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须苞石竹——塞尔维亚番茄 stolbur 植原体的新寄主。

Dianthus barbatus-A New Host of Stolbur Phytoplasma in Serbia.

作者信息

Josic D, Starović M, Kojic S, Pivic R, Stanojkovic-Sebic A, Zdravkovic M, Pavlovic S

机构信息

Institute of Soil Science, Genetic Lab, Belgrade, Serbia.

Institute for Plant Protection and Environment, Plant Pathology, Belgrade, Serbia.

出版信息

Plant Dis. 2015 Feb;99(2):283. doi: 10.1094/PDIS-08-14-0875-PDN.

DOI:10.1094/PDIS-08-14-0875-PDN
PMID:30699573
Abstract

Sweet William (Dianthus barbatus, Caryophyllaceae) is a biennial or short-lived perennial plant native to southern Europe, from the Pyrenees to the Carpathians and the Balkans. During the summers of 2012 and 2013, phytoplasma-like symptoms were observed on D. barbatus plants on a Serbian plantation (Pancevo, 44°51'49″ N, 20°39'33″ E, 80 m ASL). Only seven symptomatic plants were observed in the summer of 2012. Disease incidence in 2013 was estimated to be less than 1% but increased during 2014 to 4%. Affected plants, showing symptoms of leaf reddening, malformation, and proliferation; flower bud deficiency; and abnormal shoot production, were tested for phytoplasmas. Samples were collected from seven symptomatic and three symptomless plants each year (20 samples), and total nucleic acid was extracted from midrib tissue using a method that includes a phytoplasma enrichment step and DNA purification by chloroform/phenol (3). Oligonucleotide primers specific to the phytoplasma 16S to 23S rRNA intergenic spacer region were used in polymerase chain reaction (PCR) assays on DNA extracted from Sweet William plants (1,3). Using phytoplasma universal primer pairs P1/P7 and P1/16S-Sr, phytoplasma-specific 1.8- and 1.5-kb amplicons were obtained from four and six symptomatic plants collected in 2012 and 2013, respectively. Nested PCR with R16F2n/R2 primers yielded ~1.2-kb amplicons from DNAs of all symptomatic plants (1). No amplicon was generated in PCRs conducted with DNA templates from symptomless plants. Restriction fragment length polymorphism (RFLP) analysis of amplified 1.2-kb fragments was performed using four endonucleases (AluI, Tru1I, HhaI, and HpaII). Comparative analysis was done using RFLP patterns of Stolbur (Stol), Aster Yellows (AY), Flavescence Doree-C (FD-C), Poinsettia Branch-Inducing (PoiBI), and Clover Yellow Edge (CYE) phytoplasmas. PCR-RFLP patterns from tested samples were identical to those of the Stol reference strain, indicating that diseased Sweet William was affected by phytoplasma belonging to the 16SrXII-A (Stolbur) group. The sequence of a 1.2-kb rDNA PCR product derived from sample Tk9 (deposited under accession number KM401436 in NCBI GenBank) showed the closest identity (100%) to those of Bulgarian corn (KF907506.1), Iranian 'Bois Noir' (KJ637208.1), and two Serbian phytoplasmas (KJ174507.1 from Calendula officinalis and KF614623.1 from Paeonia tenuifolia), all belonging to the 'Candidatus Phytoplasma solani' Stolbur subgroup. Previously, Aster Yellows Phytoplasma (16SrI) had been detected in two Dianthus species: D. barbatus (Sweet William) and D. caryophyllus (carnation) (2). This is the first record of the 16SrXII-A phytoplasma subgroup being associated with yellowing and reddening of D. barbatus in Serbia. The Stolbur phytoplasma occurrence on Sweet William is significant for the management of the disease in Serbia. References: (1) I. M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (2) P. Northover et al. http://www.umanitoba.ca/faculties/afs/MAC_proceedings/proceedings/ 2007/Philip_Northover.pdf , 2007. (3) J. P. Prince et al. Phytopathology 83:1130, 1993.

摘要

麝香石竹(Dianthus barbatus,石竹科)是一种二年生或短命多年生植物,原产于欧洲南部,从比利牛斯山脉到喀尔巴阡山脉和巴尔干半岛。在2012年和2013年夏季,塞尔维亚一个种植园(潘切沃,北纬44°51'49″,东经20°39'33″,海拔80米)的麝香石竹植株上观察到类植原体症状。2012年夏季仅观察到7株有症状的植株。2013年的发病率估计低于1%,但在2014年增至4%。对表现出叶片变红、畸形和增生;花芽缺失;以及异常枝条产生等症状的受影响植株进行了植原体检测。每年从7株有症状和3株无症状植株上采集样本(共20个样本),使用一种包括植原体富集步骤和通过氯仿/苯酚进行DNA纯化的方法,从叶脉组织中提取总核酸(3)。在对从麝香石竹植株中提取的DNA进行聚合酶链反应(PCR)分析时,使用了针对植原体16S至23S rRNA基因间隔区的寡核苷酸引物(1,3)。使用植原体通用引物对P1/P7和P1/16S-Sr,分别从2012年和2013年采集的4株和6株有症状植株中获得了植原体特异性的1.8 kb和1.5 kb扩增子。用R16F2n/R2引物进行巢式PCR,从所有有症状植株的DNA中产生了约1.2 kb的扩增子(1)。用无症状植株的DNA模板进行PCR时未产生扩增子。使用四种内切酶(AluI、Tru1I、HhaI和HpaII)对扩增的1.2 kb片段进行限制性片段长度多态性(RFLP)分析。使用Stolbur(Stol)、翠菊黄化(AY)、黄萎病-C(FD-C)、一品红分枝诱导(PoiBI)和三叶草黄边(CYE)植原体的RFLP模式进行比较分析。测试样本的PCR-RFLP模式与Stol参考菌株的模式相同,表明患病的麝香石竹受到属于XII-A(Stolbur)组的植原体影响。来自样本Tk9(在NCBI GenBank中登录号为KM401436)的1.2 kb rDNA PCR产物序列与保加利亚玉米(KF907506.1)、伊朗“Bois Noir”(KJ637208.1)以及两个塞尔维亚植原体(来自金盏花的KJ174507.1和来自细叶芍药的KF614623.1)的序列显示出最接近的同一性(100%),它们均属于“Ca. Phytoplasma solani”Stolbur亚组。此前,在两种石竹属植物中检测到翠菊黄化植原体(16SrI):麝香石竹(Sweet William)和香石竹(康乃馨)(2)。这是塞尔维亚首次记录到XII-A植原体亚组与麝香石竹黄化和变红有关。麝香石竹上Stolbur植原体的出现对塞尔维亚该病的管理具有重要意义。参考文献:(1)I.M. Lee等人,《国际系统细菌学杂志》48:1153,1998年。(2)P. Northover等人,http://www.umanitoba.ca/faculties/afs/MAC_proceedings/proceedings/2007/Philip_Northover.pdf,2007年。(3)J.P. Prince等人,《植物病理学》83:1130,1993年。

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