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塞尔维亚与月见草变红相关的16SrXII - A亚组植原体(斯托尔布尔)的首次报道

First Report of 16SrXII-A Subgroup Phytoplasma (Stolbur) Associated with Reddening of Oenothera biennis in Serbia.

作者信息

Adamovic D, Djalovic I, Mitrovic P, Kojic S, Starovic M, Purar B, Josic D

机构信息

Institute of Field and Vegetable Crops, Maksima Gorkog 30, 21000 Novi Sad, Serbia.

Institute for Molecular Genetic and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, 11000 Belgrade, Serbia.

出版信息

Plant Dis. 2014 Jun;98(6):841. doi: 10.1094/PDIS-12-13-1225-PDN.

DOI:10.1094/PDIS-12-13-1225-PDN
PMID:30708653
Abstract

Evening primrose (Oenothera biennis L.) is a biennial medicinal, edible, and ornamental plant species. It has attracted great interest for its seed oil that contains gamma linolenic acid, thus distinguishing this plant as a main commercial source of this essential fatty acid (4). This species has been grown as a permanent member of a medicinal plant collection established near Backi Petrovac (northern Serbia) for 22 years. The first disease symptoms were recognized as red spots on leaf rosette in July 2011, spreading gradually during vegetative growth and covering 1/3 to 1/2 of the leaf surface. Symptoms, observed on 16% of the plants (32 of 200) in the second half of May 2012 and on 23% (69 of 300) at the beginning of May 2013, appeared as reddening of lower leaves of flower-bearing stems. Affected plants exhibited stunted growth, while reddening spread over other leaves of flower-bearing stems. In severely affected plants, the flower-bearing stems were poorly developed, frequently forming witches' brooms. For that reason, 30 reddened and 20 symptomless leaves (2 leaves per plant) were sampled in both July 2012 and 2013 and total nucleic acids were extracted. Direct PCR assays were performed using phytoplasma universal primer pair P1/P7 (2) to amplify 1,800-bp fragments (the 16S rRNA gene, the 16S-23S intergenic spacer region, and a part of the 5' region of the 23S rRNA gene). PCR products were used in nested PCR with primers R16F2n/R2 (2) to amplify 1,200-bp fragments. The identification of phytoplasmas was done using RFLP (restriction fragments length polymorphisms) analyses of R16F2n/R2 amplicons digested with AluI, Kpn I, HpaII, TruI1, or HhaI endonucleases (Thermo Scientific, Lithuania) (2). RFLP patterns were identical to that of STOL reference strain of the 16SrXII-A subgroup, indicating that symptomatic plants were infected with phytoplasma (2). The 16S rDNA nucleotide sequence of representative strain E7 was deposited in GenBank under accession number KF850526. The BLASTn search showed 100% homology to an Iranian strain (KF263684.1) from peach and Serbian strains JQ730742.1 and JQ730750 from valerian and corn, respectively, all belonging to 'Candidatus Phytoplasma solani' (Stolbur). Sequencing data confirmed the association of Stolbur phytoplasma with affected O. biennis plants. It has already been reported that phytoplasma infection caused yellows disease of O. biennis (1). Also, the virescence of O. hookeri was associated with phytoplasma strain OAY from aster yellows (AY) group (subgroups 16SrI-B), and selected as the reference strain for the novel taxon 'Ca. P. asteris' (3). Here we provide the first report of naturally occurring Stolbur phytoplasma disease of O. biennis in Serbia. References: (1) S. F. Hwang et al. Z. Pflanzenkr. Pflanzenschutz 105:64, 1998. (2) I.-M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (3) I.-M. Lee et al. Int. J. Syst. Evol. Microbiol. 54:1037, 2004. (4) E. Small and P. M. Catling. Canadian Medicinal Crops. NRC Research Press, Ottawa, Ontario, Canada, 1999.

摘要

月见草(Oenothera biennis L.)是一种二年生药用、食用及观赏植物。它因种子油中含有γ-亚麻酸而备受关注,使其成为这种必需脂肪酸的主要商业来源(4)。该物种作为位于巴茨基彼得罗瓦茨(塞尔维亚北部)附近建立的药用植物收集区的永久成员,已种植了22年。2011年7月,最初的病害症状表现为莲座叶上出现红斑,在营养生长期间逐渐蔓延,覆盖叶片表面的1/3至1/2。2012年5月下旬在16%的植株(200株中的32株)上观察到症状,2013年5月初在23%(300株中的69株)的植株上观察到症状,症状表现为开花茎下部叶片发红。受影响的植株生长发育不良,而发红现象蔓延至开花茎的其他叶片。在严重受影响的植株中,开花茎发育不良,常形成扫帚状丛生枝。因此,在2012年7月和2013年分别采集了30片发红叶片和20片无症状叶片(每株2片叶),并提取了总核酸。使用植原体通用引物对P1/P7(2)进行直接PCR分析,以扩增1800 bp片段(16S rRNA基因、16S - 23S基因间隔区以及23S rRNA基因5'区域的一部分)。PCR产物用于引物R16F2n/R2(2)的巢式PCR,以扩增1200 bp片段。使用AluI、Kpn I、HpaII、TruI1或HhaI核酸内切酶(立陶宛赛默飞世尔科技公司)对R16F2n/R2扩增子进行RFLP(限制性片段长度多态性)分析,以鉴定植原体(2)。RFLP图谱与16SrXII - A亚组的STOL参考菌株相同,表明有症状的植株感染了植原体(2)。代表性菌株E7的16S rDNA核苷酸序列已提交至GenBank,登录号为KF850526。BLASTn搜索显示,与来自桃的伊朗菌株(KF263684.1)、来自缬草和玉米的塞尔维亚菌株JQ730742.1和JQ730750分别具有100%的同源性,这些菌株均属于'Ca. Phytoplasma solani'( stolbur)。测序数据证实了stolbur植原体与受影响的月见草植株之间的关联。已有报道称植原体感染导致月见草黄化病(1)。此外,O. hookeri的返绿与来自翠菊黄化病(AY)组(16SrI - B亚组)的植原体菌株OAY有关,并被选为新分类单元'Ca. P. asteris'的参考菌株(3)。在此,我们首次报道了塞尔维亚月见草自然发生的stolbur植原体病害。参考文献:(1)S. F. Hwang等人,《植物病害杂志》105:64,1998年。(2)I.-M. Lee等人,《国际系统细菌学杂志》48:1153,1998年。(3)I.-M. Lee等人,《国际系统与进化微生物学杂志》54:1037,2004年。(4)E. Small和P. M. Catling,《加拿大药用作物》,加拿大国家研究委员会出版社,渥太华,安大略省,加拿大,1999年。

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