Jain Vaibhav, Plaisance-Bonstaff Karlie, Sangani Rajnikumar, Lanier Curtis, Dolce Alexander, Hu Jianhong, Brulois Kevin, Haecker Irina, Turner Peter, Renne Rolf, Krueger Brian
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610, USA.
Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Viruses. 2016 Feb 19;8(2):54. doi: 10.3390/v8020054.
Kaposi's sarcoma-associated herpesvirus (KSHV) encodes 12 viral microRNAs (miRNAs) that are expressed during latency. Research into KSHV miRNA function has suffered from a lack of genetic systems to study viral miRNA mutations in the context of the viral genome. We used the Escherichia coli Red recombination system together with a new bacmid background, BAC16, to create mutants for all known KSHV miRNAs. The specific miRNA deletions or mutations and the integrity of the bacmids have been strictly quality controlled using PCR, restriction digestion, and sequencing. In addition, stable viral producer cell lines based on iSLK cells have been created for wildtype KSHV, for 12 individual miRNA knock-out mutants (ΔmiR-K12-1 through -12), and for mutants deleted for 10 of 12 (ΔmiR-cluster) or all 12 miRNAs (ΔmiR-all). NGS, in combination with SureSelect technology, was employed to sequence the entire latent genome within all producer cell lines. qPCR assays were used to verify the expression of the remaining viral miRNAs in a subset of mutants. Induction of the lytic cycle leads to efficient production of progeny viruses that have been used to infect endothelial cells. Wt BAC16 and miR mutant iSLK producer cell lines are now available to the research community.
卡波西肉瘤相关疱疹病毒(KSHV)编码12种在潜伏期表达的病毒微小RNA(miRNA)。对KSHV miRNA功能的研究因缺乏在病毒基因组背景下研究病毒miRNA突变的遗传系统而受到阻碍。我们使用大肠杆菌Red重组系统以及新的杆粒背景BAC16,为所有已知的KSHV miRNA创建突变体。通过PCR、限制性酶切和测序对特定miRNA的缺失或突变以及杆粒的完整性进行了严格的质量控制。此外,还基于iSLK细胞创建了野生型KSHV、12个单个miRNA敲除突变体(ΔmiR-K12-1至-12)、12个中缺失10个的突变体(ΔmiR-簇)或所有12个miRNA缺失的突变体(ΔmiR-全部)的稳定病毒生产细胞系。结合SureSelect技术,利用二代测序(NGS)对所有生产细胞系中的整个潜伏基因组进行测序。采用定量PCR分析来验证一部分突变体中剩余病毒miRNA的表达。裂解周期的诱导导致子代病毒的高效产生,这些子代病毒已被用于感染内皮细胞。野生型BAC16和miR突变体iSLK生产细胞系现已可供研究界使用。