生物技术通报 ›› 2025, Vol. 41 ›› Issue (8): 175-185.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0377

• 研究报告 • 上一篇    

哈茨木霉T9131对黄芪幼苗的促生机理

白雨果1(), 李婉迪1, 梁建萍1,2, 石志勇1,2, 卢庚龙1, 刘红军1, 牛景萍1,2()   

  1. 1.山西农业大学生命科学学院,太谷 030801
    2.中兽医药现代化山西省重点实验室,太谷 030801
  • 收稿日期:2025-04-11 出版日期:2025-08-26 发布日期:2025-08-14
  • 通讯作者: 牛景萍,女,博士,讲师,研究方向 :黄芪抗病和促生机理;E-mail: niujingping@sxau.edu.cn
  • 作者简介:白雨果,男,硕士研究生,研究方向 :黄芪生态种植;E-mail: 15837071231@163.com
  • 基金资助:
    山西省现代农业中药材产业技术体系专项(2025ZYC09);山西省科技重大专项计划“揭榜挂帅”项目(202405018);山西省科技成果转化引导专项(202304021301059);2025年度山西农业大学特优农业高质量发展科技支撑工程项目(TYGC25-79);2025年度山西农业大学特优农业高质量发展科技支撑工程项目(TYGC25-80)

Growth-promoting Mechanism of Trichoderma harzianum T9131 on Astragalus membranaceus Seedlings

BAI Yu-guo1(), LI Wan-di1, LIANG Jian-ping1,2, SHI Zhi-yong1,2, LU Geng-long1, LIU Hong-jun1, NIU Jing-ping1,2()   

  1. 1.College of Life Sciences, Shanxi Agricultural University, Taigu 030801
    2.Shanxi Key Laboratory of Chinese Veterinary Medicine Modernization, Taigu 030801
  • Received:2025-04-11 Published:2025-08-26 Online:2025-08-14

摘要:

目的 探究哈茨木霉T9131对黄芪幼苗促生的调控机制,为T9131提高黄芪产量提供理论依据。 方法 对生长30 d的黄芪幼苗进行哈茨木霉T9131孢子悬浮液灌根处理,分别在灌根后的0 h、24 h、48 h和45 d对黄芪幼苗根部进行取样,并在45 d测定黄芪幼苗的株高、根长和植株鲜重。通过RNA-Seq构建3个时间点0、24和48 h的转录组文库,利用DESeq2软件获得3个比较组(T_24 h vs T_0 h、T_48 h vs T_0 h、T_48 h vs T_24 h)中的差异表达基因(DEGs),对3组DEGs进行韦恩分析,明确3组共有DEGs;对共有DEGs进行KEGG富集分析筛选促生相关基因,并通过RT-qPCR分析T9131诱导45 d和外源激素ABA诱导初期黄芪幼苗促生相关基因的表达情况;对0 h、48 h和45 d的根部样品通过LC-MS/MS方法进行15种激素含量测定。 结果 T9131能显著促进黄芪幼苗的株高和鲜重。T9131诱导黄芪幼苗转录组分析表明,3个比较组中共有差异表达基因149个。KEGG富集通路分析表明,与促生相关的通路主要有萜类骨架生物合成、类胡萝卜素生物合成、二萜生物合成、氰基氨基酸代谢、玉米素生物合成和植物激素信号转导;通路中富集的基因类型有HMGRCYP707A2GA2ox2E3.2.1.21UGT73C6PYL4GH3.1JAZ,共包括14个基因,除基因UGT73C6(DN24891_c1_g1)受T9131诱导下调表达外,其余基因均上调表达;在T9131诱导黄芪幼苗45 d时HMGR(DN10463_c0_g2、DN989_c0_g1、DN113450_c0_g1、DN989_c2_g1)、CYP707A2JAZ等7个基因显著上调表达,其余基因均下调表达。14个基因受ABA诱导表达分析表明,HMGR(DN10463_c0_g2、DN989_c0_g1、DN113450_c0_g1、DN989_c2_g1)、CYP707A2(DN397_c0_g2)和E3.2.1.21(DN2073_c0_g1)等6个基因受ABA诱导表达显著下调,其余基因均上调表达。激素测定表明,T9131能显著降低ABA含量。 结论 哈茨木霉T9131可能通过调控黄芪促生相关基因HMGRCYP707A2JAZ的上调表达和降低ABA含量促进黄芪生长;外源ABA能降低HMGRCYP707A2的表达。

关键词: 哈茨木霉, 黄芪, 生长指标, 促生调控, 转录组, 液相色谱?串联质谱法, 激素含量, 表达分析

Abstract:

Objective To explore the regulatory mechanism of Trichoderma harzianum T9131 on the growth promotion of Astragalus membranaceus seedlings and provide a theoretical basis for T9131 to increase the yield of A. membranaceus. Method The A. membranaceus seedlings grown for 30 d were treated by root irrigation with T. harzianum T9131 spores suspension. Samples were taken from the roots of the A. membranaceus seedlings at 0, 24 h, 48 h and 45 d after root irrigation, and the plant height, root length and fresh weight of the A. membranaceus seedlings at 45 d were determined. Transcriptome libraries were constructed at three time points of 0, 24 and 48 h by RNA-Seq. Differentially expressed genes (DEGs) in the three comparison groups (T_24 h vs T_0 h, T_48 h vs T_0 h, and T_48 h vs T_24 h) were obtained by using DESeq2 software. Venn analysis was conducted on the three groups of DEGs to clarify that the three groups had a total of DEGs. KEGG enrichment analysis was performed on the common DEGs to screen the growth-promoting related genes, and the expression of growth-promoting-related genes in A. membranaceus seedlings in the early stage after 45 d of induction with T9131 and induction with exogenous hormone ABA was analyzed by RT-qPCR. The contents of 15 hormones in the root samples at 0 h, 48 h and 45 d were determined by the LC-MS/MS method. Result T9131 could significantly promote the plant height and fresh weight of A. membranaceus seedlings.Transcriptome analysis of A. membranaceus seedlings induced by T9131 indicated that there were 149 differentially expressed genes in the three comparison groups. KEGG enrichment pathway analysis showed that the pathways related to growth promotion mainly included terpenoid backbone biosynthesis, carotenoid biosynthesis, diterpenoid biosynthesis, cyanoamino acid metabolism, zeatin biosynthesis, and plant hormone signal transduction. The gene types enriched in the pathway include HMGR, CYP707A2, GA2ox2, E3.2.1.21, UGT73C6, PYL4, GH3.1, and JAZ, totaling 14 genes. Except for the gene UGT73C6 (DN24891_c1_g1) down-regulated by T9131 induction, the remaining genes were all up-regulated in expression. Fourteen genes induced A. membranaceus seedlings in T9131 at 45 d, seven genes including HMGR (DN10463_c0_g2, DN989_c0_g1, DN113450_c0_g1, DN989_c2_g1), CYP707A2 and JAZ were significantly up-regulated, while the remaining genes were down-regulated. Analysis of the expressions of the 14 genes induced by ABA showed that the expressions of 6 genes, including HMGR (DN10463_c0_g2, DN989_c0_g1, DN113450_c0_g1, DN989_c2_g1), CYP707A2 (DN397_c0_g2), and E3.2.1.21 (DN2073_c0_g1), were significantly down-regulated by ABA induction, while the expressions of the remaining genes were up-regulated. Hormone determination indicated that T9131 significantly reduced the content of ABA. Conclusion T. harzianum T9131 may promote the growth of A. membranaceus by regulating the up-regulated expressions of genes related to the growth promotion of A. membranaceus, such as HMGR, CYP707A2 and JAZ, and by reducing the content of ABA. Exogenous ABA can reduce the expressions of HMGR and CYP707A2.

Key words: Trichoderma harzianum, Astragalus membranaceus, growth index, growth-promoting regulation, transcriptome, LC-MS/MS, hormone content, expression analysis