Universidade Federal do Rio de Janeiro, Instituto de Microbiologia Paulo de Góes, Departamento de Virologia, Laboratório de Virologia e Espectrometria de Massas, Rio de Janeiro, RJ, Brasil.
Universidade Federal Fluminense, Instituto Biomédico, Departamento de Microbiologia e Parasitologia, Niterói, RJ, Brasil.
Mem Inst Oswaldo Cruz. 2024 Jul 22;119:e230186. doi: 10.1590/0074-02760230186. eCollection 2024.
Giant viruses have brought new insights into different aspects of virus-cell interactions. The resulting cytopathic effects from these interactions are one of the main aspects of infection assessment in a laboratory routine, mainly reflecting on the morphological features of an infected cell.
In this work, we follow the entire kinetics of the cytopathic effect in cells infected by viruses of the Mimiviridae family, spatiotemporally quantifying typical features such as cell roundness, loss of motility, decrease in cell area and cell lysis.
Infections by Acanthamoeba polyphaga mimivirus (APMV), Tupanvirus (TPV) and M4 were carried out at multiplicity of infection (MOI) 1 and MOI 10 in Acanthamoeba castellanii. Monitoring of infections was carried out using time lapse microscopy for up to 72 hours. The images were analyzed using ImageJ software.
The data obtained indicate that APMV is the slowest virus in inducing the cytopathic effects of rounding, decrease in cell area, mobility and cell lysis. However, it is the only virus whose MOI increase accelerates the lysis process of infected cells. In turn, TPV and M4 rapidly induce morphological and behavioral changes.
Our results indicate that mimiviruses induce different temporal responses within the host cell and that it is possible to use these kinetic data to facilitate the understanding of infection by these viruses.
巨型病毒为病毒-细胞相互作用的不同方面带来了新的认识。这些相互作用所导致的细胞病变效应是实验室常规中评估感染的主要方面之一,主要反映了受感染细胞的形态特征。
在这项工作中,我们跟踪感染 mimiviridae 科病毒的细胞中细胞病变效应的整个动力学,时空定量分析细胞圆度、运动能力丧失、细胞面积减小和细胞裂解等典型特征。
在粘菌性阿米巴(Acanthamoeba castellanii)中以感染复数(MOI)1 和 MOI 10 进行 Polyphaga mimivirus(APMV)、Tupanvirus(TPV)和 M4 的感染。使用延时显微镜对感染进行监测,最长达 72 小时。使用 ImageJ 软件对图像进行分析。
获得的数据表明,APMV 是诱导细胞病变效应(细胞变圆、细胞面积减小、运动能力丧失和细胞裂解)最慢的病毒。然而,它是唯一一种增加 MOI 会加速感染细胞裂解过程的病毒。相反,TPV 和 M4 会迅速诱导形态和行为变化。
我们的结果表明,巨型病毒在宿主细胞内诱导不同的时间反应,并且可以使用这些动力学数据来促进对这些病毒感染的理解。