Univ Lyon, Université Lyon 1, CNRS, INSA-Lyon, Bayer SAS Crop Science Division, UMR 5240 MAP, Microbiologie, Adaptation et Pathogénie, 14 Impasse Pierre Baizet BP 99163, 69263, Lyon Cedex 09, France.
Bayer SAS, Crop Science Division, 14 Impasse Pierre Baizet, BP 99163, 69263, Lyon Cedex 09, France.
BMC Biotechnol. 2021 Mar 25;21(1):27. doi: 10.1186/s12896-021-00684-9.
Phakopsora pachyrhizi is a biotrophic fungal pathogen responsible for the Asian soybean rust disease causing important yield losses in tropical and subtropical soybean-producing countries. P. pachyrhizi triggers important transcriptional changes in soybean plants during infection, with several hundreds of genes being either up- or downregulated.
Based on published transcriptomic data, we identified a predicted chitinase gene, referred to as GmCHIT1, that was upregulated in the first hours of infection. We first confirmed this early induction and showed that this gene was expressed as early as 8 h after P. pachyrhizi inoculation. To investigate the promoter of GmCHIT1, transgenic soybean plants expressing the green fluorescence protein (GFP) under the control of the GmCHIT1 promoter were generated. Following inoculation of these transgenic plants with P. pachyrhizi, GFP fluorescence was detected in a limited area located around appressoria, the fungal penetration structures. Fluorescence was also observed after mechanical wounding whereas no variation in fluorescence of pGmCHIT1:GFP transgenic plants was detected after a treatment with an ethylene precursor or a methyl jasmonate analogue.
We identified a soybean chitinase promoter exhibiting an early induction by P. pachyrhizi located in the first infected soybean leaf cells. Our results on the induction of GmCHIT1 promoter by P. pachyrhizi contribute to the identification of a new pathogen inducible promoter in soybean and beyond to the development of a strategy for the Asian soybean rust disease control using biotechnological approaches.
Phakopsora pachyrhizi 是一种专性寄生真菌病原体,可引起亚洲大豆锈病,导致热带和亚热带大豆生产国的产量严重损失。P. pachyrhizi 在感染过程中可引发大豆植株的重要转录变化,几百个基因被上调或下调。
基于已发表的转录组数据,我们鉴定了一个预测的几丁质酶基因,称为 GmCHIT1,该基因在感染初期被上调。我们首先证实了这种早期诱导,并表明该基因在 P. pachyrhizi 接种后 8 小时即可表达。为了研究 GmCHIT1 的启动子,我们生成了表达 GFP 的转基因大豆植株,GFP 受 GmCHIT1 启动子的控制。用 P. pachyrhizi 接种这些转基因植株后,在靠近附着胞(真菌穿透结构)的有限区域检测到 GFP 荧光。在机械损伤后也观察到荧光,而在用乙烯前体或茉莉酸甲酯类似物处理后,pGmCHIT1:GFP 转基因植物的荧光没有变化。
我们鉴定了一个在第一个被感染的大豆叶细胞中被 P. pachyrhizi 早期诱导的大豆几丁质酶启动子。我们对 P. pachyrhizi 诱导 GmCHIT1 启动子的研究结果有助于鉴定大豆中的一个新的病原体诱导启动子,并为利用生物技术方法控制亚洲大豆锈病提供了一种策略。