Rodrigues Rodrigo Araújo Lima, Louazani Amina Cherif, Picorelli Agnello, Oliveira Graziele Pereira, Lobo Francisco Pereira, Colson Philippe, La Scola Bernard, Abrahão Jônatas Santos
Laboratório de Vírus, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Microbes, Evolution, Phylogeny and Infection (MEΦI), IRD 198, Assistance Publique-Hopitaux de Marseille (AP-HM), Aix-Marseille Université UM63, Marseille, France.
Front Microbiol. 2020 Apr 14;11:651. doi: 10.3389/fmicb.2020.00651. eCollection 2020.
Marseilleviruses comprise a family of large double-stranded DNA viruses belonging to the proposed order "Megavirales." These viruses have a circular genome of ∼370 kbp, coding hundreds of genes. Over a half of their genes are associated with AT-rich putative promoter motifs, which have been demonstrated to be important for gene regulation. However, the transcriptional profile of Marseilleviruses is currently unknown. Here we used RNA sequencing technology to get a general transcriptional profile of Marseilleviruses. Eight million 75-bp-long nucleotide sequences were robustly mapped to all 457 genes initially predicted for Marseillevirus isolate T19, the prototype strain of the family, and we were able to assemble 359 viral contigs using a genome-guided approach with stringent parameters. These reads were differentially mapped to the genes according to the replicative cycle time point from which they were obtained. Cluster analysis indicated the existence of three main temporal categories of gene expression, early, intermediate and late, which were validated by quantitative reverse transcription polymerase chain reaction assays targeting several genes. Genes belonging to different functional groups exhibited distinct expression levels throughout the infection cycle. We observed that the previously predicted promoter motif, AAATATTT, as well as new predicted motifs, were not specifically related to any of the temporal or functional classes of genes, suggesting that other components are involved in temporally regulating virus transcription. Moreover, the host transcription machinery is heavily altered, and many genes are down regulated, including those related to translation process. This study provides an overview of the transcriptional landscape of Marseilleviruses.
马赛病毒属于一个大型双链DNA病毒家族,隶属于拟议中的“巨病毒目”。这些病毒拥有一个约370千碱基对的环状基因组,编码数百个基因。它们超过一半的基因与富含AT的假定启动子基序相关,这些基序已被证明对基因调控很重要。然而,马赛病毒的转录谱目前尚不清楚。在此,我们使用RNA测序技术来获取马赛病毒的总体转录谱。八百万条75个碱基长的核苷酸序列被可靠地映射到最初为该病毒家族的原型菌株马赛病毒分离株T19预测的所有457个基因上,并且我们能够使用具有严格参数的基因组引导方法组装359个病毒重叠群。这些读数根据其获得的复制周期时间点被差异映射到各个基因上。聚类分析表明存在基因表达的三个主要时间类别,即早期、中期和晚期,这通过针对几个基因的定量逆转录聚合酶链反应测定得到了验证。属于不同功能组的基因在整个感染周期中表现出不同的表达水平。我们观察到,先前预测的启动子基序AAATATTT以及新预测的基序与任何时间或功能类别的基因均无特异性关联,这表明其他成分参与了病毒转录的时间调控。此外,宿主转录机制发生了重大改变,许多基因被下调,包括那些与翻译过程相关的基因。本研究提供了马赛病毒转录图谱的概述。