。测试了基于逆转录聚合酶链反应(RT-PCR)的方案,以评估其在甘薯病毒检测中的适用性。结果表明,RT-PCR是无需进行病毒纯化即可对甘薯病毒进行分子鉴定的有效方法。但是,它与常规诊断并不一致。使用组合的引物(Pot1-Pot2和Pot2-P89),扩增了14个分离株的保守区,但不包括从紫单胞菌中获得的病毒。来自包括SPFMV-C的三个分离株的RT-PCR产物被克隆和测序。所选分离物的cDNA的5,限制性片段长度多态性和单链构象多态性分析的比较未发现可能与不同生物学特性有关的基因组差异。使用针对马铃薯病毒的特异性单克隆抗体进行的酶联免疫吸附试验,检测到有症状植物中存在马铃薯病毒。

著录项

  • 作者单位

    Louisiana State University and Agricultural & Mechanical College.;

  • 授予单位 Louisiana State University and Agricultural & Mechanical College.;
  • 学科 Plant pathology.;Microbiology.
  • 学位 Ph.D.
  • 年度 1998
  • 页码 97 p.
  • 总页数 97
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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