Genetic and Phenotypic Variation of Foot-and-Mouth Disease Virus during Serial Passages in a Natural Host
Open Access
- 15 October 2007
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 81 (20) , 11341-11351
- https://doi.org/10.1128/jvi.00930-07
Abstract
Foot-and-mouth disease virus (FMDV), like other RNA viruses, exhibits high mutation rates during replication that have been suggested to be of adaptive value. However, even though genetic variation in RNA viruses and, more specifically, FMDV has been extensively examined during virus replication in a wide variety of in vitro cell cultures, very little is known regarding the generation and effects of genetic variability of virus replication in the natural host under experimental conditions and no genetic data are available regarding the effects of serial passage in natural hosts. Here, we present the results of 20 serial contact transmissions of the highly pathogenic, pig-adapted O Taiwan 97 (O Tw97) isolate of FMDV in swine. We examined the virus genomic consensus sequences for a total of 37 full-length viral genomes recovered from 20 in vivo passages. The characteristics and distributions of changes in the sequences during the series of pig infections were analyzed in comparison to the O Tw97 genomes recovered from serially infected BHK-21 cell cultures. Unexpectedly, a significant reduction of virulence upon pig passages was observed, and finally, interruption of the viral transmission chain occurred after the14th pig passage (T14). Virus was, however, isolated from the tonsils and nasal swabs of the asymptomatic T15 pigs at 26 days postcontact, consistent with a natural establishment of the carrier state previously described only for ruminants. Surprisingly, the region encoding the capsid protein VP1 (1D) did not show amino acid changes during in vivo passages. These data demonstrate that contact transmission of FMDV O Tw97 in pigs mimics the fitness loss induced by the bottleneck effect, which was previously observed by others during plaque-to-plaque FMDV passage in vitro, suggesting that unknown mechanisms of virulence recovery might be necessary during the evolution and perpetuation of FMDV in nature.Keywords
This publication has 59 references indexed in Scilit:
- Recombination Patterns in Aphthoviruses Mirror Those Found in Other PicornavirusesJournal of Virology, 2006
- Molecular Epidemiology of the Foot-and-Mouth Disease Virus Outbreak in the United Kingdom in 2001Journal of Virology, 2006
- Increased Fidelity Reduces Poliovirus Fitness and Virulence under Selective Pressure in MicePLoS Pathogens, 2005
- Action of mutagenic agents and antiviral inhibitors on foot-and-mouth disease virusVirus Research, 2004
- PrefaceVirus Research, 2003
- Ribavirin Causes Error Catastrophe during Hantaan Virus ReplicationJournal of Virology, 2003
- Resistance to extinction of low fitness virus subjected to plaque-to-plaque transfers: diversification by mutation clusteringJournal of Molecular Biology, 2002
- Efficient Virus Extinction by Combinations of a Mutagen and Antiviral InhibitorsJournal of Virology, 2001
- EFFECT OF DELETERIOUS MUTATION-ACCUMULATION ON THE FITNESS OF RNA BACTERIOPHAGE MS2Evolution, 2000
- Genetic Lesions Associated with Muller's Ratchet in an RNA VirusJournal of Molecular Biology, 1996