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. 2011 Jul;5(7):e1231.
doi: 10.1371/journal.pntd.0001231. Epub 2011 Jul 5.

Genotype v Japanese encephalitis virus is emerging

Affiliations

Genotype v Japanese encephalitis virus is emerging

Ming-Hua Li et al. PLoS Negl Trop Dis. 2011 Jul.

Abstract

Japanese encephalitis (JE) is a global public health issue that has spread widely to more than 20 countries in Asia and has extended its geographic range to the south Pacific region including Australia. JE has become the most important cause of viral encephalitis in the world. Japanese encephalitis viruses (JEV) are divided into five genotypes, based on the nucleotide sequence of the envelope (E) gene. The Muar strain, isolated from patient in Malaya in 1952, is the sole example of genotype V JEV. Here, the XZ0934 strain of JEV was isolated from Culex tritaeniorhynchus, collected in China. The complete nucleotide and amino acid sequence of XZ0934 strain have been determined. The nucleotide divergence ranged from 20.3% to 21.4% and amino acid divergence ranged from 8.4% to 10.0% when compared with the 62 known JEV isolates that belong to genotype I-IV. It reveals low similarity between XZ0934 and genotype I-IV JEVs. Phylogenetic analysis using both complete genome and structural gene nucleotide sequences demonstrates that XZ0934 belongs to genotype V. This, in turn, suggests that genotype V JEV is emerging in JEV endemic areas. Thus, increased surveillance and diagnosis of viral encephalitis caused by genotype V JEV is an issue of great concern to nations in which JEV is endemic.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Phylogenetic analysis of XZ0934 and other JEV strains based on the nucleotide sequences.
A) complete genome; B) C gene; C) PrM gene; D) M gene; E) E gene. Phylogenetic analyses were performed by the neighbor-joining method using MEGA version 4.0.2 software package (www.megasoftware.net). The tree was rooted using Murray Valley encephalitis virus (MVEV) strain MVE-1-51 as an outgroup. Bootstrap probabilities of each node were calculated using 1000 replicates. Scale bars indicate the number of nucleotide substitutions per site.
Figure 2
Figure 2. Phylogenetic analysis of XZ0934 and other flaviviruses constructed using complete genome sequences.
Phylogenetic analyses were performed by the neighbor-joining method using MEGA version 4.0.2 software package (www.megasoftware.net). Bootstrap probabilities of each node were calculated using 1000 replicates. Scale bars indicate the number of nucleotide substitutions per site.

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