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南非洋葱种子作物中的鸢尾黄斑病毒。

Iris yellow spot virus in Onion Seed Crops in South Africa.

作者信息

Toit L J du, Burger J T, McLeod A, Engelbrecht M, Viljoen A

机构信息

Washington State University Mount Vernon NWREC, Mount Vernon 98273.

Department of Genetics, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa.

出版信息

Plant Dis. 2007 Sep;91(9):1203. doi: 10.1094/PDIS-91-9-1203A.

Abstract

In December 2006, symptoms typical of iris yellow spot caused by Iris yellow spot virus (IYSV; genus Tospovirus, family Bunyaviridae) were observed on scapes (seed stalks) in an onion (Allium cepa L.) seed crop in the Klein Karoo of the Western Cape Province, South Africa. Symptoms included diamond-shaped chlorotic or necrotic lesions on the scapes, some of which had 'green-islands' with nested diamond-shaped lesions, as well as indistinct, circular to irregular, chlorotic or necrotic lesions of various sizes. At the time symptoms were observed, approximately 5% of the scapes had lodged as a result of extensive lesions resembling those caused by IYSV. The crop was 2 to 3 weeks from harvest. Symptomatic tissue from two plants (two samples from one plant and four samples from the other plant) was tested for IYSV by reverse-transcriptase (RT)-PCR. Total RNA was extracted from symptomatic scape tissue with the SV Total RNA Isolation System (Promega, Madison, WI) according to the manufacturer's instructions. First strand cDNA was synthesized with the RevertAid H Minus First Strand cDNA Synthesis kit (Fermentas Inc., Hanover, MD), followed by PCR amplification with primers IYSV-For (TGG YGG AGA TGY RGA TGT GGT) and IYSV-Rev (ATT YTT GGG TTT AGA AGA CTC ACC), which amplify the nucleocapsid (NP) gene of IYSV. An amplicon of expected size (approximately 750 bp) was observed for each of the symptomatic plants assayed and was sequenced. Comparison of the sequence (GenBank Accession No. EF579801) with GenBank sequences revealed 95% sequence identity with the NP gene of IYSV GenBank Accession No. EF419888, with eight amino acid differences. The known geographic distribution of IYSV in onion bulb or seed crops has increased rapidly in recent years in many areas of the world (1). To our knowledge, this is the first confirmation of IYSV in South Africa. Approximately 6,100 ha of onion bulb crops are grown annually in South Africa in the Western Cape, Kwazulu Natal, Limpopo, and Northern Cape provinces, and 600 ha of onion seed crops are grown primarily in the semi-arid regions of the Western Cape. Examination of an additional 10 onion seed crops in the Klein Karoo during January 2007 revealed the presence of iris yellow spot in three more crops at approximately 5% incidence in each crop. The four symptomatic crops had all been planted as bulb-to-seed crops, using vernalized bulbs produced on the same farm. This suggests that IYSV may have been disseminated into the seed crops on the vernalized bulbs, either as infected bulb tissue or in viruliferous thrips on the bulbs. Reference: (1) D. H. Gent et al. Plant Dis. 90:1468, 2006.

摘要

2006年12月,在南非西开普省小卡鲁地区的一个洋葱(Allium cepa L.)种子田中,在花茎(种茎)上观察到了由鸢尾黄斑病毒(IYSV;番茄斑萎病毒属,布尼亚病毒科)引起的典型鸢尾黄斑症状。症状包括花茎上出现菱形褪绿或坏死斑,其中一些有“绿岛”,伴有嵌套的菱形斑,以及大小不一、不明显的圆形至不规则褪绿或坏死斑。在观察到症状时,约5%的花茎因类似IYSV引起的广泛病斑而倒伏。该作物距收获还有2至3周。通过逆转录酶(RT)-PCR对两株植物的有症状组织(一株植物的两个样本和另一株植物的四个样本)进行IYSV检测。根据制造商的说明,使用SV总RNA分离系统(Promega公司,威斯康星州麦迪逊)从有症状的花茎组织中提取总RNA。使用RevertAid H Minus第一链cDNA合成试剂盒(Fermentas公司,马里兰州汉诺威)合成第一链cDNA,随后用引物IYSV-For(TGG YGG AGA TGY RGA TGT GGT)和IYSV-Rev(ATT YTT GGG TTT AGA AGA CTC ACC)进行PCR扩增,这对引物可扩增IYSV的核衣壳(NP)基因。对每个检测的有症状植物都观察到了预期大小(约750 bp)的扩增子,并进行了测序。将该序列(GenBank登录号EF579801)与GenBank序列进行比较,发现与IYSV GenBank登录号EF419888的NP基因有95%的序列同一性,有8个氨基酸差异。近年来,IYSV在世界许多地区洋葱鳞茎或种子作物中的已知地理分布迅速增加(1)。据我们所知,这是IYSV在南非的首次确认。南非每年在西开普省、夸祖鲁-纳塔尔省、林波波省和北开普省种植约6100公顷洋葱鳞茎作物,600公顷洋葱种子作物主要种植在西开普省半干旱地区。2007年1月对小卡鲁地区另外10个洋葱种子作物进行检查发现,又有3个作物出现鸢尾黄斑,每个作物的发病率约为5%。这四个有症状的作物都是作为球茎到种子作物种植的,使用的是同一农场生产的经过春化处理的球茎。这表明IYSV可能通过受感染的球茎组织或球茎上带毒的蓟马传播到种子作物中。参考文献:(1)D. H. Gent等人,《植物病害》90:1468,2

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