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doi: 10.1371/journal.pone.0055165. Epub 2013 Feb 4.

Molecular detection and genotyping of Japanese encephalitis virus in mosquitoes during a 2010 outbreak in the Republic of Korea

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Molecular detection and genotyping of Japanese encephalitis virus in mosquitoes during a 2010 outbreak in the Republic of Korea

Hyun-Ji Seo et al. PLoS One. 2013.

Abstract

Japanese encephalitis virus (JEV), a mosquito-borne zoonotic pathogen, is one of the major causes of viral encephalitis. To reduce the impact of Japanese encephalitis among children in the Republic of Korea (ROK), the government established a mandatory vaccination program in 1967. Through the efforts of this program only 0-7 (mean 2.1) cases of Japanese encephalitis were reported annually in the ROK during the period of 1984-2009. However, in 2010 there was an outbreak of 26 confirmed cases of Japanese encephalitis, including 7 deaths. This represented a >12-fold increase in the number of confirmed cases of Japanese encephalitis in the ROK as compared to the mean number reported over the last 26 years and a 3.7-fold increase over the highest annual number of cases during this same period (7 cases). Surveillance of adult mosquitoes was conducted during the 2010 outbreak of Japanese encephalitis in the ROK. A total of 6,328 culicine mosquitoes belonging to 12 species from 5 genera were collected at 6 survey sites from June through October 2010 and assayed by reverse-transcription polymerase chain reaction (RT-PCR) for the presence of JEV. A total of 34/371 pooled samples tested positive for JEV (29/121 Culex tritaeniorhynchus, 4/64 Cx. pipiens, and 1/26 Cx. bitaeniorhynchus) as confirmed by sequencing of the pre-membrane and envelope protein coding genes. The maximum likelihood estimates of JEV positive individuals per 1,000 culicine vectors for Cx. tritaeniorhynchus, Cx. pipiens, and Cx. bitaeniorhynchus were 11.8, 5.6, and 2.8, respectively. Sequences of the JEV pre-membrane and envelope protein coding genes amplified from the culicine mosquitoes by RT-PCR were compared with those of JEV genotypes I-V. Phylogenetic analyses support the detection of a single genotype (I) among samples collected from the ROK in 2010.

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Conflict of interest statement

Competing Interests: SGK are employed by Korea Racing Authority; AMR is employed by Alaska Science Center. There are no patents, products in development or marketed products to declare. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.

Figures

Figure 1
Figure 1. Clinical cases and deaths of Japanese encephalitis in Republic of Korea, 1984–2010.
Figure is based on data provided by the Korea Center for Disease Control and Prevention, 2011.
Figure 2
Figure 2. Collection sites and of Japanese encephalitis virus-positive pools, Republic of Korea, 2010.
Abbreviations in parentheses indicate the number of Japanese encephalitis virus-positive pools by mosquito species.
Figure 3
Figure 3. Phylogenetic tree illustrating the genetic relationship of nucleotide sequences for pre-membrane protein genes of Japanese encephalitis virus (JEV) strains identified in mosquitoes, Republic of Korea, 2010 (indicated in bold font) and reference sequences from other geographic regions as reported on GenBank.
Genotypes of JEV strains are indicated on the right of the phylogenetic tree and were assigned according to Chen et al. , . Bootstrap support values are shown. The scale bar indicates the number of mutations. Abbreviations for strains reported in this study are as follows: K10CT = Republic of Korea (ROK), 2010, Culex tritaeniorhynchus; K10CB = ROK, 2010, Culex bitaeniorhynchus; and K10CP = ROK, 2010, Culex pipiens. Vaccine strains that have been used in ROK are indicated in bold font and with an asterisk (*).
Figure 4
Figure 4. Phylogenetic tree illustrating the genetic relationship of nucleotide sequences for envelope protein coding genes of Japanese encephalitis virus (JEV) strains identified in mosquitoes, Republic of Korea, 2010 (indicated in bold font) and reference sequences for JEV strains from other geographic regions as reported on GenBank.
Genotypes of JEV strains are indicated on the right of the phylogenetic tree and were assigned according to Chen et al. , . Bootstrap support values are shown. The scale bar indicates the number of mutations. Abbreviations for strains reported in this study are as follows: K10CT = Republic of Korea (ROK), 2010, Culex tritaeniorhynchus; K10CB = ROK, 2010, Culex bitaeniorhynchus; and K10CP = ROK, 2010, Culex pipiens. Vaccine strains that have been used in ROK are indicated in bold font and with an asterisk (*).

References

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