Suppr超能文献

应用激光微切割技术研究模式植物拟南芥中植原体的特异性基因表达。

Application of laser microdissection to study phytoplasma site-specific gene expression in the model plant Arabidopsis thaliana.

机构信息

Institute for Sustainable Plant Protection, National Research Council of Italy, IPSP-CNR Headquarter, Strada delle Cacce 73, 10135, Turin, Italy.

Institute for Sustainable Plant Protection, National Research Council of Italy, IPSP-CNR Headquarter, Strada delle Cacce 73, 10135, Turin, Italy; Institute for Sustainable Plant Protection, National Research Council of Italy, IPSP-CNR Turin Unit, Viale Mattioli 25, 10125, Turin, Italy.

出版信息

Microbiol Res. 2018 Dec;217:60-68. doi: 10.1016/j.micres.2018.09.001. Epub 2018 Sep 10.

Abstract

Many aspects of plant diseases caused by phytoplasmas are still unknown, as these pathogens are phloem restricted, uncultivable wall-less bacteria and must be studied always in association with their host. Phytoplasma transcripts are strongly underrepresented within host tissues and this poses problems for gene expression analyses. In this study, a procedure was established to infect the model plant Arabidopsis thaliana with the phytoplasma Flavescence dorée, a serious threat to European viticulture. Rates of phytoplasma infective insects and transmission efficiency to A. thaliana as well as pathogen loads were measured in different tissues of infected A. thaliana plants, and modification of phloem cell ultrastructure was observed in infected plant tissues at microscopic level. Moreover, a protocol for the application of laser microdissection to analyze plant and phytoplasma gene expression profiles in the specific colonized tissue was designed. The procedure allowed a good preservation of the plant tissue anatomy. Results showed that the extracted RNA was suitable for qualitative and quantitative RT-PCR, since both plant and pathogen transcripts, either abundant or rare ones, could be detected without any pre-amplification step. The combined use of laser microdissection approach and A. thaliana to study phytoplasmas opens the way to exploit biological, molecular and bioinformatic tools available for the model plant and to elucidate key pathways of the infection mechanisms of these important plant pathogen.

摘要

植原体引起的许多植物病害的方面仍然未知,因为这些病原体是韧皮部限制的、无细胞壁的不可培养细菌,并且必须始终与其宿主一起研究。在宿主组织中,植原体转录本的含量严重不足,这给基因表达分析带来了问题。在这项研究中,建立了一种用严重威胁欧洲葡萄种植业的植原体 Flavescence dorée 感染模式植物拟南芥的程序。在感染拟南芥植物的不同组织中测量了感染昆虫的植原体比率和向拟南芥的传播效率以及病原体载量,并在微观水平上观察了感染植物组织中韧皮部细胞超微结构的变化。此外,还设计了一种应用激光微切割来分析特定定殖组织中植物和植原体基因表达谱的方案。该程序很好地保存了植物组织解剖结构。结果表明,提取的 RNA 适用于定性和定量 RT-PCR,因为无需任何预扩增步骤即可检测到丰富或稀有植物和病原体转录本。激光微切割方法与拟南芥的联合使用为研究植原体开辟了道路,可以利用模式植物的生物、分子和生物信息学工具来阐明这些重要植物病原体感染机制的关键途径。

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