龙葵F1C1运动基因的综合实验与转录组学分析。

IF 3.3 4区 生物学 Q2 MICROBIOLOGY
Sharmilee Sarkar, Mohit Yadav, Diganta Pegu, Aditya Kumar
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引用次数: 0

摘要

植物病原体Ralstonia solanacearum是世界上几种作物的“细菌性枯萎病”的罪魁祸首,即番茄、茄子、辣椒、土豆、花生等。这导致寄主植物变黄,枯萎,最终死亡。运动性是植物病原体的基本要求,这有助于它们感染和穿越寄主组织并在寄主植物内传播。植物病原菌solanacearum表现出抽搐和游动等运动性,这些运动性分别由毛和鞭毛控制。本研究旨在通过识别毛和鞭毛编码基因(如pilY_1, fliP和fliG)及其相关途径来描述其作用。这些基因的破坏导致了R. solanacearum F1C1菌株的三个运动突变体的产生。运动试验表明,ΔfliP和ΔfliG突变体在游泳能力方面发生了显著变化。此外,转录组学分析确定了不同突变体中差异表达的基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated Experimental and Transcriptomic Analyses of Motility Genes in Ralstonia solanacearum F1C1

The phytopathogen Ralstonia solanacearum is responsible for the “bacterial wilt disease” in several crop species worldwide, viz., tomato, brinjal, chilli, potato, groundnut, etc. This results in the yellowing of host plants, wilting, and finally their death. Motility is an essential requirement of plant pathogens, which helps them to infect and navigate through the host tissues and spread inside the host plant. The phytopathogen R. solanacearum exhibits motility such as twitching and swimming, which are governed by pili and flagella, respectively. This study aims to delineate the role of pili and flagella encoding genes, such as pilY_1, fliP, and fliG, by recognising the genes and their associated pathways. Disruption of these genes led to the creation of three motility mutants of the R. solanacearum F1C1 strain. Motility assays showed that the ΔfliP and ΔfliG mutants were significantly altered in terms of swimming ability. Further, transcriptomic analysis identified the differentially expressed genes in the respective altered mutants.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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