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小麦线条花叶病毒在新西兰小麦上的首次报道。

First Report of Wheat streak mosaic virus on Wheat in New Zealand.

作者信息

Lebas B S M, Ochoa-Corona F M, Alexander B J R, Lister R A, Fletcher J D F, Bithell S L, Burnip G M

机构信息

Ministry of Agriculture and Forestry, P.O. Box 2095, Auckland 1140, New Zealand.

Crop and Food Research, Private Bag 4704, Christchurch, New Zealand.

出版信息

Plant Dis. 2009 Apr;93(4):430. doi: 10.1094/PDIS-93-4-0430B.

Abstract

In August of 2005, seeds of wheat (Triticum aestivum) breeding line 6065.3 tested positive for Wheat streak mosaic virus (WSMV; genus Tritimovirus) by a WSMV-specific reverse transcription (RT)-PCR assay (2). The sequence of the 200-bp amplicon (GenBank Accession No. FJ434246) was 99% identical with WSMV isolates from Turkey and the United States (GenBank Accession Nos. AF454455 and AF057533) and 96 to 97% identical to isolates from Australia (GenBank Accession Nos. DQ888801 to DQ888805 and DQ462279), which belong to the subclade D (1). As a result, an extensive survey of three cereal experimental trials and 105 commercial wheat crops grown on the South Island of New Zealand was conducted during the 2005-2006 summer to determine the distribution of WSMV. Wherever possible, only symptomatic plants were collected. Symptoms on wheat leaf samples ranged from very mild mosaic to symptomless. In total, 591 leaf samples suspected to be symptomatic were tested for WSMV by a double-antibody sandwich (DAS)-ELISA (DSMZ, Braunschweig, Germany). Of the 591 symptomatic samples, 81 tested positive. ELISA results were confirmed by RT-PCR with novel forward (WSMV-F1; 5'-TTGAGGATTTGGAGGAAGGT-3') and reverse (WSMV-R1; 5'-GGATGTTGCCGAGTTGATTT-3') primers designed to amplify a 391-nt fragment encoding a region of the P3 and CI proteins. Total RNA was extracted from the 81 ELISA-positive leaf samples using the Plant RNeasy Kit (Qiagen Inc., Chatsworth, CA). The expected size fragment was amplified from each of the 81 ELISA-positive samples. The positive samples represent 30 of 56 wheat cultivars (54%) collected from 28 of 108 sites (26%) sampled in the growing regions from mid-Canterbury to North Otago. These results suggest that WSMV is widespread in New Zealand both geographically and within cultivars. WSMV is transmitted by the wheat curl mite (Aceria tosichella) (3), which had not been detected in New Zealand despite repeated and targeted surveys. WSMV is of great economic importance in some countries, where the disease has been reported to cause total yield loss (3). Although WSMV is transmitted by seeds at low rates (0.1 to 0.2%) (4), it is the most likely explanation of the spread of the disease in New Zealand. References: (1) G. I. Dwyer et al. Plant Dis. 91:164, 2007. (2) R. French and N. L. Robertson. J. Virol. Methods 49:93, 1994. (3) R. French and D. C. Stenger. Descriptions of Plant Viruses. Online publication. No. 393, 2002. (4) R. A. C. Jones et al. Plant Dis. 89:1048, 2005.

摘要

2005年8月,通过小麦线条花叶病毒(WSMV;小麦病毒属)特异性逆转录(RT)-PCR检测,小麦(Triticum aestivum)育种系6065.3的种子检测出WSMV呈阳性(2)。200碱基对扩增子的序列(GenBank登录号FJ434246)与来自土耳其和美国的WSMV分离株(GenBank登录号AF454455和AF057533)有99%的同一性,与来自澳大利亚的分离株(GenBank登录号DQ888801至DQ888805以及DQ462279)有96%至97%的同一性,这些澳大利亚分离株属于D亚分支(1)。因此,在2005 - 2006年夏季,对新西兰南岛种植的三项谷类作物试验和105种商业小麦作物进行了广泛调查,以确定WSMV的分布情况。只要有可能,只采集有症状的植株。小麦叶片样本的症状从非常轻微的花叶病到无症状不等。总共对591份疑似有症状的叶片样本进行了双抗体夹心(DAS)-ELISA检测(德国不伦瑞克的DSMZ公司)以检测WSMV。在这591份有症状的样本中,81份检测呈阳性。ELISA结果通过RT-PCR得到证实,使用新设计并用于扩增一段391核苷酸片段的正向引物(WSMV-F1;5'-TTGAGGATTTGGAGGAAGGT-3')和反向引物(WSMV-R1;5'-GGATGTTGCCGAGTTGATTT-3'),该片段编码P3和CI蛋白的一个区域。使用植物RNA提取试剂盒(Qiagen公司,加利福尼亚州查茨沃思)从81份ELISA阳性叶片样本中提取总RNA。从81份ELISA阳性样本中的每一份都扩增出了预期大小的片段。阳性样本代表了从坎特伯雷中部到北奥塔哥种植区采样的108个地点中的28个地点(26%)采集的56个小麦品种中的30个(54%)。这些结果表明WSMV在新西兰无论是地理分布还是品种内分布都很广泛。WSMV由小麦卷叶螨(Aceria tosichella)传播(3),尽管进行了多次有针对性的调查,但在新西兰尚未检测到这种螨。WSMV在一些国家具有重大经济重要性,据报道在这些国家该病害会导致总产量损失(3)。虽然WSMV通过种子传播的比率较低(0.1%至0.2%)(4),但这是该病害在新西兰传播的最可能原因。参考文献:(1)G.I.德怀尔等人,《植物病害》91:164,2007年。(2)R.弗伦奇和N.L.罗伯逊,《病毒学方法杂志》49:93,1994年。(3)R.弗伦奇和D.C.斯滕格,《植物病毒描述》。在线出版物。第393号,2002年。(4)R.A.C.琼斯等人,《植物病害》89:1048,2005年。

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