An Engineered Citrus Tristeza Virus (T36CA)-Based Vector Induces Gene-Specific RNA Silencing and Is Graft Transmissible to Commercial Citrus Varieties.

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES
Robert R Krueger, Angel Y S Chen, Jaclyn S Zhou, Si Liu, Huaying Karen Xu, James C K Ng
{"title":"An Engineered Citrus Tristeza Virus (T36CA)-Based Vector Induces Gene-Specific RNA Silencing and Is Graft Transmissible to Commercial Citrus Varieties.","authors":"Robert R Krueger, Angel Y S Chen, Jaclyn S Zhou, Si Liu, Huaying Karen Xu, James C K Ng","doi":"10.1094/PHYTO-05-24-0167-R","DOIUrl":null,"url":null,"abstract":"<p><p>A protein-expressing citrus tristeza virus-based vector construct, pT36CA-V1.3, obtained from a California isolate of the T36 strain (T36CA), was retooled into a virus-induced gene silencing system intended for use with studies of California citrus. Virus-induced gene silencing constructs engineered with a truncated <i>Citrus macrophylla PHYTOENE DESATURASE</i> (<i>CmPDS</i>) gene sequence in the sense or antisense orientation worked equally well to silence the endogenous <i>CmPDS</i> gene. In a parallel effort to optimize vector performance, two nonsynonymous nucleotides in open reading frame 1a of pT36CA-V1.3 were replaced with those conserved in the reference sequences from the T36CA cDNA library. The resulting viruses, T36CA-V1.4 (with one amino acid modification: D760N) and T36CA-V1.5 (with two amino acid modifications: D760N and P1174L), along with T36CA-V1.3, were individually propagated in <i>Nicotiana benthamiana</i> and <i>C. macrophylla</i> plants. Enzyme-linked immunosorbent assay (ELISA) measurements of extracts of the newly emerged leaves suggested that all three viruses accumulated to similar levels in <i>N. benthamiana</i> plants at 5 weeks postinoculation. ELISA values of T36CA-V1.4- and -V1.5-infected <i>C. macrophylla</i> samples were significantly higher than that of T36CA-V1.3-infected samples within an 8- to 12-month postinoculation window, suggesting a higher accumulation of T36CA-V1.4 and -V1.5 than T36CA-V1.3. However, at 36 months postinoculation, the ELISA values suggested that all three viruses accumulated to similar levels. When <i>C. macrophylla</i> plants infected with each of the three viruses were grafted to commercial citrus varieties, a limited number of receptor plants became infected, demonstrating a weak but nonetheless (the first) successful delivery of T36CA to California-grown commercial citrus.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"PHYTO05240167R"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-05-24-0167-R","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

A protein-expressing citrus tristeza virus-based vector construct, pT36CA-V1.3, obtained from a California isolate of the T36 strain (T36CA), was retooled into a virus-induced gene silencing system intended for use with studies of California citrus. Virus-induced gene silencing constructs engineered with a truncated Citrus macrophylla PHYTOENE DESATURASE (CmPDS) gene sequence in the sense or antisense orientation worked equally well to silence the endogenous CmPDS gene. In a parallel effort to optimize vector performance, two nonsynonymous nucleotides in open reading frame 1a of pT36CA-V1.3 were replaced with those conserved in the reference sequences from the T36CA cDNA library. The resulting viruses, T36CA-V1.4 (with one amino acid modification: D760N) and T36CA-V1.5 (with two amino acid modifications: D760N and P1174L), along with T36CA-V1.3, were individually propagated in Nicotiana benthamiana and C. macrophylla plants. Enzyme-linked immunosorbent assay (ELISA) measurements of extracts of the newly emerged leaves suggested that all three viruses accumulated to similar levels in N. benthamiana plants at 5 weeks postinoculation. ELISA values of T36CA-V1.4- and -V1.5-infected C. macrophylla samples were significantly higher than that of T36CA-V1.3-infected samples within an 8- to 12-month postinoculation window, suggesting a higher accumulation of T36CA-V1.4 and -V1.5 than T36CA-V1.3. However, at 36 months postinoculation, the ELISA values suggested that all three viruses accumulated to similar levels. When C. macrophylla plants infected with each of the three viruses were grafted to commercial citrus varieties, a limited number of receptor plants became infected, demonstrating a weak but nonetheless (the first) successful delivery of T36CA to California-grown commercial citrus.

一种基于柑橘三叶虫病毒(T36CA)的工程载体可诱导基因特异性 RNA 沉默,并可嫁接传播到商业柑橘品种上。
从加利福尼亚州分离的 T36 株系(T36CA)中获得了一种基于蛋白表达的柑橘三尖杉病毒(CTV)载体构建体 pT36CA-V1.3,并将其改造成病毒诱导基因沉默(VIGS)系统,用于加利福尼亚柑橘的研究。用截短的大叶柑橘(Cm)芳香烃脱酸酶(PDS)基因序列设计的 VIGS 构建体在有义或无义方向上都能很好地抑制内源 CmPDS 基因。在优化载体性能的同时,pT36CA-V1.3 开放阅读框 1a 中的两个非同义核苷酸被替换为 T36CA cDNA 文库参考序列中保留的核苷酸。得到的病毒 T36CA-V1.4(有一个氨基酸修饰:D760N)和 T36CA-V1.5(有两个氨基酸修饰:D760N 和 P1174L)与 T36CA-V1.3 一起分别在烟草和 C. macrophylla 植物中繁殖。对新萌发叶片提取物的酶联免疫吸附测定(ELISA)结果表明,在接种后 5 周,三种病毒在 N. benthamiana 植物体内的积累水平相似。受 T36CA-V1.4 和 -V1.5 感染的 C. macrophylla 样本的 ELISA 值在接种后 8 至 12 个月 (mpi) 的窗口期内明显高于受 T36CA-V1.3 感染的样本,这表明 T36CA-V1.4 和 -V1.5 的积累量高于 T36CA-V1.3。然而,在 36 mpi 时,ELISA 值表明三种病毒的积累水平相似。将感染了这三种病毒的 C. macrophylla 植株嫁接到商业柑橘品种上时,受体植株受感染的数量有限,这表明 T36CA 对加利福尼亚种植的商业柑橘的传播虽然微弱,但还是成功的(第一次)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Phytopathology
Phytopathology 生物-植物科学
CiteScore
5.90
自引率
9.40%
发文量
505
审稿时长
4-8 weeks
期刊介绍: Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信