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对根部的全转录组和靶向代谢物分析揭示了两个抗性马铃薯品种针对感染的不同防御机制。

Global transcriptome and targeted metabolite analyses of roots reveal different defence mechanisms against infection in two resistant potato cultivars.

作者信息

Jose Jeny, Éva Csaba, Bozsó Zoltán, Hamow Kamirán Áron, Fekete Zsófia, Fábián Attila, Bánfalvi Zsófia, Sági László

机构信息

Agricultural Institute, Centre for Agricultural Research, Martonvásár, Hungary.

Doctoral School of Plant Sciences, Hungarian University of Agriculture and Life Sciences, Gödöllő, Hungary.

出版信息

Front Plant Sci. 2023 Jan 9;13:1065419. doi: 10.3389/fpls.2022.1065419. eCollection 2022.

DOI:10.3389/fpls.2022.1065419
PMID:36733596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9889091/
Abstract

(), the causal agent of bacterial wilt disease in an unusually wide range of host plants, including potato (), is one of the most destructive phytopathogens that seriously reduces crop yields worldwide. Identification of defence mechanisms underlying bacterial wilt resistance is a prerequisite for biotechnological approaches to resistance breeding. Resistance to has been reported only in a few potato landraces and cultivars. Our inoculation bioassays confirmed that the cultivars 'Calalo Gaspar' (CG) and 'Cruza 148' (CR) are resistant to infection. Comparative transcriptome analyses of CG and CR roots, as well as of the roots of an -susceptible cultivar, 'Désirée' (DES), were carried out two days after infection, in parallel with their respective noninfected controls. In CR and DES, the upregulation of chitin interactions and cell wall-related genes was detected. The phenylpropanoid biosynthesis and glutathione metabolism pathways were induced only in CR, as confirmed by high levels of lignification over the whole stele in CR roots six days after infection. At the same time, infection greatly increased the concentrations of chlorogenic acid and quercetin derivatives in CG roots as it was detected using ultra-performance liquid chromatography - tandem mass spectrometry. Characteristic increases in the expression of MAP kinase signalling pathway genes and in the concentrations of jasmonic, salicylic, abscisic and indoleacetic acid were measured in DES roots. These results indicate different defence mechanisms in the two resistant potato cultivars and a different response to infection in the susceptible cultivar.

摘要

茄科劳尔氏菌(Ralstonia solanacearum)是一种能感染异常广泛寄主植物的病原菌,包括马铃薯(Solanum tuberosum),它是最具破坏性的植物病原体之一,在全球范围内严重降低作物产量。鉴定抗青枯病的防御机制是抗病育种生物技术方法的前提条件。仅在少数马铃薯地方品种和栽培品种中报道了对茄科劳尔氏菌的抗性。我们的茄科劳尔氏菌接种生物测定证实,“Calalo Gaspar”(CG)和“Cruza 148”(CR)品种对茄科劳尔氏菌感染具有抗性。在茄科劳尔氏菌感染两天后,对CG和CR根系以及感病品种“Desirée”(DES)的根系进行了比较转录组分析,并与各自未感染的对照同时进行。在CR和DES中,检测到几丁质相互作用和细胞壁相关基因的上调。苯丙烷生物合成和谷胱甘肽代谢途径仅在CR中被诱导,茄科劳尔氏菌感染六天后CR根系整个中柱的木质化水平升高证实了这一点。同时,通过超高效液相色谱 - 串联质谱法检测发现,茄科劳尔氏菌感染极大地增加了CG根系中绿原酸和槲皮素衍生物的浓度。在DES根系中检测到促分裂原活化蛋白激酶信号通路基因表达以及茉莉酸、水杨酸、脱落酸和吲哚乙酸浓度的特征性增加。这些结果表明两个抗性马铃薯品种中存在不同的抗茄科劳尔氏菌防御机制,以及感病品种对茄科劳尔氏菌感染的不同反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/fc9fd3e6efa3/fpls-13-1065419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/093dd2f45a31/fpls-13-1065419-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/683b88171c16/fpls-13-1065419-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/b2aac56565f1/fpls-13-1065419-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/e190386cc8ed/fpls-13-1065419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/4ca842f54672/fpls-13-1065419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/b52fa1bb42d2/fpls-13-1065419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/e79ed17eab2d/fpls-13-1065419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/fc9fd3e6efa3/fpls-13-1065419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/093dd2f45a31/fpls-13-1065419-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/683b88171c16/fpls-13-1065419-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/b2aac56565f1/fpls-13-1065419-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/e190386cc8ed/fpls-13-1065419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/4ca842f54672/fpls-13-1065419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/b52fa1bb42d2/fpls-13-1065419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/e79ed17eab2d/fpls-13-1065419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b32/9889091/fc9fd3e6efa3/fpls-13-1065419-g008.jpg

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