• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

花椰菜花叶病毒,一种植物拟反转录病毒的时间演化和全球传播。

The temporal evolution and global spread of Cauliflower mosaic virus, a plant pararetrovirus.

机构信息

Laboratory of Plant Virology, Faculty of Agriculture, Saga University, Saga, Japan.

Laboratory of Plant Virology, Faculty of Agriculture, Saga University, Saga, Japan ; The United Graduate School of Agricultural Sciences, Kagoshima University, Kagoshima, Japan.

出版信息

PLoS One. 2014 Jan 21;9(1):e85641. doi: 10.1371/journal.pone.0085641. eCollection 2014.

DOI:10.1371/journal.pone.0085641
PMID:24465629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3897471/
Abstract

Cauliflower mosaic virus (CaMV) is a plant pararetrovirus with a double-stranded DNA genome. It is the type member of the genus Caulimovirus in the family Caulimoviridae. CaMV is transmitted by sap inoculation and in nature by aphids in a semi-persistent manner. To investigate the patterns and timescale of CaMV migration and evolution, we sequenced and analyzed the genomes of 67 isolates of CaMV collected mostly in Greece, Iran, Turkey, and Japan together with nine published sequences. We identified the open-reading frames (ORFs) in the genomes and inferred their phylogeny. After removing recombinant sequences, we estimated the substitution rates, divergence times, and phylogeographic patterns of the virus populations. We found that recombination has been a common feature of CaMV evolution, and that ORFs I-V have a different evolutionary history from ORF VI. The ORFs have evolved at rates between 1.71 and 5.81×10(-4) substitutions/site/year, similar to those of viruses with RNA or ssDNA genomes. We found four geographically confined lineages. CaMV probably spread from a single population to other parts of the world around 400-500 years ago, and is now widely distributed among Eurasian countries. Our results revealed evidence of frequent gene flow between populations in Turkey and those of its neighboring countries, with similar patterns observed for Japan and the USA. Our study represents the first report on the spatial and temporal spread of a plant pararetrovirus.

摘要

花椰菜花叶病毒 (CaMV) 是一种具有双链 DNA 基因组的植物拟反转录病毒。它是花椰菜花叶病毒科花椰菜花叶病毒属的模式成员。CaMV 通过汁液接种在植物间传播,在自然界中通过蚜虫以半持久方式传播。为了研究 CaMV 的迁移和进化模式和时间尺度,我们对主要在希腊、伊朗、土耳其和日本收集的 67 个 CaMV 分离株的基因组进行了测序和分析,同时还分析了 9 个已发表的序列。我们确定了基因组中的开放阅读框 (ORF),并推断了它们的系统发育。在去除重组序列后,我们估计了病毒群体的取代率、分歧时间和系统地理学模式。我们发现重组是 CaMV 进化的一个共同特征,并且 ORF I-V 与 ORF VI 具有不同的进化历史。ORF 以 1.71 到 5.81×10(-4)个替换/位点/年的速率进化,与具有 RNA 或 ssDNA 基因组的病毒相似。我们发现了四个具有地理局限性的谱系。CaMV 可能在 400-500 年前从一个单一种群传播到世界其他地区,现在在欧亚国家广泛分布。我们的研究结果揭示了土耳其及其邻国之间种群间频繁基因流动的证据,日本和美国也观察到了类似的模式。我们的研究代表了对植物拟反转录病毒时空传播的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/564b5384ebe7/pone.0085641.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/ef54e59b9f5e/pone.0085641.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/a07eb388c362/pone.0085641.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/3813e61a0c17/pone.0085641.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/564b5384ebe7/pone.0085641.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/ef54e59b9f5e/pone.0085641.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/a07eb388c362/pone.0085641.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/3813e61a0c17/pone.0085641.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f2/3897471/564b5384ebe7/pone.0085641.g004.jpg

相似文献

1
The temporal evolution and global spread of Cauliflower mosaic virus, a plant pararetrovirus.花椰菜花叶病毒,一种植物拟反转录病毒的时间演化和全球传播。
PLoS One. 2014 Jan 21;9(1):e85641. doi: 10.1371/journal.pone.0085641. eCollection 2014.
2
A phylogeographical study of the cauliflower mosaic virus population in mid-Eurasia Iran using complete genome analysis.中欧亚地区伊朗的芜菁花叶病毒种群的系统地理学研究:基于全基因组分析。
Arch Virol. 2014 Jun;159(6):1329-40. doi: 10.1007/s00705-013-1910-5. Epub 2013 Dec 17.
3
Biological and molecular variation of Iranian Cauliflower mosaic virus (CaMV) isolates.伊朗花椰菜花叶病毒(CaMV)分离株的生物学和分子变异
Virus Genes. 2013 Oct;47(2):347-56. doi: 10.1007/s11262-013-0948-5. Epub 2013 Jul 5.
4
Investigation of CaMV-host co-evolution through synonymous codon pattern.通过同义密码子模式研究花椰菜花叶病毒与宿主的共同进化
J Basic Microbiol. 2024 May;64(5):e2300664. doi: 10.1002/jobm.202300664. Epub 2024 Mar 4.
5
Nucleotide sequence and genome organization of a member of a new and distinct Caulimovirus species from dahlia.来自大丽花的一种新的独特花椰菜花叶病毒属病毒成员的核苷酸序列和基因组结构
Arch Virol. 2008;153(11):2145-8. doi: 10.1007/s00705-008-0235-2. Epub 2008 Oct 31.
6
Mapping regions of the cauliflower mosaic virus ORF III product required for infectivity.绘制花椰菜花叶病毒ORF III产物感染性所需的区域。
Virology. 1998 Mar 15;242(2):395-402. doi: 10.1006/viro.1997.8995.
7
Cauliflower mosaic virus is preferentially acquired from the phloem by its aphid vectors.花椰菜花叶病毒优先通过其蚜虫传播媒介从韧皮部获取。
J Gen Virol. 2002 Dec;83(Pt 12):3163-3171. doi: 10.1099/0022-1317-83-12-3163.
8
Patterns of nucleotide sequence variation among cauliflower mosaic virus isolates.花椰菜花叶病毒分离株间的核苷酸序列变异模式。
Biochimie. 1994;76(1):3-8. doi: 10.1016/0300-9084(94)90056-6.
9
Cassava vein mosaic virus (CsVMV), type species for a new genus of plant double stranded DNA viruses?木薯叶脉花叶病毒(CsVMV),一种植物双链DNA病毒新属的模式种?
Arch Virol. 1998;143(5):945-62. doi: 10.1007/s007050050344.
10
The genome of the Cauliflower mosaic virus, a plant pararetrovirus, is highly methylated in the nucleus.花椰菜花叶病毒的基因组是一种植物拟反转录病毒,在细胞核中高度甲基化。
FEBS Lett. 2020 Jun;594(12):1974-1988. doi: 10.1002/1873-3468.13852.

引用本文的文献

1
Metagenomics-based novel Caulimoviridae virus discovery and its development of identification markers in Lilium lancifolium thunb.基于宏基因组学在卷丹中发现新型花椰菜花叶病毒科病毒及其鉴定标记的开发
Virol J. 2025 Jul 5;22(1):221. doi: 10.1186/s12985-025-02837-0.
2
Host Plants Shape the Codon Usage Pattern of Turnip Mosaic Virus.寄主植物塑造了芜菁花叶病毒的密码子使用模式。
Viruses. 2022 Oct 15;14(10):2267. doi: 10.3390/v14102267.
3
Determinants of Virus Variation, Evolution, and Host Adaptation.病毒变异、进化和宿主适应性的决定因素。

本文引用的文献

1
Plant pararetroviruses: interactions of cauliflower mosaic virus with plants and insects.植物拟反转录病毒:花椰菜花叶病毒与植物和昆虫的相互作用。
Curr Opin Virol. 2013 Dec;3(6):629-38. doi: 10.1016/j.coviro.2013.08.014. Epub 2013 Sep 25.
2
Biological and molecular variation of Iranian Cauliflower mosaic virus (CaMV) isolates.伊朗花椰菜花叶病毒(CaMV)分离株的生物学和分子变异
Virus Genes. 2013 Oct;47(2):347-56. doi: 10.1007/s11262-013-0948-5. Epub 2013 Jul 5.
3
Brazilian begomovirus populations are highly recombinant, rapidly evolving, and segregated based on geographical location.
Pathogens. 2022 Sep 13;11(9):1039. doi: 10.3390/pathogens11091039.
4
The recombinogenic history of turnip mosaic potyvirus reveals its introduction to Japan in the 19th century.芜菁花叶马铃薯Y病毒的重组历史揭示了其于19世纪传入日本的情况。
Virus Evol. 2022 Jun 24;8(2):veac060. doi: 10.1093/ve/veac060. eCollection 2022.
5
Functional analysis of a viral promoter from a strawberry vein banding virus isolate from China.中国草莓皱果病毒分离物病毒启动子的功能分析。
Virol J. 2022 Mar 31;19(1):60. doi: 10.1186/s12985-022-01778-2.
6
Molecular characterization of strawberry vein banding virus from China and the development of loop‑mediated isothermal amplification assays for their detection.中国草莓皱果病毒的分子特征及环介导等温扩增检测方法的建立。
Sci Rep. 2022 Mar 22;12(1):4912. doi: 10.1038/s41598-022-08981-9.
7
Complete Genome Sequence of Isolate Bari 1, a Mild Strain of Cauliflower Mosaic Virus.花椰菜花叶病毒温和株系巴里1分离株的全基因组序列
Microbiol Resour Announc. 2021 Jul 8;10(27):e0053421. doi: 10.1128/MRA.00534-21.
8
Genomic analysis of the brassica pathogen turnip mosaic potyvirus reveals its spread along the former trade routes of the Silk Road.对芸薹菜花叶病毒的基因组分析揭示了其沿着丝绸之路的前贸易路线传播。
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12). doi: 10.1073/pnas.2021221118.
9
Enhancing Capsid Proteins Capacity in Plant Virus-Vector Interactions and Virus Transmission.增强衣壳蛋白在植物病毒-介体互作和病毒传播中的作用。
Cells. 2021 Jan 7;10(1):90. doi: 10.3390/cells10010090.
10
A Complex of Badnavirus Species Infecting Cacao Reveals Mixed Infections, Extensive Genomic Variability, and Interspecific Recombination.一种侵染可可的复杂 Badnavirus 物种揭示了混合感染、广泛的基因组变异性和种间重组。
Viruses. 2020 Apr 14;12(4):443. doi: 10.3390/v12040443.
巴西曲叶病毒种群具有高度重组性、快速进化性,并根据地理位置进行隔离。
J Virol. 2013 May;87(10):5784-99. doi: 10.1128/JVI.00155-13. Epub 2013 Mar 13.
4
Turnip mosaic potyvirus probably first spread to Eurasian brassica crops from wild orchids about 1000 years ago.芜菁花叶病毒可能在大约 1000 年前首次从野生兰花传播到欧亚大陆的芸薹属作物上。
PLoS One. 2013;8(2):e55336. doi: 10.1371/journal.pone.0055336. Epub 2013 Feb 6.
5
Landscape heterogeneity shapes host-parasite interactions and results in apparent plant-virus codivergence.景观异质性塑造了宿主-寄生虫相互作用,并导致明显的植物-病毒协同进化。
Mol Ecol. 2013 Apr;22(8):2325-40. doi: 10.1111/mec.12232. Epub 2013 Feb 4.
6
Possible consequences of the overlap between the CaMV 35S promoter regions in plant transformation vectors used and the viral gene VI in transgenic plants.植物转化载体中 CaMV 35S 启动子区域与转基因植物中病毒基因 VI 重叠可能产生的后果。
GM Crops Food. 2012 Oct-Dec;3(4):296-300. doi: 10.4161/gmcr.21406. Epub 2012 Aug 15.
7
SPREAD: spatial phylogenetic reconstruction of evolutionary dynamics.SPREAD:进化动态的空间系统发生重建。
Bioinformatics. 2011 Oct 15;27(20):2910-2. doi: 10.1093/bioinformatics/btr481. Epub 2011 Sep 11.
8
Reconstructing the history of maize streak virus strain a dispersal to reveal diversification hot spots and its origin in southern Africa.重建玉米线条病毒 A 株系的扩散历史,揭示多样化热点及其在非洲南部的起源。
J Virol. 2011 Sep;85(18):9623-36. doi: 10.1128/JVI.00640-11. Epub 2011 Jun 29.
9
Inferring weak population structure with the assistance of sample group information.借助样本群组信息推断较弱的群体结构。
Mol Ecol Resour. 2009 Sep;9(5):1322-32. doi: 10.1111/j.1755-0998.2009.02591.x. Epub 2009 Apr 1.
10
MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.MEGA5:用于最大似然法、进化距离法和最大简约法的分子进化遗传学分析。
Mol Biol Evol. 2011 Oct;28(10):2731-9. doi: 10.1093/molbev/msr121. Epub 2011 May 4.