Water Transport and Enzyme Recycling in Tenebrio molitor Midgut: Insights From Transcriptomics, Proteomics, and In Vivo Inhibition Assays

IF 1.9 4区 农林科学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of Insect Biochemistry and Physiology Pub Date : 2025-04-08 DOI:10.1002/arch.70059
Ignacio G. Barroso, Clelia Ferreira, Walter R. Terra
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Abstract

The low excretory rates of secreted digestive enzymes, such as trypsins, in insect species with peritrophic membranes led to the hypothesis of ectoperitrophic countercurrent water fluxes causing enzyme recycling. The midgut water flux model of Tenebrio molitor (T. molitor) is revisited and supported by in vivo experiments. Sequences from proteins putatively involved in water transport were retrieved from the T. molitor transcriptome by Blast and analyzed using bioinformatics tools. Gene expression of selected proteins was determined in three midgut sections (anterior, AM; middle, MM; posterior, PM) by RNA-seq, and transporter proteins were verified in microvillar-membrane-enriched midgut samples by proteomics. Genes encoding three cation chloride cotransporters (CCC) and four aquaporins were expressed in the midgut. TmNaCCC2, TmPrip, and TmEglp1 showed higher expression in the front half, while TmKCC, TmNKCC1, TmDrip, and TmEglp2 were more highly expressed in the back half. However, only TmNaCCC2 was found by proteomics. Midgut water fluxes were quantified by feeding T. molitor larvae with nonabsorbable dye and measuring its concentration along the midgut. The results suggest water absorption in AM and secretion in MM and PM, potentially caused by TmNaCCC2 and TmPrip in AM, and TmKCC and TmDrip in PM, whereas MM serves as a transition region. Larvae fed on furosemide, an NKCC and KCC inhibitor, showed altered midgut water fluxes, resulting in higher trypsin excretion into the hindgut, thus reinforcing the hypothesis of a countercurrent water flux generated by CCCs powering enzyme recycling in insect midguts.

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黄粉虫中肠的水运输和酶循环:来自转录组学、蛋白质组学和体内抑制分析的见解
在具有周营养膜的昆虫物种中,分泌的消化酶(如胰蛋白酶)的排泄率较低,这导致了非周营养逆流水通量导致酶循环的假设。本文对黄粉虫(tenbrio molitor, T. molitor)中肠水通量模型进行了重新研究,并得到了体内实验的支持。利用Blast从T. molitor转录组中检索了推测与水转运有关的蛋白质序列,并使用生物信息学工具进行了分析。选定蛋白的基因表达在三个中肠切片(前,AM;中间,MM;在富含微绒毛膜的中肠样品中,通过蛋白质组学验证了转运蛋白。编码3种阳离子氯共转运体(CCC)和4种水通道蛋白的基因在中肠中表达。TmNaCCC2、TmPrip、TmEglp1在前半程表达较高,TmKCC、TmNKCC1、TmDrip、TmEglp2在后半程表达较高。然而,通过蛋白质组学只发现了TmNaCCC2。用不可吸收染料饲喂黑斑田鼠幼虫,测定其沿中肠的浓度,定量测定中肠水分通量。结果表明AM的吸水和MM和PM的分泌可能是由AM中的TmNaCCC2和TmPrip以及PM中的TmKCC和TmDrip引起的,而MM则是一个过渡区。喂食NKCC和KCC抑制剂速尿(furosemide)的幼虫显示出中肠水通量的改变,导致胰蛋白酶排泄到后肠的量增加,从而加强了CCCs驱动昆虫中肠酶循环产生逆流水通量的假设。
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来源期刊
CiteScore
4.30
自引率
4.50%
发文量
115
审稿时长
12 months
期刊介绍: Archives of Insect Biochemistry and Physiology is an international journal that publishes articles in English that are of interest to insect biochemists and physiologists. Generally these articles will be in, or related to, one of the following subject areas: Behavior, Bioinformatics, Carbohydrates, Cell Line Development, Cell Signalling, Development, Drug Discovery, Endocrinology, Enzymes, Lipids, Molecular Biology, Neurobiology, Nucleic Acids, Nutrition, Peptides, Pharmacology, Pollinators, Proteins, Toxicology. Archives will publish only original articles. Articles that are confirmatory in nature or deal with analytical methods previously described will not be accepted.
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