White-backed planthopper, Sogatella furcifera (Horváth) (Hemiptera: Delphacidae), is known as a long-range migratory pest in Asia. Although exact primary source of S. furcifera in Korea remains unknown. We used twelve microsatellite markers (SSR) to analyze the population genetic structure of the pest. We collected S. furcifera from Asia in 2012 (Korea, Laos, Nepal, Thailand, Vietnam and four different sites of Bangladesh), 2013 (China, Nepal, Thailand, two different sites of Bangladesh, and fifteen different sites of Korea), and 2014 (four different sites of China and ten different sites of Korea). To verify the genetic variance, we used STRUCTURE program to obtain structure analysis of K and K showed in three components in genetic clustering. Result in sample 2012, similar genetic structure showed in Korea and Vietnam. In 2013 and 2014, various genetic structure revealed in different sites of Korea and Asian population genetic structure appeared as on large panmictic population. Furthermore, we tested migration pathway to see the probable source and reciplent populations of first generation migrants in S. furcifera. In 2012, Laos, Nepal, Thailand, Vietnam and four different sites of Bangladesh showed the potential source of S. furcifera. In 2013, we observed S. furcifera in Korea was more likely originated from Nepal and Bangladesh. Various migration pathway showed in fifteen different sites of Korea as panmictic population. Lastly in 2014, the migration pathway indicated that S. furcifera migrates from China to Korea. Seemingly, S. furcifera in Asia display as large panmictic population and more study is acquire to verify the origin source.

White-backed planthopper, Sogatella furcifera (Horvath) (Hemiptera: Delphacidae), has been a serious migratory pest in Korea. It is important to figure out the migration route and gene flow of S. furcifera. Microsatellite marker (SSR) shows high efficiency as molecular markers. Unfortunately, various microsatellite marker of S. furcifera has not been developed to see genetic diversity. S. furcifera samples were collected from Vietnam, Laos and three different sites of Bangladesh in 2012. We extracted DNA by using QIAamp DNA Mini Kit and ran next generation DNA sequencer (NGS) Roche 454 to develop a new microsatellite marker. Roughly, about 18 singleton primers and 14 contigs primers were found. We will test these primers with S. fucifera DNA samples, and figure out the accurate new microstatellite marker.