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Detection and characterization of tomato leaf curl New Delhi virus association with mosaic disease of ivy gourd (Coccinia grandis (L.) Voigt) in North India

机译:北印度甘草甘露甘草叶片番茄叶卷曲新德里病毒与马赛克病的检测与鉴定(Coccinia Grandis(L.)voigt)

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摘要

Sixteen ivy gourd (Coccinia grandis (L.) Voigt) plant samples showing severe mosaic symptoms were collected from New Delhi and Varanasi (Uttar Pradesh) in India. Begomovirus infection was confirmed by PCR using begomovirusspecific primers. Amplified PCR products (1.2 kb fragments) were cloned and the sequence was characterized. Based on sequence analysis, begomovirus associated with the majority of ivy gourd samples (16) was found to be a member of a bipartite begomovirus species, which is closely related to tomato leaf curl New Delhi virus (ToLCNDV). Therefore, two samples of ivy gourd, IVG1-ND and IVG2-Var, were selected for full-length genome (DNA-A and DNA-B-like sequence) amplification by the rolling circle DNA amplification (RCA) method. Sequence analysis performed using the Species Demarcation Tool (SDT) program revealed that they share 89.5-91.3% (IVG1-ND) and 93.4-96.8% (IVG2-Var) nucleotide (nt) identity with the DNA-A-like sequence of ToLCNDV isolated from cucurbits and chilli, respectively. The IVG1-ND and IVG2-Var isolates shared 90% nt identity among themselves, indicating that they are two different strains of ToLCNDV. Similarly, SDT analysis of the DNA-B-like sequence of IVG1-ND and IVG2-Var exhibited showed 82.7-93.3% nt identity with the DNA-B-like sequences of ToLCNDV infecting cucurbits. The recombination analysis of DNA-A and DNB-B-like sequences showed that the greater part of their genome most likely originated from previously reported begomoviruses that are known to infect chilli and cucurbits through recombination.
机译:出现严重马赛克征十六常春藤葫芦(红瓜(L.)Voigt的)植物样本来自于印度新德里和瓦拉纳西(北方邦)收集。双生病毒感染,通过PCR引物begomovirusspecific证实。扩增的PCR产物(1.2kb的片段)进行克隆和序列表征。基于序列分析,大部分常春藤葫芦样品的(16)相关联的双生病毒被认为是二分双生病毒物质,其是密切相关的番茄曲叶新德里病毒(ToLCNDV)的成员。因此,被选择用于全长基因组(DNA-A和DNA-B样序列)扩增由所述滚环DNA扩增(RCA)法常春藤葫芦,IVG1-ND和IVG2-VAR,两个样品。使用物种划界工具(SDT)程序显示,它们共享89.5-91.3%(IVG1-ND)和93.4-96.8%的序列分析来进行(IVG2-VAR)个核苷酸(nt)与ToLCNDV的DNA-A样序列同一性从葫芦科植物和辣椒分别分离。所述IVG1-ND和IVG2-瓦尔株共享90%的同一性NT本身之间,表明它们是ToLCNDV的两种不同的菌株。与类似地,SDT的分析DNA-B样IVG1-ND和IVG2-瓦尔序列表现出表明82.7-93.3%NT同一性DNA-B样ToLCNDV感染葫芦科植物的序列。 DNA-A和的复合分析DNB-B样序列表明,它们的基因组的较大部分最有可能是源于已知通过重组感染辣椒和葫芦先前报道begomoviruses。

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