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猪流行性腹泻病毒细胞入侵途径中观察到的生物力学现象:综述

The biomechanical phenomena observed in the cell invasion pathway of porcine epidemic diarrhea virus: a review.

作者信息

Zou Hong, Wang Yi, Luo Gan, Huang Shilei

机构信息

College of Animal Science & Technology, Chongqing Three Gouges Vocational College, Chongqing, China.

Wanzhou Center for Animal Husbandry Industry Development of Chongqing, Chongqing, China.

出版信息

Arch Virol. 2025 May 26;170(7):139. doi: 10.1007/s00705-025-06326-1.

DOI:10.1007/s00705-025-06326-1
PMID:40418401
Abstract

Porcine epidemic diarrhea virus (PEDV) is the primary pathogen responsible for highly contagious intestinal infections in pigs, which results in significant economic losses to the global animal husbandry industry. PEDV is an enveloped virus that enters cells via endocytosis, a process that is dependent on the binding of the viral surface S protein to a receptor on the host cell membrane. This results in a series of biomechanical alterations that drive the fusion of the viral and host cell membranes. These alterations stabilise the binding of the virus to the receptor and also affect the tension and the curvature of the plasma membrane and the formation of endocytic vesicles. A comprehensive understanding of the mechanism by which PEDV enters cells and the biomechanical changes that accompany this process is of paramount importance for the development of PEDV inhibitors, vaccines, and disease prevention and control strategies. Here, we review the general mechanism of PEDV entry, the biomechanical phenomena that occur during endocytosis, and the potential applications of biomechanics in antiviral therapy. It is anticipated that by gaining insight into these mechanisms, novel approaches to regulating viral entry pathways through mechanical interference, vaccine development, and antiviral drug design can be explored.

摘要

猪流行性腹泻病毒(PEDV)是导致猪高度传染性肠道感染的主要病原体,给全球畜牧业造成重大经济损失。PEDV是一种包膜病毒,通过内吞作用进入细胞,这一过程依赖于病毒表面S蛋白与宿主细胞膜上受体的结合。这会导致一系列生物力学改变,驱动病毒膜与宿主细胞膜融合。这些改变稳定了病毒与受体的结合,还影响质膜的张力和曲率以及内吞小泡的形成。全面了解PEDV进入细胞的机制以及伴随这一过程的生物力学变化,对于开发PEDV抑制剂、疫苗以及疾病防控策略至关重要。在此,我们综述了PEDV进入的一般机制、内吞作用过程中发生的生物力学现象以及生物力学在抗病毒治疗中的潜在应用。预计通过深入了解这些机制,可以探索通过机械干扰调节病毒进入途径、疫苗开发和抗病毒药物设计的新方法。

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本文引用的文献

1
Establishment and Application of a Triplex Real-Time Reverse-Transcription Polymerase Chain Reaction Assay for Differentiation of PEDV, TGEV and PKV.一种用于鉴别猪流行性腹泻病毒(PEDV)、猪传染性胃肠炎病毒(TGEV)和猪轮状病毒(PKV)的三重实时逆转录聚合酶链反应检测方法的建立与应用
Vet Sci. 2024 Sep 6;11(9):413. doi: 10.3390/vetsci11090413.
2
Time-resolved proximity proteomics uncovers a membrane tension-sensitive caveolin-1 interactome at the rear of migrating cells.时间分辨临近蛋白质组学揭示了迁移细胞后部的膜张力敏感的窖蛋白-1相互作用组。
Elife. 2024 Sep 24;13:e85601. doi: 10.7554/eLife.85601.
3
Isolation and characterization of a novel S1-gene insertion porcine epidemic diarrhea virus with low pathogenicity in newborn piglets.
一株对新生仔猪致病性低的新型S1基因插入型猪流行性腹泻病毒的分离与鉴定
Virulence. 2024 Dec;15(1):2397512. doi: 10.1080/21505594.2024.2397512. Epub 2024 Sep 16.
4
The Mechanism of Action of the Active Ingredients of against Porcine Epidemic Diarrhea Was Investigated Using Network Pharmacology and Molecular Docking Technology.采用网络药理学和分子对接技术研究 对猪流行性腹泻的活性成分的作用机制。
Viruses. 2024 Jul 31;16(8):1229. doi: 10.3390/v16081229.
5
An extended interaction site determines binding between AP180 and AP2 in clathrin mediated endocytosis.一个扩展的相互作用位点决定了网格蛋白介导的内吞作用中 AP180 和 AP2 之间的结合。
Nat Commun. 2024 Jul 13;15(1):5884. doi: 10.1038/s41467-024-50212-4.
6
A novel and cost-effective real-time RT-PCR targeting 24 nucleotides deletion to differentiate PEDV wild-type and classical attenuated vaccine strains.针对 PEDV 野毒株和经典弱毒疫苗株 24 个核苷酸缺失的新型且经济有效的实时 RT-PCR 检测方法。
J Virol Methods. 2024 Sep;329:114986. doi: 10.1016/j.jviromet.2024.114986. Epub 2024 Jun 22.
7
Research progress of porcine epidemic diarrhea virus S protein.猪流行性腹泻病毒S蛋白的研究进展
Front Microbiol. 2024 May 30;15:1396894. doi: 10.3389/fmicb.2024.1396894. eCollection 2024.
8
Establishment and application of a quadruplex real-time RT-qPCR assay for differentiation of TGEV, PEDV, PDCoV, and PoRVA.用于区分猪传染性胃肠炎病毒(TGEV)、猪流行性腹泻病毒(PEDV)、猪德尔塔冠状病毒(PDCoV)和猪轮状病毒A(PoRVA)的四重实时逆转录定量聚合酶链反应(RT-qPCR)检测方法的建立与应用
Microb Pathog. 2024 Jun;191:106646. doi: 10.1016/j.micpath.2024.106646. Epub 2024 Apr 16.
9
Epidemiological monitoring and genetic variation analysis of pathogens associated with porcine viral diarrhea in southern China from 2021 to 2023.2021年至2023年中国南方猪病毒性腹泻相关病原体的流行病学监测与基因变异分析
Front Microbiol. 2024 Mar 20;15:1303915. doi: 10.3389/fmicb.2024.1303915. eCollection 2024.
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ALIX and TSG101 are essential for cellular entry and replication of two porcine alphacoronaviruses.Alix 和 TSG101 对于两种猪α冠状病毒的细胞进入和复制是必不可少的。
PLoS Pathog. 2024 Mar 15;20(3):e1012103. doi: 10.1371/journal.ppat.1012103. eCollection 2024 Mar.