Key result
Sabin 1 vaccine strains exhibited hypermutations with preferences similar to adenosine deaminases acting on RNA (ADAR), suggesting ADARs may participate in poliovirus vaccine evolution.
Poliovirus, the causative agent of poliomyelitis, is a human enterovirus and member of the Picornaviridae family. An effective live-attenuated poliovirus vaccine strain (Sabin 1) has been developed and has protected humans from polio. However, a few cases of vaccine virulence reversion have been documented in several countries. For instance, circulating type 1 vaccine-derived poliovirus is a highly pathogenic poliovirus that evolved from an avirulent strain, but the mechanism by which vaccine strains undergo reversion remains unclear. In this study, vaccine strains exhibited A to G/U to C and G to A/C to U hypermutations in the reversed evolution of Sabin 1. Furthermore, the mutation ratios of U to C and C to U were higher than those of other mutation types. Dinucleotide editing context was then analyzed. Results showed that A to G and U to C mutations exhibited preferences similar to adenosine deaminases acting on RNA (ADAR). Hence, ADARs may participate in poliovirus vaccine evolution.
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Liu et al. (2014) studied Poliovirus. Adenosine deaminases acting on RNA (ADAR) was evaluated on Mutation ratios and dinucleotide editing context. Sabin 1 vaccine strains exhibited hypermutations with preferences similar to adenosine deaminases acting on RNA (ADAR), suggesting ADARs may participate in poliovirus vaccine evolution.
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