Picornavirus Morphogenesis
Author(s) -
Ping Jiang,
Ying Liu,
Hsin-Chieh Ma,
Aniko V. Paul,
Eckard Wimmer
Publication year - 2014
Publication title -
microbiology and molecular biology reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.358
H-Index - 247
eISSN - 1098-5557
pISSN - 1092-2172
DOI - 10.1128/mmbr.00012-14
Subject(s) - picornavirus , biology , picornaviridae , rna , translation (biology) , computational biology , viral life cycle , morphogenesis , genetics , ribosome , mechanism (biology) , genome , rna binding protein , virology , viral replication , capsid , microbiology and biotechnology , non coding rna , nucleic acid structure , helicase , model organism , virus , rna virus , viral evolution
SUMMARY ThePicornaviridae represent a large family of small plus-strand RNA viruses that cause a bewildering array of important human and animal diseases. Morphogenesis is the least-understood step in the life cycle of these viruses, and this process is difficult to study because encapsidation is tightly coupled to genome translation and RNA replication. Although the basic steps of assembly have been known for some time, very few details are available about the mechanism and factors that regulate this process. Most of the information available has been derived from studies of enteroviruses, in particular poliovirus, where recent evidence has shown that, surprisingly, the specificity of encapsidation is governed by a viral protein-protein interaction that does not involve an RNA packaging signal. In this review, we make an attempt to summarize what is currently known about the following topics: (i) encapsidation intermediates, (ii) the specificity of encapsidation (iii), viral and cellular factors that are required for encapsidation, (iv) inhibitors of encapsidation, and (v) a model of enterovirus encapsidation. Finally, we compare some features of picornavirus morphogenesis with those of other plus-strand RNA viruses.
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