Pfeiffer Julie K, Kirkegaard Karla
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California, USA.
PLoS Pathog. 2005 Oct;1(2):e11. doi: 10.1371/journal.ppat.0010011. Epub 2005 Oct 7.
RNA viruses have high error rates, and the resulting quasispecies may aid survival of the virus population in the presence of selective pressure. Therefore, it has been theorized that RNA viruses require high error rates for survival, and that a virus with high fidelity would be less able to cope in complex environments. We previously isolated and characterized poliovirus with a mutation in the viral polymerase, 3D-G64S, which confers resistance to mutagenic nucleotide analogs via increased fidelity. The 3D-G64S virus was less pathogenic than wild-type virus in poliovirus-receptor transgenic mice, even though only slight growth defects were observed in tissue culture. To determine whether the high-fidelity phenotype of the 3D-G64S virus could decrease its fitness under a defined selective pressure, we compared growth of the 3D-G64S virus and 3D wild-type virus in the context of a revertible attenuating point mutation, 2C-F28S. Even with a 10-fold input advantage, the 3D-G64S virus was unable to compete with 3D wild-type virus in the context of the revertible attenuating mutation; however, in the context of a non-revertible version of the 2C-F28S attenuating mutation, 3D-G64S virus matched the replication of 3D wild-type virus. Therefore, the 3D-G64S high-fidelity phenotype reduced viral fitness under a defined selective pressure, making it likely that the reduced spread in murine tissue could be caused by the increased fidelity of the viral polymerase.
RNA病毒具有很高的错误率,由此产生的准种可能有助于病毒群体在选择性压力存在的情况下存活。因此,从理论上来说,RNA病毒需要高错误率才能生存,而具有高保真度的病毒在复杂环境中的应对能力会较弱。我们之前分离并鉴定了一种在病毒聚合酶中发生突变的脊髓灰质炎病毒,即3D-G64S,它通过提高保真度赋予了对诱变核苷酸类似物的抗性。在脊髓灰质炎病毒受体转基因小鼠中,3D-G64S病毒的致病性低于野生型病毒,尽管在组织培养中仅观察到轻微的生长缺陷。为了确定3D-G64S病毒的高保真表型在特定的选择性压力下是否会降低其适应性,我们在一个可回复的减毒点突变2C-F28S的背景下比较了3D-G64S病毒和3D野生型病毒的生长情况。即使具有10倍的初始优势,在可回复的减毒突变背景下,3D-G64S病毒仍无法与3D野生型病毒竞争;然而,在2C-F28S减毒突变的不可回复版本的背景下,3D-G64S病毒的复制与3D野生型病毒相当。因此,3D-G64S的高保真表型在特定的选择性压力下降低了病毒的适应性,这使得其在鼠类组织中传播减少很可能是由病毒聚合酶保真度的提高所致。