Abstract
HBB [2-(alpha-hydroxybenzyl)-benzimidazole] selectively inhibits RNA synthesis of most enteroviruses. However, isolation of HBB-dependent variants is possible. Sequence analysis and characterization of recombinant viruses revealed that HBB dependence maps to the nonstructural protein 2C. A single point mutation at position C(4782)U is sufficient to establish the HBB-dependent phenotype in our echovirus 9 model.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antiviral Agents / pharmacology*
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Benzimidazoles / pharmacology*
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Cloning, Molecular
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Enterovirus B, Human / drug effects*
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Enterovirus B, Human / enzymology
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Enterovirus B, Human / genetics
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Enterovirus B, Human / physiology
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Humans
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Point Mutation
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RNA Helicases / genetics*
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RNA, Viral / biosynthesis
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Viral Proteins
Substances
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Antiviral Agents
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Benzimidazoles
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RNA, Viral
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Viral Proteins
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HBBPC
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2C helicase
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RNA Helicases