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与西瓜叶卷曲和黄化病相关的番茄曲叶新德里病毒的特性鉴定及其环介导等温扩增检测方法的建立

Characterization of Tomato leaf curl New Delhi virus associated with leaf curl and yellowing disease of Watermelon and development of LAMP assay for its detection.

作者信息

Venkataravanappa V, Ashwathappa K V, Reddy C N Lakshminarayana, Shankarappa K S, Reddy M Krishna

机构信息

ICAR-Indian Institute of Horticultural Research, Hessaraghatta Lake PO, Bangalore, 560089 Karnataka India.

Division of Plant Pathology, Central Horticultural Experiment Station, Chettalli, ICAR-Indian Institute of Horticultural Research, Hessaraghatta Lake PO, Bangalore, India.

出版信息

3 Biotech. 2020 Jun;10(6):282. doi: 10.1007/s13205-020-02245-x. Epub 2020 Jun 2.

Abstract

Diseases caused by begomoviruses are becoming the major limiting factors for the production of watermelon in India. Survey for the incidence of plants showing symptoms typical to begomovirus infection was conducted in watermelon fields. The study revealed that 40% of the watermelon plants were showing the yellowing and downward curling symptoms. Twenty infected samples were collected from the different farmer's fields to know the association of begomoviruses. The PCR amplification using begomovirus-specific primers resulted in an expected 1.2 kb PCR product indicating the begomovirus association with the watermelon samples. The sequence comparison results of 1.2 kb representing partial genome revealed that all sequences obtained from watermelon samples have a nucleotide (nt) identity of more than 98% among them and are maximum homology with Tomato leaf curl New Delhi virus (ToLCNDV). One watermelon sample (WM1) was selected for complete genome amplification using RCA method (rolling-circle amplification). Amplification of DNA B and no amplification of betasatellites and alphasatellite indicated this virus as bipartite. Sequence Demarcation Tool (SDT) analysis of the DNA A component of the WM1 isolate showed the maximum nt identity of 94.6-97.9% and 85.2-95.8% with ToLCNDV infecting cucurbits. The recombinant analysis showed that the genome was likely to be derived from the recombination of already reported begomoviruses (ToLCNDV, ToLCPalV, and MYMIV) infecting diverse crops. The whitefly cryptic species predominant in the begomovirus-infected watermelon fields were identified as Asia-II-5 group. The LAMP assay developed based on coat protein gene sequence was able to detect the ToLCNDV in the infected samples. Visual detection of the LAMP-amplified products was observed with the hydroxy naphthol blue. LAMP assay was also validated with ToLCNDV infected sponge gourd, spine gourd, ivy gourd, ridge gourd, and cucumber. This is the first report of ToLCNDV association with leaf curl and yellowing disease of watermelon from India and World based on complete genome sequencing.

摘要

双生病毒引起的病害正成为印度西瓜生产的主要限制因素。在西瓜田中对表现出双生病毒感染典型症状的植株发病率进行了调查。研究表明,40%的西瓜植株出现黄化和向下卷曲症状。从不同农户的田地中采集了20个感染样本,以了解双生病毒的关联情况。使用双生病毒特异性引物进行PCR扩增,得到了预期的1.2 kb PCR产物,表明双生病毒与西瓜样本有关联。对代表部分基因组的1.2 kb序列进行比较的结果显示,从西瓜样本中获得的所有序列之间的核苷酸(nt)同一性超过98%,并且与番茄曲叶新德里病毒(ToLCNDV)具有最大同源性。选择了一个西瓜样本(WM1),使用滚环扩增(RCA)方法进行全基因组扩增。DNA B的扩增以及β卫星和α卫星未扩增表明该病毒为双分体病毒。对WM1分离株的DNA A组分进行序列划分工具(SDT)分析,结果显示与感染葫芦科作物的ToLCNDV的最大nt同一性为94.6 - 97.9%和85.2 - 95.8%。重组分析表明,该基因组可能源自已报道的感染多种作物的双生病毒(ToLCNDV、ToLCPalV和MYMIV)的重组。在双生病毒感染的西瓜田中占主导地位的粉虱隐性物种被鉴定为亚洲-II-5组。基于外壳蛋白基因序列开发的环介导等温扩增(LAMP)检测方法能够检测感染样本中的ToLCNDV。使用羟基萘酚蓝可对LAMP扩增产物进行可视化检测。LAMP检测方法也在感染ToLCNDV的丝瓜、棱角丝瓜、佛手瓜、瓠瓜和黄瓜上进行了验证。这是基于全基因组测序首次报道ToLCNDV与印度乃至全球西瓜叶卷曲和黄化病的关联。

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