Li Hanlue, Zhou Zijie, Chang Chuanyu, Shi Weiwei, Li Yuzhen, Wei Qiaolin, Meng Fanxing, Tian Jianxia, Hao Qiqi, Liu Jinming, Liu Haijin, Yang Zengqi, Xiao Sa
College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, People's Republic of China.
Sci Rep. 2025 Aug 13;15(1):29744. doi: 10.1038/s41598-025-14404-2.
Newcastle disease virus (NDV), as an avian pathogen, can infect a broad spectrum of cell lines in vitro. However, noncarcinoma cell lines possessing nonsusceptibility to NDV are rare. Here, we isolated primary mouse embryonic fibroblasts (MEFs), which are nonsusceptible to NDV. MEF-derived cells were generated by passaging the cells over fifty times to achieve spontaneous immortalization. Two of the resulting cell lines were named SLM-21 and MEF50. Karyotype analysis revealed that SLM-21 has a near-tetraploid karyotype and that MEF50 shows a near-tetraploid and near-hexaploid chimeric karyotype. NDV exerted a significant cytopathic effect on MEF50, and substantial viral replication was observed. In contrast, NDV did not have a significant effect on SLM-21, indicating that SLM-21 was a nonsusceptible cell line to NDV, while MEF50 was a susceptible cell line. The NDV authentic sialic acid (SA) receptors SA 2,3-Gal and SA 2,6-Gal were expressed in SLM-21. Transcriptomic analysis revealed that the non-susceptibility of SLM-21 may be related to its broadly activated antiviral pathways and fine-tuned regulation of the cell cycle and DNA damage. This study provides a basic cell platform for exploring viral susceptibility and pathogenesis as well as host-virus interactions during NDV infection.
新城疫病毒(NDV)作为一种禽类病原体,在体外可感染多种细胞系。然而,对NDV不敏感的非癌细胞系却很罕见。在此,我们分离出了对NDV不敏感的原代小鼠胚胎成纤维细胞(MEF)。通过将细胞传代五十多次以实现自发永生化,从而获得了MEF衍生细胞。所得的两个细胞系分别命名为SLM - 21和MEF50。核型分析显示,SLM - 21具有近四倍体核型,而MEF50呈现近四倍体和近六倍体的嵌合核型。NDV对MEF50产生了显著的细胞病变效应,并观察到大量病毒复制。相比之下,NDV对SLM - 21没有显著影响,这表明SLM - 21是对NDV不敏感的细胞系,而MEF50是敏感细胞系。NDV真正的唾液酸(SA)受体SA 2,3 - Gal和SA 2,6 - Gal在SLM - 21中表达。转录组分析表明,SLM - 21的不敏感性可能与其广泛激活的抗病毒途径以及对细胞周期和DNA损伤的精细调节有关。本研究为探索NDV感染期间的病毒易感性、发病机制以及宿主 - 病毒相互作用提供了一个基础细胞平台。