Suppr超能文献

番茄斑萎病毒感染塞尔维亚洋葱和大蒜的首次报告。

First Report of Tomato spotted wilt virus Infecting Onion and Garlic in Serbia.

作者信息

Stanković I, Bulajić A, Vučurović A, Ristić D, Milojević K, Nikolić D, Krstić B

机构信息

Institute of Plant Protection, Department of Phytopathology, University of Belgrade-Faculty of Agriculture, Nemanjina 6, 11080 Belgrade, Serbia. This research was supported by grant III-43001 of the Ministry of Education and Science, Republic of Serbia.

出版信息

Plant Dis. 2012 Jun;96(6):918. doi: 10.1094/PDIS-02-12-0157-PDN.

Abstract

In June 2011, extensive bleaching and numerous small whitish spots on leaves were observed in an onion (Allium cepa) seed crop as well as chlorotic spots and streaks in the neighboring garlic (A. sativum) bulb crop in the Aleksandrovo locality (Central Banat District, Serbia). Affected plants occurred throughout the field and disease incidence was estimated at 60% in the onion and 40% in the garlic crop. A high population of Thrips tabaci that was found in both crops, and local necrotic spots on Petunia × hybrida mechanically inoculated with infected onion or garlic sap by a chilled 0.01 M phosphate buffer, pH 7.0, containing 0.1% sodium sulfite (1), suggested the presence of a Tospovirus. For these reasons, sampled symptomatic onion and garlic plants were tested for the presence of Tomato spotted wilt virus (TSWV) and Iris yellow spot virus (IYSV) using commercial double-antibody sandwich-ELISA diagnostic kits (Bioreba AG, Reinach, Switzerland). Commercial positive and negative controls and extracts from healthy onion and garlic tissue were included in each ELISA. Of the 18 onion and 10 garlic plants tested, 16 and 7 samples, respectively, were positive for TSWV, and all were negative for IYSV. The identity of TSWV was further confirmed by conventional reverse transcription (RT)-PCR analysis. Total RNAs were extracted with an RNeasy Plant Mini Kit (Qiagen, Hilden, Germany) and RT-PCR was performed with the One-Step RT-PCR Kit (Qiagen) using TSWV-specific forward (5'-GGTTAAGCTCACTAAGAAARCA-3') and reverse primers (5'-TTTAACYCCRAACATTTCATAGA-3'), designed to amplify a 738-bp fragment of the nucleocapsid protein (N) gene. Total RNAs obtained from plants infected with a Serbian isolate of TSWV (GenBank Accession No. GQ373173) and healthy onion garlic plants were used as positive and negative controls, respectively. An amplicon of the expected size was produced from the 16 onion and 7 garlic ELISA-positive plants, but not from healthy controls. The amplified products derived from the two selected isolates, 114-11 from onion and 115-11 from garlic, were sequenced directly after purification with the QIAquick PCR Purification kit (Qiagen); the sequences obtained were allocated GenBank Accession Nos. JQ619234 and JQ619235, respectively. Sequence analysis of the partial N gene, conducted with MEGA5 software (4), revealed 99.9% nucleotide identity (100% amino acid identity) between the two Serbian Allium isolates. Serbian onion and garlic isolates showed the highest nucleotide identities of 100% and 99.9% with Serbian summer squash isolate (JF303081) and tobacco isolate from Montenegro (GU369729), respectively. Well-established in many European countries, TSWV has been reported as an important constraint to the production of tomato, pepper, tobacco, and ornamentals (2), but the information on TSWV naturally infecting Allium spp. is limited. The presence of TSWV on onion and garlic in Serbia revealed that its known host range has expanded in Europe. To our knowledge, other than Marchoux's unpublished data (3), there are no other reports of garlic as a natural host of TSWV. The TSWV presence on Allium spp. represents a serious threat for these crops in Serbia, considering that it is prevalent in other crops in the area and its vectors are widespread. References: (1) Anonymous. OEPP/EPPO Bull. 34:271, 2004. (2) H. R. Pappu et al. Virus Res. 141:219, 2009. (3) G. Parrella et al. J. Plant Pathol. 85:227, 2003. (4) K. Tamura et al. Mol. Biol. Evol. 28:2731, 2011.

摘要

2011年6月,在塞尔维亚中部巴纳特地区的亚历山德罗沃,一块洋葱(葱属)种子田中观察到叶片大面积白化以及众多小白斑,相邻的大蒜(蒜属)鳞茎作物上出现了褪绿斑点和条纹。病害植株遍布整块田地,据估计洋葱作物的发病率为60%,大蒜作物为40%。在两种作物中均发现了大量烟蓟马,并且用含0.1%亚硫酸钠的0.01 M、pH 7.0的冷磷酸缓冲液将感染的洋葱或大蒜汁液机械接种到矮牵牛上后出现了局部坏死斑,这表明存在番茄斑萎病毒属病毒。基于这些原因,采集有症状的洋葱和大蒜植株样本,使用商用双抗体夹心酶联免疫吸附测定(ELISA)诊断试剂盒(瑞士雷纳赫的Bioreba AG公司)检测番茄斑萎病毒(TSWV)和鸢尾黄斑病毒(IYSV)的存在情况。每次ELISA检测均包括商用阳性和阴性对照以及健康洋葱和大蒜组织的提取物。在检测的18株洋葱和10株大蒜植株中,分别有16个和7个样本对TSWV呈阳性反应,对IYSV均呈阴性反应。通过常规逆转录(RT)-PCR分析进一步确认了TSWV的身份。使用RNeasy植物微量提取试剂盒(德国希尔德的Qiagen公司)提取总RNA,并使用一步RT-PCR试剂盒(Qiagen公司)进行RT-PCR,使用TSWV特异性正向引物(5'-GGTTAAGCTCACTAAGAAARCA-3')和反向引物(5'-TTTAACYCCRAACATTTCATAGA-3'),该引物旨在扩增核衣壳蛋白(N)基因的一个738 bp片段。分别从感染塞尔维亚TSWV分离株(GenBank登录号:GQ373173)的植株和健康洋葱大蒜植株中获得的总RNA用作阳性和阴性对照。从16株洋葱和7株大蒜ELISA阳性植株中产生了预期大小的扩增子,但健康对照植株未产生。从两个选定的分离株(洋葱的114-11和大蒜的115-11)获得的扩增产物用QIAquick PCR纯化试剂盒(Qiagen公司)纯化后直接测序;获得的序列分别被分配GenBank登录号JQ619234和JQ619235。使用MEGA5软件(4)对部分N基因进行序列分析,结果显示两个塞尔维亚葱属分离株之间的核苷酸同一性为99.9%(氨基酸同一性为100%)。塞尔维亚洋葱和大蒜分离株与塞尔维亚西葫芦分离株(JF303081)和黑山烟草分离株(GU369729)的核苷酸同一性最高,分别为100%和99.9%。TSWV在许多欧洲国家早已存在,据报道它是番茄、辣椒、烟草和观赏植物生产的重要限制因素(2),但关于TSWV自然感染葱属植物的信息有限。塞尔维亚洋葱和大蒜上TSWV的存在表明其已知宿主范围在欧洲有所扩大。据我们所知,除了马尔舒未发表的数据(3)外,没有其他关于大蒜是TSWV自然宿主的报道。考虑到TSWV在该地区的其他作物中普遍存在且其传播媒介广泛分布,TSWV在葱属植物上的存在对塞尔维亚的这些作物构成了严重威胁。参考文献:(1)匿名。《OEPP/EPPO通报》34:271,2004年。(2)H. R. 帕普等人。《病毒研究》141:219,2009年。(3)G. 帕雷拉等人。《植物病理学杂志》85:227,2003年。(4)K. 田村等人。《分子生物学与进化》28:2731,2011年。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验