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探索猪水疱性口炎病毒发病机制的分子基础:来自感染M51R突变病毒的原代巨噬细胞表达谱分析的见解

Exploring the Molecular Basis of Vesicular Stomatitis Virus Pathogenesis in Swine: Insights from Expression Profiling of Primary Macrophages Infected with M51R Mutant Virus.

作者信息

Velazquez-Salinas Lauro, Medina Gisselle N, Valdez Federico, Zarate Selene, Collinson Shannon, Zhu James J, Rodriguez Luis L

机构信息

Plum Island Animal Disease Center (PIADC), Agricultural Research Service, USDA, Greenport, NY 11944, USA.

National Bio and Agro-Defense Facility (NBAF), ARS, USDA, Manhattan, KS 66502, USA.

出版信息

Pathogens. 2023 Jun 30;12(7):896. doi: 10.3390/pathogens12070896.

Abstract

Vesicular stomatitis virus (VSV) is an emergent virus affecting livestock in the US. Previously, using a recombinant VSV carrying the M51R mutation in the matrix protein (rNJ0612NME6-M51R), we evaluated the pathogenesis of this virus in pigs. Our results indicated that rNJ0612NME6-M51R represented an attenuated phenotype in in-vivo and in ex-vivo in pig macrophages, resembling certain clinical features observed in field VSV isolates. In order to gain more insight into the molecular basis leading to the attenuation of rNJ0612NME6-M51R in pigs, we conducted a microarray analysis to assess the gene expression profiles of primary porcine macrophages infected with rNJ0612NME6-M51R compared to its parental virus (rNJ0612NME6). Our results showed an overall higher gene expression in macrophages infected with rNJ0612NME6-M51R. Specifically, we observed that the pathways related with immune cytokine signaling and interferon (IFN)-related responses (including activation, signaling, induction, and antiviral mechanisms) were the ones comprising most of the relevant genes identified during this study. Collectively, the results presented herein highlight the relevance of type I interferon during the pathogenesis of VSV in pigs. The information generated from this study may represent a framework for future studies intended to understand the molecular bases of the pathogenesis of field strains in livestock.

摘要

水泡性口炎病毒(VSV)是一种在美国影响家畜的新兴病毒。此前,我们使用一种在基质蛋白中携带M51R突变的重组VSV(rNJ0612NME6-M51R),评估了该病毒在猪体内的发病机制。我们的结果表明,rNJ0612NME6-M51R在猪巨噬细胞的体内和体外均表现出减毒表型,类似于在野外VSV分离株中观察到的某些临床特征。为了更深入了解导致rNJ0612NME6-M51R在猪体内减毒的分子基础,我们进行了微阵列分析,以评估感染rNJ0612NME6-M51R与其亲本病毒(rNJ0612NME6)的原代猪巨噬细胞的基因表达谱。我们的结果显示,感染rNJ0612NME6-M51R的巨噬细胞中基因表达总体较高。具体而言,我们观察到与免疫细胞因子信号传导和干扰素(IFN)相关反应(包括激活、信号传导、诱导和抗病毒机制)相关的途径是本研究中鉴定出的大多数相关基因所包含的途径。总体而言,本文呈现的结果突出了I型干扰素在VSV感染猪发病机制中的相关性。本研究产生的信息可能为未来旨在了解家畜野外毒株发病机制分子基础的研究提供一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0d1/10384765/2f3dbea56b53/pathogens-12-00896-g001.jpg

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