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厚垣轮枝菌 Tr-92 在产厚垣孢子条件下的全转录组测序和基因表达分析。

Whole RNA-sequencing and gene expression analysis of Trichoderma harzianum Tr-92 under chlamydospore-producing condition.

机构信息

College of Life Sciences, North China University of Science and Technology, Tangshan, 063210, People's Republic of China.

Biology Institute, Hebei Academy of Sciences, Shijiazhuang, 050081, People's Republic of China.

出版信息

Genes Genomics. 2019 Jun;41(6):689-699. doi: 10.1007/s13258-019-00812-y. Epub 2019 Apr 9.

Abstract

BACKGROUND

Trichoderma is one of the most important biocontrol fungi, which could produce mycelia, conidiospores, and chlamydospores three types of propagules under different conditions. Chlamydospores are produced in harsh conditions in various fungi, and may be more resistant to adverse conditions. However, the knowledge associated with the mechanism of chlamydospore formation remained unclear in Trichoderma.

OBJECTIVES

This study is aimed to explore the essential genes and regulatory pathways associated with chlamydospore formation in Trichoderma.

METHODS

The culture condition, survival rate, and biocontrol effects of chlamydospores and conidiospores from Trichoderma.harzianum Tr-92 were determined. Furthermore, the whole transcriptome profiles of T. harzianum Tr-92 under chlamydospore-producing and chlamydospore-nonproducing conditions were performed.

RESULTS

T. harzianum Tr-92 produced chlamydospores under particular conditions, and chlamydospore-based formulation of T. harzianum Tr-92 exhibited higher biocontrol ability against Botrytis cinerea in cucumber than conidoiospore-based formulation. In the transcriptome analysis, a total of 2,029 differentially expressed genes (DEGs) were identified in T. harzianum Tr-92 under chlamydospore-producing condition, compared to that under chlamydospore-nonproducing condition. GO classification indicated that the DEGs were significantly enriched in 284 terms among biological process, cellular components and molecular function categories. A total of 19 pathways were observed with DEGs by KEGG analysis. Furthermore, fifteen DEGs were verified by quantitative real-time PCR, and the expression profiles were consistent with the transcriptome data.

CONCLUSION

The results would provide a basis on the molecular mechanisms underlying Trichoderma sporulation, which would assist the development and application of fungal biocontrol agents.

摘要

背景

木霉是最重要的生防真菌之一,可在不同条件下产生菌丝体、分生孢子和厚垣孢子三种类型的繁殖体。厚垣孢子是各种真菌在恶劣条件下产生的,可能对不利条件更具抗性。然而,木霉中厚垣孢子形成的机制相关知识仍不清楚。

目的

本研究旨在探讨与木霉厚垣孢子形成相关的必需基因和调控途径。

方法

测定了木霉 Tr-92 的厚垣孢子和分生孢子的培养条件、存活率和生防效果。此外,还对木霉 Tr-92 在产生厚垣孢子和不产生厚垣孢子条件下的全转录组谱进行了分析。

结果

木霉 Tr-92 在特定条件下产生厚垣孢子,基于厚垣孢子的木霉 Tr-92 制剂对黄瓜灰霉病的生防能力高于基于分生孢子的制剂。在转录组分析中,与不产生厚垣孢子条件相比,木霉 Tr-92 在产生厚垣孢子条件下共鉴定出 2029 个差异表达基因(DEGs)。GO 分类表明,在生物过程、细胞成分和分子功能类别中,DEGs 显著富集在 284 个术语中。KEGG 分析共观察到 19 条与 DEGs 相关的通路。此外,通过定量实时 PCR 验证了 15 个 DEGs,其表达谱与转录组数据一致。

结论

这些结果为木霉孢子形成的分子机制提供了基础,有助于真菌生防剂的开发和应用。

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