College of Horticulture and Plant Protection, Henan University of Science and Technology, Luoyang 471023, PR China.
College of Horticulture and Plant Protection, Henan University of Science and Technology, Luoyang 471023, PR China.
J Hazard Mater. 2024 Jun 5;471:134299. doi: 10.1016/j.jhazmat.2024.134299. Epub 2024 Apr 12.
Trichoderma can enhance the metabolism of organophosphate pesticides in plants, but the mechanism is unclear. Here, we performed high-throughput transcriptome sequencing of roots upon Trichoderma asperellum (TM) inoculation and phoxim (P) application in tomato (Solanum lycopersicum L.). A total of 4059 differentially expressed genes (DEGs) were obtained, including 2110 up-regulated and 1949 down-regulated DEGs in P vs TM+P. COG and KOG analysis indicated that DEGs were mainly enriched in signal transduction mechanisms. We then focused on the pesticide detoxification pathway and screened out cytochrome P450 CYP736A12 as a putative gene for functional analysis. We suppressed the expression of CYP736A12 in tomato plants by virus-induced gene silencing and analyzed tissue-specific phoxim residues, oxidative stress markers, glutathione pool, GST activity and related gene expression. Silencing CYP736A12 significantly increased phoxim residue and induced oxidative stress in tomato plants, by attenuating the TM-induced increased activity of antioxidant and detoxification enzymes, redox homeostasis and transcripts of detoxification genes including CYP724B2, GSH1, GSH2, GR, GPX, GST1, GST2, GST3, and ABC. The study revealed a critical mechanism by which TM promotes the metabolism of phoxim in tomato roots, which can be useful for further understanding the Trichoderma-induced xenobiotic detoxification and improving food safety.
木霉可以增强植物有机磷农药的代谢,但机制尚不清楚。在这里,我们对番茄根进行了高通量转录组测序,研究了木霉(TM)接种和辛硫磷(P)处理后基因的表达变化。共获得 4059 个差异表达基因(DEGs),其中 P 处理与 TM+P 处理相比,有 2110 个上调基因和 1949 个下调基因。COG 和 KOG 分析表明,DEGs 主要富集在信号转导机制。我们进一步关注了农药解毒途径,并筛选出细胞色素 P450 CYP736A12 作为功能分析的候选基因。我们通过病毒诱导的基因沉默抑制番茄中 CYP736A12 的表达,并分析了组织特异性辛硫磷残留、氧化应激标志物、谷胱甘肽池、GST 活性和相关基因表达。沉默 CYP736A12 显著增加了番茄植株中的辛硫磷残留,并诱导了氧化应激,通过减弱 TM 诱导的抗氧化和解毒酶活性的增加、氧化还原平衡以及解毒基因 CYP724B2、GSH1、GSH2、GR、GPX、GST1、GST2、GST3 和 ABC 的转录。该研究揭示了 TM 促进番茄根系中辛硫磷代谢的关键机制,这对于进一步理解木霉诱导的外源解毒和提高食品安全具有重要意义。