Parvoviral Host Range and Cell Entry Mechanisms

• Published in: Advances in Virus Research Vol. 70; pp. 183 - 232
• Main Authors: Cotmore, Susan F., Tattersall, Peter
• Format: Book Chapter Journal Article
• Language: English
• Published: United States Elsevier Science & Technology 2007
• Subjects: Amino Acid Sequence; Animals; Canine parvovirus; Cats; Cell Line; Dogs; Humans; Mice; Minute virus of mice; Minute Virus of Mice - chemistry; Minute Virus of Mice - pathogenicity; Minute Virus of Mice - ultrastructure; Models, Molecular; Molecular Sequence Data; Parvoviridae Infections - physiopathology; Parvoviridae Infections - virology; Parvovirus - chemistry; Parvovirus - pathogenicity; Parvovirus - ultrastructure; Parvovirus, Canine - chemistry; Parvovirus, Canine - pathogenicity; Parvovirus, Canine - ultrastructure; Rats; Species Specificity; Virion - chemistry; Virion - ultrastructure; Virology
• DOI: 10.1016/S0065-3527(07)70005-2
• ISBN: 9780123737281; 0123737281
• ISSN: 0065-3527

Parvoviruses elaborate rugged nonenveloped icosahedral capsids of ∼260 Å in diameter that comprise just 60 copies of a common core structural polypeptide. While serving as exceptionally durable shells, capable of protecting the single‐stranded DNA genome from environmental extremes, the capsid also undergoes sequential conformational changes that allow it to translocate the genome from its initial host cell nucleus all the way into the nucleus of its subsequent host. Lacking a duplex transcription template, the virus must then wait for its host to enter S‐phase before it can initiate transcription and usurp the cell's synthetic pathways. Here we review cell entry mechanisms used by parvoviruses. We explore two apparently distinct modes of host cell specificity, first that used by Minute virus of mice, where subtle glycan‐specific interactions between host receptors and residues surrounding twofold symmetry axes on the virion surface mediate differentiated cell type target specificity, while the second involves novel protein interactions with the canine transferrin receptor that allow a mutant of the feline leukopenia serotype, Canine parvovirus, to bind to and infect dog cells. We then discuss conformational shifts in the virion that accompany cell entry, causing exposure of a capsid‐tethered phospholipase A2 enzymatic core that acts as an endosomolytic agent to mediate virion translocation across the lipid bilayer into the cell cytoplasm. Finally, we discuss virion delivery into the nucleus, and consider the nature of transcriptionally silent DNA species that, escaping detection by the cell, might allow unhampered progress into S‐phase and hence unleash the parvoviral Trojan horse.