Abstract:
In this study, the possibility of using Ceratitis capitata (medfly)-derived
microsatellites both for developing an SSR-based species-diagnostic peR assay and
studying the genetic structures of a range of congeneric, economically important African
fruit fly species has been investigated. The medfly SSR primers used were based on
published sequences obtained from the GenBank database.
Twenty-four medfly SSR were screened for amplification on the genomic DNA of
C rosa, Cjasciventris and C cosyra. All primer pairs produced PCR products in at least
one of the three species examined. Amplification success ranged from 79.2% (C cosyra)
to 91.3% (in both C rosa and C jasciventris). Specifically, a number of loci
differentially amplified in the four species examined: of the 24 loci screened, 17 were
common to all, five were PCR-negative in C cosyra, two were negative in C rosa and in
C jasciventris, while one locus amplified only in C capitata. The majority of the
amplicons were similar, if not identical in size to those expected in the medf1y. The
structures of the repeat motifs and their flanking=sequences were examined at a total of
repeat units were (CA)nI(TG)". Some species-specific nucleotide differences were
observed among the four species.
Ten of the cross-species SSRs markers were used to survey the levels of genetic
variability and analyse the genetic aspects of the population dynamics of C rosa, C
fasciventris in Africa, in comparison with variability data from C capitata. The loci
proved to be informative. The degree of microsatellite polymorphism in C rosa and C