4.6 Article

RNA Structure in the 5' Untranslated Region of Enterovirus D68 Strains with Differing Neurovirulence Phenotypes

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VIRUSES-BASEL
卷 15, 期 2, 页码 -

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MDPI
DOI: 10.3390/v15020295

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5 ' untranslated region; enterovirus D68; RNA structure; internal ribosome entry site; neurovirulence

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In this study, the secondary and tertiary structures of EV-D68 5'UTR RNA were analyzed and compared. Significant changes in secondary structures were observed in domains II, IV, and V of the 2014 isolate KT347251.1 compared to the historical Fermon strain. These structure variations may be related to the neurovirulence of EV-D68 and provide potential targets for the treatment of neurotropic enteroviruses.
Enterovirus-D68 (EV-D68) is a positive-sense single-stranded RNA virus within the family Picornaviridae. EV-D68 was initially considered a respiratory virus that primarily affected children. However, in 2014, EV-D68 outbreaks occurred causing the expected increase in respiratory illness cases, but also an increase in acute flaccid myelitis cases (AFM). Sequencing of 2014 outbreak isolates revealed variations in the 5 & PRIME; UTR of the genome compared to the historical Fermon strain. The structure of the 5 & PRIME; UTR RNA contributes to enterovirus virulence, including neurovirulence in poliovirus, and could contribute to neurovirulence in contemporary EV-D68 strains. In this study, the secondary and tertiary structures of 5 ' UTR RNA from the Fermon strain and 2014 isolate KT347251.1 are analyzed and compared. Secondary structures were determined using SHAPE-MaP and TurboFold II and tertiary structures were predicted using 3dRNAv2.0. Comparison of RNA structures between the EV-D68 strains shows significant remodeling at the secondary and tertiary levels. Notable secondary structure changes occurred in domains II, IV and V. Shifts in the secondary structure changed the tertiary structure of the individual domains and the orientation of the domains. Our comparative structural models for EV-D68 5 & PRIME; UTR RNA highlight regions of the molecule that could be targeted for treatment of neurotropic enteroviruses.

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