Biological relevance of in vitro cellular models to study varicella-zoster virus-host cell interactome: current limitations and future perspectives.

IF 7.8 1区 生物学 Q1 MICROBIOLOGY
Microbiology and Molecular Biology Reviews Pub Date : 2025-09-25 Epub Date: 2025-08-06 DOI:10.1128/mmbr.00165-25
Jonas Govaerts, Charlotte Goethals, Elise Van Breedam, Catherine Sadzot-Delvaux, Peter Delputte, Benson Ogunjimi, Marielle Lebrun, Peter Ponsaerts
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引用次数: 0

Abstract

SUMMARYWith varicella-zoster virus (VZV) being a strictly human-specific pathogen, in vitro cell culture models to study the VZV-host cell interactome predominantly rely on the use of primary human cells, immortalized cell lines, and-more recently-stem cell-derived models. In this work, based on literature reports published within the past 15 years, we attempted to summarize major lessons learned from in vitro VZV research, with a specific focus on whether and how a variety of host cells respond upon VZV infection at the cellular level. Following this specific approach, we describe the cellular events occurring following VZV infection in a neural cell type context, an immune cell type context, and a skin cell type context. Highly relevant, and for sure subject to the development of future VZV research, cell types within each of the three compartments reviewed display similarities but also significant differences in cellular response to VZV infection. Clearly, these need further clarification on a cell-type and/or VZV strain-specific level. Finally, to increase physiological relevance, we propose an integrated approach for future VZV-host cell interactome studies on a systems level by using advanced human-induced pluripotent stem cell-derived skin, peripheral, and central nervous system compartments that can be complemented with an isogenic immune cell component. Combined with the implementation of state-of-the-art multi-omics analyses, as well as electrophysiological recordings, this next-generation toolbox for advanced virus-host cell interactome studies may help to elucidate important aspects of VZV biology, including the suggested link between VZV pathology and neurodegenerative diseases.

体外细胞模型研究水痘-带状疱疹病毒-宿主细胞相互作用的生物学相关性:目前的局限性和未来的前景。
由于水痘带状疱疹病毒(VZV)是一种严格意义上的人类特异性病原体,研究水痘-带状疱疹病毒-宿主细胞相互作用的体外细胞培养模型主要依赖于使用原代人细胞、永活细胞系和最近的干细胞衍生模型。在这项工作中,基于过去15年发表的文献报告,我们试图总结体外VZV研究的主要经验教训,特别关注各种宿主细胞在细胞水平上是否以及如何对VZV感染作出反应。根据这种特定的方法,我们描述了在神经细胞类型背景下,免疫细胞类型背景下和皮肤细胞类型背景下VZV感染后发生的细胞事件。高度相关的,并且肯定会受到未来VZV研究发展的影响,三个室内的细胞类型在对VZV感染的细胞反应中表现出相似性,但也有显着差异。显然,这些需要在细胞类型和/或VZV株特异性水平上进一步澄清。最后,为了增加生理相关性,我们提出了一种综合方法,用于未来vzv -宿主细胞相互作用组在系统水平上的研究,通过使用先进的人类诱导的多能干细胞衍生的皮肤、外周和中枢神经系统区室,可以与等基因免疫细胞成分相补充。结合实施最先进的多组学分析,以及电生理记录,这个下一代高级病毒-宿主细胞相互作用组研究工具箱可能有助于阐明VZV生物学的重要方面,包括VZV病理与神经退行性疾病之间的联系。
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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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