Abrahams Rhiannon R, Majumder Kinjal
Institute for Molecular Virology and McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, WI 53707, USA.
Viruses. 2025 Mar 29;17(4):494. doi: 10.3390/v17040494.
Parvoviruses are small, single-stranded DNA viruses that have evolved sophisticated mechanisms to hijack host cell machinery for replication and persistence. One critical aspect of this interaction involves the manipulation of the host's DNA Damage Response (DDR) pathways. While the viral genome is comparatively simple, parvoviruses have developed strategies that cause significant DNA damage, activate DDR pathways, and disrupt the host cell cycle. This review will explore the impact of parvovirus infections on host genome stability, focusing on key viral species such as Adeno-Associated Virus (AAV), Minute Virus of Mice (MVM), and Human Bocavirus (HBoV), and their interactions with DDR proteins. Since parvoviruses are used as oncolytic agents and gene therapy vectors, a better understanding of cellular DDR pathways will aid in engineering potent anti-cancer agents and gene therapies for chronic diseases.
细小病毒是小型单链DNA病毒,它们已经进化出复杂的机制来劫持宿主细胞机制以进行复制和持续存在。这种相互作用的一个关键方面涉及对宿主DNA损伤反应(DDR)途径的操纵。虽然病毒基因组相对简单,但细小病毒已经开发出导致显著DNA损伤、激活DDR途径并破坏宿主细胞周期的策略。本综述将探讨细小病毒感染对宿主基因组稳定性的影响,重点关注腺相关病毒(AAV)、小鼠微小病毒(MVM)和人博卡病毒(HBoV)等关键病毒种类,以及它们与DDR蛋白的相互作用。由于细小病毒被用作溶瘤剂和基因治疗载体,更好地理解细胞DDR途径将有助于设计有效的抗癌药物和针对慢性疾病的基因疗法。