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阿尔德黄化植原体侵染黑山普通桤木和灰桤木(欧洲桤木和灰毛桤木)的首次报道

First Report of Alder Yellows Phytoplasma Infecting Common and Grey Alder (Alnus glutinosa and A. incana) in Montenegro.

作者信息

Radonjić S, Hrnčić S, Krstić O, Cvrković T, Mitrović M, Jović J, Toševski I

机构信息

University of Montenegro, Biotechnical Faculty, Centre for Plant Protection, Mihaila Lalića 1, 81000 Podgorica, Montenegro.

Institute for Plant Protection and Environment, Department of Plant Pests, Banatska 33, 11080 Zemun, Serbia.

出版信息

Plant Dis. 2013 May;97(5):686. doi: 10.1094/PDIS-11-12-1087-PDN.

DOI:10.1094/PDIS-11-12-1087-PDN
PMID:30722214
Abstract

Alder yellows phytoplasmas (AldYp) of the 16SrV-group associated with common alder (Alnus glutinosa) and grey alder (A. incana) are closely related to the grapevine yellows (GY)-associated quarantine phytoplasma Flavescence dorée (FDp). AldYp have been reported in several countries where epidemic appearance of FDp has been confirmed (France, Italy, and Serbia) (1,2). To date, the presence of 16SrV-group of phytoplasmas has not been reported in Montenegro; however, the main vector of FD phytoplasma, Scaphoideus titanus, has been identified in Montenegrin vineyards since 2008. During a survey in September 2011, in the northern part of Montenegro, 12 symptomatic alder trees showing symptoms of leaf discoloration, ranging from yellow to light green, were sampled. Six samples, each comprising several symptomatic leaves, were collected from A. glutinosa at streamside in woodlands near the town Kolašin and other six samples from A. incana close to the river Lim near the town of Bijelo Polje. Leaves of six young A. glutinosa seedlings were used as controls. Total DNA was extracted from fresh leaf midribs and petioles using the DNeasy Plant Mini Kit (Qiagen, Hilden, Germany). Nested PCR assay was conducted on 16S rRNA gene using phytoplasma generic primers P1/P7 and F2n/R2 followed by RFLP with MseI endonuclease (Fermentas, Vilnius, Lithuania) (3). Confirmation of identification and characterization of phytoplasma positive samples was performed by amplifying the non-ribosomal metionine aminopeptidase (map) gene using FD9f5/MAPr1 and FD9f6/MAPr2 primer set (1), specific for the members of the 16SrV group phytoplasmas. Amplification products were sequenced and deposited in GenBank (KC188998 through 9001). Comparison of the map gene sequences was performed by phylogenetic analysis along with 20 reference sequences of the 16SrV-group members (1), using the neighbor-joining method in MEGA5 software (4). 16S rRNA gene amplification revealed the presence of phytoplasmas in 11 out of 12 symptomatic samples, while Mse I restriction analysis and comparison with reference strains (AldYp and FDp from Serbia) enabled affiliation of detected phytoplasmas to the 16SrV-group. None of the controls were positive for any phytoplasma. Phylogenetic analysis of the Montenegrin AldYp map gene sequences revealed presence of four different strains clustering within the previously defined clusters of the 16SrV-group members (1). Three different strains associated with symptomatic A. glutinosa were identified and they clustered either within the FD1, FD2, or PGY-C cluster, while a single detected strain from A. incana proved to be identical with PGY-A isolate of AldY phytoplasma infecting grapevine in Germany (AM384892). To our knowledge, this is the first report of the association of 16SrV-group phytoplasmas with common and grey alder in Montenegro, as well as the first report of FD-related phytoplasmas in Montenegro. Since alder trees are considered as a possible natural reservoir of the FD phytoplasmas (1), the finding of alders naturally infected with strains related to the FDp (FD1 and FD2 clusters) indicate a possible threat of economic importance to the grape production in Montenegro, which should be addressed in further research. References: (1) G. Arnaud et al. Appl. Environ. Microbiol. 73:4001, 2007. (2) T. Cvrkovic et al. Plant Pathol. 57:773, 2008. (3) I-M. Lee et al. Int. J. Syst. Evol. Bacteriol. 48:1153, 1998. (4) K. Tamura et al. Mol. Biol. Evol. 28:2731, 2011.

摘要

与欧洲桤木(Alnus glutinosa)和灰桤木(A. incana)相关的16SrV组桤木黄化植原体(AldYp)与葡萄黄化病(GY)相关的检疫性植原体葡萄黄化病植原体(FDp)密切相关。在几个已证实出现FDp流行的国家(法国、意大利和塞尔维亚)均已报道过AldYp(1,2)。迄今为止,黑山尚未报道过16SrV组植原体的存在;然而,自2008年以来,在黑山的葡萄园已鉴定出FD植原体的主要传播媒介——葡萄叶蝉(Scaphoideus titanus)。在2011年9月的一项调查中,在黑山北部,对12棵出现症状的桤木树进行了采样,这些树表现出从黄色到浅绿色的叶片变色症状。从科拉欣镇附近林地溪边的欧洲桤木采集了6个样本,每个样本包含几片有症状的叶子,从比耶洛波列镇附近利姆河附近的灰桤木采集了另外6个样本。6株欧洲桤木幼苗的叶子用作对照。使用DNeasy植物微量提取试剂盒(Qiagen,德国希尔德)从新鲜叶片中脉和叶柄中提取总DNA。使用植原体通用引物P1/P7和F2n/R2对16S rRNA基因进行巢式PCR分析,随后用MseI核酸内切酶(Fermentas,立陶宛维尔纽斯)进行RFLP分析(3)。通过使用FD9f5/MAPr1和FD9f6/MAPr2引物对(1)扩增非核糖体甲硫氨酸氨基肽酶(map)基因,对植原体阳性样本进行鉴定和特征确认,该引物对是16SrV组植原体成员的特异性引物。扩增产物进行测序并保存在GenBank中(KC188998至9001)。通过系统发育分析,将map基因序列与16SrV组成员的20个参考序列(1)进行比较,使用MEGA5软件中的邻接法(4)。16S rRNA基因扩增显示12个有症状样本中有11个存在植原体,而Mse I限制性分析以及与参考菌株(来自塞尔维亚的AldYp和FDp)的比较使得检测到的植原体归属于16SrV组。所有对照样本均未检测到任何植原体呈阳性。对黑山AldYp map基因序列的系统发育分析显示,存在四种不同的菌株,它们聚集在先前定义的16SrV组成员聚类中(1)。鉴定出与有症状的欧洲桤木相关的三种不同菌株,它们分别聚集在FD1、FD2或PGY-C聚类中,而从灰桤木中检测到的单个菌株被证明与德国感染葡萄的AldY植原体的PGY-A分离株相同(AM384892)。据我们所知,这是黑山首次报道16SrV组植原体与欧洲桤木和灰桤木相关,也是黑山首次报道与FD相关的植原体。由于桤木树被认为是FD植原体的可能天然宿主(1),发现自然感染与FDp相关菌株(FD1和FD2聚类)的桤木表明对黑山葡萄生产可能具有经济重要性的威胁,应在进一步研究中加以解决。参考文献:(1)G. Arnaud等人,《应用与环境微生物学》73:4001,2007。(2)T. Cvrkovic等人,《植物病理学》57:773,2008。(3)I-M. Lee等人,《国际系统与进化微生物学杂志》48:1153,1998。(4)K. Tamura等人,《分子生物学与进化》28:2731,2011。