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榆树黄化病植原体的分子检测与鉴定
引用本文:ZHU Tian-sheng,潘一展,CUI Ting-tao,高瑞,LI Xiang-dong,朱水芳.榆树黄化病植原体的分子检测与鉴定[J].植物病理学报,2008,38(4):401-406.
作者姓名:ZHU Tian-sheng  潘一展  CUI Ting-tao  高瑞  LI Xiang-dong  朱水芳
作者单位:1. 山东农业大学植物保护学院植物病理学系, 泰安 271018;2. 塔里木大学植物科技学院, 阿拉尔 843300;3. 商丘职业技术学院, 商丘 476100;4. 中国检验检疫科学研究院动植物检疫研究所, 北京 100029
基金项目:教育部跨世纪优秀人才培养计划,国家科技支撑计划,泰安市大学生科技创新计划 
摘    要: 利用植原体16SrRNA基因的通用引物R16rrLF2/R16mR1和R16F2n/R16R2对山东泰山上发生的榆树(Ulmus parvifolia)黄化病感病植株总DNA进行巢式PCR扩增,得到了约1.2kb的特异性片段,从分子水平证实了榆树黄化病的病原(EY-China)为植原体。将扩增到的片段测序,并进行一致性和系统进化树分析。结果表明,该分离物属于植原体榆树黄化组(Candidatus Phytoplasma ulmi),与该组成员16SrRNA序列的一致性均在98.2%以上,其中与16SrV-B亚组中的纸桑丛枝(Paper mulberry wiches'-broom)和枣疯病(Jujube witches'-broom)植原体一致性最高,达到99.4%,在系统进化树中与该亚组成员聚类到同一个分支,说明该分离物属于植原体16SrV-B亚组。本研究首次对在中国引致榆树黄化病的植原体进行了分子检测,并通过核酸序列分析将其鉴定到亚组水平。

关 键 词:榆树黄化病  植原体  16S  RRNA基因  巢式PCR  系统进化分析  

Molecular detection and identification of the phytoplasma associated with Elm yellows in China
ZHU Tian-sheng,PAN Yi-zhan,CUI Ting-tao,GAO Rui,LI Xiang-dong,ZHU Shui-fang.Molecular detection and identification of the phytoplasma associated with Elm yellows in China[J].Acta Phytopathologica Sinica,2008,38(4):401-406.
Authors:ZHU Tian-sheng  PAN Yi-zhan  CUI Ting-tao  GAO Rui  LI Xiang-dong  ZHU Shui-fang
Institution:1. Department of Plant Pathology, College of Plant Protection, Shandong Agricultural University, Tai'an 271018, China;2. College of Plant Science and Technology, Tarimu University, Alar 843300, China;3. Shangqiu Vocational and Technical College, Shangqiu 476100, China;4. Institute of Animal and Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing 100029, China
Abstract:By use of nested-PCR, the 16S rRNA gene of phytoplasma associated with Elm yellows in China (EY-china) was amplified with universal primer pairs R16mF2/R16mRl and R16F2n/R16R2. DNA fragments of ca. 1.2 kb were obtained from the total DNA of diseased elm samples. The fragment was sequenced and subjected to RFLP and phylogenetic analyses. The results indicated that the phytoplasma EY-China was a member of Candidatus Phytoplasma ulmi (16SrV), and shared identities of more than 98.2% with other members in this group. It had the highest identity of 99.4%, and formed the same branch in phylogentic tree with phytoplasmas associated with paper mulberry witches'-broom and jujube witches'-broom of subgroup 16SrV-B. These results indicate that EY-China belong to subgroup 16SrV-B. This is the first report of phytoplasma associated with elm yellows disease identified to subgroup level according to molecular evidences in China.
Keywords:Elm yellows  phytoplasma  16S rRNA gene  nested-PCR  phylogenetic analysis  
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