印度首次报道感染蝴蝶豌豆的铃花黄花叶病毒。

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2025-02-09 DOI:10.1094/PDIS-10-24-2175-PDN
Subham Dutta, Souvik Chhandogi, Mritunjoy Barman, Swati Chakraborty, Tarique Ahmed, Poorvasandhya R, Jayanta Tarafdar
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引用次数: 0

摘要

蝶豆(Clitoria ternatea),又称亚洲鸽,是豆科多年生草本植物,是天然食用色素和抗氧化剂的重要来源(Suarna et al., 2021)。它是一种多用途饲料,可以产生生物活性化合物,作为覆盖作物,并通过固氮提高土壤肥力(Gomez等,2003)。由白蝇(烟粉虱)传播的黄花叶病毒(RhYMV)首次报道于巴基斯坦豆科杂草最少的豆豆,最小的Rhynchosia minima (Illias等,2009)。在印度或世界上任何地方都没有蝴蝶豌豆感染RhYMV的记录。在2022年和2023年,从印度西孟加拉省10个地区(Alipurduar、Darjeeling、Jalpaiguri、Cooch Behar、Malda、Nadia、Birbhum、Hoogly、Purulia和East Midnapore)的几个家庭菜园中收集了250株完整的蝴蝶豌豆,显示出广泛的黄色花叶症状和花瓣蓝色褪色的扭曲花(补充文件1)。印度西孟加拉邦的Bidhan Chandra Krishi Viswavidyalaya。DNA提取采用植物基因组DNA分离试剂盒(Sigma-Aldrich, St Louis, USA)。采用DeNovix-DS11分光光度计测定DNA样品的浓度和纯度。利用begomovirus特异性退化引物(Li et al., 2004)和RhYMV特异性引物(Ilyas et al., 2009),通过聚合酶链反应(PCR)证实了该病毒的存在。在250份检测样品中,有241份呈begomvirus特异性退化引物阳性(96.40%),178份呈RhYMV特异性引物阳性(73.85%)。通过滚动圈扩增(RCA) (TempliPhi 100扩增试剂盒,Cytiva)确认病毒全基因组后进行测序。在CLC Genomics version Workbench 21.0.5 (Matvienko, 2015)中对数据进行组装和分析后,将DNA-A全基因组序列存入NCBI GenBank数据库(登录号:PP735226)。序列的BLASTn分析表明,来自西孟加拉邦的分离物与来自巴基斯坦小豆(Rhyncosia minima)的RhYMV分离物(FM208847)具有95.44%的同源性(2616 bp / 2741 bp)。致病性试验(补充文件2),在多室条件下饲养的白蝇,在感染植株上获得24小时的病毒(AAP),然后让有病毒的白蝇接种健康植株24小时(IAP),并在防虫笼中监测症状。接种后2周左右,所有阴蒂植株均表现出轻微的黄色花叶症状。在28 dpi时,叶片呈亮黄绿色马赛克状,向下卷曲,起皱,卷须薄,花严重扭曲,与不同地区采集的样品相似。为进一步证实,对感染样本进行RCA和全基因组测序,检测到RhYMV特异性引物阳性,发现了相同的RhYMV谱系(登录号- PQ360900)。据我们所知,这是第一次报道在牛虻豌豆中发生RhYMV,牛虻豌豆被认为是印度RhYMV的新宿主,也可以作为病毒进一步传播到其他豆科植物的储存库。
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First report of Rhynchosia yellow mosaic virus (RhYMV) infecting butterfly pea (Clitoria ternatea) in India.

Butterfly pea (Clitoria ternatea), also known as Asian pigeonwings is a perennial herbaceous plant belongs to the Fabaceae family has a great source of natural food colorants and antioxidants (Suarna et al., 2021). It is a multipurpose forage that produces bioactive compounds, acts as a cover crop and improves soil fertility through nitrogen fixation (Gomez et al, 2003). Rhynchosia Yellow Mosaic Virus (RhYMV) which is transmitted by the whitefly (Bemisia tabaci) was first reported from Pakistan in leguminous weed least snoutbean, Rhynchosia minima (Illias et al., 2009). There is no record on the infection of RhYMV in butterfly pea in India or anywhere in the world. In 2022 and 2023, 250 whole butterfly pea plants were collected from few home stead gardens from ten districts (Alipurduar, Darjeeling, Jalpaiguri, Cooch Behar, Malda, Nadia, Birbhum, Hoogly, Purulia and East Midnapore) within the West Bengal province in India, showed extensive yellow mosaic symptoms and distorted flower with bleaching of blue color of petals (Supplementary file 1). The detection of the virus was carried out in the Advanced Plant Virus Diagnostic Centre, Bidhan Chandra Krishi Viswavidyalaya, West Bengal, India. DNA extraction was conducted by using plant genomic DNA isolation kit (Sigma-Aldrich, St Louis, USA). The concentration and purity of DNA samples were determined by DeNovix-DS11 spectrophotometer. The presence of the virus was confirmed through polymerase chain reaction (PCR) using begomovirus-specific degenerated primer (Li et al., 2004) followed by RhYMV specific primer (Ilyas et al., 2009). Out of total 250 test samples, 241 were positive for begomovirus specific degenerated primer (96.40%) and out of 241 positive samples, 178 plants were positive to RhYMV specific primer which confirmed 73.85% samples infected to RhYMV. After confirmation of the virus whole genome obtained through Rolling Circle Amplification (RCA) (TempliPhi 100 Amplification Kit, Cytiva) followed by sequencing. After assembled and analyzing the data in CLC Genomics version Workbench 21.0.5 (Matvienko, 2015) whole genome of DNA-A sequence was depositd in the NCBI GenBank database (accession number- PP735226). The BLASTn analyses of the sequence indicated that the isolate from West Bengal, had the 95.44% identity (2616 bp out of 2741 bp) with a RhYMV isolate from snoutbean (Rhyncosia minima) from Pakistan (FM208847). For pathogenecity test (Supplementary file 2), whiteflies reared under polyhouse conditions, acquired the virus from infected plants over 24 hrs (AAP) then allowed viruliferous whiteflies to inoculate the healthy plants for 24 hrs (IAP) and symptoms were monitored under an insect-proof cage. Around two weeks of post- inoculation, all Clitoria plants exhibited mild yellow mosaic symptoms. At 28 dpi, bright yellow to green mosaic appearance, downward curling, and wrinkling of the leaves accompanied with thin tendril with severely distorted flowers were seen which was similar to the samples collected from the different districts. For further confirmation, the infected samples tested positive for RhYMV specific primer were subjected to RCA and whole genome sequencing and found same lineage of RhYMV (accession number- PQ360900). To the best of our knowledge, this is the first report on the incidence of RhYMV in butter fly pea which is to be considered as a new host of RhYMV in India could also act as a reservoir of the virus for further spread to other leguminous plants.

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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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