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中国番茄()上番茄曲叶新德里病毒的发生情况

Occurrence of Tomato leaf curl New Delhi virus in tomato () in China.

作者信息

Li Ruichen, Liu Yi, Yin Chuanlin, Sun Kai, Zhang Pengjun

机构信息

China Jiliang University, 92270, College of Life Sciences, Hangzhou, China;

China Jiliang University, 92270, College of Life Sciences, room 508,Gebei hall, Xueyuan street 258, Hangzhou, China, 310018.

出版信息

Plant Dis. 2022 Oct 24. doi: 10.1094/PDIS-06-22-1427-PDN.

Abstract

Tomato leaf curl New Delhi virus (ToLCNDV), a member of the genus Begomovirus in the family Geminiviridae is naturally transmitted by the whitefly Bemisia tabaci (order Hemiptera, family Aleyrodidae) in a circulative and persistent manner (Moriones et al. 2017). ToLCNDV has occurred in Bangladesh, India, Indonesia, Iran, Italy, Malaysia, Pakistan, Sri Lanka, Spain, Thailand and Tunisia (Moriones et al. 2017). To date, The primary cultivated host of ToLCNDV has been identified as tomato (Lycopersicon esculentum), but the virus is also known to infect 43 other plant species from a range of families including Cucurbitaceae, Euphorbiaceae, Solanaceae, Malvaceae and Fabaceae (Zaidi et al. 2017). In August 2021, virus-like symptoms including leaf deformation and curing were observed on tomato (Lycopersicon esculentum) in a greenhouse of about 0.5 hectares in Zhejiang Province, China. To identify viral agents potentially associated with this disease, an Oxford Nanopore cDNA library from a symptomatic sample was generated and sequenced. Total RNA was extracted using RNAiso Plus (TaKaRa, Tokyo, Japan). Libraries were constructed using Oxford Nanopore PCR-cDNA Sequencing Kit (SQK-PCS109; Oxford Nanopore Technologies, Oxford, UK), as recommended. Approximately 8.7 million reads were obtained from the Oxford MinION platform. After removing the adapters and low-quality reads, the clean reads were subjected to BLASTn analysis against the nt database. Approximately 797 and 168 reads produced high nt identities to the genome of ToLCNDV DNA-A (GeneBank Accession No. U15015.2) and ToLCNDV DNA-B (GeneBank Accession No. U15017.2) respectively. We designed 6 primer pairs (Table S1) to obtain the sequence of ToLCNDV Zhejiang (ToLCNDV-ZJ) isolate DNA-A and DNA-B. Briefly, total DNA from ToLCNDV-infected tomato was extracted using standard cetyl trimethylammonium bromide method. Segments of ToLCNDV DNA-A and DNA-B were amplified using high-fidelity DNA polymerase KOD-Plus-Neo (Toyobo, Osaka, Japan). PCR products were cloned into the pLB vector (Tiangen, Beijing, China) and Sanger sequenced. The obtained sequences were assembled into complete sequences of ToLCNDV-ZJ DNA-A (2,739 nt, GeneBank Accession No. OP356207) and DNA-B (2,693 nt, GeneBank Accession No. OP356208). Pairwise sequence comparison revealed that the ToLCNDV -ZJ shared the highest nt sequence identities of 98.7% and 98.4% with the genome segments of New Delhi isolate (genome A: HM159454) and India:Delhi:Cucumis:2012 isolate (genome B: KC545813) respectively. Furthermore, we performed PCR detection on 10 collected samples using the primer pair P1F and P1R. All eight symptomatic plants showing upward leaf curling and leaf distortion tested positive for ToLCNDV infection, whereas two asymptomatic plants were ToLCNDV free. To our knowledge, this is the first report of ToLCNDV infecting tomato in China, and with the widespread presence of B. tabaci in green houses, ToLCNDV may be a potential threat to the cultivation of tomato in China. In addition, ToLCNDV is an exceptional Old World bipartite begomovirus. In China, monopartite DNA satellite-associated begomoviruses with mostly narrow geographical ranges predominate, and are widespread (Li et al., 2022). The occurrence of ToLCNDV in China, which indicates that the success of this virus would become an emerging threat to vegetable and fiber crops.

摘要

番茄曲叶新德里病毒(ToLCNDV)是双生病毒科菜豆金色花叶病毒属的成员,由烟粉虱(半翅目,粉虱科)以循环持久的方式自然传播(莫里内斯等人,2017年)。ToLCNDV已在孟加拉国、印度、印度尼西亚、伊朗、意大利、马来西亚、巴基斯坦、斯里兰卡、西班牙、泰国和突尼斯出现(莫里内斯等人,2017年)。迄今为止,ToLCNDV的主要栽培寄主已被确定为番茄(番茄),但已知该病毒还感染来自葫芦科、大戟科、茄科、锦葵科和豆科等一系列科的其他43种植物(扎伊迪等人,2017年)。2021年8月,在中国浙江省一个约0.5公顷的温室中,番茄(番茄)上观察到了包括叶片变形和卷曲在内的病毒样症状。为了鉴定可能与这种疾病相关的病毒病原体,从一个有症状的样本中构建了牛津纳米孔cDNA文库并进行了测序。使用RNAiso Plus(Takara,东京,日本)提取总RNA。按照推荐,使用牛津纳米孔PCR-cDNA测序试剂盒(SQK-PCS109;牛津纳米孔技术公司,牛津,英国)构建文库。从牛津MinION平台获得了约870万个读数。去除接头和低质量读数后,将干净的读数与nt数据库进行BLASTn分析。分别有约797个和168个读数与ToLCNDV DNA-A(基因库登录号U15015.2)和ToLCNDV DNA-B(基因库登录号U15017.2)的基因组产生了高nt同一性。我们设计了6对引物(表S1)以获得ToLCNDV浙江分离株(ToLCNDV-ZJ)DNA-A和DNA-B的序列。简要地说,使用标准的十六烷基三甲基溴化铵方法从感染ToLCNDV的番茄中提取总DNA。使用高保真DNA聚合酶KOD-Plus-Neo(东洋纺,大阪,日本)扩增ToLCNDV DNA-A和DNA-B的片段。PCR产物克隆到pLB载体(天根,北京,中国)中并进行Sanger测序。获得的序列组装成ToLCNDV-ZJ DNA-A(2739 nt,基因库登录号OP356207)和DNA-B(2693 nt,基因库登录号OP356208)的完整序列。成对序列比较显示,ToLCNDV-ZJ与新德里分离株(基因组A:HM159454)和印度:德里:黄瓜:2012分离株(基因组B:KC545813)的基因组片段分别具有98.7%和98.4%的最高nt序列同一性。此外,我们使用引物对P1F和P1R对10个采集的样本进行了PCR检测。所有八株表现出向上叶片卷曲和叶片变形的有症状植株检测出ToLCNDV感染呈阳性,而两株无症状植株未感染ToLCNDV。据我们所知,这是ToLCNDV在中国感染番茄的首次报道,并且由于温室中广泛存在烟粉虱,ToLCNDV可能对中国的番茄种植构成潜在威胁。此外,ToLCNDV是一种特殊的旧世界双分体菜豆金色花叶病毒。在中国,主要具有狭窄地理范围的单分体DNA卫星相关菜豆金色花叶病毒占主导地位且分布广泛(李等人,2022年)。ToLCNDV在中国的出现表明这种病毒的成功将会对蔬菜和纤维作物成为一种新出现的威胁。

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1
Occurrence of Tomato leaf curl New Delhi virus in tomato () in China.
Plant Dis. 2022 Oct 24. doi: 10.1094/PDIS-06-22-1427-PDN.

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