Venkataravanappa V, Reddy C N Lakshminarayana, Nandan M, Hiremath Shridhar, Ashwathappa K V, Shankarappa K S, Vinay Kumar H D, Reddy M Krishna
Division of Plant Pathology, CHES, ICAR-Indian Institute of Horticultural Research, Chettalli, Madikeri District, Bangalore, Karnataka, 571248 India.
Department of Plant Pathology, College of Agriculture, University of Agricultural Sciences, GKVK, Bengaluru, Karnataka 563125 India.
3 Biotech. 2021 Jun;11(6):265. doi: 10.1007/s13205-021-02821-9. Epub 2021 May 12.
Summer squash is one of the important vegetable crops and its production is hampered by various abiotic and biotic stresses. Of the different biotic stresses, viral infections are responsible for causing great losses to this crop. Diseases caused by begomoviruses are becoming a major constraint in the cultivation of summer squash. Samples from summer squash plants exhibiting severe yellow mosaic and leaf curl symptoms were collected from the Varanasi district of Uttar Pradesh (India) and begomovirus associated with these plants was transmitted through whiteflies () to healthy squash plants. The relationship between causal virus and whitefly vector was determined. The minimum acquisition access period (AAP) and inoculation feeding period (IFP) required by to transmit the virus was determined to be 10 min and female insects have greater efficiency in transmitting virus than male insects. The partial genome of the virus was amplified by PCR (1.2 kb), cloned and sequenced from the ten infected plant samples collected from field. Partial genome sequence analysis (1.2 kb) obtained from the ten samples revealed that they are associated with begomovirus species closely related to the Indian strain of (SLCCNV). Therefore, one representative sample (Sq-1) was selected and complete genome of the virus was amplified by rolling circle amplification (RCA) method. Sequence analysis by Sequence Demarcation Tool (SDT) showed that the current isolate has maximum nucleotide (nt) identity of 93.7-98.4% and 89-98.1% with respect to DNA A DNA B, respectively with Indian strains of SLCCNV infecting cucurbits in India. Recombination analysis of genomes (DNA A and DNA B components) showed that a major part of genomes likely to be originated from already known begomoviruses (ToLCNDV, SLCCNV-CN and SLCCNV-IN) are infecting cucurbitaceous crops. Serological assays such as triple antibody sandwich-enzyme-linked immune-sorbent (TAS-ELISA) assay, dot blot immunobinding assay (DIBA), immuno-capture polymerase chain reaction (IC-PCR) were developed for the detection of SLCCNV.
The online version contains supplementary material available at 10.1007/s13205-021-02821-9.
西葫芦是重要的蔬菜作物之一,其产量受到各种非生物和生物胁迫的影响。在不同的生物胁迫中,病毒感染对这种作物造成了巨大损失。由双生病毒引起的病害正成为西葫芦种植的主要限制因素。从印度北方邦瓦拉纳西地区采集了表现出严重黄花叶和卷叶症状的西葫芦植株样本,与这些植株相关的双生病毒通过烟粉虱传播到健康的西葫芦植株上。确定了致病病毒与烟粉虱载体之间的关系。烟粉虱传播该病毒所需的最短获毒饲育期(AAP)和接种饲育期(IFP)分别为10分钟,且雌虫传播病毒的效率高于雄虫。通过PCR扩增(1.2 kb)病毒的部分基因组,从田间采集的10个感染植株样本中进行克隆和测序。从这10个样本获得的部分基因组序列分析(1.2 kb)表明,它们与与印度番茄曲叶新德里病毒株(SLCCNV)密切相关的双生病毒种有关。因此,选择了一个代表性样本(Sq-1),并通过滚环扩增(RCA)方法扩增病毒的完整基因组。序列分界工具(SDT)的序列分析表明,当前分离株与感染印度葫芦科作物的印度SLCCNV株在DNA A和DNA B上的最大核苷酸(nt)同一性分别为93.7-98.4%和89-98.1%。基因组(DNA A和DNA B组分)的重组分析表明,基因组的主要部分可能起源于已经已知的感染葫芦科作物的双生病毒(番茄褪绿曲叶病毒、SLCCNV-CN和SLCCNV-IN)。开发了用于检测SLCCNV的血清学检测方法,如三抗体夹心酶联免疫吸附(TAS-ELISA)检测、斑点印迹免疫结合检测(DIBA)、免疫捕获聚合酶链反应(IC-PCR)。
在线版本包含可在10.1007/s13205-021-02821-9获取的补充材料。