Gonzalez Victoria, Word Cierra, Guerra-Pilaquinga Nahomi, Mazinani Mitra, Fawcett Stephen, Portfors Christine, Falzarano Darryl, Kell Alison M, Jangra Rohit K, Banerjee Arinjay, Seifert Stephanie N, Letko Michael
Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK S7N 5E3 Canada.
Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada.
bioRxiv. 2024 Nov 19:2024.11.19.624190. doi: 10.1101/2024.11.19.624190.
Multiple viruses that are highly pathogenic in humans are known to have evolved in bats. How bats tolerate infection with these viruses, however, is poorly understood. As viruses engage in a wide range of interactions with their hosts, it is essential to study bat viruses in a system that resembles their natural environment like bat-derived cellular models. However, stable and accessible bat cell lines are not widely available for the broader scientific community. Here, we generated reagents for the Seba's short-tailed bat (), tested multiple methods of immortalization, and characterized their susceptibility to virus infection and response to immune stimulation. Using a pseudotyped virus library and authentic virus infections, we show that these cell lines derived from a diverse array of tissues are susceptible to viruses bearing the glycoprotein of numerous orthohantaviruses, including Andes and Hantaan virus and are also susceptible to live hantavirus infection. Furthermore, stimulation with synthetic double-stranded RNA prior to infection with VSV and MERS-CoV induced a protective antiviral response, demonstrating the suitability of our cell lines to study the bat antiviral immune response. Taken together, the approaches outlined here will inform future efforts to develop tools for virology from non-model organisms and these cell lines will enable studies on virus-host interactions in bats.
已知多种对人类具有高致病性的病毒是在蝙蝠体内进化而来的。然而,蝙蝠如何耐受这些病毒的感染,目前却知之甚少。由于病毒与其宿主之间存在广泛的相互作用,因此在类似于蝙蝠自然环境的系统(如源自蝙蝠的细胞模型)中研究蝙蝠病毒至关重要。然而,稳定且易于获取的蝙蝠细胞系并未广泛提供给广大科学界。在此,我们为西氏鼠尾蝠()制备了试剂,测试了多种永生化方法,并对它们对病毒感染的敏感性以及对免疫刺激的反应进行了表征。使用假型病毒库和真实病毒感染,我们表明这些源自多种组织的细胞系对携带多种正汉坦病毒糖蛋白的病毒敏感,包括安第斯病毒和汉坦病毒,并且也对活汉坦病毒感染敏感。此外,在用水泡性口炎病毒(VSV)和中东呼吸综合征冠状病毒(MERS-CoV)感染之前,用合成双链RNA进行刺激可诱导保护性抗病毒反应,这证明了我们的细胞系适用于研究蝙蝠的抗病毒免疫反应。综上所述,本文概述的方法将为未来从非模式生物开发病毒学工具的工作提供参考,并且这些细胞系将有助于研究蝙蝠中的病毒-宿主相互作用。