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The codling moth, Cydia pomonella (Lep., Tortricidae), is a significant pest of orchard crops such as apple and pear in Southern Germany, and can cause severe economic damage to apple crops. Due to resistance to conventional pesticides and the growing market for organic fruit, Cydia pomonella Granulovirus (CpGV) has been used to control C. pomonella in Germany for over 10 years. Recently, populations exhibiting resistance to CpGV have been reported. In this study, we have used amplified fragment length polymorphism (AFLP) markers to estimate genetic variations between eight different C. pomonella populations, which were obtained from different locations exhibiting varying levels of resistance to CpGV. Three different AFLP primer combinations generated a total of 194 AFLP fragments, ranging from 57.84 to 424.11 bp, with an average of 59.23 amplified fragments per primer combination. The total number of segregating fragments ranged from 181 to 115 and resulted in a high loci polymorphism of 100% in most cases, except for two populations, where it was found to be 88.1% and 93.3%. An analysis of genetic variation based on the obtained AFLP markers resulted in high gene diversity (Hj) values, ranging between 0.2884 to 0.3508. Hj values also indicated a loss in gene diversity within a population over time. The Wright Fixation Index (FST) values indicated a low to moderate genetic differentiation in the populations. The cluster analysis (UPGMA), based on genetic distance values, showed that the majority of C. pomonella populations from different locations were clearly distributed into distinct groups and showed a large genetic variability.
The entomopathogenic hyphomycete Beauveria brongniartii is a promising candidate for biocontrol of economically important agricultural and forest pests. Assessment of genetic relatedness of this species appears to be essential to gain insight into the monitoring of such biocontrol products. Distinction of Beauveria spp. strains with different virulence to target organisms revealed to be a serious constraint in the development of successful biocontrol using these important species. Thus, there is a need to find ways to monitor these strains when applied to natural agents. We have used amplified fragment length polymorphism (AFLPs) markers to estimate genetic variations among fourteen isolates (ten B. brongniartii, two B. bassiana (BALSAMO) VUILLEMIN and two Nomuraea rileyi (FARLOW) SAMSON) obtained from different geographical origins and hosts with differing virulence to scarabs. Seven different AFLP primer combinations yielded a total of 229 AFLP fragments comprised between 30 (EcoRI-ACA/Tru1l-C) to 57 (EcoRI-AAG/Tru1l-CTT) AFLP markers with an average of 54 amplified fragments per primer combination. Fragment size varied between 50-541 base pairs (bp) among the ten B. brongniartii isolates analysed in this study achieving a good resolution between the isolates. The cluster analysis based on genetic distance values clustered all isolates at above 0.40 similarity and demonstrated that some B. brongniartii isolates from distinct geographical origins and various hosts showed a greater genetic variability.