Simas J P, Swann D, Bowden R, Efstathiou S
J Gen Virol. 1999 Jan;80 ( Pt 1):75-82. doi: 10.1099/0022-1317-80-1-75.
Murine gammaherpesvirus-68 (MHV-68) is a gamma2-herpesvirus that upon experimental infection of laboratory mice establishes a latent infection in B lymphocytes. To date, no virus-encoded gene products have been reported to be expressed during latent infection. In this study, viral transcription has been analysed in a persistently infected B-cell line and abundant and preferential transcription of open reading frame M3 has been identified. Significantly, in situ hybridization analysis of latently infected mouse spleens with probes corresponding to 20 MHV-68 ORFs demonstrated active transcription of a single ORF, corresponding to M3. The kinetics and pattern of transcription of M3 were compared with that of the virally encoded tRNAs (vtRNAs), previously demonstrated to constitute a marker for latent infection in the spleen. Transcription of vtRNAs in splenic tissue could be first detected at 7 days post-inoculation (p.i.) in scattered cells in periarteriolar lymphoid sheaths (PALS). At 10 days p.i., vtRNA transcription was widespread and localized not only to cells in PALS but also to cells within developing germinal centres and from 21 days p.i. expression was detected exclusively within lymphoid follicles. Transcription of vtRNAs could be detected as late as 70 days p.i. In contrast, the histological localization of M3 transcription, which was first detected at 7 days p.i. in scattered cells in PALS, never changed and transcription could not be detected beyond 21 days p.i. These results suggest that M3 is an ORF that is expressed early during the establishment of latency in vivo.
鼠γ疱疹病毒68(MHV-68)是一种γ2疱疹病毒,在对实验室小鼠进行实验性感染后,它会在B淋巴细胞中建立潜伏感染。迄今为止,尚未有报道称在潜伏感染期间有病毒编码的基因产物表达。在本研究中,对一个持续感染的B细胞系中的病毒转录进行了分析,发现开放阅读框M3存在丰富且优先的转录。值得注意的是,用对应于20个MHV-68开放阅读框的探针,对潜伏感染的小鼠脾脏进行原位杂交分析,结果显示只有一个对应于M3的开放阅读框有活跃转录。将M3的转录动力学和模式与病毒编码的tRNA(vtRNA)进行了比较,之前已证明vtRNA是脾脏潜伏感染的一个标志物。在接种后7天(p.i.),可在脾动脉周围淋巴鞘(PALS)中的散在细胞中首次检测到脾组织中vtRNA的转录。在接种后10天,vtRNA转录广泛存在,不仅定位于PALS中的细胞,还定位于生发中心内的细胞,从接种后21天起,仅在淋巴滤泡内检测到表达。vtRNA转录最晚可在接种后70天检测到。相比之下,M3转录的组织学定位在接种后7天首次在PALS中的散在细胞中检测到,此后从未改变,在接种后21天之后无法检测到转录。这些结果表明,M3是一个在体内潜伏建立早期就表达的开放阅读框。