首页> 外文期刊>Journal of Phytopathology >Quantitative RT-PCR Expression Analysis of Lipodepsipeptides Synthetase and Defence-related Genes in Orange Fruit in Response to Antagonist-pathogen Interaction
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Quantitative RT-PCR Expression Analysis of Lipodepsipeptides Synthetase and Defence-related Genes in Orange Fruit in Response to Antagonist-pathogen Interaction

机译:拮抗物-病原体相互作用对橙皮果脂肽肽合成酶及防御相关基因的定量RT-PCR表达分析

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Strains of Pseudomonas syringae are effective in controlling postharvest diseases of citrus fruits, and antagonistic activity has been correlated with in vitro production of lipodepsipeptides. Additionally, biocontrol agents can induce a range of defence mechanisms of resistance in citrus tissue that result in a broad spectrum of metabolic modifications, such as systemic acquired resistance, induced systemic resistance and production of reactive oxygen species. The aim of this study was to evaluate the expression of syringomycin (syrB1) and syringopeptin (sypA) synthetase genes from P. syringae pv. syringae biocontrol strains in vitro on different culture media and in vivo on citrus fruits (Citrus sinensis cv. Tarocco) during the interaction with Penicillium digitatum by quantitative RT-PCR. Similarly, gene transcript levels of chitinase (CHI1), allene oxide synthase (AOS), glutathione peroxidase (GPX1) and phenylalanine ammonia-lyase (PAL1) were measured. SyrB1 and sypA genes were more actively expressed when antagonistic Pseudomonas strains were grown on orange peel broth as compared to NB and PDB. Penicillium digitatum resulted to be strongly stimulatory only to syrB1 expression, thus suggesting that syrB1 gene could be involved in biocontrol activity. QRT-PCR showed that both P. s. pv. syringae and P. digitatum strains increase CHI1 transcription in inoculated flavedo tissues relative to the untreated control. Interestingly, CHI1 transcription was markedly induced by co-inoculation of P. s. pv syringae and P. digitatum strains. Pseudomonas syringae pv. syringae, alone or co-inoculated with P. digitatum, was weakly effective in enhancing GPX1, AOS and PAL1 gene expression, whereas P. digitatum alone strongly enhanced GPX1, AOS and PAL1 expression. Moreover, we assume that CHI1 gene is most likely part of the molecular mechanisms involved in pathogen defence responses in citrus fruit. This is the first example of monitoring the expression of syrB1-sypA and CHI1, GPX1, AOS and PAL1 genes in interactions between P. s. pv. syringae biocontrol agents and P. digitatum in vitro and in vivo.
机译:丁香假单胞菌菌株可有效控制柑橘类水果的采后病,并且拮抗活性与脂肽肽的体外产生有关。另外,生物防治剂可以诱导柑桔组织中一系列抵抗力的防御机制,从而导致广泛的代谢修饰,例如系统性获得性抵抗力,诱导的系统性抵抗力和活性氧的产生。这项研究的目的是评估丁香假单胞菌PV中丁香霉素(syrB1)和丁香肽素(sypA)合成酶基因的表达。定量RT-PCR与丁香青霉相互作用期间,在不同培养基上体外和在柑橘类水果(Citrus sinensis cv。Tarocco)上对丁香紫丁香生物防治菌株进行体内研究。同样,测量了几丁质酶(CHI1),丙二烯氧化合酶(AOS),谷胱甘肽过氧化物酶(GPX1)和苯丙氨酸氨裂合酶(PAL1)的基因转录水平。与NB和PDB相比,当在桔皮肉汤上培养拮抗假单胞菌菌株时,SyrB1和sypA基因更活跃地表达。指状青霉菌仅对syrB1表达具有强烈的刺激作用,因此表明syrB1基因可能参与生物防治活动。 QRT-PCR显示两个P。 pv。丁香和丁香假单胞菌菌株相对于未处理的对照,增加了接种的黄褐色组织中的CHI1转录。有趣的是,CHI1的转录明显地被P. s的共同接种所诱导。 pv丁香和数指假单胞菌菌株。丁香假单胞菌PV。丁香假单胞菌单独或与洋地黄假单胞菌共接种,在增强GPX1,AOS和PAL1基因表达方面效果不佳,而单独地洋地黄假单胞菌则强烈增强GPX1,AOS和PAL1表达。此外,我们认为CHI1基因最有可能是参与柑橘类水果病原体防御反应的分子机制的一部分。这是监测P.s之间相互作用中syrB1-sypA和CHI1,GPX1,AOS和PAL1基因表达的第一个例子。 pv。丁香生物防治剂和洋地黄假单胞菌。

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