Adamovic D, Djalovic I, Mitrovic P, Kojic S, Pivic R, Josic D
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.
Plant Dis. 2014 Apr;98(4):565. doi: 10.1094/PDIS-07-13-0702-PDN.
Peony (Paeonia tenuifolia L.) is a herbaceous perennial plant known for its beautiful and showy flowers. In Serbia it is native to the Deliblato Sands and is used as an ornamental and medicinal plant in folk medicine. This plant species has become a rarity and for that reason peony was introduced into a botanical collection near Backi Petrovac (northern Serbia), where it has been maintained since 1988. Reddening of lower leaves observed on 10% of plants (5 of 50) in the collection at flowering in May 2012 gradually progressed throughout affected plants by the seed maturation stage. Five leaves from each of three reddened and three symptomless plants were sampled at the end of July 2012. Total nucleic acid was extracted separately from individual leaves (30 samples) using the CTAB (cetyltrimethylammonium bromide) method (2). A nested PCR assay using universal primer pairs P1/P7, followed by R16F2n/R16R2 (4), amplified 16S rDNA fragments of 1.8 and 1.2 kb, respectively. DNA from all three reddened plants (15 samples) yielded 1.2-kb amplicons after nested PCRs. Restriction fragment length polymorphism (RFLP) patterns obtained by digestion of nested products with endonucleases AluI, TruI, HpaII, or HhaI (Thermo Scientific, Lithuania) (4) were identical to those of the STOL reference strain included for comparative purposes, indicating that symptoms were consistently associated with plant infection by 'Ca. Phytoplasma solani' (Stolbur) phytoplasma. The 16S rDNA amplicons from two peony plants (1.2 kb from B15 and 1.8 from B18) were sequenced (GenBank Accession No. KC960487 and KF614623, respectively). BLAST analysis revealed a 100% identity between the sequences and GenBank sequences of Stolbur phytoplasma, subgroup 16SrXII-A phytoplasma, previously detected in maize (JQ730750) in Serbia and red clover (EU814644.1) in the Czech Republic. Phytoplasma associated diseases of other species of the genus Paeonia (P. lactiflora Pall. and P. suffruticosa Andrews) have been described elsewhere. Disease symptoms on P. lactiflora from Chile were associated with the phytoplasma that belongs to the ribosomal subgroup 16SrVII-A ('Ca. Phytoplasma fraxini') (1). Also, Stolbur phytoplasma from the 16SrXII group was detected on P. suffruticosa plants in China, manifesting yellowing symptoms (3). To our knowledge, this is the first report of naturally occurring Stolbur phytoplasma disease of P. tenuifolia L. in Serbia. References: (1) N. Arismendi et al. Bull. Insectol. 64:S95, 2011. (2) X. Daire et al. Eur. J. Plant Pathol. 103:507, 1997. (3) Y. Gao et al. J. Phytopathol. 161:197, 2013. (4) I. M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998.
细叶芍药(Paeonia tenuifolia L.)是一种多年生草本植物,以其美丽艳丽的花朵而闻名。在塞尔维亚,它原产于德利布拉托沙丘,在民间医学中被用作观赏植物和药用植物。该植物物种已变得稀有,因此芍药被引入了巴茨基彼得罗瓦茨(塞尔维亚北部)附近的一个植物标本馆,自1988年以来一直在那里保存。2012年5月开花时,在标本馆中观察到10%的植株(50株中的5株)下部叶片发红,到种子成熟阶段,受影响的植株上这种症状逐渐加重。2012年7月底,从三株发红植株和三株无症状植株上分别采集了五片叶子。使用CTAB(十六烷基三甲基溴化铵)法(2)从单株叶片(30个样本)中分别提取总核酸。使用通用引物对P1/P7进行巢式PCR分析,随后使用R16F2n/R16R2(4),分别扩增出1.8 kb和1.2 kb的16S rDNA片段。经过巢式PCR后,所有三株发红植株(15个样本)的DNA都产生了1.2 kb的扩增产物。用核酸内切酶AluI、TruI、HpaII或HhaI(立陶宛赛默飞世尔科技公司)消化巢式产物获得的限制性片段长度多态性(RFLP)图谱与用于比较目的的STOL参考菌株的图谱相同,这表明这些症状始终与‘Ca. Phytoplasma solani’(Stolbur)植原体感染植株有关。对两株芍药植株的16S rDNA扩增产物(B15的1.2 kb和B18的1.8 kb)进行了测序(GenBank登录号分别为KC960487和KF614623)。BLAST分析显示,这些序列与之前在塞尔维亚玉米(JQ730750)和捷克共和国红三叶草(EU814644.1)中检测到的Stolbur植原体、亚组16SrXII - A植原体的GenBank序列具有100%的同一性。芍药属其他物种(P. lactiflora Pall.和P. suffruticosa Andrews)的植原体相关病害在其他地方已有描述。智利芍药P. lactiflora上的病害症状与属于核糖体亚组16SrVII - A(‘Ca. Phytoplasma fraxini’)的植原体有关(1)。此外,在中国的牡丹P. suffruticosa植株上检测到了来自16SrXII组的Stolbur植原体,表现出黄化症状(3)。据我们所知,这是塞尔维亚首次关于细叶芍药自然发生Stolbur植原体病害的报道。参考文献:(1)N. Arismendi等人,《昆虫学通报》64:S95,2011年。(2)X. Daire等人,《欧洲植物病理学杂志》103:507,1997年。(3)Y. Gao等人,《植物病理学杂志》161:197,2013年。(4)I. M. Lee等人,《国际系统细菌学杂志》48:1153,1998年。