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. 2011 Aug;17(8):1498-501.
doi: 10.3201/eid1708.110077.

Bagaza virus in partridges and pheasants, Spain, 2010

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Bagaza virus in partridges and pheasants, Spain, 2010

Montserrat Agüero et al. Emerg Infect Dis. 2011 Aug.

Abstract

In September 2010, an unusually high number of wild birds (partridges and pheasants) died in Cádiz in southwestern Spain. Reverse transcription PCR and virus isolation detected flavivirus infections. Complete nucleotide sequence analysis identified Bagaza virus, a flavivirus with a known distribution that includes sub-Saharan Africa and India, as the causative agent.

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Figures

Figure 1
Figure 1
Phylogenetic relationships between a full-length genomic sequence for Bagaza virus identified in Cádiz, Spain, 2010 (solid circle) and 32 full-length flavivirus sequences, including 2 Bagaza virus isolates from GenBank. The phylogenetic tree was inferred by using the maximum-likelihood method. Percentage of 500 successful bootstrap replicates is indicated at the nodes. Evolutionary distances were computed by using the optimal general time reversible + Γ + proportion invariant model. A discrete Γ distribution was used to model evolutionary rate differences among sites (5 categories, G parameter = 2.0552). The rate variation model enabled some sites to be evolutionarily invariable (+I, 10.1524% sites). The tree is drawn to scale, and branch lengths are indicated as number of nucleotide substitutions per site. There were 9,803 positions in the final dataset. Phylogenetic analyses were conducted by using MEGA5 (www.megasoftware.net). GenBank accession numbers are indicated beside each isolate/strain name.
Figure 2
Figure 2
Phylogenetic relationships between partial envelope protein–coding gene sequence for Bagaza virus identified in Cádiz, Spain, 2010 (solid circle) and 38 equivalent flavivirus nucleotide sequences, including those for 3 Bagaza virus isolates, 1 Israel turkey meningoencephalitis virus, 1 Ntaya virus, and 2 Tembusu viruses from GenBank. The phylogenetic tree was inferred by using the maximum-likelihood method. Percentage of 500 successful bootstrap replicates is indicated at the nodes. The optimal Tamura-Nei with Γ distribution model was selected to compute evolutionary distances. A discrete Γ distribution was used to model evolutionary rate differences among sites (5 categories, G parameter = 1.8944). The tree is drawn to scale, and branch lengths are indicated as number of nucleotide substitutions per site. There were 941 positions in the final dataset. Phylogenetic analyses were conducted by using MEGA5 (www.megasoftware.net). GenBank accession numbers are indicated beside each isolate/strain name.

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