Department of Medical Microbiology & Immunology and Li Ka Shing Institute of Virology, University of Alberta, Edmonton, Alberta, Canada.
J Virol. 2014 May;88(10):5277-86. doi: 10.1128/JVI.00022-14. Epub 2014 Feb 26.
Recombination plays a critical role in virus evolution. It helps avoid genetic decline and creates novel phenotypes. This promotes survival, and genome sequencing suggests that recombination has facilitated the evolution of human pathogens, including orthopoxviruses such as variola virus. Recombination can also be used to map genes, but although recombinant poxviruses are easily produced in culture, classical attempts to map the vaccinia virus (VACV) genome this way met with little success. We have sequenced recombinants formed when VACV strains TianTan and Dryvax are crossed under different conditions. These were a single round of growth in coinfected cells, five rounds of sequential passage, or recombinants obtained using leporipoxvirus-mediated DNA reactivation. Our studies showed that recombinants contain a patchwork of DNA, with the number of exchanges increasing with passage. Further passage also selected for TianTan DNA and correlated with increased plaque size. The recombinants produced through a single round of coinfection contain a disproportionate number of short conversion tracks (<1 kbp) and exhibited 1 exchange per 12 kbp, close to the ∼1 per 8 kbp in the literature. One by-product of this study was that rare mutations were also detected; VACV replication produces ∼1×10(-8) mutation per nucleotide copied per cycle of replication and ∼1 large (21 kbp) deletion per 70 rounds of passage. Viruses produced using DNA reactivation appeared no different from recombinants produced using ordinary methods. An attractive feature of this approach is that when it is combined with selection for a particular phenotype, it provides a way of mapping and dissecting more complex virus traits.
When two closely related viruses coinfect the same cell, they can swap genetic information through a process called recombination. Recombination produces new viruses bearing different combinations of genes, and it plays an important role in virus evolution. Poxviruses are a family of viruses that includes variola (or smallpox) virus, and although poxviruses are known to recombine, no one has previously mapped the patterns of DNAs exchanged between viruses. We coinfected cells with two different vaccinia poxviruses, isolated the progeny, and sequenced them. We show that poxvirus recombination is a very accurate process that assembles viruses containing DNA copied from both parents. In a single round of infection, DNA is swapped back and forth ∼18 times per genome to make recombinant viruses that are a mosaic of the two parental DNAs. This mixes many different genes in complex combinations and illustrates how recombination can produce viruses with greatly altered disease potential.
重组在病毒进化中起着关键作用。它有助于避免遗传衰退并创造新的表型。这促进了生存,基因组测序表明,重组促进了人类病原体的进化,包括正痘病毒(如天花病毒)。重组也可用于基因定位,但尽管在培养物中很容易产生重组痘病毒,但以这种方式对牛痘病毒(VACV)基因组进行经典定位尝试的成功率却很低。我们已经对在不同条件下交叉的天坛株和干燥株进行了测序,这些是在共感染细胞中进行的一轮生长,五轮连续传代,或者使用兔痘病毒介导的 DNA 再激活获得的重组体。我们的研究表明,重组体包含 DNA 的拼凑,随着传代次数的增加,交换的数量也会增加。进一步的传代还选择了天坛株 DNA,并与斑块大小的增加相关。通过一轮共感染产生的重组体包含不成比例数量的短转换轨迹(<1 kbp),并表现出每 12 kbp 交换 1 次,接近文献中的每 8 kbp 交换 1 次。这项研究的一个副产品是还检测到了罕见的突变;VACV 复制在每个复制周期中产生约 1×10(-8)个核苷酸拷贝的突变,并且在 70 轮传代中产生约 1 个大(21 kbp)缺失。使用 DNA 再激活产生的病毒与使用普通方法产生的重组体没有区别。这种方法的一个吸引人的特点是,当它与特定表型的选择结合使用时,它为绘制和剖析更复杂的病毒特征提供了一种方法。
当两种密切相关的病毒共同感染同一细胞时,它们可以通过称为重组的过程交换遗传信息。重组产生了带有不同基因组合的新病毒,并且在病毒进化中起着重要作用。正痘病毒是包括天花病毒在内的病毒家族,尽管已知正痘病毒会发生重组,但以前没有人对病毒之间交换的 DNA 模式进行过定位。我们用两种不同的牛痘病毒共感染细胞,分离出后代并对其进行了测序。我们表明,痘病毒重组是一个非常准确的过程,它组装了包含来自双亲 DNA 的病毒。在一轮感染中,每个基因组之间来回交换 DNA 约 18 次,从而产生了由两种亲本 DNA 组成的嵌合体重组病毒。这将许多不同的基因混合在一起,并说明了重组如何产生具有大大改变的疾病潜力的病毒。