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青枯雷尔氏菌对荧光假单胞菌SN15-2抗菌代谢产物的转录组反应

Transcriptomic response of Ralstonia solanacearum to antimicrobial Pseudomonas fluorescens SN15-2 metabolites.

作者信息

Lou Haibo, Wang Xiaobing, Chen Jun, Wang Bozhi, Wang Wei

机构信息

a State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.

b School of Information Science and Technology, Fudan University, Shanghai, 200433, China.

出版信息

Can J Microbiol. 2018 Nov;64(11):816-825. doi: 10.1139/cjm-2018-0094. Epub 2018 May 31.

Abstract

To develop efficient biocontrol agents, it is essential to investigate the response of soil-borne plant pathogens to such agents. For example, the response of Ralstonia solanacearum, the tomato wilt pathogen, to antimicrobial metabolites of Pseudomonas fluorescens is unknown. Thus, we assessed the effects of P. fluorescens SN15-2 fermentation broth on R. solanacearum by transmission electron microscopy and transcriptome technology. RNA sequencing identified 109 and 155 genes that are significantly upregulated and downregulated, respectively, in response to P. fluorescens metabolites, many of which are associated with the cell membrane and cell wall, and with nucleotide acid metabolism, iron absorption, and response to oxidative stress. This study highlights the effectiveness of P. fluorescens metabolites against the tomato wilt pathogen and helps clarify the underlying molecular mechanisms.

摘要

为了开发高效的生物防治剂,研究土壤传播的植物病原体对此类制剂的反应至关重要。例如,番茄青枯病菌(Ralstonia solanacearum)对荧光假单胞菌(Pseudomonas fluorescens)抗菌代谢产物的反应尚不清楚。因此,我们通过透射电子显微镜和转录组技术评估了荧光假单胞菌SN15 - 2发酵液对番茄青枯病菌的影响。RNA测序鉴定出分别因荧光假单胞菌代谢产物而显著上调和下调的109个和155个基因,其中许多基因与细胞膜、细胞壁、核苷酸代谢、铁吸收以及氧化应激反应有关。本研究突出了荧光假单胞菌代谢产物对番茄青枯病菌的防治效果,并有助于阐明其潜在的分子机制。

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