Yan-qi Yang, Yu-jian Liang, Jun-rui Zhi, Ding-yin Li, Cao Li
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Compared with the control, <i>S. frugiperda</i> exhibited varying degrees of mortality after treatment with four concentrations of validamycin, showing a dose-dependent increase in mortality rate. The mortality rates 24 and 48 h after treatment with 0.07 mg μL<sup>−1</sup> validamycin were 35.6% and 42.2%, respectively, indicating the effective lethal concentration. Treatment with 0.07 mg μL<sup>−1</sup> validamycin led to developmental delay, abnormal molting, and death in <i>S. frugiperda</i>, but it exerted no lasting effects on the survival rate, pupal weight, and phenotype during its subsequent developmental stages. At 24 h after validamycin treatment, TRE1 and TRE2 activities and glucose content decreased significantly, whereas the trehalose content increased significantly. Treatment with validamycin significantly upregulated <i>TRE1</i> and <i>TRE2</i> expression after 24 and 48 h and downregulated the mRNA expression of chitin synthase A and B genes. However, after 72 h, chitin content was not significantly affected. Hence, validamycin can destroy the dynamic transformation balance of trehalose and glucose by inhibiting the activities of the two TREs, and further affect the expression of downstream chitin synthase genes. 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引用次数: 0
摘要
海藻糖酶(Trehalase)是降解海藻糖的关键酶,海藻糖在昆虫的生长发育中起着至关重要的作用。虽然validamycin是一类有效的抗生素和杀菌剂,它可以通过抑制TRE活性来控制害虫,但它是否同时作用于玉米(Zea mays L., Poaceae)的主要害虫——夜蛾(Spodoptera frugiperda, J. E. Smith)的海藻糖和几丁质代谢尚不清楚。本研究探讨了缬霉素处理后藻糖代谢的变化及其对下游几丁质合成途径的影响。与对照相比,4种浓度的缬霉素处理后,frugiperda的死亡率呈现不同程度的升高,且呈剂量依赖性。0.07 mg μL−1缬霉素处理后24 h和48 h的死亡率分别为35.6%和42.2%,为有效致死浓度。0.07 mg μL−1 validamycin处理会导致果蝇发育迟缓、蜕皮异常和死亡,但对其后续发育阶段的存活率、蛹重和表型没有持久影响。在处理24 h后,TRE1、TRE2活性和葡萄糖含量显著降低,海藻糖含量显著升高。治疗24和48 h后,缬霉素显著上调TRE1和TRE2的表达,下调几丁质合成酶A和B基因的mRNA表达。72h后,几丁质含量无明显变化。因此,缬霉素可以通过抑制两种TREs的活性,破坏海藻糖和葡萄糖的动态转化平衡,进而影响下游几丁质合成酶基因的表达。这些发现为利用TRE抑制剂防治frugiperda提供了理论依据。
Regulation of trehalose metabolism mediated by validamycin on chitin synthesis in Spodoptera frugiperda
Trehalase (TRE) is a key enzyme for degrading trehalose, which plays a vital role in the growth and development of insects. Although validamycin, a compound belonging to a class of efficient antibiotics and fungicides, can control pests by suppressing TRE activities, it remains unknown whether it acts on both trehalose and chitin metabolism in Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae), a major pest of maize (Zea mays L., Poaceae). This study investigated the changes in trehalose metabolism after validamycin treatment in S. frugiperda and its effects on the downstream chitin synthesis pathway. Compared with the control, S. frugiperda exhibited varying degrees of mortality after treatment with four concentrations of validamycin, showing a dose-dependent increase in mortality rate. The mortality rates 24 and 48 h after treatment with 0.07 mg μL−1 validamycin were 35.6% and 42.2%, respectively, indicating the effective lethal concentration. Treatment with 0.07 mg μL−1 validamycin led to developmental delay, abnormal molting, and death in S. frugiperda, but it exerted no lasting effects on the survival rate, pupal weight, and phenotype during its subsequent developmental stages. At 24 h after validamycin treatment, TRE1 and TRE2 activities and glucose content decreased significantly, whereas the trehalose content increased significantly. Treatment with validamycin significantly upregulated TRE1 and TRE2 expression after 24 and 48 h and downregulated the mRNA expression of chitin synthase A and B genes. However, after 72 h, chitin content was not significantly affected. Hence, validamycin can destroy the dynamic transformation balance of trehalose and glucose by inhibiting the activities of the two TREs, and further affect the expression of downstream chitin synthase genes. These findings provide a theoretical basis for using TRE inhibitors to control S. frugiperda.
期刊介绍:
Entomologia Experimentalis et Applicata publishes top quality original research papers in the fields of experimental biology and ecology of insects and other terrestrial arthropods, with both pure and applied scopes. Mini-reviews, technical notes and media reviews are also published. Although the scope of the journal covers the entire scientific field of entomology, it has established itself as the preferred medium for the communication of results in the areas of the physiological, ecological, and morphological inter-relations between phytophagous arthropods and their food plants, their parasitoids, predators, and pathogens. Examples of specific areas that are covered frequently are:
host-plant selection mechanisms
chemical and sensory ecology and infochemicals
parasitoid-host interactions
behavioural ecology
biosystematics
(co-)evolution
migration and dispersal
population modelling
sampling strategies
developmental and behavioural responses to photoperiod and temperature
nutrition
natural and transgenic plant resistance.