口蹄疫病毒顺式复制元件变异与宿主易感性测定相关

H. Kang, Mi So Seong, B. Ku, J. Cheong
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摘要

口蹄疫病毒(FMDV)是小核糖核酸病毒科Aphthovirus属的一员,影响野生和家养反刍动物和猪。在FMDV RNA(核糖核酸)基因组复制过程中,FMDV编码RNA聚合酶3D以高度位置特异性的方式起作用。这表明FMDV基因组非编码区域内3D聚合酶识别的特定RNA结构有助于在复制过程中结合。其中一个区域是顺式作用复制元件(CRE),它的功能是作为RNA复制的模板。FMDV CRE采用具有扩展双茎的茎环构象,支持一个新的15-17个核苷酸环,该环从碱基堆叠相互作用中获得稳定性,CRE的确切RNA核苷酸序列产生不同的RNA二级结构。在这里,我们发现2010年至2017年在韩国分离的fmdv的CRE序列表现为A和O基因型。有趣的是,韩国FMDV RNA二级结构的变化与这些病毒之间的系统发育关系是一致的,并揭示了FMDV感染对特定宿主物种的特异性。因此,我们得出结论,韩国FMDV的每个遗传分支都具有独特的功能CRE,并且新遗传谱系的进化成功可能与新的CRE基序的发明有关。因此,我们提出CRE的特定RNA结构是FMDV根据宿主物种分类的附加标准。这些发现将有助于正确分析CRE序列,并指出未来FMDV流行的宿主物种特异性。
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Cis-acting Replication Element Variation of the Foot-and-mouth Disease Virus is Associated with the Determination of Host Susceptibility
The foot-and-mouth disease virus (FMDV), a member of the Aphthovirus genus in the Picornaviridae family, affects wild and domesticated ruminants and pigs. During replication of the FMDV RNA (ribonucleic acid) genome, FMDV-encoding RNA polymerase 3D acts in a highly location-specific manner. This suggests that specific RNA structures recognized by 3D polymerase within non-coding regions of the FMDV genome assist with binding during replication. One such region is the cis-acting replication element (CRE), which functions as a template for RNA replication. The FMDV CRE adopts a stem-loop conformation with an extended duplex stem, supporting a novel 15-17 nucleotide loop that derives stability from base-stacking interactions, with the exact RNA nucleotide sequence of the CRE producing different RNA secondary structures. Here, we show that CRE sequences of FMDVs isolated in Korea from 2010 to 2017 exhibit A and O genotypes. Interestingly, variations in the RNA secondary structure of the Korean FMDVs are consistent with the phylogenetic relationships between these viruses and reveal the specificity of FMDV infections for particular host species. Therefore, we conclude that each genetic clade of Korean FMDV is characterized by a unique functional CRE and that the evolutionary success of new genetic lineages may be associated with the invention of a novel CRE motif. Therefore, we propose that the specific RNA structure of a CRE is an additional criterion for FMDV classification dependent on the host species. These findings will help correctly analyze CRE sequences and indicate the specificity of host species for future FMDV epidemics.
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