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Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors

机译:相互的Polydnaviruses与致病祖先共享基本的复制基因功能。

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摘要

Viruses are usually thought to form parasitic associations with hosts, but all members of the family Polydnaviridae are obligate mutualists of insects called parasitoid wasps. Phylogenetic data founded on sequence comparisons of viral genes indicate that polydnaviruses in the genus Bracovirus (BV) are closely related to pathogenic nudiviruses and baculoviruses. However, pronounced differences in the biology of BVs and baculoviruses together with high divergence of many shared genes make it unclear whether BV homologs still retain baculovirus-like functions. Here we report that virions from Microplitis demolitor bracovirus (MdBV) contain multiple baculovirus-like and nudivirus-like conserved gene products. We further show that RNA interference effectively and specifically knocks down MdBV gene expression. Coupling RNAi knockdown methods with functional assays, we examined the activity of six genes in the MdBV conserved gene set that are known to have essential roles in transcription (lef-4, lef-9), capsid assembly (vp39, vlf-1), and envelope formation (p74, pif-1) during baculovirus replication. Our results indicated that MdBV produces a baculovirus-like RNA polymerase that transcribes virus structural genes. Our results also supported a conserved role for vp39, vlf-1, p74, and pif-1 as structural components of MdBV virions. Additional experiments suggested that vlf-1 together with the nudivirus-like gene int-1 also have novel functions in regulating excision of MdBV proviral DNAs for packaging into virions. Overall, these data provide the first experimental insights into the function of BV genes in virion formation.
机译:通常认为病毒与宿主形成寄生联系,但Polydnaviridae家族的所有成员都是专一的昆虫共生者,称为寄生蜂。建立在病毒基因序列比较基础上的系统发育数据表明,Bracovirus(BV)属中的polydnaviruses与致病性nudiviruses和杆状病毒密切相关。然而,BV和杆状病毒生物学上的显着差异以及许多共享基因的高度差异使得尚不清楚BV同源物是否仍保留杆状病毒样功能。在这里,我们报告从小支原体微博克病毒(MdBV)产生的病毒体包含多个杆状病毒样和诺迪病毒样保守基因产物。我们进一步表明,RNA干扰有效且特异性地敲低了MdBV基因表达。将RNAi敲除方法与功能测定结合起来,我们检查了MdBV保守基因集中六个基因的活性,这些基因在转录(lef-4,lef-9),衣壳装配(vp39,vlf-1),和杆状病毒复制过程中的包膜形成(p74,pif-1)。我们的结果表明,MdBV产生杆状病毒样RNA聚合酶,可转录病毒结构基因。我们的结果还支持了vp39,vlf-1,p74和pif-1作为MdBV病毒体的结构成分的保守作用。额外的实验表明,vlf-1与类似纽迪克病毒的基因int-1在调节MdBV前病毒DNA的切割以包装成病毒体方面也具有新功能。总体而言,这些数据为BV基因在病毒体形成中的功能提供了初步的实验见解。

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