Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO, USA.
The Connecticut Agricultural Experiment Station, Department of Environmental Sciences, Center for Vector Biology and Zoonotic Diseases, New Haven, CT, USA.
Virology. 2018 Aug;521:175-180. doi: 10.1016/j.virol.2018.06.007. Epub 2018 Jun 26.
Mosquito cell lines have been used extensively in research to isolate and propagate arthropod-borne viruses and understand virus-vector interactions. Despite their utility as an in vitro tool, these cell lines are poorly defined and may harbor insect-specific viruses. Accordingly, we screened four commonly-used mosquito cell lines, C6/36 and U4.4 cells from Aedes albopictus, Aag2 cells from Aedes aegypti, and Hsu cells from Culex quinquefasciatus, for the presence of adventitious (i.e. exogenous) viruses. All four cell lines stained positive for double-stranded RNA, indicative of RNA virus replication. We subsequently identified viruses infecting Aag2, U4.4 and Hsu cell lines using untargeted next-generation sequencing, but not C6/36 cells. PCR confirmation revealed that these sequences stem from active viral replication and/or integration into the cellular genome. Our results show that these commonly-used mosquito cell lines are persistently-infected with several viruses. This finding may be critical to interpreting data generated in these systems.
蚊细胞系已广泛应用于研究中,以分离和繁殖节肢动物传播的病毒,并了解病毒-媒介的相互作用。尽管它们作为体外工具具有实用性,但这些细胞系的定义很差,并且可能携带有昆虫特异性病毒。因此,我们筛选了四种常用的蚊细胞系,即来自白纹伊蚊的 C6/36 和 U4.4 细胞、来自埃及伊蚊的 Aag2 细胞和来自致倦库蚊的 Hsu 细胞,以检测是否存在外来(即外源)病毒。所有四种细胞系均对双链 RNA 呈阳性染色,表明存在 RNA 病毒复制。随后,我们使用非靶向下一代测序鉴定了感染 Aag2、U4.4 和 Hsu 细胞系的病毒,但未鉴定出感染 C6/36 细胞的病毒。PCR 确认表明这些序列源自病毒的活跃复制和/或整合到细胞基因组中。我们的结果表明,这些常用的蚊细胞系持续感染了几种病毒。这一发现可能对解释这些系统中产生的数据至关重要。