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甜菜对致病卵菌甜菜根腐病菌响应的转录组分析

Transcriptome analysis of sugar beet in response to the pathogenic oomycete Aphanomyces cochlioides.

作者信息

Rossi Valentina, Holmquist Louise, Alexandersson Erik, Grenville-Briggs Laura

机构信息

Department of Plant Protection Biology, Swedish University of Agricultural Sciences, P.O. Box 190, Lomma, SE-234 22, Sweden.

DLF Beet Seed, Säbyholmsvägen 24, Landskrona, SE-261 91, Sweden.

出版信息

BMC Plant Biol. 2024 Dec 18;24(1):1177. doi: 10.1186/s12870-024-05910-y.

DOI:10.1186/s12870-024-05910-y
PMID:39690418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11653986/
Abstract

BACKGROUND

Aphanomyces root rot is one of the most severe diseases in sugar beet (Beta vulgaris L.), resulting in drastic losses in sugar yield and plant degeneration. The causal agent is the soil-borne pathogen Aphanomyces cochlioides, a phytopathogenic oomycete able to infect sugar beet roots from the seedling stage until harvest. Reliable control measures and fully resistant varieties to prevent the disease on mature roots are currently not available. Furthermore, the quantitative nature of the resistance mechanisms to the root rot disease remain unclear. With the aim to identify key genes involved in plant defense responses against the root rot, we performed a transcriptome analysis of sugar beet interactions with A. cochlioides. The transcriptome responses of two partially resistant and two susceptible sugar beet breeding lines, inoculated with three A. cochlioides isolates with different geographical origins have been investigated in this study.

RESULTS

The results showed that the transcriptional responses to A. cochlioides infection were mainly genotype-dependent. Comparisons of transcriptome profiles of partially resistant and susceptible breeding lines revealed the presence of differentially expressed genes that play a key role in defense mechanisms during the initial stages of infection. Gene Ontology (GO) categories associated with hydrogen peroxide (HO) metabolism, detoxification and cell wall organization were significantly enriched in the differentially expressed gene set from the two partially resistant lines, while photosynthesis-related GO terms were significantly enriched in the two susceptible lines. Unique and overlapping GO categories were over-represented in specific genotype-isolate-time point interactions, indicating that different genotypes respond with common defense strategies as well as specialized responses to different isolates and time points. Transcription factors belonging to the WRKY and ERF families were up-regulated in all genotypes. Furthermore, increased expression of genes encoding for disease resistant proteins have been identified in the two partially resistant genotypes.

CONCLUSIONS

This research offers new insights into the transcriptomic events that regulate the sugar beet defense responses to A. cochlioides infection. The findings of this study emphasize the importance of genotype-specific interactions in response to different A. cochlioides isolates. Moreover, the results showed the up-regulation of genes that may play important roles in the defense responses to A. cochlioides which can be used to improve future breeding and to assist in the development of resistant cultivars.

摘要

背景

腐皮镰孢根腐病是甜菜(Beta vulgaris L.)最严重的病害之一,会导致糖分产量大幅损失和植株退化。病原菌是土壤传播的病原体腐皮镰孢(Aphanomyces cochlioides),一种植物致病卵菌,能够从幼苗期到收获期感染甜菜根。目前尚无可靠的防治措施和对成熟根具有完全抗性的品种。此外,对根腐病抗性机制的定量性质仍不清楚。为了鉴定参与植物对根腐病防御反应的关键基因,我们对甜菜与腐皮镰孢的相互作用进行了转录组分析。本研究调查了两个部分抗性和两个感病甜菜育种系接种三种不同地理来源的腐皮镰孢分离株后的转录组反应。

结果

结果表明,对腐皮镰孢感染的转录反应主要取决于基因型。部分抗性和感病育种系转录组图谱的比较揭示了在感染初始阶段防御机制中起关键作用的差异表达基因的存在。与过氧化氢(HO)代谢、解毒和细胞壁组织相关的基因本体(GO)类别在两个部分抗性系的差异表达基因集中显著富集,而与光合作用相关的GO术语在两个感病系中显著富集。独特和重叠的GO类别在特定的基因型-分离株-时间点相互作用中过度代表,表明不同基因型以共同的防御策略以及对不同分离株和时间点的特异性反应做出响应。属于WRKY和ERF家族的转录因子在所有基因型中均上调。此外,在两个部分抗性基因型中鉴定出编码抗病蛋白的基因表达增加。

结论

本研究为调控甜菜对腐皮镰孢感染防御反应的转录组事件提供了新的见解。本研究结果强调了基因型特异性相互作用在应对不同腐皮镰孢分离株中的重要性。此外,结果显示了可能在对腐皮镰孢防御反应中起重要作用的基因上调,这可用于改进未来的育种并协助开发抗性品种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/11653986/20744ca1c329/12870_2024_5910_Fig9_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/11653986/f4c4f445188e/12870_2024_5910_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/11653986/a83380d6c139/12870_2024_5910_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad97/11653986/d09c388c31c6/12870_2024_5910_Fig8_HTML.jpg
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