Kara M
Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Bursa Uludag University, Bursa, 16059 Turkey.
Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, FL 3261 USA.
Mol Biol (Mosk). 2024 Jan-Feb;58(1):154-156. doi: 10.31857/S0026898424010148.
Murine gammaherpesvirus 68 (MHV68) establishes latency mainly in B cells and causes lymphomas reminiscent of human gammaherpesvirus diseases in laboratory mice. To study the molecular mechanism of virus infection and how the viral determinants control cell and eventually cause tumorigenesis, readily available latently infected cell lines are essential. For in vitro MHV68 latency studies, only two cell culture systems have been available. Gammaherpesviruses are known to infect developing B cells and macrophages, therefore we aimed to expand the MHV68 latently infected cell line repertoire. Here, several latently infected immature B cell and macrophage-like cell line clones were generated. Hygromycin-resistant recombinant MHV68 was isolated from a laboratory-made latent cell line, HE2.1, and propagated to develop stable cell lines that carry the viral genome under hygromycin selection. Subclones of these cells lines were analyzed for viral miRNA expression by TaqMan qPCR and assessed for expression of a lytic viral transcript M3. The cell lines maintain the viral genome as an episome shown by the digestion-circularization PCR assay. Latently infected cell lines generated here do not express viral miRNAs higher than the parental cell line. However, these cell lines may provide an alternative tool to study latency mechanisms and miRNA target identification studies.
鼠γ疱疹病毒68(MHV68)主要在B细胞中建立潜伏感染,并在实验小鼠中引发类似于人类γ疱疹病毒疾病的淋巴瘤。为了研究病毒感染的分子机制以及病毒决定因素如何控制细胞并最终导致肿瘤发生,易于获得的潜伏感染细胞系至关重要。对于体外MHV68潜伏感染研究,仅有两种细胞培养系统可用。已知γ疱疹病毒会感染发育中的B细胞和巨噬细胞,因此我们旨在扩充MHV68潜伏感染细胞系库。在此,我们生成了多个潜伏感染的未成熟B细胞和巨噬细胞样细胞系克隆。从实验室构建的潜伏细胞系HE2.1中分离出潮霉素抗性重组MHV68,并在潮霉素选择下进行传代培养,以建立携带病毒基因组的稳定细胞系。通过TaqMan qPCR分析这些细胞系的亚克隆的病毒miRNA表达,并评估裂解性病毒转录本M3的表达。通过消化-环化PCR分析表明,这些细胞系将病毒基因组维持为附加体。此处生成的潜伏感染细胞系表达的病毒miRNA并不高于亲本细胞系。然而,这些细胞系可能为研究潜伏机制和miRNA靶标鉴定研究提供一种替代工具。