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海藻糖支持细胞生长,并改变基因表达和登革病毒复制。

Trehalose supports the growth of cells and modifies gene expression and dengue virus replication.

作者信息

Marten Andrew D, Haslitt Douglas P, Martin Chad A, Swanson Daniel H, Kalera Karishma, Johnson Ulysses G, Swarts Benjamin M, Conway Michael J

机构信息

Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48859, USA.

Department of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, USA.

出版信息

bioRxiv. 2024 Dec 4:2024.12.03.626538. doi: 10.1101/2024.12.03.626538.

DOI:10.1101/2024.12.03.626538
PMID:39677712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11643125/
Abstract

Trehalose is a non-reducing disaccharide that is the major sugar found in insect hemolymph fluid. Trehalose provides energy, and promotes growth, metamorphosis, stress recovery, chitin synthesis, and insect flight. Trehalase is the only enzyme responsible for the hydrolysis of trehalose, which makes it an attractive molecular target. Here we show that Aedes aegypti (Aag2) cells express trehalase and that they can grow on trehalose-containing cell culture media. Trehalase activity was confirmed by treating Aag2 cells with trehalase inhibitors, which inhibited conversion of trehalose to glucose and reduced cell proliferation. Cell entry of a fluorescent trehalose probe was dependent on trehalose concentration, suggesting that trehalose moves across the cell membrane via passive transport. Culturing Aag2 cells with trehalose-containing cell culture media led to significant changes in gene expression, intracellular lipids, and dengue virus replication and specific infectivity, and increased their susceptibility to trehalase inhibitors. These data describe an in vitro model that can be used to rapidly screen novel trehalase inhibitors and probes and underscores the importance of trehalose metabolism in Ae. aegypti physiology and transmission of a mosquito-borne virus.

摘要

海藻糖是一种非还原性二糖,是昆虫血淋巴液中发现的主要糖类。海藻糖提供能量,并促进生长、变态、应激恢复、几丁质合成和昆虫飞行。海藻糖酶是唯一负责水解海藻糖的酶,这使其成为一个有吸引力的分子靶点。在这里,我们表明埃及伊蚊(Aag2)细胞表达海藻糖酶,并且它们可以在含海藻糖的细胞培养基上生长。通过用海藻糖酶抑制剂处理Aag2细胞来证实海藻糖酶活性,该抑制剂抑制海藻糖向葡萄糖的转化并减少细胞增殖。荧光海藻糖探针的细胞摄取取决于海藻糖浓度,这表明海藻糖通过被动运输穿过细胞膜。用含海藻糖的细胞培养基培养Aag2细胞导致基因表达、细胞内脂质、登革病毒复制和特异性感染性发生显著变化,并增加了它们对海藻糖酶抑制剂的敏感性。这些数据描述了一种可用于快速筛选新型海藻糖酶抑制剂和探针的体外模型,并强调了海藻糖代谢在埃及伊蚊生理学和蚊媒病毒传播中的重要性。

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本文引用的文献

1
Targeting Persistence through Inhibition of the Trehalose Catalytic Shift.通过抑制海藻糖催化转变来靶向持久性。
ACS Infect Dis. 2024 Apr 12;10(4):1391-1404. doi: 10.1021/acsinfecdis.4c00138. Epub 2024 Mar 14.
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Targeting Metabolism with Next-Generation Insecticides.靶向代谢的下一代杀虫剂。
Viruses. 2023 Feb 8;15(2):469. doi: 10.3390/v15020469.
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Trehalose in Biomedical Cryopreservation-Properties, Mechanisms, Delivery Methods, Applications, Benefits, and Problems.海藻糖在生物医学低温保存中的应用-性质、机制、传递方法、应用、益处和问题。
ACS Biomater Sci Eng. 2023 Mar 13;9(3):1190-1204. doi: 10.1021/acsbiomaterials.2c01225. Epub 2023 Feb 13.
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Discovery of super-insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations.亚洲发现超级抗杀虫剂登革热蚊子:伴随击倒抗性突变的威胁。
Sci Adv. 2022 Dec 21;8(51):eabq7345. doi: 10.1126/sciadv.abq7345.
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Updating the Insecticide Resistance Status of and in Asia: A Systematic Review and Meta-Analysis.更新亚洲[具体昆虫名称1]和[具体昆虫名称2]的抗药性状况:系统评价与荟萃分析
Trop Med Infect Dis. 2022 Oct 17;7(10):306. doi: 10.3390/tropicalmed7100306.
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Chronic depletion of vertebrate lipids in Aedes aegypti cells dysregulates lipid metabolism and inhibits innate immunity without altering dengue infectivity.在埃及伊蚊细胞中慢性耗尽脊椎动物脂质会扰乱脂质代谢并抑制先天免疫,而不会改变登革热感染性。
PLoS Negl Trop Dis. 2022 Oct 24;16(10):e0010890. doi: 10.1371/journal.pntd.0010890. eCollection 2022 Oct.
7
Activation of the autophagy pathway decreases dengue virus infection in Aedes aegypti cells.自噬途径的激活可降低登革热病毒在埃及伊蚊细胞中的感染。
Parasit Vectors. 2021 Oct 26;14(1):551. doi: 10.1186/s13071-021-05066-w.
8
Current Trends and Limitations in Dengue Antiviral Research.登革热抗病毒研究的当前趋势与局限
Trop Med Infect Dis. 2021 Sep 30;6(4):180. doi: 10.3390/tropicalmed6040180.
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Regen Ther. 2020 Sep 8;15:173-179. doi: 10.1016/j.reth.2020.08.003. eCollection 2020 Dec.
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J Virol. 2021 Mar 1;95(5). doi: 10.1128/JVI.02024-20. Epub 2020 Dec 16.