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2
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Future Med Chem. 2017 Apr;9(6):541-552. doi: 10.4155/fmc-2016-0233. Epub 2017 Apr 12.
3
Interactions between the Dengue Virus Polymerase NS5 and Stem-Loop A.登革病毒聚合酶NS5与茎环A之间的相互作用
J Virol. 2017 May 12;91(11). doi: 10.1128/JVI.00047-17. Print 2017 Jun 1.
4
Viral RNA switch mediates the dynamic control of flavivirus replicase recruitment by genome cyclization.病毒RNA开关通过基因组环化介导黄病毒复制酶募集的动态控制。
Elife. 2016 Oct 1;5:e17636. doi: 10.7554/eLife.17636.
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Dengue Hemorrhagic Fever at 60 Years: Early Evolution of Concepts of Causation and Treatment.登革出血热60年:病因与治疗概念的早期演变
Microbiol Mol Biol Rev. 2015 Sep;79(3):281-91. doi: 10.1128/MMBR.00009-15.
6
Dengue serotype-specific differences in clinical manifestation, laboratory parameters and risk of severe disease in adults, singapore.新加坡成年人登革热血清型在临床表现、实验室参数及重症疾病风险方面的差异
Am J Trop Med Hyg. 2015 May;92(5):999-1005. doi: 10.4269/ajtmh.14-0628. Epub 2015 Mar 30.
7
Clustal omega.Clustal欧米伽
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10
Differential RNA sequence requirement for dengue virus replication in mosquito and mammalian cells.登革病毒在蚊源和哺乳细胞中复制的差异 RNA 序列需求。
J Virol. 2013 Aug;87(16):9365-72. doi: 10.1128/JVI.00567-13. Epub 2013 Jun 12.

登革热病毒基因组环化元件中的RNA二级结构变异及其在致病性方面的潜在影响。

The RNA secondary structural variation in the cyclization elements of the dengue genome and the possible implications in pathogenicity.

作者信息

Mishra Bibhudutta, Balaji Advait, Beesetti Hemalatha, Swaminathan Sathyamangalam, Aduri Raviprasad

机构信息

Department of Biological Sciences, Birla Institute of Technology and Science, Pilani, K K Birla Goa Campus, Zuarinagar, South Goa, Goa 403 726 India.

Department of Biological Sciences, Birla Institute of Technology and Science, Pilani, Hyderabad Campus, Jawahar Nagar, Shameerpet Mandal, Hyderabad, Telangana 500 078 India.

出版信息

Virusdisease. 2020 Sep;31(3):299-307. doi: 10.1007/s13337-020-00615-w. Epub 2020 Jul 30.

DOI:10.1007/s13337-020-00615-w
PMID:32904896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7458965/
Abstract

Dengue virus (DENV), the causative agent of dengue fever and severe dengue, exists as four antigenically different serotypes. These serotypes are further classified into genotypes and have varying degrees of pathogenicity. The 5' and 3' ends of the genomic RNA play a critical role in the viral life cycle. A global scale study of the RNA structural variation among the sero- and genotypes was carried out to correlate RNA structure with pathogenicity. We found that the GC rich stem and rigid loop structure of the 5' end of the genomic RNA of DENV 2 differs significantly from the others. The observed variation in base composition and base pairing may confer structural and functional advantage in highly virulent strains. This variation in the structure may influence the ease of cyclization and recruitment of viral RNA polymerase, NS5 RdRp, thereby affecting the pathogenicity of these strains.

摘要

登革病毒(DENV)是登革热和重症登革热的病原体,有四种抗原性不同的血清型。这些血清型进一步分为基因型,且具有不同程度的致病性。基因组RNA的5'端和3'端在病毒生命周期中起关键作用。开展了一项关于血清型和基因型之间RNA结构变异的全球规模研究,以关联RNA结构与致病性。我们发现,登革病毒2型基因组RNA 5'端富含GC的茎环结构与其他血清型和基因型显著不同。观察到的碱基组成和碱基配对的变化可能赋予高毒力毒株结构和功能上的优势。这种结构变化可能会影响病毒RNA环化的难易程度以及病毒RNA聚合酶NS5 RdRp的募集,从而影响这些毒株的致病性。