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关于彩叶草类病毒感染印度彩叶草的首次报道。

First Report of Coleus blumei viroid Infecting Coleus in India.

作者信息

Adkar-Purushothama C R, Nagaraja H, Sreenivasa M Y, Sano T

机构信息

Faculty of Agriculture and Life Science, Hirosaki University, Bunkyo-cho 3, Hirosaki 036-8561, Japan.

Department of Studies in Microbiology, University of Mysore, Manasagangothri, Mysore 570 006, India.

出版信息

Plant Dis. 2013 Jan;97(1):149. doi: 10.1094/PDIS-08-12-0715-PDN.

DOI:10.1094/PDIS-08-12-0715-PDN
PMID:30722272
Abstract

Members of the genus Coleviroid (Coleus blumei viroid [CbVd]), family Pospiviroidae have been reported to infect Coleus (Solenostemon sp.). CbVd-1 was first reported from Brazil, CbVd-2, -3, and -4 were first reported from Germany, whereas CbVd-5 and -6 were recently identified in China (2). In India, Coleus is extensively cultivated as an ornamental plant in home gardens. In March to June 2012, Coleus leaf samples with irregular chlorotic spots/patches were collected from home gardens of two different districts of Karnataka (Kodagu and Mysore districts), India, suspecting the presence of Coleus blumei viroids (CbVd 1 to 6). Low molecular weight RNAs were extracted using 2% CTAB buffer containing 1.4 M NaCl, 20 mM EDTA, pH 8.0 and 100 mM Tris-Cl, pH 8.0 (1). Viroid-like RNA was enriched by fractionation 2M LiCl soluble nucleic acids (4). A DNA fragment with the expected size of CbVd-1 was detected in 10 (including both districts) of 14 analyzed (incident rate of 71%) from reverse transcription (RT)-PCR assay using Coleviroid specific primers (forward 5'-TGGATCCAGCGCTGCAACGGAATCCA-3' and reverse 5'-TTGGATCCGCCAGGGAACCCAGGTAAG-3'). RT was performed at 37°C for 60 min in 25 μl reaction mix containing 5 μl RNA extracts, 1 μl reverse primer, 1× first strand buffer, 10 mM dNTPs, and 200U M-MuLV-RT (Invitrogen, USA). For PCR, 2 μl RT was mixed in 25 μl PCR mix containing 0.2 μM each forward and reverse primers and 2U LA Taq (Takara-Bio, Japan) according to the manufacturer's instruction. PCR parameter was one cycle at 94°C for 2 min, 35 cycles at 94°C for 45 s, 53°C for 30 s, and 72°C for 60 s, followed by final extension at 72°C for 10 min (4). Sequence analysis of cloned amplicons detected CbVd-1 in India. To confirm the sequence of the primer regions, an additional set of tail-tail primers were designed, CbVd1-136F (5'-CTTCGTGGAACGGCTCCGCG-3') and CbVd1-136Rev (5'-GAAGAAGCCGAAGCAACTCTC-3') and were used for RT-PCR. Amplified products were cloned, sequenced and compared with previously obtained data. Further, the presences of CbVd-1 in Coleus samples was confirmed by a RNA gel blot assay using digoxigenin-labeled CbVd-1 cRNA probe (3). Alignment of 19 sequences obtained from four representative Coleus samples found the presence of two sequence variants of CbVd-1, namely Ind-1 (GenBank Accession No. AB740017) and Ind-2 (AB740018). Ind-1 was found to differ from Ind-2 by two nucleotide substitutions at position 40 (C to T) and 211 (T to C). BLAST analysis of Ind-1 showed 100% sequence similarity with CbVd-1 isolates from China (DQ178399) and South Korea (EU 410620), whereas Ind-2 was 99% identical to these two Chinese and Koreans isolates. Furthermore, 97% and 96% sequence identity with CbVd 1-RL RNA (Accession no. X95366) was observed for Ind-1 and Ind-2, respectively. Isolates from India were 88% similar with Coleus blumei viroid 1-RG (X95291). To the best of our knowledge, this is the first molecular evidence for the presence of CbVd-1 infecting Coleus in India. Coleus harbors various viroid species and CbVd-1, reported widely, can transmit efficiently through seed and also could infect the other herbaceous plants (3). This report from India will contribute further understanding of a potential risk of Coleus viroids in ornamental species. References: (1) J. J. Doyle and J. L. Doyle. Phytochem. Bull. 19:11, 1987. (2) F. H. Fu et al. Plant Dis. 95:494, 2011. (3) Ishiguro et al. Ann. Phytopathol. Soc. Jpn. 62:84, 1996. (4) S.-F. Li et al., Plant Pathol. 55:565, 2006.

摘要

据报道,马铃薯纺锤形块茎类病毒科(Coleus blumei类病毒[CbVd])的成员可感染彩叶草(Solenostemon属)。CbVd - 1最早在巴西被报道,CbVd - 2、- 3和- 4最早在德国被报道,而CbVd - 5和- 6最近在中国被鉴定出来(2)。在印度,彩叶草作为观赏植物在家庭花园中广泛种植。2012年3月至6月,从印度卡纳塔克邦两个不同地区(科达古和迈索尔地区)的家庭花园中采集了带有不规则褪绿斑点/斑块的彩叶草叶片样本,怀疑存在彩叶草类病毒(CbVd 1至6)。使用含有1.4 M NaCl、20 mM EDTA(pH 8.0)和100 mM Tris - Cl(pH 8.0)的2% CTAB缓冲液提取低分子量RNA(1)。通过对2M LiCl可溶性核酸进行分级分离来富集类病毒样RNA(4)。使用类病毒特异性引物(正向5'-TGGATCCAGCGCTGCAACGGAATCCA-3'和反向5'-TTGGATCCGCCAGGGAACCCAGGTAAG-3')进行逆转录(RT)-PCR分析,在14个分析样本中的10个(包括两个地区)检测到了预期大小的CbVd - 1 DNA片段(发病率为71%)。RT在37°C下于25 μl反应混合物中进行60分钟,该反应混合物包含5 μl RNA提取物、1 μl反向引物、1×第一链缓冲液、10 mM dNTPs和200U M - MuLV - RT(美国英杰公司)。对于PCR,根据制造商的说明,将2 μl RT与25 μl PCR混合物混合,该混合物包含每种正向和反向引物0.2 μM以及2U LA Taq(日本宝生物公司)。PCR参数为94°C下1个循环2分钟,94°C下35个循环,每个循环45秒,53°C下30秒,72°C下60秒,随后在72°C下进行最终延伸10分钟(4)。对克隆扩增子的序列分析在印度检测到了CbVd - 1。为了确认引物区域的序列,设计了另一组首尾引物,CbVd1 - 136F(5'-CTTCGTGGAACGGCTCCGCG-3')和CbVd1 - 136Rev(5'-GAAGAAGCCGAAGCAACTCTC-3'),并用于RT - PCR。扩增产物被克隆、测序并与先前获得的数据进行比较。此外,使用地高辛标记的CbVd - 1 cRNA探针通过RNA凝胶印迹分析确认了彩叶草样本中CbVd - 1的存在(3)。对从四个代表性彩叶草样本获得的19个序列进行比对,发现存在CbVd - 1的两个序列变体,即Ind - 1(GenBank登录号AB740017)和Ind - 2(AB740018)。发现Ind - 1与Ind - 2在第40位(C到T)和211位(T到C)有两个核苷酸替换。对Ind - 1的BLAST分析显示与来自中国(DQ l78399)和韩国(EU 410620)的CbVd - 1分离株具有100%的序列相似性,而Ind - 2与这两个中国和韩国分离株的同一性为99%。此外,Ind - 1和Ind - 2分别与CbVd 1 - RL RNA(登录号X95366)具有97%和96%的序列同一性。来自印度的分离株与彩叶草类病毒1 - RG(X95291)的相似性为88%。据我们所知,这是印度存在感染彩叶草CbVd - 1的首个分子证据。彩叶草含有多种类病毒物种,广泛报道的CbVd - 1可通过种子有效传播,还可感染其他草本植物(3)。来自印度的这份报告将有助于进一步了解彩叶草类病毒在观赏植物中的潜在风险。参考文献:(1)J. J. Doyle和J. L. Doyle。植物化学通报。19:11,1987。(2)F. H. Fu等人。植物疾病。95:494,2011。(3)石黑等人。日本植物病理学会年报。62:84,1996。(4)S.-F. Li等人,植物病理学。5:565,2006。