Key result
Structural and modeling studies of the enterovirus 5' cloverleaf RNA and associated virus proteins provide insight into the replication mechanism and potential targets for inhibition.
Structural analysis of enterovirus RNA and proteins provides insights into viral replication mechanisms and potential targets for inhibition.
Reveals conserved oriL platform for enterovirus replication; leaves open pan-serotype antiviral targeting.
Although enteroviruses are associated with a wide variety of diseases and conditions, their mode of replication is well conserved. Their genome is carried as a single, positive-sense RNA strand. At the 5' end of the strand is an approximately 90-nucleotide self-complementary region called the 5' cloverleaf, or the oriL. This noncoding region serves as a platform upon which host and virus proteins, including the 3B, 3C, and 3D virus proteins, assemble in order to initiate replication of a negative-sense RNA strand. The negative strand in turn serves as a template for synthesis of multiple positive-sense RNA strands. Building on structural studies of individual RNA stem-loops, the structure of the intact 5' cloverleaf from rhinovirus has recently been determined via nuclear magnetic resonance/small-angle X-ray scattering (NMR/SAXS)-based methods, while structures have also been determined for enterovirus 3A, 3B, 3C, and 3D proteins. Analysis of these structures, together with structural and modeling studies of interactions between host and virus proteins and RNA, has begun to provide insight into the enterovirus replication mechanism and the potential to inhibit replication by blocking these interactions.
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Pascal et al. (2020) conducted a review in Enterovirus infection. Structural and modeling studies of the enterovirus 5' cloverleaf RNA and associated virus proteins provide insight into the replication mechanism and potential targets for inhibition.
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