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In vitro inhibition of feline coronavirus replication by small interfering RNAs

机译:小干扰RNA在体外抑制猫冠状病毒复制

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Infection with virulent biotypes of feline coronavirus (FCoV) can result in the development of feline infectious peritonitis (FIP), a typically fatal immune mediated disease for which there is currently no effective antiviral treatment. In this study we demonstrate the ability of small interfering RNA (siRNA) mediated RNA interference (RNAi) to inhibit the replication of virulent FCoV strain FIPV WSU 79-1146 in an immortalised feline cell line. A panel of eight synthetic siRNAs targeting four different regions of the FCoV genome were tested for antiviral effects. Efficacy was determined by qRT-PCR of intracellular viral genomic and messenger RNA, TCID50 infectivity assay of extracellular virus, and direct IFA for viral protein expression. All siRNAs demonstrated an inhibitory effect on viral replication in vitro. The two most effective siRNAs, targeting the untranslated 5' leader sequence (L2) and the nucleocapsid gene (N1), resulted in a > 95% reduction in extracellular viral titre. Further characterisation of these two siRNAs demonstrated their efficacy when used at low concentrations and in cells challenged with high viral loads. Taken together these findings provide important information for the potential therapeutic application of RNAi in treating FIP
机译:猫冠状病毒(FCoV)的强毒生物型感染可导致猫传染性腹膜炎(FIP)的发展,这是一种典型的致命免疫介导性疾病,目前尚无有效的抗病毒治疗方法。在这项研究中,我们证明了小干扰RNA(siRNA)介导的RNA干扰(RNAi)抑制永生猫细胞系中有毒FCoV株FIPV WSU​​ 79-1146复制的能力。测试了针对FCoV基因组四个不同区域的一组八个合成siRNA的抗病毒作用。通过细胞内病毒基因组和信使RNA的qRT-PCR,细胞外病毒的TCID50感染性测定以及直接IFA进行病毒蛋白表达来确定功效。所有siRNA均显示出对体外病毒复制的抑制作用。靶向未翻译的5'前导序列(L2)和核衣壳基因(N1)的两种最有效的siRNA,导致细胞外病毒滴度降低> 95%。这两种siRNA的进一步表征证明了它们在低浓度下以及在高病毒载量挑战的细胞中使用时的功效。综上所述,这些发现为RNAi在治疗FIP中的潜在治疗应用提供了重要信息。

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