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宿主菌株对小鼠肺炎病毒感染的特异性反应:病变、病毒载量和细胞因子表达的研究。

Host-Strain-Specific Responses to Pneumonia Virus of Mice Infection: A Study of Lesions, Viral Load, and Cytokine Expression.

作者信息

Levy Etienne, Gilliaux Gautier, Sarlet Michaël, Desmecht Daniel, Van Laere Anne-Sophie

机构信息

Department of Pathology, FARAH Research Center, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium.

出版信息

Viruses. 2025 Apr 9;17(4):548. doi: 10.3390/v17040548.

Abstract

Pneumonia virus of mice (PVM) infection is a reference animal model for human respiratory syncytial virus (hRSV), a leading cause of lower respiratory tract disease in children under 5 years of age and in the elderly. This longitudinal study employed necropsy to examine macroscopic lesions, histological slides to assess microscopic lesions, and qRT-PCR to measure lung viral load and cytokine expression in PVM-infected mice from three different genetic backgrounds, spanning from day 1 to day 6 post-infection. Our analysis reveals a strong correlation between viral load and microscopic lesions across the 129/Sv, BALB/c, and SJL/J mouse lines, indicating that PVM pathogenicity is partially driven by the virus itself. Additionally, a significant correlation between cytokine levels and lesion severity was observed in 129/Sv and BALB/c mice, suggesting an important role of cytokines in disease progression. This study emphasizes the interplay between viral load and cytokine-driven tissue damage, with genetic background significantly influencing disease outcomes.

摘要

小鼠肺炎病毒(PVM)感染是人类呼吸道合胞病毒(hRSV)的一种参考动物模型,hRSV是5岁以下儿童和老年人下呼吸道疾病的主要病因。这项纵向研究采用尸检来检查宏观病变,用组织学切片评估微观病变,并通过qRT-PCR测量感染PVM的来自三种不同遗传背景的小鼠从感染后第1天到第6天的肺病毒载量和细胞因子表达。我们的分析揭示了在129/Sv、BALB/c和SJL/J小鼠品系中病毒载量与微观病变之间存在很强的相关性,表明PVM致病性部分由病毒本身驱动。此外,在129/Sv和BALB/c小鼠中观察到细胞因子水平与病变严重程度之间存在显著相关性,提示细胞因子在疾病进展中起重要作用。这项研究强调了病毒载量与细胞因子驱动的组织损伤之间的相互作用,遗传背景对疾病结果有显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9159/12031304/185fc79d4786/viruses-17-00548-g001.jpg

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