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柯萨奇病毒 A7 和肠道病毒 A71 在细胞和动物模型中显著减少 SARS-CoV-2 感染。

Coxsackievirus A7 and Enterovirus A71 Significantly Reduce SARS-CoV-2 Infection in Cell and Animal Models.

机构信息

State Research Center of Virology and Biotechnology "Vector", Koltsovo 630559, Novosibirsk Region, Russia.

出版信息

Viruses. 2024 Jun 4;16(6):909. doi: 10.3390/v16060909.

DOI:10.3390/v16060909
PMID:38932201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11209502/
Abstract

In this study, we investigated the features of co-infection with SARS-CoV-2 and the enterovirus vaccine strain LEV8 of coxsackievirus A7 or enterovirus A71 for Vero E6 cells and Syrian hamsters. The investigation of co-infection with SARS-CoV-2 and LEV-8 or EV-A71 in the cell model showed that a competitive inhibitory effect for these viruses was especially significant against SARS-CoV-2. Pre-infection with enteroviruses in the animals caused more than a 100-fold decrease in the levels of SARS-CoV-2 virus replication in the respiratory tract and more rapid clearance of infectious SARS-CoV-2 from the lower respiratory tract. Co-infection with SARS-CoV-2 and LEV-8 or EV-A71 also reduced the severity of clinical manifestations of the SARS-CoV-2 infection in the animals. Additionally, the histological data illustrated that co-infection with strain LEV8 of coxsackievirus A7 decreased the level of pathological changes induced by SARS-CoV-2 in the lungs. Research into the chemokine/cytokine profile demonstrated that the studied enteroviruses efficiently triggered this part of the antiviral immune response, which is associated with the significant inhibition of SARS-CoV-2 infection. These results demonstrate that there is significant viral interference between the studied strain LEV-8 of coxsackievirus A7 or enterovirus A71 and SARS-CoV-2 in vitro and in vivo.

摘要

在这项研究中,我们研究了 SARS-CoV-2 与柯萨奇病毒 A7 的肠道病毒疫苗株 LEV8 或肠道病毒 A71 共同感染 Vero E6 细胞和叙利亚仓鼠的特征。在细胞模型中研究 SARS-CoV-2 与 LEV-8 或 EV-A71 的共同感染表明,这些病毒对 SARS-CoV-2 具有特别显著的竞争性抑制作用。在动物中预先感染肠道病毒会导致呼吸道中 SARS-CoV-2 病毒复制水平降低 100 倍以上,并从下呼吸道更快地清除传染性 SARS-CoV-2。SARS-CoV-2 与 LEV-8 或 EV-A71 的共同感染也降低了动物 SARS-CoV-2 感染的临床表现严重程度。此外,组织学数据表明,柯萨奇病毒 A7 的 LEV8 株的共同感染降低了 SARS-CoV-2 在肺部引起的病变水平。对趋化因子/细胞因子谱的研究表明,研究中的肠道病毒有效地触发了这部分抗病毒免疫反应,这与 SARS-CoV-2 感染的显著抑制有关。这些结果表明,在体外和体内,研究的柯萨奇病毒 A7 的 LEV-8 株或肠道病毒 A71 与 SARS-CoV-2 之间存在显著的病毒干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/66d0e0cc1450/viruses-16-00909-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/2bc39ca930fe/viruses-16-00909-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/f46ed45bfadc/viruses-16-00909-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/83037e92e9da/viruses-16-00909-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/66d0e0cc1450/viruses-16-00909-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/2bc39ca930fe/viruses-16-00909-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/f46ed45bfadc/viruses-16-00909-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/83037e92e9da/viruses-16-00909-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb6/11209502/66d0e0cc1450/viruses-16-00909-g004.jpg

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Influenza A(H1N1)pdm09 Virus but Not Respiratory Syncytial Virus Interferes with SARS-CoV-2 Replication during Sequential Infections in Human Nasal Epithelial Cells.
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