Increased Fidelity Reduces Poliovirus Fitness and Virulence under Selective Pressure in Mice

RNA viruses have high error rates, and the resulting quasispecies may aid survival of the virus population in the presence of selective pressure. Therefore, it has been theorized that RNA viruses require high error rates for survival, and that a virus with high fidelity would be less able to cope in complex environments. We previously isolated and characterized poliovirus with a mutation in the viral polymerase, 3D-G64S, which confers resistance to mutagenic nucleotide analogs via increased fidelity. The 3D-G64S virus was less pathogenic than wild-type virus in poliovirus-receptor transgenic mice, even though only slight growth defects were observed in tissue culture. To determine whether the high-fidelity phenotype of the 3D-G64S virus could decrease its fitness under a defined selective pressure, we compared growth of the 3D-G64S virus and 3D wild-type virus in the context of a revertible attenuating point mutation, 2C-F28S. Even with a 10-fold input advantage, the 3D-G64S virus was unable to compete with 3D wild-type virus in the context of the revertible attenuating mutation; however, in the context of a non-revertible version of the 2C-F28S attenuating mutation, 3D-G64S virus matched the replication of 3D wild-type virus. Therefore, the 3D-G64S high-fidelity phenotype reduced viral fitness under a defined selective pressure, making it likely that the reduced spread in murine tissue could be caused by the increased fidelity of the viral polymerase.

[1]  D. Baltimore,et al.  Molecular cloning of poliovirus cDNA and determination of the complete nucleotide sequence of the viral genome. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[2]  B. Stocker,et al.  Colonization of the mouse intestine by an avirulent Salmonella typhimurium strain and its lipopolysaccharide-defective mutants , 1985, Infection and immunity.

[3]  K. Kirkegaard,et al.  The mechanism of RNA recombination in poliovirus , 1986, Cell.

[4]  F. Costantini,et al.  Transgenic mice expressing a human poliovirus receptor: A new model for poliomyelitis , 1990, Cell.

[5]  Succession of mutations in the Sabin strain of type 3 poliovirus replicating in the central nervous system of monkeys. , 1996, Virology.

[6]  E. Domingo,et al.  RNA virus mutations and fitness for survival. , 1997, Annual review of microbiology.

[7]  E. Domingo,et al.  RNA virus fitness , 1997, Reviews in medical virology.

[8]  R. Connor,et al.  Change in Coreceptor Use Correlates with Disease Progression in HIV-1–Infected Individuals , 1997, The Journal of experimental medicine.

[9]  M. Georgescu,et al.  Random selection: a model for poliovirus infection of the central nervous system. , 1997, The Journal of general virology.

[10]  A. Nomoto,et al.  Retrograde transport of intact poliovirus through the axon via the fast transport system. , 1998, Virology.

[11]  J. Drake,et al.  Rates of spontaneous mutation. , 1998, Genetics.

[12]  A. Sylwester,et al.  Evidence for the HIV-1 phenotype switch as a causal factor in acquired immunodeficiency , 1998, Nature Medicine.

[13]  S. Rubino,et al.  Role of the Salmonella abortusovis virulence plasmid in the infection of BALB/c mice. , 2000, FEMS microbiology letters.

[14]  J. Arnold,et al.  The broad-spectrum antiviral ribonucleoside ribavirin is an RNA virus mutagen , 2000, Nature Medicine.

[15]  A. Nomoto,et al.  Recent insights into poliovirus pathogenesis. , 2001, Trends in microbiology.

[16]  C. Cameron,et al.  RNA virus error catastrophe: Direct molecular test by using ribavirin , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[17]  R. Andino,et al.  Poliovirus pathogenesis in a new poliovirus receptor transgenic mouse model: age-dependent paralysis and a mucosal route of infection. , 2002, The Journal of general virology.

[18]  Julie K. Pfeiffer,et al.  A single mutation in poliovirus RNA-dependent RNA polymerase confers resistance to mutagenic nucleotide analogs via increased fidelity , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[19]  J. Stringer,et al.  Diversity at the Locus Associated with Transcription of a Variable Surface Antigen of Pneumocystis carinii as an Index of Population Structure and Dynamics in Infected Rats , 2003, Infection and Immunity.

[20]  Hongye Li,et al.  Genetic Bottlenecks Reduce Population Variation in an Experimental RNA Virus Population , 2004, Journal of Virology.

[21]  T. Hovi,et al.  Evolution of wild-type 1 poliovirus in two healthy siblings excreting the virus over a period of 6 months. , 2004, The Journal of general virology.

[22]  H. Yonekawa,et al.  Characterization of three different transgenic mouse lines that carry human poliovirus receptor gene—influence of the transgene expression on pathogenesis , 2005, Archives of Virology.

[23]  M. Vignuzzi,et al.  Remote Site Control of an Active Site Fidelity Checkpoint in a Viral RNA-dependent RNA Polymerase* , 2005, Journal of Biological Chemistry.

[24]  Manfred Eigen,et al.  The error threshold. , 2005, Virus research.

[25]  K. Kirkegaard,et al.  Trans-dominant inhibition of RNA viral replication can slow growth of drug-resistant viruses , 2005, Nature Genetics.