Mark Denison
Last active: 2/22/2016

A live, impaired-fidelity coronavirus vaccine protects in an aged, immunocompromised mouse model of lethal disease.

Graham RL, Becker MM, Eckerle LD, Bolles M, Denison MR, Baric RS
Nat Med. 2012 18 (12): 1820-6

PMID: 23142821 · PMCID: PMC3518599 · DOI:10.1038/nm.2972

Live, attenuated RNA virus vaccines are efficacious but subject to reversion to virulence. Among RNA viruses, replication fidelity is recognized as a key determinant of virulence and escape from antiviral therapy; increased fidelity is attenuating for some viruses. Coronavirus (CoV) replication fidelity is approximately 20-fold greater than that of other RNA viruses and is mediated by a 3'→5' exonuclease (ExoN) activity that probably functions in RNA proofreading. In this study we demonstrate that engineered inactivation of severe acute respiratory syndrome (SARS)-CoV ExoN activity results in a stable mutator phenotype with profoundly decreased fidelity in vivo and attenuation of pathogenesis in young, aged and immunocompromised mice. The ExoN inactivation genotype and mutator phenotype are stable and do not revert to virulence, even after serial passage or long-term persistent infection in vivo. ExoN inactivation has potential for broad applications in the stable attenuation of CoVs and, perhaps, other RNA viruses.

MeSH Terms (19)

Age Factors Animals Base Sequence DNA Primers Drug Design Exoribonucleases Female Immunocompromised Host Mice Mice, Inbred BALB C Molecular Sequence Data Plasmids Real-Time Polymerase Chain Reaction SARS Virus Sequence Analysis, DNA Severe Acute Respiratory Syndrome Statistics, Nonparametric Viral Vaccines Virus Replication

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