Suppr超能文献

阿曼芝麻(Sesamum indicum)扫帚病的首次报告。

First Report of Witches'-Broom Disease of Sesame (Sesamum indicum) in Oman.

作者信息

Al-Sakeiti M A, Al-Subhi A M, Al-Saady N A, Deadman M L

机构信息

Department of Crop Sciences, Sultan Qaboos University, Box 34, Al Khod 123, Oman. Plant Dis. 89:530, 2005.

出版信息

Plant Dis. 2005 May;89(5):530. doi: 10.1094/PD-89-0530C.

Abstract

Sesame is the major oil seed crop in Oman. During 2004, disease symptoms were observed at Nizwa, 175 km south of Muscat. Symptoms included phyllody and excessive development of short shoots and internodes resulting in little leaves. Total genomic DNA was extracted from healthy and symptomatic plants with a modified cetyltrimethylammoniumbromide (CTAB) buffer method (2). DNA samples were assayed by polymerase chain reaction (PCR), with the 16S rDNA amplified using primers P1 and P7. Direct PCR products were used as template DNA for nested PCR with primers R16F2n and R16R2. Direct PCR products were analyzed by restriction fragment length polymorphism (RFLP) with four restriction enzymes, Tru9I, HaeIII, HhaI, and RsaI. DNAs from alfalfa and lime plants infected by witches'-broom phytoplasmas were used as positive controls and DNA from healthy plants and water were negative controls. The results showed the presence of a 1.8-kb product amplified with the direct PCR and a 1.2-kb product of the nested PCR from infected sesame and the positive controls. No PCR product was observed in the negative control. The PCR assay confirmed the presence of phytoplasma causing witches'-broom disease in sesame. The RFLP results showed the sesame phytoplasma to be most similar to the alfalfa phytoplasma, a member of 16SrII group (1). To our knowledge, this is the first report of a phytoplasma of the 16Sr II group causing witches'-broom disease on sesame in the Sultanate of Oman. References: (1) A. J. Khan et al. Phytopathology 92:1038, 2002. (2) M. A. Saghai-Maroof et al. Proc. Natl. Acad. Sci. USA, 81:8014, 1984.

摘要

芝麻是阿曼的主要油料作物。2004年期间,在马斯喀特以南175公里处的尼兹瓦发现了病害症状。症状包括叶变花以及短枝和节间过度发育,导致叶片变小。采用改良的十六烷基三甲基溴化铵(CTAB)缓冲液法(2)从健康和有症状的植株中提取总基因组DNA。DNA样本通过聚合酶链反应(PCR)进行检测,使用引物P1和P7扩增16S rDNA。直接PCR产物用作模板DNA进行巢式PCR,使用引物R16F2n和R16R2。直接PCR产物用四种限制性内切酶Tru9I、HaeIII、HhaI和RsaI进行限制性片段长度多态性(RFLP)分析。来自感染了扫帚病植原体的苜蓿和酸橙植株的DNA用作阳性对照,来自健康植株的DNA和水用作阴性对照。结果显示,从感染的芝麻和阳性对照中,直接PCR扩增出了1.8kb的产物,巢式PCR扩增出了1.2kb的产物。阴性对照中未观察到PCR产物。PCR检测证实芝麻中存在导致扫帚病的植原体。RFLP结果表明,芝麻植原体与苜蓿植原体最为相似,苜蓿植原体是16SrII组的成员(1)。据我们所知,这是关于16Sr II组植原体在阿曼苏丹国导致芝麻扫帚病的首次报道。参考文献:(1)A. J. Khan等人,《植物病理学》92:1038,2002年。(2)M. A. Saghai-Maroof等人,《美国国家科学院院刊》,81:8014,1984年。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验