食品科学 ›› 2025, Vol. 46 ›› Issue (19): 107-115.doi: 10.7506/spkx1002-6630-20250408-056

• 生物工程 • 上一篇    

扩展青霉Rho4基因缺失关联苹果果实病健交界处苯丙烷代谢的激活

范高丽,张学梅,王雪雪,朱丹丹,项芯悦,宗元元,Dov PRUSKY,毕阳   

  1. (1.甘肃农业大学食品科学与工程学院,甘肃 兰州 730070;2.农业研究组织新鲜农产品采后科学部,以色列 里雄莱锡安 7505101)
  • 发布日期:2025-09-16
  • 基金资助:
    国家自然科学基金国际(地区)合作与交流项目(31861143046)

Association of Rho4 Gene Deletion in Penicillium expansum with Activation of Phenylpropanoid Metabolism at the Disease-Health Interface of Apple Fruits

FAN Gaoli, ZHANG Xuemei, WANG Xuexue, ZHU Dandan, XIANG Xinyue, ZONG Yuanyuan, Dov PRUSKY, BI Yang   

  1. (1. College of Food Science and Engineering, Gansu Agricultural University, Lanzhou 730070, China; 2. Department of Postharvest Science of Fresh Produce, Agricultural Research Organization, Rishon LeZion 7505101, Israel)
  • Published:2025-09-16

摘要: 为研究小G蛋白(小GTPases)Rho4在果实-病原互作中对宿主抗性的影响,以苹果果实为材料,分别接种扩展青霉(Penicillium expansum)野生型菌株(WT)、Rho4缺失突变株(ΔPeRho4)和回补菌株(ΔPeRho4-C),评估发病情况,并对病健交界处组织进行转录组分析,筛选差异表达基因(differentially expressed genes,DEGs)。同时,测定苯丙烷代谢关键酶的表达与活性,以及相关代谢产物的变化。结果表明,ΔPeRho4接种果实的病斑直径显著低于野生型,而ΔPeRho4-C接种后果实病斑直径恢复至WT水平。转录组分析共筛选出216 个DEGs,其中4 个参与苯丙烷代谢的基因上调表达。进一步分析显示,ΔPeRho4接种显著提高了苯丙氨酸解氨酶、肉桂酸-4-羟化酶、4-香豆酰辅酶A连接酶和肉桂醇脱氢酶的基因表达量和活性,促进了酚酸类物质、木质素单体、总酚、类黄酮和木质素的积累。综上所述,Rho4基因缺失削弱了P. expansum的致病性,可能间接诱导果实病健交界处苯丙烷代谢的激活,增强了果实的防御反应。该研究为真菌小GTPases调控宿主抗病机制提供了新见解,并为采后果实病害防控提供了潜在策略。

关键词: 扩展青霉;小G蛋白;Rho4缺失;苹果果实;苯丙烷代谢;诱导抗性

Abstract: To investigate the role of Rho4, a small GTPase, in host resistance during fruit-pathogen interactions, we inoculated apple fruits separately with a wild-type (WT) strain, a Rho4-deleted mutant (ΔPeRho4) and a complemented strain (ΔPeRho4-C) of Penicillium expansum. The lesion size was assessed, and transcriptomic analysis of tissues at the disease-health interface was performed to identify differentially expressed genes (DEGs). The expression and activity of key enzymes involved in phenylpropanoid metabolism were measured and changes in related metabolites were examined. Our results showed that fruits inoculated with ΔPeRho4 exhibited significantly smaller lesions compared with those inoculated with the WT strain, and the lesion size of ΔPeRho4-C was similar to the WT level. Transcriptomic profiling identified 216 DEGs, among which four were associated with the phenylpropanoid pathway and up-regulated in ΔPeRho4 inoculated tissues. Moreover, ΔPeRho4 inoculation significantly increased the expression and activities of phenylalanine ammonia lyase (PAL), cinnamate-4-hydroxylase (C4H), 4-coumaroyl-coenzyme A ligase (4CL), and cinnamyl alcohol dehydrogenase (CAD). It also promoted the accumulation of phenolic acids, lignin monomers, total phenolics, flavonoids, and lignin. These results suggest that the deletion of Rho4 attenuated the pathogenicity of P. expansum, which may indirectly trigger the activation of phenylpropanoid metabolism at the disease-health interface and enhance defense responses in apple fruits. This study provides new insights into the molecular mechanisms by which fungal small GTPases influence host resistance and offers potential strategies for postharvest disease control.

Key words: Penicillium expansum; small GTPase; Rho4 deletion; apple fruit; phenylpropanoid metabolism; induced resistance

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