Nanocarrier-mediated RNAi of CYP9E2 and CYB5R enhance susceptibility of invasive tomato pest, Tuta absoluta to cyantraniliprole.

IF 4.1 2区 生物学 Q1 PLANT SCIENCES
Frontiers in Plant Science Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI:10.3389/fpls.2025.1573634
Farman Ullah, Guru-Pirasanna-Pandi G, Hina Gul, Rudra Madhab Panda, Ghulam Murtaza, Zhijun Zhang, Jun Huang, Xiaowei Li, Nicolas Desneux, Yaobin Lu
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引用次数: 0

Abstract

Cyantraniliprole, a second-generation anthranilic diamide, is widely used to manage lepidopteran pests, including the invasive tomato pinworm Tuta absoluta (Meyrick). However, cyantraniliprole's resistance mechanisms and associated fitness costs in T. absoluta remain underexplored. Here, we investigated the fitness costs and resistance mechanisms of cyantraniliprole-resistant strain (CyanRS) via nanocarrier-mediated RNA interference (RNAi). Results showed that the egg incubation period and developmental durations of larval and pupal stages were significantly prolonged in the CyanRS population of T. absoluta compared to the susceptible strain (SS). Further, the adult emergence, longevities of male and female, fecundity, and hatching rate were significantly reduced in CyanRS individuals. The mRNA expression levels of cytochrome b5 reductase (CYB5R) and cytochrome P450 (CYP9E2) were analyzed using RT-qPCR to explore their potential involvement in cyantraniliprole resistance in T. absoluta. Phylogenetic and motif analysis of CYB5R and CYP9E2 indicated their evolutionary and functional conservation with other insect species, especially Lepidopterans. Notably, nanocarrier-encapsulated dsRNA targeting CYB5R and CYP9E2 genes significantly reduced their expression levels. Further, the activity of cytochrome P450 was substantially decreased after the knockdown of the CYB5R and CYP92 genes. This increased susceptibility of the resistant population of T. absoluta to cyantraniliprole, leading to a higher mortality rate than the controls. These findings show that CYB5R and CYP9E2 might play a key role in cyantraniliprole resistance evolution in T. absoluta. The current study provides in-depth insights to understand the underlying mechanisms of cyantraniliprole resistance in this key invasive herbivore.

纳米载体介导的CYP9E2和CYB5R的RNAi增强了入侵番茄害虫绝对土塔对氰虫虫的敏感性。
Cyantraniliprole是一种第二代邻氨基二胺,被广泛用于防治鳞翅目害虫,包括入侵性番茄蛲虫(Tuta absoluta) (Meyrick)。然而,对氰氨虫的抗性机制和相关的适应成本仍未深入研究。本研究通过纳米载体介导的RNA干扰(RNAi)技术研究了氰氨酰胺抗性菌株(cyantranilprole resistant strain, CyanRS)的适应度成本和抗性机制。结果表明,与敏感品系(SS)相比,赤眼蜂的卵潜伏期、幼虫期和蛹期发育时间显著延长。此外,青虫个体的成虫羽化、雌雄寿命、繁殖力和孵化率均显著降低。采用RT-qPCR方法分析细胞色素b5还原酶(CYB5R)和细胞色素P450 (CYP9E2) mRNA表达水平,探讨其在绝对白蝇对氰氨酰胺耐药中的作用。系统发育和基序分析表明,cypb5r和CYP9E2在进化和功能上与其他昆虫物种,特别是鳞翅目昆虫保持一致。值得注意的是,靶向CYB5R和CYP9E2基因的纳米载体封装dsRNA显著降低了它们的表达水平。此外,CYB5R和CYP92基因敲除后,细胞色素P450的活性显著降低。这增加了抗药性种群对氰胺虫胺的易感性,导致死亡率高于对照。这些结果表明,CYB5R和CYP9E2可能在赤潮田鼠对氰氨酰胺的抗性进化中起关键作用。目前的研究为深入了解这种关键入侵食草动物对氰氨酰胺抗性的潜在机制提供了深入的见解。
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来源期刊
Frontiers in Plant Science
Frontiers in Plant Science PLANT SCIENCES-
CiteScore
7.30
自引率
14.30%
发文量
4844
审稿时长
14 weeks
期刊介绍: In an ever changing world, plant science is of the utmost importance for securing the future well-being of humankind. Plants provide oxygen, food, feed, fibers, and building materials. In addition, they are a diverse source of industrial and pharmaceutical chemicals. Plants are centrally important to the health of ecosystems, and their understanding is critical for learning how to manage and maintain a sustainable biosphere. Plant science is extremely interdisciplinary, reaching from agricultural science to paleobotany, and molecular physiology to ecology. It uses the latest developments in computer science, optics, molecular biology and genomics to address challenges in model systems, agricultural crops, and ecosystems. Plant science research inquires into the form, function, development, diversity, reproduction, evolution and uses of both higher and lower plants and their interactions with other organisms throughout the biosphere. Frontiers in Plant Science welcomes outstanding contributions in any field of plant science from basic to applied research, from organismal to molecular studies, from single plant analysis to studies of populations and whole ecosystems, and from molecular to biophysical to computational approaches. Frontiers in Plant Science publishes articles on the most outstanding discoveries across a wide research spectrum of Plant Science. The mission of Frontiers in Plant Science is to bring all relevant Plant Science areas together on a single platform.
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