Plant Molecular Virology, CSIR-National Botanical Research Institute, Rana Pratap Marg, Lucknow 226001, Uttar Pradesh, India.
Plant Molecular Virology, CSIR-National Botanical Research Institute, Rana Pratap Marg, Lucknow 226001, Uttar Pradesh, India.
Virus Res. 2015 Apr 2;201:41-9. doi: 10.1016/j.virusres.2015.02.015. Epub 2015 Feb 23.
Severe yellow mosaic disease was observed in three ornamental species of Jatropha: J. integerrima, J. podagrica and J. multifida grown in gardens at Lucknow, India, during a survey in 2013. The causal pathogen was successfully transmitted from diseased to healthy plants of these species by whitefly (Bemisia tabaci). The infection of begomovirus was initially detected in naturally infected plant samples by PCR using begomovirus universal primers. The begomovirus was characterized having a monopartite genome based on sequence analyses of the cloned ∼2.9kb DNA-A genome amplified by rolling circle amplification using Phi-29 DNA polymerase. The genome contained 2844 nucleotides that could be translated into seven potential open reading frames. The nucleotide sequences of DNA-A genome of the begomovirus isolates: JI (KC513823), JP (KF652078) and JM (KF652077) shared 94-95% identities together and 93-95% identities with an uncharacterized begomovirus isolated from J. curcas (the only sequences available in GenBank database as GU451249 and EU798996 under the name jatropha leaf curl virus). These shared highest identity of 61% and highly distant phylogenetic relationships with other begomoviruses reported worldwide. Based on 61% sequence identities (much less than 89%, the species demarcation criteria for a new begomovirus) the isolates under study were identified as members of a new Begomovirus species for which the name was proposed as "Jatropha mosaic Lucknow virus (JMLV)". The recombination analysis also suggested that JMLV was not a recombinant species, hence considered as unidentified Begomovirus species. Koch's postulates were also established by agroinfiltration assay of agroinfectious clone of JMLV. Characterization of JMLV associated with yellow mosaic disease of J. integerrima, J. podagrica and J. multifida is being reported for the first time.
2013 年在印度勒克瑙的花园中进行调查时,观察到三种观赏麻疯树属植物(Jatropha integerrima、J. podagrica 和 J. multifida)发生严重的黄色花叶病。通过粉虱(Bemisia tabaci),成功地将病原体从病株传播到这些物种的健康植株上。通过使用黄症病毒通用引物的 PCR,从自然感染的植物样本中最初检测到黄症病毒的感染。根据使用 Phi-29 DNA 聚合酶进行滚环扩增克隆的约 2.9kb DNA-A 基因组的序列分析,鉴定出黄症病毒具有单分体基因组。基因组包含 2844 个核苷酸,可翻译成七个潜在的开放阅读框。从麻疯树分离物中扩增的 DNA-A 基因组的核苷酸序列:JI(KC513823)、JP(KF652078)和 JM(KF652077)与一种未鉴定的黄症病毒共享 94-95%的身份,与从 J. curcas 分离的未鉴定的黄症病毒共享 93-95%的身份(唯一在 GenBank 数据库中可用的序列作为名称为“麻疯树卷叶病毒”的 GU451249 和 EU798996)。这些序列与世界各地报道的其他黄症病毒具有最高的 61%身份和高度遥远的系统发育关系。基于 61%的序列同一性(远小于 89%,这是新黄症病毒的物种划分标准),研究中的分离物被鉴定为新的黄症病毒物种的成员,该病毒被提议命名为“麻疯树花叶勒克瑙病毒(JMLV)”。重组分析还表明,JMLV 不是重组种,因此被认为是未鉴定的黄症病毒种。还通过 JMLV 的农杆菌侵染克隆的农业浸染测定确立了 Koch 的假设。这是首次报道 JMLV 与黄麻属植物黄化病的关系。