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大豆矮缩病毒在威斯康星州大豆上的首次报道。

First Report of Soybean dwarf virus on Soybean in Wisconsin.

作者信息

Phibbs A, Barta A, Domier L L

机构信息

Wisconsin Department of Agriculture, Trade and Consumer Protection, 4702 University Ave, Madison 53707.

USDA-ARS, University of Illinois, Urbana 61801.

出版信息

Plant Dis. 2004 Nov;88(11):1285. doi: 10.1094/PDIS.2004.88.11.1285A.

Abstract

Soybean dwarf virus (SbDV) causes widespread economic losses on soybean (Glycine max (L.) Merr.) in Japan (4), and has been reported on soybean in Virginia (2), in various legumes in the southeastern United States (1), and in peas in California (3). During late July and early August of 2003, soybean plants in Wisconsin were surveyed for SbDV. In 286 soybean fields at the R2-R4 growth stage, the uppermost fully unfurled leaf was collected from 10 plants at each of five sites. Samples were collected at random without regard to symptoms. SbDV symptom information was not recorded. Samples were stored on ice until frozen at -80°C. Five fields in four Wisconsin counties (Columbia, Lafayette, Sauk, and Waushara) tested positive for SbDV using double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). DAS-ELISA testing was conducted with reagents from Agdia, Inc (Elkhart, IN) following the manufacturer's protocol. Absorbance was read at 405 nm with a Stat Fax 2100 microplate reader (Awareness Technology, Inc., Palm City, FL) or visually evaluated. DAS-ELISA did not discriminate between strains of SbDV. The presence of SbDV was confirmed, and strain identity was inferred as dwarfing strain using reverse transcription-polymerase chain reaction (RT-PCR). Total RNA was extracted from homogenized leaf tissue, reverse transcribed, and amplified with the SuperScript One Step RT-PCR System (Invitrogen, Carlsbad, CA) and SbDV-specific primers (5'-CTGCTTCTGGTGATTACACTGCCG-3' and 5'-CGCTTTCATTTAACGYCATCAAAGGG-3'). Size of the RT-PCR products (110 bp) was consistent with the dwarfing strain, SbDV-D. All locations that tested positive for SbDV showed soybean aphids, Aphis glycines Matsumura (Homoptera: Aphididae), on 100% of soybean plants. Several aphid species have been reported to vector SbDV, but at this time, vector relations in the Wisconsin infections are unknown. To our knowledge, this is the first report of SbDV infecting soybean in Wisconsin. References: (1) V. D. Damsteegt et al. Plant Dis. 79:48, 1995. (2) A. Fayad et al. Phytopathology (Abstr.) 90(Suppl.):S132, 2000. (3) G. R. Johnstone et al. Phytopathology (Abstr.) 74:795(A43), 1984. (4) T. Tamada et al. Ann. Phytopathol. Soc. Jpn. 35:282, 1969.

摘要

大豆矮缩病毒(SbDV)在日本给大豆(Glycine max (L.) Merr.)造成了广泛的经济损失(4),并且在弗吉尼亚州的大豆上有过报道(2),在美国东南部的各种豆类作物上(1)以及加利福尼亚州的豌豆上(3)也有发现。2003年7月下旬至8月初,对威斯康星州的大豆植株进行了SbDV调查。在处于R2-R4生长阶段的286个大豆田中,从五个地点的每10株植株上采集最上部完全展开的叶片。随机采集样本,不考虑症状。未记录SbDV症状信息。样本在冰上保存,直至在-80°C下冷冻。使用双抗体夹心酶联免疫吸附测定(DAS-ELISA)对威斯康星州四个县(哥伦比亚、拉斐特、索克和沃沙拉)的五个田块进行检测,结果显示SbDV呈阳性。按照制造商的方案,使用来自Agdia公司(印第安纳州埃尔克哈特)的试剂进行DAS-ELISA检测。使用Stat Fax 2100酶标仪(佛罗里达州棕榈城的Aware Technology公司)在405 nm处读取吸光度,或者进行目视评估。DAS-ELISA无法区分SbDV的不同毒株。通过反转录聚合酶链反应(RT-PCR)确认了SbDV的存在,并推断毒株类型为矮化毒株。从匀浆的叶片组织中提取总RNA,进行反转录,然后使用SuperScript One Step RT-PCR System(加利福尼亚州卡尔斯巴德的Invitrogen公司)和SbDV特异性引物(5'-CTGCTTCTGGTGATTACACTGCCG-3'和5'-CGCTTTCATTTAACGYCATCAAAGGG-3')进行扩增。RT-PCR产物的大小(110 bp)与矮化毒株SbDV-D一致。所有检测出SbDV呈阳性的地点,100%的大豆植株上都发现了大豆蚜,Aphis glycines Matsumura(同翅目:蚜科)。据报道,有几种蚜虫可传播SbDV,但目前尚不清楚威斯康星州感染病例中的传毒关系。据我们所知,这是SbDV在威斯康星州感染大豆的首次报道。参考文献:(1)V. D. Damsteegt等人,《植物病害》79:48,1995年。(2)A. Fayad等人,《植物病理学(摘要)》90(增刊):S132,2000年。(3)G. R. Johnstone等人,《植物病理学(摘要)》74:795(A43),1984年。(4)T. Tamada等人,《日本植物病理学会年报》35:282,1969年。

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