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. 2005 Aug;79(16):10487-97.
doi: 10.1128/JVI.79.16.10487-10497.2005.

Phylogeography, population dynamics, and molecular evolution of European bat lyssaviruses

Affiliations

Phylogeography, population dynamics, and molecular evolution of European bat lyssaviruses

Patricia L Davis et al. J Virol. 2005 Aug.

Abstract

European bat lyssaviruses types 1 and 2 (EBLV-1 and EBLV-2) are widespread in Europe, although little is known of their evolutionary history. We undertook a comprehensive sequence analysis to infer the selection pressures, rates of nucleotide substitution, age of genetic diversity, geographical origin, and population growth rates of EBLV-1. Our study encompassed data from 12 countries collected over a time span of 35 years and focused on the glycoprotein (G) and nucleoprotein (N) genes. We show that although the two subtypes of EBLV-1--EBLV-1a and EBLV-1b--have both grown at a low exponential rate since their introduction into Europe, they have differing population structures and dispersal patterns. Furthermore, there were strong constraints against amino acid change in both EBLV-1 and EBLV-2, as reflected in a low ratio of nonsynonymous to synonymous substitutions per site, particularly in EBLV-1b. Our inferred rate of nucleotide substitution in EBLV-1, approximately 5 x 10(-5) substitutions per site per year, was also one of the lowest recorded for RNA viruses and implied that the current genetic diversity in the virus arose 500 to 750 years ago. We propose that the slow evolution of EBLVs reflects their distinctive epidemiology in bats, where they occupy a relatively stable fitness peak.

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Figures

FIG. 1.
FIG. 1.
Maximum-likelihood phylogenetic tree depicting the evolutionary relationships among 63 complete N gene sequences from EBLV-1 and EBLV-2 and two isolates of DUVV. Horizontal branches are drawn to scale, and the numbers at specific nodes indicate the degree of bootstrap support where it is >90%. The tree is midpoint rooted for purposes of clarity only. The “N” before each isolate name signifies the N gene.
FIG. 2.
FIG. 2.
Maximum-likelihood phylogenetic tree of 55 N gene sequences of EBLV-1. Horizontal branches are drawn to scale, and nodes with >95% bootstrap support are indicated. The tree is rooted between EBLV-1a and EBLV-1b. The “N” before each isolate name signifies the N gene.
FIG. 3.
FIG. 3.
Maximum-likelihood phylogenetic tree of 47 G gene sequences of EBLV-1. Horizontal branches are drawn to scale, and nodes with >95% bootstrap support are indicated. The tree is rooted between EBLV-1a and EBLV-1b. The “G” before each isolate name signifies the G gene.
FIG. 4.
FIG. 4.
Sampling locations of all EBLV-1 strains (G, N, and noncoding region) used in this study. EBLV-1a strains are indicated by closed stars, while EBLV-1b strains are indicated by open circles.

References

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