Purine nucleoside phosphorylase mediates midgut physiological functions in Aedes aegypti by orchestrating uric acid biosynthesis and oxidative stress homeostasis.

IF 3 1区 农林科学 Q1 ENTOMOLOGY
Houming Ren, Xiaolin Yang, Huixuan Tang, Xin Wang, Zhuanzhuan Su, Qingshan Ou, Yujiao Han, Yuqi Lou, Symphony Kashyap, Qian Pu, Shiping Liu
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Abstract

Insects excrete nitrogenous waste primarily through the synthesis of uric acid, with purine nucleoside phosphorylase (PNP; AAEL002269) serving as a critical enzyme in this metabolic pathway. Downregulation of PNP has been shown to significantly disrupt blood digestion, ovarian development, and adult longevity in mosquitoes following a blood meal. However, the precise molecular mechanisms underlying these phenotypic consequences remain poorly understood. In this study, we employed clustered regularly interspaced small palindromic repeats (CRISPR) / CRISPR-associated nuclease 9-mediated gene editing to knockout the PNP gene in Aedes aegypti, thereby providing further evidence for the essential biological roles of PNP. Comprehensive transcriptomic and proteomic analyses revealed 5 238 differentially expressed transcripts and 145 differentially expressed proteins in PNP-deficient mosquitoes. These molecular changes were associated with key biological processes, including oxidative stress, energy metabolism, and xenobiotic detoxification. Notably, the downregulation of uric acid synthesis pathway genes, 5'-nucleotidase II (NT2; AAEL024497), and xanthine dehydrogenase 1 (XDH1; AAEL002683), recapitulated the phenotypic defects observed in PNP-deficient mosquitoes. Further mechanistic investigations demonstrated that PNP depletion led to mitochondrial dysfunction in midgut cells, reduced expression of digestive enzymes, impaired uric acid synthesis, elevated ammonia accumulation, and increased reactive oxygen species (ROS) levels. Our results indicate that the disruption of uric acid synthesis was closely linked to ROS overproduction. PNP maintains physiological homeostasis in mosquitoes by coordinately regulating uric acid synthesis and ROS levels. This study not only advances our understanding of antioxidant defense mechanisms and nitrogen metabolism in mosquitoes but also identifies potential molecular targets for the development of novel strategies to control mosquito-borne diseases.

嘌呤核苷磷酸化酶通过协调尿酸生物合成和氧化应激稳态介导埃及伊蚊中肠生理功能。
昆虫排泄含氮废物主要通过合成尿酸,嘌呤核苷磷酸化酶(PNP; AAEL002269)在这一代谢途径中起关键作用。PNP的下调已被证明会显著破坏吸血后蚊子的血液消化、卵巢发育和成年寿命。然而,这些表型结果背后的精确分子机制仍然知之甚少。在本研究中,我们采用集群规则间隔小回文重复序列(CRISPR) / CRISPR相关核酸酶9介导的基因编辑技术敲除埃及伊蚊的PNP基因,从而进一步证明了PNP的重要生物学作用。综合转录组学和蛋白质组学分析显示,pnp缺失的蚊子有5 238个差异表达转录物和145个差异表达蛋白。这些分子变化与关键的生物过程有关,包括氧化应激、能量代谢和外源解毒。值得注意的是,尿酸合成途径基因5′-核苷酸酶II (NT2; AAEL024497)和黄嘌呤脱氢酶1 (XDH1; AAEL002683)的下调重现了pnp缺乏蚊子的表型缺陷。进一步的机制研究表明,PNP消耗导致中肠细胞线粒体功能障碍,消化酶表达降低,尿酸合成受损,氨积累升高,活性氧(ROS)水平升高。我们的研究结果表明,尿酸合成的破坏与活性氧过量生产密切相关。PNP通过协调调节尿酸合成和活性氧水平来维持蚊子的生理稳态。本研究不仅促进了我们对蚊子抗氧化防御机制和氮代谢的理解,而且为开发控制蚊媒疾病的新策略确定了潜在的分子靶点。
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来源期刊
Insect Science
Insect Science 生物-昆虫学
CiteScore
7.80
自引率
5.00%
发文量
1379
审稿时长
6.0 months
期刊介绍: Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.
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