伪狂犬病毒抑制神经母细胞瘤细胞死亡途径的转录组学启示。

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2024-09-19 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1430396
Shinuo Cao, Li Zhang, Mo Zhou, Shanyuan Zhu
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引用次数: 0

摘要

伪狂犬病毒(PRV)主要通过调节宿主细胞死亡途径来优化其在神经-2a细胞中的复制和传播,表现出宿主与病原体之间复杂的相互作用。通过高通量 RNA 测序,我们发现了 2,382 个上调的差异表达基因(DEGs)和 3,998 个下调的差异表达基因(DEGs),这表明病毒致病机制与宿主细胞反应之间存在着错综复杂的相互作用。这项研究为我们提供了有关 PRV 感染分子过程的宝贵见解,突出了神经-2a 细胞中关键细胞死亡途径的实质性抑制,包括坏死、热噬、自噬、铁噬和杯噬。感染了 PRV 的细胞会减少这些通路中关键基因的表达,这可能是一种避免宿主免疫反应、确保细胞存活以支持病毒持续复制的机制。这种对细胞凋亡和新陈代谢改变的广泛抑制凸显了 PRV 所使用的复杂策略,增强了我们对疱疹病毒生物学的理解,并提高了创造特异性抗病毒疗法的可行性。这项研究有助于我们了解病毒是如何操纵宿主细胞死亡的,并为破坏病毒生命周期的治疗干预提供了潜在的机会。
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Transcriptomic insights into pseudorabies virus suppressed cell death pathways in neuroblastoma cells.

Pseudorabies virus (PRV) exhibits a complex interplay of host-pathogen interactions, primarily by modulating host cell death pathways to optimize its replication and spread in Neuro-2a cells. Using high-throughput RNA sequencing, we identified 2,382 upregulated differentially expressed genes (DEGs) and 3,998 downregulated DEGs, indicating a intricate interaction between viral pathogenesis and host cellular responses. This research offers valuable insights into the molecular processes involved in PRV infection, highlighting the substantial inhibition of crucial cell death pathways in Neuro-2a cells, including necroptosis, pyroptosis, autophagy, ferroptosis, and cuproptosis. Cells infected with PRV exhibit decreased expression of genes critical in these pathways, potentially as a mechanism to avoid host immune reactions and ensure cell survival to support ongoing viral replication. This extensive inhibition of apoptosis and metabolic alterations highlights the sophisticated tactics utilized by PRV, enhancing our comprehension of herpesvirus biology and the feasibility of creating specific antiviral treatments. This research contributes to our understanding of how viruses manipulate host cell death and presents potential opportunities for therapeutic interventions to disrupt the virus's lifecycle.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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