Akad F, Jacobi J C, Polston J E
Department of Plant Pathology, University of Florida, Gainesville 32607.
Alabama Cooperative Extension System, Birmingham 35223.
Plant Dis. 2007 Jul;91(7):906. doi: 10.1094/PDIS-91-7-0906C.
During July 2005, approximately 23% of tomato plants (Solanum lycopersicum L. 'Sebring') in a commercial field in St. Clair County, Alabama showed symptoms of stunting, leaf deformation, mottling, and reduced leaf size, which resembled symptoms of Tomato yellow leaf curl virus (TYLCV). A high population of whiteflies (Bemisia tabaci) was observed in this field, and as the season progressed, 100% of the plants became symptomatic. During October 2006, similar symptoms in tomato were observed at low incidences (less than 10%) in a commercial greenhouse in Jefferson County. Two samples from St. Clair County and six from Jefferson County were collected and tested for the presence of a begomovirus by PCR using three pairs of primers, PAR1c496 and PAL1v1978, a degenerate primer pair designed to amplify regions of the begomovirus A component, PBL1v2040 and PCRc154, a degenerate primer pair that amplifies a hypervariable region of the begomovirus B component (3), and C473 and PTYC1v2406, which are specific to TYLCV (1,2). Primer pair PAR1c496 and PAL1v1978 produced two amplicons (1,360 and 1,159 bp) in all samples tested, which suggests the presence of a monopartite and bipartite begomovirus. Primer pair pBL1v2040 and PCRc154 produced a 678-bp amplicon that would be consistent with the presence of a bipartite begomovirus. Primer pair C473 and PTYC1v2406 produced an 850-bp amplicon that would be consistent with the presence of TYLCV. Sequence analysis revealed that the 1,360-bp amplicon had 98% sequence identity to isolates of TYLCV from Cuba (GenBank Accession No. AJ223505), the Dominican Republic (GenBank Accession No. (AF04715), Florida (GenBank Accession Nos. AF260331 and AY530931), Egypt (GenBank Accession No. AY594174), and Almeria (GenBank Accession No. AJ489258). The 1,159-bp amplicon had a 97 to 99% sequence identity to the A component of Tomato mottle virus (ToMoV) Florida (GenBank Accession Nos. L14460, EF028241, and M90495) and Puerto Rico (GenBank Accession No. AY965900). Each of the eight tomato samples were shown to be infected with TYLCV and ToMoV. Symptoms of plants infected with both viruses resembled those of TYLCV because the milder symptoms of ToMoV are masked in the field by the more severe symptoms of TYLCV. To our knowledge, this is the first report of ToMoV and TYLCV in the state of Alabama. Reference: (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.
2005年7月期间,阿拉巴马州圣克莱尔县一片商业种植地里,约23%的番茄植株(茄属番茄‘赛布灵’)出现了发育迟缓、叶片变形、斑驳及叶片变小的症状,这些症状与番茄黄化曲叶病毒(TYLCV)的症状相似。在这片地里观察到大量烟粉虱(烟粉虱),随着季节推移,所有植株都出现了症状。2006年10月,杰斐逊县一个商业温室里的番茄出现了类似症状,但发病率较低(不到10%)。从圣克莱尔县采集了2个样本,从杰斐逊县采集了6个样本,使用三对引物通过PCR检测双生病毒的存在,这三对引物分别是PAR1c496和PAL1v1978,这是一对简并引物,用于扩增双生病毒A组分区域;PBL1v2040和PCRc154,这是一对简并引物,用于扩增双生病毒B组分的一个高变区(3);以及C473和PTYC1v2406,它们是TYLCV特异性引物(1,2)。引物对PAR1c496和PAL1v1978在所有测试样本中产生了两个扩增子(1360和1159 bp),这表明存在单分体和双分体双生病毒。引物对pBL1v2040和PCRc154产生了一个678 bp的扩增子,这与双分体双生病毒的存在一致。引物对C473和PTYC1v2406产生了一个850 bp的扩增子,这与TYLCV的存在一致。序列分析表明,1360 bp的扩增子与来自古巴(GenBank登录号AJ223505)、多米尼加共和国(GenBank登录号(AF04715))、佛罗里达(GenBank登录号AF260331和AY530931)、埃及(GenBank登录号AY594174)和阿尔梅里亚(GenBank登录号AJ489258)的TYLCV分离株具有98%的序列同一性。1159 bp的扩增子与佛罗里达(GenBank登录号L14460、EF028241和M90495)和波多黎各(GenBank登录号AY965900)的番茄斑驳病毒(ToMoV)A组分具有97%至99%的序列同一性。八个番茄样本均显示感染了TYLCV和ToMoV。感染两种病毒的植株症状与TYLCV相似,因为ToMoV较轻的症状在田间被TYLCV更严重的症状掩盖了。据我们所知,这是阿拉巴马州首次报道ToMoV和TYLCV。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。