Ling K-S, Sfetcu D
USDA-ARS, U.S. Vegetable Laboratory, Charleston, SC 29414.
Houweling Nurseries Oxnard, Inc., 645 W. Laguna Road, Carmarillo, CA 92012.
Plant Dis. 2010 Nov;94(11):1376. doi: 10.1094/PDIS-07-10-0516.
In April 2009, a large number of tomato plants (Solanum lycopersicum L.) grown in a commercial greenhouse facility near Los Angles, CA exhibited general plant stunting (short internodes) and foliar symptoms that included distortion, chlorosis, and scattered necrotic spotting. Over time, the leaves began to exhibit a purple color and curling. Diseased plants were often elongated and frail with spindly shoots. The disease resulted in a significant yield loss due to reduced fruit size. Disease symptoms described above are generally different from those of Pepino mosaic virus (PepMV) infection, which causes yellow mosaic or patches on leaves and marbling of fruits. The disease was initially localized in certain areas in a greenhouse despite using a number of cultural management efforts including vigorous scouting, roguing of diseased plants, and strict hygiene and cleaning practices. The disease was also observed in neighboring greenhouses by the spring of 2010. A standard panel of tests for common tomato viruses and viroids were conducted using the appropriate serological or PCR assays. Reverse transcription (RT) PCR analysis of nine symptomatic plants with pospiviroid-specific primers, Pospil-RE and Pospil-FW (3), produced an amplicon of the expected size (~196 bp) while three healthy looking tomato plants did not. Subsequently, full viroid genomic sequences were obtained through RT-PCR with primer sets specific for Potato spindle tuber viroid (PSTVd), 3H1/2H1 (2), as well as for the pospiviroid genus, MTTVd-F and MTTVd-R (1). Sequences obtained from direct sequencing of amplicons or cloned PCR products from one isolate were identical and consisted of a full viroid genome of 358 nt, which was named PSTVd-CA1 (GenBank Accession No. HM753555). BLASTn queries of the NCBI database showed that this isolate had a high sequence identity (98%) to other PSTVd isolates (i.e., EF044304, X52037, and Y09577). The disease was reproducible upon mechanical transmission (1) on three tomato 'Moneymaker' plants, which expressed symptoms that were similar to those on the source plants. Recovery of PSTVd on the inoculated tomato plants was confirmed by RT-PCR and sequencing. Because of its susceptibility to viroid infection, tomato 'Moneymaker' plants are commonly used as indicators for the study of pospiviroids, including PSTVd. Natural PSTVd infection on greenhouse tomatoes has been reported in Europe (3) and New Zealand. Although a number of reports in the United States have been published on naturally occurring PSTVd infections of potatoes, to our knowledge, this is the first report of a natural PSTVd infection on tomatoes in the United States. The exact source of the PSTVd inoculum in the current disease outbreak is unknown, but it could have been introduced from infected potato or ornamental plants (4) or through infected tomato seeds. The disease epidemic might have been enhanced by frequent hands-on activities in greenhouse tomato production and the environmental conditions (high temperature and intense lighting) in the greenhouse that favor symptom expression. References: (1) K.-S. Ling and W. Zhang, Plant Dis. 93:1216, 2009. (2). A. M. Shamloul et al. Can. J. Plant Pathol. 19:89, 1997. (3) J. Th. J. Verhoeven et al. Eur. J. Plant Pathol. 110:823, 2004. (4) J. Th. J. Verhoeven et al. Plant Pathol. 59:3, 2010.
2009年4月,加利福尼亚州洛杉矶附近一家商业温室设施中种植的大量番茄植株(Solanum lycopersicum L.)出现植株普遍矮化(节间短)和叶片症状,包括变形、黄化和散在的坏死斑点。随着时间的推移,叶片开始呈现紫色并卷曲。患病植株通常细长且脆弱,嫩枝细长。由于果实大小减小,该病导致产量大幅损失。上述病害症状通常与 Pepino 花叶病毒(PepMV)感染的症状不同,PepMV 感染会导致叶片出现黄色花叶或斑块以及果实出现大理石花纹。尽管采取了多种栽培管理措施,包括积极巡查、拔除患病植株以及严格的卫生和清洁措施,但该病最初仍局限于温室的某些区域。到2010年春季,相邻温室中也观察到了这种病害。使用适当的血清学或PCR检测方法对常见番茄病毒和类病毒进行了标准检测。用马铃薯纺锤块茎类病毒特异性引物Pospil - RE和Pospil - FW(3)对9株有症状的植株进行逆转录(RT)PCR分析,产生了预期大小(约196 bp)的扩增子,而3株外观健康的番茄植株未产生。随后,通过使用针对马铃薯纺锤块茎类病毒(PSTVd)的引物对3H1/2H1(2)以及针对马铃薯纺锤块茎类病毒属的引物对MTTVd - F和MTTVd - R(1)进行RT - PCR获得了完整的类病毒基因组序列。从一个分离株的扩增子直接测序或克隆的PCR产物获得的序列相同,由一个358 nt的完整类病毒基因组组成,命名为PSTVd - CA1(GenBank登录号HM753555)。对NCBI数据库的BLASTn查询显示,该分离株与其他PSTVd分离株(即EF044304、X52037和Y09577)具有高度的序列同一性(98%)。通过机械接种(1)在3株番茄“Money maker”植株上再现了该病,这些植株表现出与源植株相似的症状。通过RT - PCR和测序证实了接种的番茄植株上存在PSTVd。由于番茄“Money maker”植株对类病毒感染敏感,通常被用作研究包括PSTVd在内的马铃薯纺锤块茎类病毒的指示植物。欧洲(3)和新西兰已报道温室番茄上自然发生的PSTVd感染。尽管美国已发表了多篇关于马铃薯自然发生PSTVd感染的报道,但据我们所知,这是美国首次报道番茄上自然发生的PSTVd感染。当前病害爆发中PSTVd接种体的确切来源尚不清楚,但可能是从受感染的马铃薯或观赏植物(4)引入的,或者是通过受感染的番茄种子引入的。温室番茄生产中频繁的人工操作以及温室中有利于症状表现的环境条件(高温和强光)可能加剧了病害流行。参考文献:(1)K.-S. Ling和W. Zhang,植物病害93:1216,2009。(2)A. M. Shamloul等人,加拿大植物病理学杂志19:89,1997。(3)J. Th. J. Verhoeven等人,欧洲植物病理学杂志110:823,2004。(4)J. Th. J. Verhoeven等人,植物病理学59:3,2010。