Short CommunicationsCharacterization of Poliovirus Conformational Alteration Mediated by Soluble Cell Receptors
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Role of class I human leukocyte antigen molecules in early steps of echovirus infection of rhabdomyosarcoma cells
2008, VirologyCitation Excerpt :The interaction between sDAF and EV7 is reversible and does not lead to the formation of A-particles (Powell et al., 1997). In contrast, the interaction of human rhinovirus 14 and the soluble form of its receptor (intercellular adhesion molecule-1: ICAM-1) or of poliovirus and the soluble poliovirus receptor (PVR, CD155) induces irreversible conformational changes leading to the formation of A-particles, suggesting that these viruses do not need additional determinants at the cell surface (Casasnovas and Springer, 1994; Gomez Yafal et al., 1993). Recent reports have suggested that β2-microglobulin (β2m) and CD59 — a GPI-anchored protein that regulates the complement cascade at a later stage than DAF — may also play a role as a coreceptor in the infectious cycle of EV7 (Goodfellow et al., 2000; Ward et al., 1998).
New (fluorescent) light on poliovirus entry
2008, Trends in MicrobiologyCitation Excerpt :It is conceivable that entry of the virion (as distinct from the RNA genome) is not required at all. After contact with soluble poliovirus receptor (PVR) in vitro, poliovirus undergoes conformational changes that culminate in release of RNA [12–14]. Hydrophobic domains within capsid proteins become exposed, and interact with membranes to form pores that might facilitate RNA transfer across the membrane [15].
Release of canine parvovirus from endocytic vesicles
2003, VirologyRecent insights into poliovirus pathogenesis
2001, Trends in Microbiology