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首页> 外文期刊>Archives of virology >Transcriptional control of Borna disease virus (BDV) in persistently BDV-infected cells.
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Transcriptional control of Borna disease virus (BDV) in persistently BDV-infected cells.

机译:持久性BDV感染细胞诞生病毒(BDV)的转录控制。

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Regulation of viral RNA levels in infected cells is considered important in the investigation of viral transcription and replication. Amounts of Borna disease virus (BDV) RNAs were increased in confluent persistently BDV-infected MDCK cells (MDCK/BDV) cells, while maintained at low levels in growing cells. The amount of 1.9-kb RNA without cap formation and polyadenylation at the 5' and 3' ends respectively were remarkably increased (200% per day) in confluent MDCK/BDV cells. Both the full-length genomic and anti-genomic RNAs were increased accompained by 1.9-kb RNA, suggesting the transcription of the 1.9-kb RNA was important for replication of BDV. Ribavirin has an inhibitory effect on replication and transcription of BDV at concentrations from 1 to 10 microgram/ml [Mizutani T et al., Arch Virol (1998)143: 2039-2 044]. BDV transcripts were decreased with ribavirin treatment and increased after its removal which indicated that ribavirin has a reversible inhibitory effect on BDV transcription. Furthermore, BDV transcription was also decreased by two agents, RMNPA and EICAR, which selectively inhibit enzyme activity related to cap formation at the 5' end of mRNA. On the contrary, when the growing MDCK/BDV cells were treated with actinomycin D, transcripts of BDV RNA were increased for 24 h. These agents and culture conditions in this study were found to be useful tools for up-and down-regulation of BDV transcription in persistently BDV-infected cells.
机译:在调查病毒转录和复制的调查中认为感染细胞病毒RNA水平的调节。在汇合持续的BDV感染的MDCK细胞(MDCK / BDV)细胞中增加了诞生病毒(BDV)RNA的量,同时在生长细胞中保持低水平。在汇合MDCK / BDV细胞中,分别在5'和3'末端的不含帽形成和聚酰基化的1.9kb rna的量显着增加(每天200%)。全长基因组和抗基因组RNA伴随着1.9kb的RNA增加,表明1.9-kB RNA的转录对于BDV的复制很重要。利巴韦林对BDV的复制和转录在1至10微克/ mL [Mizutani T等人,拱病毒(1998)143:2039-2 044]上具有抑制作用和转录BDV的复制和转录。通过利巴韦林治疗降低BDV转录物并在去除后增加,表明利巴韦林对BDV转录具有可逆抑制作用。此外,BDV转录也通过两个药剂,RMNPA和EICAR降低,其选择性地抑制与mRNA的5'末端有关的胶质形成有关的酶活性。相反,当用放线霉素D处理生长的MDCK / BDV细胞时,BDV RNA的转录物增加24小时。发现本研究中的这些药剂和培养条件是在持续BDV感染细胞中的BDV转录的上下调节的有用工具。

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