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Complex nature of infection associated with yellow vein mosaic disease in Bhendi (Abelmoschus esculentus)

机译:Bhendi(Abelmoschus esculentus)的黄色静脉花叶病相关感染的复杂性

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摘要

Abelmoschus esculentus (Bhendi) is a traditional vegetable crop widely cultivated and consumed commonly in India. Yellow vein mosaic disease (YVMD) caused by Bhendi yellow vein mosaic virus (BYVMV) is a major constraint for Bhendi cultivation in India. To study the nature of infection in the field, we collected leaves which showed typical YVMD in Madurai (9 plants) and carried out rolling circle amplification (RCA) for plant #6. Intriguingly, the digestion of RCA product did not yield expected fragments. This suggests that there may be new viruses due to recombination or mutation or mixed infection. However, on digesting the RCA product of plant #1 with SacI, monomers of 2.7 and 1.3 kb were released and each was cloned into the pOK12 vector. Sequenced RCA digested products showed mixed infection by BYVMV DNA A, Okra enation leaf curl virus (OELCuV) DNA A, beta, alphasatellite with the nanovirus origin of replication. Consequently, mixed infection was also confirmed by Southern hybridization and qPCR in all the analysed plant samples. In the mixed infection of BYVMV and OELCuV, we examined high level of OELCuV DNA A accumulation.
机译:Abelmoschus esculentus(Bhendi)是一种传统的蔬菜作物,在印度广泛种植和消费。 Bhendi黄脉花叶病毒(BYVMV)引起的黄脉花叶病(YVMD)是印度Bhendi种植的主要限制因素。为了研究田间感染的性质,我们收集了在Madurai(9株植物)中表现出典型YVMD的叶片,并对6号植物进行了滚环扩增(RCA)。有趣的是,RCA产物的消化未产生预期的片段。这表明可能由于重组或突变或混合感染而出现了新病毒。然而,在用SacI消化植物#1的RCA产物时,释放了2.7和1.3kb的单体,并将其分别克隆到pOK12载体中。测序的RCA消化产物显示BYVMV DNA A,黄秋葵叶卷曲病毒(OELCuV)DNA A,β,α卫星混合感染,具有纳米病毒复制起点。因此,在所有分析的植物样品中,还通过Southern杂交和qPCR证实了混合感染。在BYVMV和OELCuV的混合感染中,我们检查了高水平的OELCuV DNA A积累。

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