Chen Songbiao, Liu Feifei, Yang Aofei, Shang Ke
Laboratory of Functional Microbiology and Animal Health, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, Henan, China.
Luoyang Key Laboratory of Live Carrier Biomaterial and Animal Disease Prevention and Control, Henan University of Science and Technology, Luoyang, Henan, China.
Front Immunol. 2024 Feb 23;15:1324531. doi: 10.3389/fimmu.2024.1324531. eCollection 2024.
Parvoviruses are a group of non-enveloped DNA viruses that have a broad spectrum of natural infections, making them important in public health. NS1 is the largest and most complex non-structural protein in the parvovirus genome, which is indispensable in the life cycle of parvovirus and is closely related to viral replication, induction of host cell apoptosis, cycle arrest, DNA damage response (DDR), and other processes. Parvovirus activates and utilizes the DDR pathway to promote viral replication through NS1, thereby increasing pathogenicity to the host cells. Here, we review the latest progress of parvovirus in regulating host cell DDR during the parvovirus lifecycle and discuss the potential of cellular consequences of regulating the DDR pathway, targeting to provide the theoretical basis for further elucidation of the pathogenesis of parvovirus and development of new antiviral drugs.
细小病毒是一组无包膜的DNA病毒,具有广泛的自然感染谱,在公共卫生领域具有重要意义。NS1是细小病毒基因组中最大且最复杂的非结构蛋白,在细小病毒的生命周期中不可或缺,与病毒复制、诱导宿主细胞凋亡、细胞周期停滞、DNA损伤反应(DDR)等过程密切相关。细小病毒通过NS1激活并利用DDR途径来促进病毒复制,从而增加对宿主细胞的致病性。在此,我们综述了细小病毒在其生命周期中调节宿主细胞DDR的最新进展,并讨论调节DDR途径的细胞后果的潜力,旨在为进一步阐明细小病毒的发病机制和开发新的抗病毒药物提供理论依据。