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Comparative Genomics of Foot-and-mouth Disease Virus

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Journal J Virol
Date 2005 Apr 29
PMID 15858032
Citations 221
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Abstract

Here we present complete genome sequences, including a comparative analysis, of 103 isolates of foot-and-mouth disease virus (FMDV) representing all seven serotypes and including the first complete sequences of the SAT1 and SAT3 genomes. The data reveal novel highly conserved genomic regions, indicating functional constraints for variability as well as novel viral genomic motifs with likely biological relevance. Previously undescribed invariant motifs were identified in the 5' and 3' untranslated regions (UTR), as was tolerance for insertions/deletions in the 5' UTR. Fifty-eight percent of the amino acids encoded by FMDV isolates are invariant, suggesting that these residues are critical for virus biology. Novel, conserved sequence motifs with likely functional significance were identified within proteins L(pro), 1B, 1D, and 3C. An analysis of the complete FMDV genomes indicated phylogenetic incongruities between different genomic regions which were suggestive of interserotypic recombination. Additionally, a novel SAT virus lineage containing nonstructural protein-encoding regions distinct from other SAT and Euroasiatic lineages was identified. Insights into viral RNA sequence conservation and variability and genetic diversity in nature will likely impact our understanding of FMDV infections, host range, and transmission.

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References
1.
Knowles N, Samuel A . Molecular epidemiology of foot-and-mouth disease virus. Virus Res. 2003; 91(1):65-80. DOI: 10.1016/s0168-1702(02)00260-5. View

2.
Murray K, Barton D . Poliovirus CRE-dependent VPg uridylylation is required for positive-strand RNA synthesis but not for negative-strand RNA synthesis. J Virol. 2003; 77(8):4739-50. PMC: 152113. DOI: 10.1128/jvi.77.8.4739-4750.2003. View

3.
Mason P, Pacheco J, Zhao Q, Knowles N . Comparisons of the complete genomes of Asian, African and European isolates of a recent foot-and-mouth disease virus type O pandemic strain (PanAsia). J Gen Virol. 2003; 84(Pt 6):1583-1593. DOI: 10.1099/vir.0.18669-0. View

4.
Hofacker I . Vienna RNA secondary structure server. Nucleic Acids Res. 2003; 31(13):3429-31. PMC: 169005. DOI: 10.1093/nar/gkg599. View

5.
Paul A, Yin J, Mugavero J, Rieder E, Liu Y, Wimmer E . A "slide-back" mechanism for the initiation of protein-primed RNA synthesis by the RNA polymerase of poliovirus. J Biol Chem. 2003; 278(45):43951-60. DOI: 10.1074/jbc.M307441200. View