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感病和抗病小麦(Triticum aestivum)品种对条锈菌(Puccinia striiformis f. sp. tritici)侵染的代谢组学分析。

Metabolite profiling of susceptible and resistant wheat (Triticum aestivum) cultivars responding to Puccinia striiformis f. sp. tritici infection.

机构信息

Research Centre for Plant Metabolomics, Department of Biochemistry, University of Johannesburg, Auckland Park, P.O. Box 524, Johannesburg, 2006, South Africa.

International Research and Development Division, Omnia Group, Ltd, Johannesburg, 2006, South Africa.

出版信息

BMC Plant Biol. 2023 Jun 1;23(1):293. doi: 10.1186/s12870-023-04313-9.

Abstract

BACKGROUND

Puccinia striiformis f. sp. tritici (Pst) is an economically devasting disease that is prominent in cereal crops such as wheat (Triticum aestivum). The fungal pathogen can cause approximately 30-70% losses in crop productivity and yields. Pst has become difficult to manage due to its ease of transmission through wind dispersal over long distances, and intercontinental dispersal has been previously reported. The ease of transmission has resulted in further destruction because of new and more virulent strains infecting crops previously resistant to a different strain.

RESULTS

In this study, a liquid chromatography-mass spectrometry-based untargeted metabolomics approach, in combination with multivariate data analytical tools, was used to elucidate the mechanistic nature of the defence systems of a Pst-resistant and a susceptible wheat cultivar infected with P. striiformis. We also investigated the time-dependant metabolic reconfiguration of infected plants over a four-week period. The untargeted metabolomic analysis revealed a time-course metabolic reprogramming involving phenylpropanoids (majority flavonoids), amino acids, lipids, benzoic acids, TCA cycle intermediates and benzoxazinoids responding to Pst infection. Interestingly, the results do not show a linear course for the decrease and increase (up-/down-regulation) of said classes of metabolites, but rather the up- or down-regulation of specific metabolites in response to the pathogen infection. The resistant Koonap cultivar had an abundance of phenolic compounds such as rutin, isoorintin-7-O-glucoside and luteolin-6-C-hexoside-O-hexoside. These compounds showed a decrease over time in control Koonap plants compared to an increase in Pst-infected plants. These metabolites were down-regulated in the susceptible Gariep cultivar, which could serve as biomarkers for plant responses to biotic stress and resistance against Pst.

CONCLUSIONS

Overall, an LC-MS-based metabolomics approach allowed for the metabolic profiling and analysis of the impact of plant-pathogen interactions on the overall plant metabolome and provided a real-time snapshot of the differential significant metabolic perturbations occurring in wheat plants responding to the Pst pathogen. The Pst-resistant Koonap cultivar showed a rapid accumulation of defence metabolites in response to pathogen infection compared to the susceptible Gariep cultivar. These findings provide insight into the mechanistic biochemical nature of plant-microbe interactions and the prospects of metabolic engineering for improved plant tolerance and resistance to biotic stresses.

摘要

背景

条锈菌(Puccinia striiformis f. sp. tritici,Pst)是一种经济上极具破坏性的疾病,在小麦(Triticum aestivum)等谷类作物中尤为突出。这种真菌病原体可导致作物产量减少约 30-70%。由于其易于通过风远距离传播,以及以前有报道过洲际传播,因此条锈菌变得难以控制。由于新的、更具毒性的菌株感染了以前对不同菌株具有抗性的作物,进一步的传播造成了更大的破坏。

结果

在这项研究中,采用基于液相色谱-质谱的非靶向代谢组学方法,结合多元数据分析工具,阐明了抗条锈病和易感小麦品种感染条锈菌后的防御系统的机制性质。我们还研究了感染后四周内植物的时间依赖性代谢重排。非靶向代谢组学分析揭示了一个涉及苯丙烷类(大多数类黄酮)、氨基酸、脂质、苯甲酸、三羧酸循环中间产物和苯并恶嗪类的时间进程代谢重编程,这些物质对条锈菌感染有反应。有趣的是,结果并没有显示出这些代谢物类别的下降和增加(上调/下调)的线性过程,而是针对病原体感染,特定代谢物的上调或下调。抗性品种 Koonap 含有丰富的酚类化合物,如芦丁、异芦丁-7-O-葡萄糖苷和木犀草素-6-C-己糖苷-O-己糖苷。与感染条锈菌的植物相比,对照 Koonap 植物中这些化合物随时间的推移而减少。在易感品种 Gariep 中,这些代谢物下调,可作为植物对生物胁迫反应和抗条锈病的生物标志物。

结论

总之,基于 LC-MS 的代谢组学方法允许对植物-病原体相互作用对整个植物代谢组的影响进行代谢谱分析,并提供了对小麦植物对 Pst 病原体反应过程中发生的差异显著代谢扰动的实时快照。与易感品种 Gariep 相比,抗性品种 Koonap 在受到病原体感染时迅速积累防御代谢物。这些发现为植物-微生物相互作用的机制生化性质以及代谢工程改善植物对生物胁迫的耐受性和抗性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a971/10233866/32dce4507382/12870_2023_4313_Fig1_HTML.jpg

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