to the oriental fruit fly, Bactrocera dorsalis (Hendel) (Wan et al. 2011), which limits the development of agriculture in many countries due to reduction in farm income; it also leads to overuse of pesticides. The difficult problems in B. tau control are to rapidly and accurately identify the morphologically similar cryptic species complexes, and reconstruct historical processes to tackle the issue of the origin and range expansion (Dujardin and Kitthawee 2013). Microsatellites, also known as simple sequence repeats (SSRs), are highly polymorphic and codominant molecular markers based on simple repeated and frequent sequences common in eukaryotic genomes, which have proven to be a powerful tool available in genetic diversity, genome mapping, molecular ecology and evolutionary studies (Goldstein and Schlötterer 1999). Microsatellites could solve many of these problems because of the power and ability for investigating population genetic differentiation. Therefore, this study was aimed at developing and characterizing a microsatellite marker set for B. tau.
Materials and methods
Insect collectionAdult flies were collected from a fruit garden in the suburb of Hainan, China. Flies were captured using traps baited with parakairomone methyl eugenol. B. tau adults were identified to species based on morphology.
Construction and sequencing of microsatellite-enriched genomic libraryTotal genomic DNA of B. tau was extracted from the adult individual with standard phenol-chloroform extraction Abstract The fruit fly, Bactrocera tau (Walker), is one of the most important invasive worldwide pests on fruits and vegetables. In order to facilitate species identification and population genetic analysis, we isolated 22 microsatellite loci through an enriched genomic library protocol. Polymorphisms were evaluated in 30 individuals. The number of alleles per locus ranged from 2 to 9, and the observed and expected heterozygosities ranged from 0.048 to 0.862 and 0.136 to 0.852, respectively. The polymorphic information content values were from 0.124 to 0.818. Eight loci had significant deviations from the Hardy-Weinberg equilibrium. These SSR markers can be used to understand the population genetics and evolutionary patterns of the B. tau complex.