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台湾番木瓜黄化病相关的16SrXII组植原体的首次报道

First Report of Group 16SrXII Phytoplasma Associated with Papaya Yellows in Taiwan.

作者信息

Bau H J, Hung S C, Chang W C, Chen Y K

机构信息

Department of Biotechnology, Transworld University, Douliu, Yunlin 640, Taiwan.

Department of Plant Protection, Chiayi Agricultural Experiment Station, Taiwan Agriculture Research Institute, Chiayi 600, Taiwan.

出版信息

Plant Dis. 2011 Dec;95(12):1581. doi: 10.1094/PDIS-05-11-0407.

Abstract

Phytoplasmas have been reported to cause various disorders in papaya (Carica papaya L.), including dieback, mosaic, and yellow crinkle in Australia, Nivun Haamir dieback in Israel, and bunchy top-like disease in Cuba (1). Papaya is an economically important crop in Taiwan, and therefore, is monitored for viral infections. In 2005, papaya plants showing chlorosis, yellows and shriveling of leaves, dieback and lateral growth of branches, bending of apical branches, latexosis of fruits, and brown necrosis in phloem tissues were observed in southern Taiwan. Examination by an electron microscope revealed the presence of pleomorphic phytoplasma cells in sieve tubes of the phloem of petioles and leaf veins of diseased plants. Total DNA was extracted individually from at least three diseased plants at each location with a commercial DNA preparation kit (Axygen Scientific, Union City, CA) and used for amplification of the phytoplasma 16S rRNA gene in PCR with universal primer pairs P1 and Tint (3). The full-length 16S rRNA gene has been amplified and cloned. Sequence analysis revealed that the fragment was 1,581 bp long (GenBank Accession No. AJ919994) and shared 99.6% sequence identity with that of the 'Candidatus Phytoplasma solani' reference strain (GenBank Accession No. AF248959). A virtual restriction fragment length polymorphism analysis of the 16S rDNA sequence amplified from the R16F2n/R16R2 primers (2) was performed with iPhyClassifier (4) and pDRAW32. In silico restriction analysis identified the studied papaya phytoplasma as a subgroup 16SrXII-A strain. The sequence had 97 to 98% sequence identity with papaya phytoplasmas of the 16SrXII group in Australia (GenBank Accession No. Y10095), Israel (GenBank Accession No. AY903951), and Cuba (GenBank Accession No. AY725234). The disease incidence was 30 to 35% during the 2006 to 2010 growing seasons, and field surveys indicated that the disease has spread to central Taiwan with sporadic occurrence in recent years. To our knowledge, this is the first report of phytoplasma associated with papaya yellows in Taiwan. References: (1) Y. Arocha et al. Int. J. Syst. Evol. Microbiol. 55:2451, 2005. (2) I. M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (3) C. D. Smart et al. Appl. Environ. Microbiol. 62:2988, 1996. (4) Y. Zhao et al. Int. J. Syst. Evol. Microbiol. 59:2582, 2009.

摘要

据报道,植原体可导致番木瓜(番木瓜属)出现多种病害,包括澳大利亚的枝条枯死、花叶病和黄化皱叶病、以色列的尼武恩哈米尔枝条枯死病以及古巴的束顶样病害(1)。番木瓜是台湾的一种重要经济作物,因此会对其病毒感染情况进行监测。2005年,在台湾南部观察到番木瓜植株出现叶片黄化、发黄和萎缩、枝条枯死及侧枝生长、顶端枝条弯曲、果实流胶以及韧皮部组织褐色坏死等症状。通过电子显微镜检查发现,患病植株叶柄和叶脉韧皮部的筛管中存在多形性植原体细胞。使用商用DNA制备试剂盒(Axygen Scientific,美国加利福尼亚州联合市)从每个地点至少三株患病植株中分别提取总DNA,并用于通过通用引物对P1和Tint进行PCR扩增植原体16S rRNA基因(3)。已扩增并克隆了全长16S rRNA基因。序列分析表明,该片段长度为1581 bp(GenBank登录号AJ919994),与‘Ca. Phytoplasma solani’参考菌株(GenBank登录号AF248959)的序列同一性为99.6%。使用iPhyClassifier(4)和pDRAW32对从R16F2n/R16R2引物扩增的16S rDNA序列进行虚拟限制性片段长度多态性分析。计算机模拟限制性分析确定所研究的番木瓜植原体为16SrXII-A亚组菌株。该序列与澳大利亚(GenBank登录号Y10095)、以色列(GenBank登录号AY903951)和古巴(GenBank登录号AY725234)的16SrXII组番木瓜植原体的序列同一性为97%至98%。在2006年至2010年生长季节,病害发生率为30%至35%,田间调查表明该病害已传播至台湾中部,近年来有零星发生。据我们所知,这是台湾首次报道与番木瓜黄化病相关的植原体。参考文献:(1)Y. Arocha等人,《国际系统与进化微生物学杂志》55:2451,2005年。(2)I. M. Lee等人,《国际系统细菌学杂志》48:1153,1998年。(3)C. D. Smart等人,《应用与环境微生物学》62:2988,1996年。(4)Y. Zhao等人,《国际系统与进化微生物学杂志》59:2582,2009年。

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