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柑橘叶斑病毒在意大利金橘上的首次报道。

First Report of Citrus leaf blotch virus on Kumquat in Italy.

作者信息

Guardo M, Sorrentino G, Marletta T, Caruso A

机构信息

CRA-Istituto Sperimentale per l'Agrumicoltura, Corso Savoia 190, 95024 Acireale (CT), Italy.

出版信息

Plant Dis. 2007 Aug;91(8):1054. doi: 10.1094/PDIS-91-8-1054A.

Abstract

During the spring of 2006, nurserymen reported observations of the bud union disorder of 'Nagami' kumquat scions propagated on Troyer citrange rootstock to the CRA-Istituto Sperimentale per l'Agrumicoltura. These plants showed reduced canopy volume and new shoots below graft points 6 months after propagation; the bud union was brittle and broke down easily after 1 year. After tests excluded common citrus viruses and viroids that might cause the incompatibility (e.g., Citrus tristeza virus, Citrus psorosis virus, Citrus exocortis viroid, and Hop stunt viroid), we tested for Citrus leaf blotch virus (CLBV), a virus previously associated with a bud union crease in kumquat (2). Leaves were collected from 100 2-year-old kumquat plants from a nursery near Messina (Sicily [Italy]); 50 were grafted on sour orange rootstock (asymptomatic) and 50 were grafted on Troyer citrange rootstock (symptomatic). Total RNA was extracted using Qiagen RNeasy Plant Mini Kit (Qiagen S.P.A. Milan, Italy). Primers previously reported (1,2) and designed from a published CLBV sequence (Genbank Accession No. AJ318061) were used in reverse transcription (RT)-PCR assays to amplify the RNA-dependent RNA polymerase gene (sense primer KU 27, 5'-GATGCAAGCCAGGATGAATAC-3', genomic positions 5321-5340 and anti-sense primer KU 15, 5'-CAGACACTCCAAGACCTTTCC-3', genomic positions 5776-5756) and the coat protein gene (sense primer KU18, 5'-TTAAGATTACAGACACGAAGG-3' genomic positions 7686-7706 and anti-sense primer KU 19 5'-CTGTTTTTGAATTTTGCTCG-3', genomic positions 8123-8104). All kumquat samples yielded amplicons of the expected size (456 and 438 bp). No amplicons were obtained from healthy plants. Amplicons for each gene were cloned into the pGEM-T Easy Vector (Promega Italy, Milan), and four clones for each plasmid DNA were sequenced in both directions. Consensus sequences of the two genes (Genbank Accession Nos. EF203229 and EF203230) had 96 and 97% nucleotide sequence identity, respectively, and both had 99% amino acid identity with the previously reported CLBV sequence (Genbank Accession No. AJ318061). Approximately 400,000 ornamental kumquats are produced annually in Italy. CLBV infection can cause serious production losses because of the decline associated with bud union disorders grafted onto trifoliate orange and trifoliate-derived rootstocks. References: (1) L. Galipienso et al. Eur. J. Plant Pathol. 110:175, 2004. (2) M. C. Vives et al. Virology 287:225, 2001.

摘要

2006年春季,苗木培育者向意大利农业柑橘试验研究所(CRA-Istituto Sperimentale per l'Agrumicoltura)报告了对嫁接到特洛亚枳橙砧木上的“长实”金柑接穗芽接结合部病害的观察情况。这些植株在繁殖6个月后,树冠体积减小,嫁接点以下出现新梢;芽接结合部变脆,1年后容易断裂。在排除了可能导致不亲和性的常见柑橘病毒和类病毒(如柑橘衰退病毒、柑橘鳞皮病毒、柑橘裂皮类病毒和柑橘速衰类病毒)后,我们对柑橘叶斑病毒(CLBV)进行了检测,该病毒此前与金柑芽接结合部皱缩有关(2)。从意大利西西里岛墨西拿附近一家苗圃的100株2年生金柑植株上采集叶片;50株嫁接到酸橙砧木上(无症状),50株嫁接到特洛亚枳橙砧木上(有症状)。使用Qiagen RNeasy植物微型试剂盒(Qiagen S.P.A.,米兰,意大利)提取总RNA。以前报道过的引物(1,2)以及根据已发表的CLBV序列(Genbank登录号AJ318061)设计的引物用于逆转录(RT)-PCR分析,以扩增RNA依赖RNA聚合酶基因(正向引物KU 27,5'-GATGCAAGCCAGGATGAATAC-3',基因组位置5321-5340;反向引物KU 15,5'-CAGACACTCCAAGACCTTTCC-3',基因组位置5776-5756)和外壳蛋白基因(正向引物KU18,5'-TTAAGATTACAGACACGAAGG-3',基因组位置7686-7706;反向引物KU 19,5'-CTGTTTTTGAATTTTGCTCG-3',基因组位置8123-8104)。所有金柑样品均产生了预期大小的扩增子(456和438 bp)。健康植株未获得扩增子。每个基因的扩增子被克隆到pGEM-T Easy载体(Promega Italy,米兰)中,每个质粒DNA的四个克隆进行双向测序。两个基因的一致序列(Genbank登录号EF203229和EF203230)的核苷酸序列同一性分别为96%和97%,两者与先前报道的CLBV序列(Genbank登录号AJ318061)的氨基酸同一性均为99%。意大利每年生产约40万株观赏金柑。CLBV感染会导致严重的生产损失,因为嫁接到枳和枳衍生砧木上会出现与芽接结合部病害相关的衰退。参考文献:(1)L. Galipienso等人,《欧洲植物病理学杂志》110:175,2004年。(2)M. C. Vives等人,《病毒学》287:225,2001年。

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