Suppr超能文献

西瓜花叶病毒在中国导致黄瓜花叶病的首次报道。

First Report of Watermelon mosaic virus causing a Mosaic Disease on Cucumis metuliferus in China.

作者信息

Gao Qiang, Ren Hai-Long, Xiao Wanyu, Zhang Yan, Zhou Bo, Xu Donglin

机构信息

Xinjiang Academy of Agricultural Sciences, 74608, Hainan Sanya Test Center of Crop Breeding, Urumqi, Xinjiang Uygur, China;

Guangzhou Academy of Agricultural Sciences, Guangzhou, Guangdong, China;

出版信息

Plant Dis. 2021 Feb 5. doi: 10.1094/PDIS-12-20-2744-PDN.

Abstract

Cucumis metuliferus, also called horned cucumber or jelly melon, is considered as a wild species in the Cucumis genus and a potential material for nematodes- or viruses-resistant breeding (Provvidenti, et al. 1977; Sigüenza et al. 2005; Chen et al. 2020). This species, originating from Africa, has been cultivated as a fruit in China in recent years. In July 2020, a mosaic disease was observed on C. metuliferus growing in five fields (approximately 0.7 hectare) in Urumqi, Xijiang, China, where more than 85100% of the field plants exhibited moderate to severe viral disease-like leaf mosaic and/or deformation symptoms. Delayed flowering and small and/or deformed fruits on the affected plants could result in yield loss of about 50%. To identify the causal pathogen, the symptomatic leaf samples were collected from the five fields (five plants/points for each field) and their total RNAs were extracted using a commercial RNA extraction kit. The universal potyviral primers (Ha et al. 2008) and specific primers for a number of frequently-occurring, cucurbit crop-infecting viruses including Papaya ringspot virus (PRSV) (Lin et al. 2013), Cucumber mosaic virus (CMV) and Watermelon mosaic virus (WMV) were designed and used for detection by RT-PCR. The result showed that only the WMV primers (forward: 5'-AAGTGTGACCAAGCTTGGACTGCA-3' and reverse: 5'-CTCACCCATTGTGCCAAAGAACGT-3') could amplify the corresponding target fragment from the total RNA templates, and direct sequencing of the RT-PCR products and GenBank BLAST confirmed the presence of WMV (genus Potyvirus) in the collected C. metuliferus samples. To complete Koch's postulates, the infected C. metuliferus leaves were ground in the sodium phosphate buffer (0.01 M, pH 7.0) and the sap was mechanically inoculated onto 30 four-leaf-stage C. metuliferus seedlings (two leaves for each seedling were inoculated) kept in an insect-proof, temperature-controlled greenhouse at 2528℃. Twenty-five of the inoculated plants were observed to have apparent leaf mosaic similar to the field symptoms two weeks after inoculation, and positive result was obtained in RT-PCR detection for the symptomatic leaves of inoculated plants using the WMV primers aforementioned, confirming the virus as the pathogen of C. metuliferus in Urumqi. To our knowledge, this is the first report of WMV naturally infecting C. metuliferus in China. We obtained the full-length sequence of the WMV Urumqi isolation (WMV-Urumqi) by sequencing the RT-PCR amplicons from seven pairs of primers spanning the viral genome and the 5'RACE and 3'RACE products. The complete sequence of WMV-Urumqi (GenBank accession no. MW345911) is 10046 nucleotides (nt) long and contains an open reading frame that encodes a polyprotein of 3220 amino acids (aa). WMV-Urumqi shares the highest nt identity (95.9%) and aa identity (98.0%) with the Cucurbita pepo-infecting isolation (KX664483) from Shanxi province, China. Our findings provide a better understanding of the host range and genetic diversity of WMV, and a useful reference for virus-resistant breeding involving C. metuliferus.

摘要

刺角瓜,也被称为非洲角瓜或火参果,被认为是黄瓜属的野生种,是抗线虫或抗病毒育种的潜在材料(普罗维登蒂等人,1977年;西根萨等人,2005年;陈等人,2020年)。该物种原产于非洲,近年来在中国作为一种水果进行种植。2020年7月,在中国新疆乌鲁木齐的五个田地(约0.7公顷)中种植的刺角瓜上观察到一种花叶病,其中超过85%至100%的田间植株表现出中度至重度的病毒病样叶花叶和/或变形症状。受影响植株上开花延迟以及果实小和/或变形可能导致产量损失约50%。为了鉴定致病病原体,从这五个田地采集了有症状的叶片样本(每个田地五株植物/采样点),并使用商业RNA提取试剂盒提取其总RNA。设计了通用的马铃薯Y病毒引物(哈等人,2008年)以及针对一些常见的感染葫芦科作物的病毒的特异性引物,包括番木瓜环斑病毒(PRSV)(林等人,2013年)、黄瓜花叶病毒(CMV)和西瓜花叶病毒(WMV),并用于通过RT-PCR进行检测。结果表明,只有WMV引物(正向:5'-AAGTGTGACCAAGCTTGGACTGCA-3';反向:5'-CTCACCCATTGTGCCAAAGAACGT-3')能够从总RNA模板中扩增出相应的目标片段,对RT-PCR产物进行直接测序并与GenBank进行BLAST比对,证实采集的刺角瓜样本中存在WMV(马铃薯Y病毒属)。为了完成柯赫氏法则,将感染的刺角瓜叶片在磷酸钠缓冲液(0.01M,pH7.0)中研磨,然后将汁液机械接种到30株处于四叶期的刺角瓜幼苗上(每株幼苗接种两片叶子),这些幼苗保存在防虫、温度控制在25至28℃的温室中。接种两周后,观察到25株接种植株出现了与田间症状相似的明显叶花叶症状,并且使用上述WMV引物对接种植株有症状的叶片进行RT-PCR检测得到阳性结果,证实该病毒是乌鲁木齐刺角瓜的病原体。据我们所知,这是WMV在中国自然感染刺角瓜的首次报道。通过对跨越病毒基因组的七对引物的RT-PCR扩增产物以及5'RACE和3'RACE产物进行测序,我们获得了WMV乌鲁木齐分离株(WMV-Urumqi)的全长序列。WMV-Urumqi的完整序列(GenBank登录号MW345911)长度为10046个核苷酸(nt),包含一个开放阅读框,编码一个由3220个氨基酸(aa)组成的多聚蛋白。WMV-Urumqi与来自中国山西省的感染西葫芦的分离株(KX664483)的核苷酸同一性最高(95.9%),氨基酸同一性最高(98.0%)。我们的研究结果有助于更好地了解WMV的寄主范围和遗传多样性,并为涉及刺角瓜的抗病毒育种提供有用的参考。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验