Suppr超能文献

寄生虫抗原在体外对 SARS-CoV-2 具有抗病毒作用。

Antigens from the Helminth Exert Antiviral Effects against SARS-CoV-2 In Vitro.

机构信息

Laboratory of Helminth Parasites of Zoonotic Importance (ATENEA), Institute of Natural Resources and Agrobiology of Salamanca (IRNASA-CSIC), C/Cordel de Merinas 40-52, 37008 Salamanca, Spain.

Institute for Integrative Systems Biology (I2SysBio), Universidad de Valencia-CSIC, 46980 Valencia, Spain.

出版信息

Int J Mol Sci. 2023 Jul 18;24(14):11597. doi: 10.3390/ijms241411597.

Abstract

SARS-CoV-2, the causal agent of COVID-19, is a new coronavirus that has rapidly spread worldwide and significantly impacted human health by causing a severe acute respiratory syndrome boosted by a pulmonary hyperinflammatory response. Previous data from our lab showed that the newly excysted juveniles of the helminth parasite (FhNEJ) modulate molecular routes within host cells related to vesicle-mediated transport and components of the innate immune response, which could potentially be relevant during viral infections. Therefore, the aim of the present study was to determine whether FhNEJ-derived molecules influence SARS-CoV-2 infection efficiency in Vero cells. Pre-treatment of Vero cells with a tegument-enriched antigenic extract of FhNEJ (FhNEJ-TEG) significantly reduced infection by both vesicular stomatitis virus particles pseudotyped with the SARS-CoV-2 Spike protein (VSV-S2) and live SARS-CoV-2. Pre-treatment of the virus itself with FhNEJ-TEG prior to infection also resulted in reduced infection efficiency similar to that obtained by remdesivir pre-treatment. Remarkably, treatment of Vero cells with FhNEJ-TEG after VSV-S2 entry also resulted in reduced infection efficiency, suggesting that FhNEJ-TEG may also affect post-entry steps of the VSV replication cycle. Altogether, our results could potentially encourage the production of FhNEJ-derived molecules in a safe, synthetic format for their application as therapeutic agents against SARS-CoV-2 and other related respiratory viruses.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是导致 COVID-19 的病原体,它是一种新型冠状病毒,在全球范围内迅速传播,通过引起肺部高度炎症反应的严重急性呼吸道综合征对人类健康造成了重大影响。我们实验室之前的数据表明,新孵化的寄生虫幼虫(FhNEJ)会调节宿主细胞内与囊泡介导的运输和先天免疫反应相关的分子途径,这在病毒感染过程中可能是相关的。因此,本研究的目的是确定 FhNEJ 衍生分子是否会影响 SARS-CoV-2 在 Vero 细胞中的感染效率。用 FhNEJ 的富含被膜的抗原性提取物(FhNEJ-TEG)预处理 Vero 细胞,可显著降低由 SARS-CoV-2 刺突蛋白(VSV-S2)假型化的水疱性口炎病毒颗粒(VSV-S2)和活 SARS-CoV-2 的感染。在感染前用 FhNEJ-TEG 预处理病毒本身也会导致感染效率降低,类似于用瑞德西韦预处理的效果。值得注意的是,用 FhNEJ-TEG 处理 Vero 细胞后,即使在 VSV-S2 进入后,也会导致感染效率降低,这表明 FhNEJ-TEG 也可能影响 VSV 复制周期的进入后步骤。总的来说,我们的研究结果可能会鼓励以安全的合成形式生产 FhNEJ 衍生分子,并将其用作治疗 SARS-CoV-2 和其他相关呼吸道病毒的治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3a/10380311/73d41168034b/ijms-24-11597-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验