Abstract

Upon infection, many RNA viruses reorganize their capsid for release of the genome into the host cell cytosol for replication. Often, this process is triggered by receptor binding and/or by the acidic environment in endosomes. In the genus Enterovirus, which includes more than 150 human rhinovirus (HRV) serotypes causing the common cold, there is persuasive evidence that the viral RNA exits single-stranded through channels formed in the protein shell. We have determined the time-dependent emergence of the RNA ends from HRV2 on incubation of virions at 56°C using hybridization with specific oligonucleotides and detection by fluorescence correlation spectroscopy. We report that psoralen UV crosslinking prevents complete RNA release, allowing for identification of the sequences remaining inside the capsid. We also present the structure of uncoating intermediates in which parts of the RNA are condensed and take the form of a rod that is directed roughly towards a two-fold icosahedral axis, the presumed RNA exit point. Taken together, in contrast to schemes frequently depicted in textbooks and reviews, our findings demonstrate that exit of the RNA starts from the 3′-end. This suggests that packaging also occurs in an ordered manner resulting in the 3′-poly-(A) tail becoming located close to a position of pore formation during conversion of the virion into a subviral particle. This directional genome release may be common to many icosahedral non-enveloped single-stranded RNA viruses.

Highlights

  • Human rhinoviruses (HRV), members of the picornavirus family, genus Enterovirus, are the major causative agent of the common cold

  • Because of its appealing and suggestive nature, schemes of enterovirus uncoating have long depicted the RNA as exiting at one of the five-fold axes; this model was never supported by experimental evidence

  • Exit at the 5-fold axis was brought into question by results of cryo-electron microscopy (cryo-electron microscopy (EM)) analysis of intermediate uncoating states of poliovirus [38], and of metastable complexes between HRV3 and a soluble form of its receptor ICAM-1 [39]

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Summary

Introduction

Human rhinoviruses (HRV), members of the picornavirus family, genus Enterovirus, are the major causative agent of the common cold. They play an important role in the exacerbation of asthma, cystic fibrosis, and chronic obstructive pulmonary disease [1]. The viral genome is a singlestranded RNA molecule of positive polarity, about 7100 bases in length. It carries a covalently linked peptide (VPg) at its 59-end and a poly-(A) tail of about 70 to 150 bases at its 39-end [2,3]. The 59nontranslated region is approximately 650 bases in length, highly structured, and involved in cap-independent translation initiation and RNA replication [4]

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