Josic D, Starovic M, Stojanovic S, Popovic T, Dolovac N, Zdravkovic J, Pavlovic S
Institute of Soil Science, Genetic Lab, Belgrade, Serbia.
Institute for Plant Protection and Environment, Belgrade, Serbia.
Plant Dis. 2013 Mar;97(3):420. doi: 10.1094/PDIS-09-12-0885-PDN.
Saponaria officinalis L. (Caryophyllaceae; also known as bouncingbet or soapwort) is a perennial medicinal plant important for the pharmaceutical industry and used as an expectorant, alterative, laxative, and ointment for some skin diseases and arthritic conditions. S. officinalis plants with typical symptoms (23% in 2011 and 47% in 2012) of phytoplasma infection were observed in Pancevo plantation, Serbia. The symptoms appeared in May with leaves changing color from green to brown with severe reddening and necrosis. Severely diseased plants died. The infected plants had a significant reduction in biomass and quality. To investigate the presence of phytoplasma, total DNA was extracted from 10 symptomatic and four asymptomatic plants by a CTAB method. The nested PCR was carried out using phytoplasma-specific primer set P1/16S-SR followed by R16F2n/R16R2, targeting the 16S rRNA gene sequence of 1.5 and 1.2 kb in length, respectively. The amplicons of expected size were obtained from the symptomatic plants, but not from the asymptomatic plants. To obtain restriction fragment length polymorphism (RFLP) patterns, the R16F2n/R2 amplicons were digested with AluI, TruI1, HpaII, and HhaI endonucleases. The resulting patterns indicated that seven plants were infected by a Stolbur phytoplasma belonging to the 16SrXII-A subgroup, since it had the identical RFLP pattern as the STOL reference strain. The 1.2 kb nested PCR products of representative isolate Sap7 were purified using PCR purification kit (Fermentas, Vilnius, Lithuania) according to the recommended protocol and sequenced using facilities of IMGGI SeqService, Belgrade, Serbia. The obtained sequence was deposited in the NCBI database (GenBank Accession No. JX866951). The phytoplasma 16S rRNA gene sequence from Sap7 had a sequence identity of 97% with GenBank accessions GQ273961.1 ('Euonymus japonicus' phytoplasma), JX311953.1 (Candidatus Phytoplasma solani clone 5043), JQ412100.1 (Iranian alfalfa phytoplasma M21), and JN561702.1 ('Convolvulus arvensis' stolbur phytoplasma clone P1/P7-Conv2/2010-Bg). To our knowledge, this is the first report of a natural infection of S. officinalis by 16SrXII-A subgroup (Stolbur) phytoplasma in Serbia. As cited by Lee et al. (1), the 16SrI-M subgroup phytoplasma in S. officinalis sample was already detected in Lithuania by Valiunas (2). The identification of phytoplasma in the Pancevo plantation caused the intensification of our biological control tests and efforts to reduce the ecological and economic impacts of these phytoplasmas. References: (1) I. M. Lee et al. Int. J. Syst. Evol. Microbiol. 54:1037, 2004. (2) D. Valiunas. PhD thesis, Institute of Botany, Vilnius, Lithuania, 2003.
肥皂草(石竹科;也被称为肥皂草或肥皂根)是一种多年生药用植物,对制药行业很重要,用作祛痰剂、变质剂、泻药以及治疗某些皮肤病和关节炎的药膏。在塞尔维亚潘切沃种植园观察到有典型植原体感染症状的肥皂草植株(2011年为23%,2012年为47%)。症状于五月出现,叶片从绿色变为褐色,伴有严重的变红和坏死。病重的植株死亡。受感染植株的生物量和质量显著下降。为了调查植原体的存在情况,通过CTAB法从10株有症状植株和4株无症状植株中提取总DNA。使用植原体特异性引物对P1/16S-SR进行巢式PCR,随后使用R16F2n/R16R2,分别靶向长度为1.5 kb和1.2 kb的16S rRNA基因序列。从有症状植株中获得了预期大小的扩增子,但无症状植株未获得。为了获得限制性片段长度多态性(RFLP)图谱,用AluI、TruI1、HpaII和HhaI核酸内切酶消化R16F2n/R2扩增子。所得图谱表明,七株植物被属于16SrXII-A亚组的 Stolbur 植原体感染,因为它具有与STOL参考菌株相同的RFLP图谱。使用PCR纯化试剂盒(Fermentas,立陶宛维尔纽斯)按照推荐方案对代表性分离株Sap7的1.2 kb巢式PCR产物进行纯化,并使用塞尔维亚贝尔格莱德IMGGI SeqService的设备进行测序。获得的序列存入NCBI数据库(GenBank登录号JX866951)。来自Sap7的植原体16S rRNA基因序列与GenBank登录号GQ273961.1('卫矛属植原体')、JX311953.1('Ca. Phytoplasma solani克隆5043') JQ412100.1(伊朗苜蓿植原体M21)和JN561702.1('旋花科植物Stolbur植原体克隆P1/P7-Conv2/2010-Bg')的序列同一性为97%。据我们所知,这是塞尔维亚首次报道肥皂草被16SrXII-A亚组(Stolbur)植原体自然感染。如Lee等人(1)所述,Valiunas(2)已在立陶宛检测到肥皂草样本中的16SrI-M亚组植原体。潘切沃种植园植原体的鉴定促使我们加强生物防治试验,并努力减少这些植原体的生态和经济影响。参考文献:(1)I. M. Lee等人,《国际系统与进化微生物学杂志》54:1037,2004年。(2)D. Valiunas,博士论文,立陶宛维尔纽斯植物研究所,2003年。