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樱桃坏死锈斑驳病毒在中国核果树上的首次报道。

First Report of Cherry necrotic rusty mottle virus on Stone Fruit Trees in China.

作者信息

Zhou J F, Wang G P, Qu L N, Deng C L, Wang Y, Wang L P, Hong N

机构信息

National Key Laboratory of Agromicrobiology, Huazhong Agricultural University, Wuhan, Hubei 430070, P. R. China.

The Key Laboratory of Plant Pathology of Hubei Province, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, P. R. China.

出版信息

Plant Dis. 2013 Feb;97(2):290. doi: 10.1094/PDIS-09-12-0836-PDN.

Abstract

During the growing seasons of 2010 through 2012, leaf tissues from 206 stone fruit trees, including one flowering cherry, three sour cherry, six nectarine (Prunus persica L. var. nucipersica Schneider), 14 apricot, 24 plum (P. domestica L.), 41 sweet cherry, and 117 peach [P. persica (L.) Batsch] trees, grown in six provinces of China, were randomly collected and tested for the CNRMV infection by RT-PCR. Out of those sampled trees, 37 showed shot holes and vein yellowing symptoms. Total RNA was extracted from leaves using the CTAB protocol reported by Li et al. (2). The primer pair CGRMV1/CGRMV2 (1) was used to amplify a fragment of 949 bp from CNRMV genome, which includes the CP gene (804 bp). PCR products with the expected size were detected in one sweet cherry, one apricot, one peach, one plum, and two sour cherry plants. However, no correlation between PCR data and symptom expression could be found. PCR products were cloned into the vector pMD18-T (TaKaRa, Dalian, China). Three independent clones from each isolate were sequenced by Genscript Corp., Nanjing, China, and sequences were deposited in the GenBank under accession nos. JX491635, JX491636, JX491637, JX648205, and JX648206. Results of sequence analysis showed that sequences of the five CNRMV isolates shared the highest nt (99.0 to 99.6%) and aa (98.9 to 100%) similarities with a cherry isolate from Germany (GenBank Accession No. AF237816). The sequence of one isolate from a peach tree (JX648205) was divergent and shared only 84.7 to 86.1% nt and 94.4 to 95.1% aa similarities with those cp sequences. Clones intra each isolate shared more than 99% nt similarities. To confirm CNRMV infection, seedlings of peach GF 305 were graft-inoculated with bud-woods from a peach and a sweet cherry tree, which was positive to CNRMV and also two other viruses: Cherry green ring mottle virus (CGRMV) and Plum bark necrosis stem pitting-associated virus (PBNSPaV), as tested by RT-PCR. Grafted seedlings were kept in an insectproof greenhouse and observed for symptom development. In May of the following year, some newly developed leaves of inoculated seedlings showed vein yellowing, ringspot, and shot hole symptoms. Results of Protein A sandwich (PAS)-ELISA using an antiserum raised against the recombinant CP of a CNRMV isolate (unpublished) and RT-PCR confirmed CNRMV infection in inoculated trees. In addition to CNRMV, tested seedlings were also found to be infected with CGRMV and PBNSPaV by RT-PCR. To our knowledge, this is the first report on the occurrence of CNRMV on stone fruit trees in China, and also the first record of the CNRMV infection in peach and plum plants. Given the economic importance of its hosts and the visible symptoms of the viral disease, it is important to prevent the virus spread by using virus-tested propagation materials. References: (1) R. Li and R. Mock. J. Virol. Methods 129:162, 2005. (2) R. Li et al. J. Virol. Methods 154:48, 2008.

摘要

在2010年至2012年的生长季节,从中国六个省份种植的206棵核果类树木上随机采集叶片组织,这些树木包括一棵樱花树、三棵酸樱桃树、六棵油桃树(Prunus persica L. var. nucipersica Schneider)、14棵杏树、24棵李树(P. domestica L.)、41棵甜樱桃树和117棵桃树[P. persica (L.) Batsch],并通过逆转录聚合酶链反应(RT-PCR)检测李痘坏死环斑病毒(CNRMV)感染情况。在这些采样树木中,有37棵表现出穿孔和叶脉黄化症状。使用Li等人(2)报道的十六烷基三甲基溴化铵(CTAB)方法从叶片中提取总RNA。引物对CGRMV1/CGRMV2(1)用于从CNRMV基因组中扩增出一段949 bp的片段,该片段包含外壳蛋白(CP)基因(804 bp)。在一棵甜樱桃树、一棵杏树、一棵桃树、一棵李树和两棵酸樱桃树中检测到了预期大小的PCR产物。然而,未发现PCR数据与症状表达之间存在相关性。PCR产物被克隆到载体pMD18-T(TaKaRa,中国大连)中。来自中国南京金斯瑞生物科技有限公司对每个分离株的三个独立克隆进行了测序,序列已提交至GenBank,登录号为JX491635、JX491636、JX491637、JX648205和JX648206。序列分析结果表明,五个CNRMV分离株的序列与来自德国的一个樱桃分离株(GenBank登录号AF237816)的核苷酸(nt)相似度最高(99.0%至99.6%),氨基酸(aa)相似度最高(98.9%至100%)。来自一棵桃树的一个分离株(JX648205)的序列存在差异,与那些CP序列的nt相似度仅为84.7%至86.1%,aa相似度为94.4%至95.1%。每个分离株内的克隆之间的nt相似度超过99%。为了确认CNRMV感染,用来自一棵桃树和一棵甜樱桃树的芽木对桃树GF 305幼苗进行嫁接接种,这两棵树经RT-PCR检测对CNRMV以及另外两种病毒呈阳性:樱桃绿环斑驳病毒(CGRMV)和李树皮坏死茎痘相关病毒(PBNSPaV)。嫁接后的幼苗置于防虫温室中,观察症状发展。次年5月,接种幼苗新长出的一些叶片出现叶脉黄化、环斑和穿孔症状。使用针对一种CNRMV分离株的重组CP产生的抗血清进行的蛋白A夹心(PAS)-酶联免疫吸附测定(ELISA)结果和RT-PCR证实接种树木感染了CNRMV。通过RT-PCR还发现,除了CNRMV外,受试幼苗还感染了CGRMV和PBNSPaV。据我们所知,这是中国核果类树木上发生CNRMV的首次报道,也是桃树和李树感染CNRMV的首次记录。鉴于其寄主的经济重要性以及该病毒病的明显症状,使用经过病毒检测的繁殖材料来防止病毒传播很重要。参考文献:(1)R. Li和R. Mock。《病毒学方法杂志》129:162,2005年。(2)R. Li等人。《病毒学方法杂志》154:48,2008年。

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