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加拿大葡萄中翠菊黄化植原体(‘Ca. Phytoplasma asteris’)的首次报道

First Report of Aster Yellow Phytoplasmas ('Candidatus Phytoplasma asteris') in Canadian Grapevines.

作者信息

Olivier C Y, Lowery D T, Stobbs L W, Vincent C, Galka B, Saguez J, Bittner L, Johnson R, Rott M, Masters C, Green M

机构信息

Agriculture and AgriFood Canada, Saskatoon, SK, Canada.

Agriculture and AgriFood Canada, Summerland BC.

出版信息

Plant Dis. 2009 Jun;93(6):669. doi: 10.1094/PDIS-93-6-0669A.

Abstract

In North America, elm yellows, aster yellows (AY), and X-disease phytoplasmas have been detected in American grapevines (1), and recently, Bois noir was detected in Canadian vineyards from British Columbia (BC) and Ontario (ON) (2). Typical symptoms of grapevine yellows (GY) include leaf rolling and chlorosis, uneven or total lack of lignification of canes, flower abortion or berry withering, and stunting. In 2006 and 2007, independent surveys were conducted by the Canadian Food Inspection Agency (CFIA) and Agriculture and Agri-Food Canada (AAFC) to detect phytoplasmas in Canadian vineyards containing different cultivars in BC, ON, Québec (QC), Nova Scotia, New Brunswick, and Prince Edward Island. The CFIA collected and tested 651 fresh leaf samples from recently imported grapevines and older grapevines in the same or neighboring blocks displaying symptoms typical of those associated with disease caused by phytoplasmas. Many vineyards were surveyed only once. AAFC collected and tested 3,485 samples from symptomatic and asymptomatic grapevines from established vineyards in ON, BC, and QC. The same vineyards were sampled in ON and BC both years; QC vineyards were only sampled in 2007. AAFC-collected leaf samples were freeze dried and stored at -20°C before processing. CFIA samples were tested by a modified real-time PCR assay and TaqMan probe targeting the 16S ribosomal RNA gene that detects a wide range of known phytoplasmas (2). Positive samples were confirmed by conventional PCR using the phytoplasma-specific primers P1/P7 (3) and the resulting ~1,800-bp fragment was cloned and sequenced as previously described (2). DNA extracted by AAFC was amplified by nested PCR technology with universal phytoplasma specific primer pairs P1/P6 and R16R2/R16F2 (3) and the resulting 1,200-bp fragment was cloned and sequenced. Two plants, one located in ON in 2006 and the other in BC in 2007, were found to be infected with an AY-like phytoplasma by the CFIA. The phytoplasmas detected in both infected plants had a 99.9% nt sequence identity with AY phytoplasma sequences from GenBank (Accession Nos. AF222063 and AY665676, respectively), with the BC isolate also showing 100% identity to a strain of AY, ash witches'-broom phytoplasma (GenBank Accession No. AY566302). AAFC detected phytoplasma DNA in both years in a total of 17 symptomatic plants and 21 asymptomatic plants from different vine varieties in ON, BC, and QC. Positive samples were found to have a 99.0% nt sequence identity to AY subgroup 16SrI-A (GenBank Accession No. AY180956). Sequences were exchanged for confirmation of phytoplasma identity and were deposited in Genbank under Accession Nos. FJ659844 and FJ824597. Phytoplasma strains were identified for all plants in which phytoplasmas were detected. Results show that AY is present in vineyards in the provinces of ON, BC, and QC. To our knowledge, this is the first report of AY being detected in grapevines in Canada. References: (1) E. Boudon-Padieu. Bull. O I V, 79:299, 2003. (2) M. Rott et al. Plant Dis. 91:1682, 2007. (3) E. Tanne et al. Phytopathology 91:741, 2001.

摘要

在北美,已在美国葡萄藤中检测到榆树黄化病菌、紫菀黄化病菌(AY)和X病植原体(1),最近,在加拿大不列颠哥伦比亚省(BC)和安大略省(ON)的葡萄园检测到了黑木病(2)。葡萄黄化病(GY)的典型症状包括叶片卷曲和黄化、茎杆木质化不均匀或完全缺乏、花败育或浆果枯萎以及植株矮化。2006年和2007年,加拿大食品检验局(CFIA)和加拿大农业及农业食品部(AAFC)进行了独立调查,以检测BC、ON、魁北克省(QC)、新斯科舍省、新不伦瑞克省和爱德华王子岛含有不同品种葡萄的加拿大葡萄园中是否存在植原体。CFIA从最近进口的葡萄藤以及同一或相邻地块表现出植原体引起疾病典型症状的老葡萄藤上采集并检测了651份新鲜叶片样本。许多葡萄园只被调查了一次。AAFC从ON、BC和QC成熟葡萄园中表现症状和无症状的葡萄藤上采集并检测了3485份样本。ON和BC的同一些葡萄园在这两年都进行了采样;QC的葡萄园只在2007年进行了采样。AAFC采集的叶片样本在处理前进行冷冻干燥并保存在-20°C。CFIA样本通过一种改良的实时PCR检测法和靶向16S核糖体RNA基因的TaqMan探针进行检测,该探针可检测多种已知的植原体(2)。阳性样本通过使用植原体特异性引物P1/P7的常规PCR进行确认(3),并将产生的约1800 bp片段克隆并测序,方法如前所述(2)。通过巢式PCR技术,使用通用的植原体特异性引物对P1/P6和R16R2/R16F2(3)对AAFC提取的DNA进行扩增,并将产生的1200 bp片段克隆并测序。CFIA发现,2006年在ON的一株植物和2007年在BC的另一株植物感染了类似AY的植原体。在两株受感染植物中检测到的植原体与来自GenBank的AY植原体序列(登录号分别为AF222063和AY665676)具有99.9%的核苷酸序列同一性,BC分离株与AY菌株、白蜡丛枝病植原体(GenBank登录号AY566302)也具有100%的同一性。AAFC在这两年中总共在ON、BC和QC不同葡萄品种的17株表现症状植物和21株无症状植物中检测到了植原体DNA。阳性样本与AY亚组16SrI-A(GenBank登录号AY180956)具有99.0%的核苷酸序列同一性。交换序列以确认植原体的同一性,并将其保存在GenBank中,登录号为FJ659844和FJ824597。对所有检测到植原体的植物鉴定了植原体菌株。结果表明,AY存在于ON、BC和QC省的葡萄园中。据我们所知,这是加拿大葡萄藤中检测到AY的首次报告。参考文献:(1)E. Boudon-Padieu。《国际葡萄与葡萄酒组织通报》,79:299,2003。(2)M. Rott等人。《植物病害》,91:1682,2007。(3)E. Tanne等人。《植物病理学》,91:741,2001。

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