Hill Tom, Unckless Robert L
Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, USA
Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, USA.
J Virol. 2017 Oct 27;91(22). doi: 10.1128/JVI.01319-17. Print 2017 Nov 15.
Hosts and viruses are locked in an evolutionary arms race. Hosts are constantly evolving to suppress virulence and replication, while viruses, which are reliant on host machinery for survival and reproduction, develop counterstrategies to escape this immune defense. Viruses must also adapt to novel conditions while establishing themselves in a host species. Both processes provide strong selection for viral adaptation. Understanding adaptive evolution in insect viruses can help us to better understand adaptive evolution in general and is important due to the use of these viruses as biocontrol agents and for protecting ecologically or economically important species from outbreaks. Here we examine the molecular evolution of baculoviruses and nudiviruses, a group of insect-infecting viruses with key roles in biocontrol. We looked for signatures of selection between genomes of baculoviruses infecting a range of species and within a population of baculoviruses. Both analyses found only a few strong signatures of positive selection, primarily in replication- and transcription-associated genes and several structural protein genes. In both analyses, we detected a conserved complex of genes, including the helicase gene, showing consistently high levels of adaptive evolution, suggesting that they may be key in antagonistic coevolution to escape host suppression. These genes are integral to the baculovirus life cycle and may be good focal genes for developing baculoviruses as effective biocontrol agents or for targeting baculoviruses infecting ecologically relevant species. Recombination and complex genomes make evolution in these double-stranded DNA viruses more efficient than that in smaller RNA viruses with error-prone replication, as seen via signatures of selection in specific genes within a population of baculoviruses. Most viral evolutionary studies focus on RNA viruses. While these viruses cause many human and animal diseases, such studies leave us with a lesser understanding of how DNA viruses adapt to hosts and how the host responds to these pathogens. In this paper, we focus on the evolution of baculoviruses, a group of insect-infecting DNA viruses, many of which have been used in biocontrol. We find that most of the genome is under purifying selection, with only a few key genes evolving adaptively. Our results provide a glimpse into how DNA viruses differ from RNA viruses in their evolutionary dynamics and identify genes that are key to DNA virus adaptation, improving our understanding of how this group of pathogens evolves.
宿主与病毒处于一场进化的军备竞赛之中。宿主不断进化以抑制病毒的毒力和复制,而依赖宿主机制进行生存和繁殖的病毒则会制定应对策略以逃避这种免疫防御。病毒在宿主物种中立足时还必须适应新的环境。这两个过程都为病毒的适应性进化提供了强大的选择压力。了解昆虫病毒的适应性进化有助于我们更好地理解一般的适应性进化,而且由于这些病毒被用作生物防治剂以及用于保护具有生态或经济重要性的物种免受疫情爆发的影响,所以这一点很重要。在此,我们研究杆状病毒和裸病毒的分子进化,这是一类在生物防治中起关键作用的感染昆虫的病毒。我们在感染一系列物种的杆状病毒基因组之间以及杆状病毒种群内部寻找选择特征。两项分析都仅发现了少数强烈的正选择特征,主要存在于与复制和转录相关的基因以及几个结构蛋白基因中。在两项分析中,我们都检测到了一组保守的基因复合体,包括解旋酶基因,其显示出持续高水平的适应性进化,这表明它们可能是逃避宿主抑制的拮抗协同进化中的关键因素。这些基因对于杆状病毒的生命周期至关重要,可能是将杆状病毒开发为有效的生物防治剂或针对感染具有生态相关性物种的杆状病毒的良好重点基因。重组和复杂的基因组使这些双链DNA病毒的进化比具有易错复制的较小RNA病毒更高效,这从杆状病毒种群中特定基因的选择特征中可见一斑。大多数病毒进化研究都集中在RNA病毒上。虽然这些病毒会引发许多人类和动物疾病,但此类研究让我们对DNA病毒如何适应宿主以及宿主如何应对这些病原体的了解较少。在本文中,我们专注于杆状病毒的进化,杆状病毒是一类感染昆虫的DNA病毒,其中许多已被用于生物防治。我们发现基因组的大部分处于纯化选择之下,只有少数关键基因在进行适应性进化。我们的研究结果让我们得以一窥DNA病毒在进化动态方面与RNA病毒的不同之处,并确定了DNA病毒适应的关键基因,从而增进了我们对这一类病原体进化方式的理解。