期刊文献+

女贞锈病发生初报 被引量:1

A Report of Rust Disease on Glossy Privet
下载PDF
导出
摘要 以从河北邯郸女贞上分离的锈菌为研究材料,经显微观测,锈菌为黄褐色,形状为卵圆形、梨形或近球形,大小为(15~21.5)μm×(16.5~22)μm。利用微波法快速提取了女贞锈病DNA,并利用保守引物扩增核糖体28 Sr DNA异变区,经聚类分析表明:女贞锈菌为柄锈菌科,与该科的白蜡柄锈菌及酸浆柄锈菌亲缘关系最近。该试验首次对女贞锈菌从分子水平进行分类及检测,对女贞锈病的防治具有重要意义。 Privet leaf samples with symptoms of a rust disease were collected from handan city in Hebei province and morphological characteristics of spore were identified based on microscopic examination.Urediniospores were tawny,globose to pear shaped and measured(15~21.5)μm×(16.5~22) μm.Rust DNA were extracted with microwave and the D1/D2/D3 domain of 28S rDNA were amplified by PCR using the conservative primer.The Phylogenic analysis revealed privet rust belong to Pucciniaceae and was most closely related to Puccinia sparganioidis.This is the first report of detection of privet rust based on PCR amplification which would provide basic information for further drawing up control measure.
出处 《北方园艺》 CAS 北大核心 2011年第9期174-176,共3页 Northern Horticulture
基金 河北邯郸市社科联基金资助项目(201053)
关键词 女贞 锈病 PCR扩增 聚类分析 Glossy privet rust disease PCR amplification phylogenic analysis
  • 相关文献

参考文献6

二级参考文献26

  • 1房德纯,傅俊范.黄瓜褐斑病病原与发病情况调查研究初报[J].植物保护,1994,20(3):23-24. 被引量:53
  • 2蔡平,毛建萍,陆小燕,包立军,张国彪,徐建方,孙振军.金叶女贞假尾孢病害的生物学特性和杀菌剂筛选[J].江苏林业科技,2005,32(2):5-7. 被引量:8
  • 3何苏琴,金秀琳,王卫成.金叶女贞褐斑病病原鉴定[J].植物保护,2006,32(2):70-72. 被引量:9
  • 4戈海泽,郭刚,张瑞,孙蓓.玻璃珠法提取基因组DNA[J].天津医科大学学报,2006,12(2):313-314. 被引量:15
  • 5观赏园艺卷编辑委员会.中国农业百科全书(观赏园艺卷)[M].北京:农业出版社,1996..
  • 6Walker WH, Fitzpatrick SL, Barrera-Saldana HA, et al. The human placental lactogen genes: structure, function, evolution and transcriptional regulation. Endocrine Reviews, 1991(12): 316-318.
  • 7CMJ van Zeijl, EHM van de Kamp, PJ Punt, et al. An improved colony-PCR method for filamentous fungi for amplification of PCR-fragments of several kilobases. Journal of Biotechnology, 1998(59): 221-224.
  • 8A1Shahni MM, Makimura K, Yamada T, et al. Direct colony PCR of several medically important fungi using ampdirect plus. Japanese Journal of Infectious Diseases, 2009, 62(2):164-167.
  • 9Murray MG, Thompson WF. Rapid isolation of high molecular weight plant DNA. Nucleic Acids Research, 1980, 8(19): 4321-4326.
  • 10Ferreira, Adlane VB, Glass N. PCR from fungal spores after microwave treatment. Fungal Genetics Newsletter, 1996(43): 25-26.

共引文献50

同被引文献97

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部