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一种在印度引起萝卜卷叶病的新型双生病毒物种。

A New Begomovirus Species Causing Leaf Curl Disease of Radish in India.

作者信息

Singh A K, Chattopadhyay B, Pandey P K, Singh A K, Chakraborty S

机构信息

Molecular Virology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi -110 067, India and Indian Institute of Vegetable Research, Varanasi, Uttar Pradesh, India.

Molecular Virology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi -110 067, India.

出版信息

Plant Dis. 2007 Aug;91(8):1053. doi: 10.1094/PDIS-91-8-1053B.

Abstract

Leaf curl disease of radish (RLCD) was observed for the first time in India in commercial fields and kitchen gardens of the Varanasi District and adjoining areas of eastern Uttar Pradesh during November 2003. Infected plants exhibited typical upward and downward leaf curling, leaf distortion, reduction of leaf area, and conspicuous enations on the underside of the leaves. Incidence of RLCD was estimated to be between 10 and 40% depending on the cultivars used. Electron microscopic observation revealed typical geminate particles in infected leaf samples. The causal virus could be transmitted to radish cv. Minu Early by whiteflies (Bemisia tabaci) and grafting. Inoculated plants developed symptoms similar to those observed in naturally infected radish plants. Viral DNA was isolated from artificially inoculated symptomatic radish plants (4) followed by concentration of super-coiled DNA by alkaline denaturation (1). The presence of a geminivirus was confirmed by PCR using DNA-A degenerate primers (3), and a 1.5-kb amplified product was obtained from six artificially and three naturally infected plants. Amplification of the full-length DNA-A was achieved using a primer combination derived from sequences obtained from a 1.5-kb amplicon. Amplification of 1.3-kb DNA-β sequences was achieved using specific primers (2) in three infected plants. Sequence analysis revealed that DNA-A (GenBank Accession No. EF 175733) contained 2,756 nt and DNA-β contained 1,358 nt (GenBank Accession No. EF 175734). DNA-A of the causal virus shares 87.7% identity with Tomato leaf curl Bangladesh virus (GenBank Accession No. AF 188481) and 62% identity with Mungbean yellow mosaic India virus (GenBank Accession No. AF126406). The begomovirus DNA-A sequence associated with RLCD contained seven open reading frames (AV1, AV2, AC1, AC2, AC3, AC4, and AC5). The DNA-β associated with RLCD shared the highest nucleotide sequence identity (84.9%) with DNA-β of Tobacco leaf curl virus isolate NIB 12-1 (GenBank Accession No. AJ316033) reported from Pakistan. Despite exhaustive attempts to amplify a putative viral B-component using degenerate primers based on the intergenic region sequence of the DNA-A or sequences that are highly conserved for other begomoviruses, no DNA-B component was detected. On the basis of DNA-A sequence analysis, the ICTV species demarcation criteria of 89% sequence identity, and genome organization, the virus causing RLCD should be considered a new Begomovirus species, for which the name Radish leaf curl virus (RLCV) is proposed. To our knowledge, this is the first report of the association of a Begomovirus with a disease of radishes in India. References: (1) H. C. Birnboim and J. Doly. Nucleic Acids Res. 7:1513, 1979. (2) R. W. Briddon et al. Mol. Biotechnol. 20:315, 2002. (3) M. R. Rojas et al. Plant Dis. 77:340, 1993. (4) K. M. Srivastava et al. J. Virol. Methods 51:297, 1995.

摘要

2003年11月,在印度北方邦东部瓦拉纳西地区及毗邻地区的商业农田和家庭菜园中首次发现了萝卜卷叶病(RLCD)。受感染植株表现出典型的叶片向上和向下卷曲、叶片扭曲、叶面积减小以及叶片下表面明显的瘤状突起。根据所种植的品种不同,萝卜卷叶病的发病率估计在10%至40%之间。电子显微镜观察在受感染的叶片样本中发现了典型的双生病毒颗粒。该致病病毒可通过烟粉虱(烟粉虱)和嫁接传播给萝卜品种Minu Early。接种后的植株出现了与自然感染的萝卜植株相似的症状。从人工接种出现症状的萝卜植株中分离出病毒DNA(4),随后通过碱性变性法浓缩超螺旋DNA(1)。使用DNA-A简并引物通过PCR确认了双生病毒的存在(3),从六株人工感染和三株自然感染的植株中获得了一个1.5 kb的扩增产物。使用从1.5 kb扩增子获得的序列衍生的引物组合实现了全长DNA-A的扩增。在三株受感染植株中使用特异性引物(2)实现了1.3 kb DNA-β序列的扩增。序列分析表明,DNA-A(GenBank登录号EF 175733)包含2756个核苷酸,DNA-β包含1358个核苷酸(GenBank登录号EF 175734)。致病病毒的DNA-A与番茄卷叶孟加拉病毒(GenBank登录号AF 188481)的序列同一性为87.7%,与绿豆黄花叶印度病毒(GenBank登录号AF126406)的序列同一性为62%。与萝卜卷叶病相关的双生病毒DNA-A序列包含七个开放阅读框(AV1、AV2、AC1、AC2、AC3、AC4和AC5)。与萝卜卷叶病相关的DNA-β与从巴基斯坦报道的烟草卷叶病毒分离株NIB 12-1(GenBank登录号AJ316033)的DNA-β具有最高的核苷酸序列同一性(84.9%)。尽管基于DNA-A的基因间隔区序列或其他双生病毒高度保守的序列使用简并引物进行了详尽的尝试以扩增假定的病毒B组分,但未检测到DNA-B组分。基于DNA-A序列分析、国际病毒分类委员会(ICTV)89%序列同一性的物种划分标准以及基因组结构,导致萝卜卷叶病的病毒应被视为一种新的双生病毒物种,为此提议将其命名为萝卜卷叶病毒(RLCV)。据我们所知,这是印度首次报道双生病毒与萝卜病害相关的研究。参考文献:(1)H. C. Birnboim和J. Doly。核酸研究。7:1513,1979年。(2)R. W. Briddon等人。分子生物技术。20:315,2002年。(3)M. R. Rojas等人。植物病害。77:340,1993年。(4)K. M. Srivastava等人。病毒学方法杂志。51:297,1995年。

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