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番茄黄化曲叶病毒在北卡罗来纳州的出现。

Appearance of Tomato yellow leaf curl virus in North Carolina.

作者信息

Polston J E, Rosebrock T R, Sherwood T, Creswell T, Shoemaker P J

机构信息

University of Florida, Gulf Coast Research and Education Center, 5007 60th St. E., Bradenton 34203.

North Carolina State University, Room 1104 Williams Hall, 100 Derieux Place, Raleigh 27695-7211.

出版信息

Plant Dis. 2002 Jan;86(1):73. doi: 10.1094/PDIS.2002.86.1.73B.

Abstract

In the summers of 2000 and 2001, tomato plants (Lycopersicon esculentum) with symptoms of stunting, curling, and marginal chlorosis of leaves, reduced leaf size, and marked reduction in fruit number, similar to those caused by Tomato yellow leaf curl virus (TYLCV), were seen in Henderson County, NC. In 2001, symptomatic plants appeared in a 40-A (18.2 ha) field in 12 foci of ≈12 plants each, at a total incidence of less than 1%. In August 2001, DNA was extracted from leaf samples from four symptomatic plants and tested by polymerase chain reaction (PCR) amplification for the presence of one or more geminiviruses. Two sets of primers were used to test for begomoviruses, AC1048 and PCRv181 (3,4), which amplify a 1,020-bp DNA product from a wide range of monopartite and bipartite (A component only) begomoviruses, and C473 and PTYC1v2406, which preferentially amplifies a 859-bp DNA product from the monopartite TYLCV (1,2). Fragments of the expected size were obtained from all four samples, and all PCR products were sequenced. The sequences of the 1,020-bp PCR product from each of the four samples were compared and found to be 100% identical. The same was found for the 859-bp products. These sequences were compared with equivalent regions of begomoviruses and were identical to sequences of TYLCV. Since the two primer sets amplify overlapping regions of the TYLCV genome, the 1,020 and 859-bp products generated by the two primer sets from one plant were combined to create a 1,464-bp sequence that represented approximately half of the TYLCV genome and encompasses the C4 ORF, the intergenic region, and most of the coat protein gene. This 1,464-bp sequence from North Carolina was 99.2 to 99.6% identical to TYLCV sequences reported from Cuba (GenBank Accession No. AJ223505), the Dominican Republic (GenBank Accession No. AF024715), and Florida, and 96.9 to 98.2% identical to TYLCV sequences reported from the Bahamas, Israel (GenBank Accession No. X15656), Jamaica (GenBank Accession No. U84146), Mexico (GenBank Accession No. AF168709), and Spain (GenBank Accession No. AF071228). Symptomatic plants appeared to be infected with an isolate of TYLCV that is most similar to TYLCV isolates reported from Florida and the northeastern Caribbean. To our knowledge, this is the first report of TYLCV in North Carolina. TYLCV may have been introduced on transplants since the infected plants showed symptoms at an early growth stage. The appearance of infected plants in clusters of limited size suggests no spread or very limited spread in the field. Reports of populations of the whitefly (Bemisia tabaci) vector in the field were not available since whiteflies are not normally a problem in this area due to the higher altitude and relatively cool temperatures characteristic of Henderson County. It is not clear at this time what threat TYLCV poses to tomato production in the county, though its appearance indicates that the geographic range of TYLCV is continuing to expand in the southeastern United States. References: (1) M. Ghanim et al. Virology 240:295, 1998. (2) M. K. Nakhla et al. Phytopathol. Mediterr. 32:163, 1993. (3) M. R. Rojas et al. Plant Dis. 77:340, 1993. (4) S. D. Wyatt et al. Phytopathology 86:1288, 1996.

摘要

2000年和2001年夏季,在北卡罗来纳州亨德森县发现番茄植株(Lycopersicon esculentum)出现发育迟缓、叶片卷曲和边缘黄化、叶面积减小以及果实数量显著减少的症状,与番茄黄化曲叶病毒(TYLCV)引起的症状相似。2001年,在一块40英亩(18.2公顷)的田地中,12个发病中心出现了有症状的植株,每个发病中心约有12株,总发病率不到1%。2001年8月,从4株有症状植株的叶片样本中提取DNA,并通过聚合酶链反应(PCR)扩增检测是否存在一种或多种双生病毒。使用两组引物检测双生病毒,即AC1048和PCRv181(3,4),它们能从多种单分体和双分体(仅A组分)双生病毒中扩增出1020 bp的DNA产物,以及C473和PTYC1v2406,它们优先从单分体TYLCV中扩增出859 bp的DNA产物(1,2)。从所有4个样本中均获得了预期大小的片段,并对所有PCR产物进行了测序。对4个样本中每个样本的1020 bp PCR产物序列进行比较,发现它们100%相同。859 bp产物的情况也是如此。将这些序列与双生病毒的等效区域进行比较,发现与TYLCV的序列相同。由于两组引物扩增的是TYLCV基因组的重叠区域,因此将两组引物从一株植物中产生的1020和859 bp产物合并,得到一个1464 bp的序列,该序列约占TYLCV基因组的一半,涵盖C4开放阅读框、基因间隔区和大部分外壳蛋白基因。来自北卡罗来纳州的这个1464 bp序列与古巴(GenBank登录号AJ223505)、多米尼加共和国(GenBank登录号AF024715)和佛罗里达州报道的TYLCV序列的同源性为99.2%至99.6%,与巴哈马、以色列(GenBank登录号X15656)、牙买加(GenBank登录号U84146)、墨西哥(GenBank登录号AF168709)和西班牙(GenBank登录号AF071228)报道的TYLCV序列的同源性为96.9%至98.2%。有症状的植株似乎感染了一种与佛罗里达州和加勒比海东北部报道的TYLCV分离株最为相似的TYLCV分离株。据我们所知,这是TYLCV在北卡罗来纳州的首次报道。由于受感染植株在生长早期就出现症状,TYLCV可能是通过移栽引入的。受感染植株呈有限大小的簇状出现,表明在田间没有传播或传播非常有限。由于该地区海拔较高且温度相对凉爽,烟粉虱(Bemisia tabaci)传播媒介的种群报告不可用,因为烟粉虱通常不是该地区的问题。目前尚不清楚TYLCV对该县番茄生产构成何种威胁,但其出现表明TYLCV在美国东南部的地理范围正在继续扩大。参考文献:(1)M. Ghanim等人,《病毒学》240:295,1998年。(2)M. K. Nakhla等人,《植物病理学报》32:163,1993年。(3)M. R. Rojas等人,《植物病害》77:340,1993年。(4)S. D. Wyatt等人,《植物病理学》86:128

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