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Inhibition of vesivirus infections in mammalian tissue culture with antisense morpholino oligomers

机译:反义吗啉代寡聚物抑制哺乳动物组织培养中的杯状病毒感染

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摘要

Caliciviruses infect and cause disease in animals and humans. They are nonenveloped, positive-stranded RNA viruses with a genome of approximately 7.5 kb that encodes viral proteins in three open reading frames (ORF). Antisense oligomers targeting one of the three ORF of caliciviruses of the genus Vesivirus significantly inhibit viral replication in tissue culture. Porcine kidney and African green monkey kidney cells were infected with Vesivirus isolates SMSV-13 and PCV Pan-1. Phosphorodiamidate morpholino oligomers (PMO) with sequence complementary to the AUG translation start site regions of ORF1, ORF2, and ORF3 were evaluated for their effect on viral titer. Scrape-loading delivered PMO to 50%-70% of the cells of the two cell lines, as measured by fluorescence microscopy and flow cytometry. A PMO targeting ORF3 caused a significant increase in viral titer. A PMO targeting ORF2, a scrambled PMO control sequence, and an unrelated PMO antisense sequence did not alter viral titer. Various PMO sequences antisense to an upstream region of ORF1 were effective in reducing viral titer up to 80% in a dose-dependent and sequence-specific manner. The extent of viral titer reduction was proportional to the delivery of PMO to cells. These observations demonstrate that antisense PMO can disrupt caliciviral gene function in a nucleic acid sequence-specific manner and are potentially effective antiviral agents.
机译:杯状病毒感染并引起动物和人类疾病。它们是非包膜的正链RNA病毒,具有大约7.5 kb的基因组,可在三个开放阅读框(ORF)中编码病毒蛋白。靶向Vesivirus属杯状病毒的三种ORF之一的反义寡聚物显着抑制组织培养中的病毒复制。猪肾和非洲绿猴肾细胞感染了病毒分离株SMSV-13和PCV Pan-1。评估其序列与ORF1,ORF2和ORF3的AUG翻译起始位点区域互补的序列的二氨基磷酸吗啉代寡聚物(PMO)对病毒滴度的影响。如通过荧光显微镜和流式细胞术所测量的,刮取装载将PMO递送至两个细胞系的50%-70%的细胞。靶向ORF3的PMO导致病毒滴度显着提高。靶向ORF2的PMO,混乱的PMO控制序列和无关的PMO反义序列不会改变病毒滴度。与ORF1上游区域反义的各种PMO序列可以有效地以剂量依赖性和序列特异性方式将病毒滴度降低至80%。病毒滴度降低的程度与PMO向细胞的输送成正比。这些观察结果表明反义PMO可以核酸序列特异性方式破坏杯状病毒基因功能,并且是潜在有效的抗病毒剂。

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