Abstract

Site-specific recombination technologies are powerful new tools for the manipulation of genomic DNA in insects that can improve transgenesis strategies such as targeting transgene insertions, allowing transgene cassette exchange and DNA mobilization for transgene stabilization. However, understanding the fitness cost implications of these manipulations for transgenic strain applications is critical. In this study independent piggyBac-mediated attP target-sites marked with DsRed were created in several genomic positions in the Mexican fruit fly, Anastrepha ludens. Two of these strains, one having an autosomal (attP_F7) and the other a Y-linked (attP_2-M6y) integration, exhibited fitness parameters (dynamic demography and sexual competitiveness) similar to wild type flies. These strains were thus selected for targeted insertion using, for the first time in mexfly, the phiC31-integrase recombination system to insert an additional EGFP-marked transgene to determine its effect on host strain fitness. Fitness tests showed that the integration event in the int_2-M6y recombinant strain had no significant effect, while the int_F7 recombinant strain exhibited significantly lower fitness relative to the original attP_F7 target-site host strain. These results indicate that while targeted transgene integrations can be achieved without an additional fitness cost, at some genomic positions insertion of additional DNA into a previously integrated transgene can have a significant negative effect. Thus, for targeted transgene insertions fitness costs must be evaluated both previous to and subsequent to new site-specific insertions in the target-site strain.

Highlights

  • Germ-line transformation has been used widely to create genetically modified insects (GMI) in pest species, and is based primarily on vectors that are Class II transposable elements such as piggyBac, Mariner, Hermes, or Minos [1,2,3,4]

  • Insect strains All target-site strains (TTSS) were derived from the Anastrepha ludens Moscafrut colony, which has been maintained in a breeding program since 1992 in the Moscafrut bio-complex near Tapachula, Chiapas, Mexico

  • The strains with the strongest fluorescence based on visual inspection were attP_M6, attP_F7, and attP_F21

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Summary

Introduction

Germ-line transformation has been used widely to create genetically modified insects (GMI) in pest species, and is based primarily on vectors that are Class II transposable elements such as piggyBac, Mariner, Hermes, or Minos [1,2,3,4]. Transposonmediated transformation has been used to create a variety of GMIs having the potential to increase the efficiency of insect control programs, especially those that use the sterile insect technique (SIT) [5]. These GMIs include those, most having fluorescent protein transformation markers that can facilitate the identification of sterile adults released into the wild [6]. Transgenic female-specific conditional lethality strains have been created that may find use for sexing in rearing [10,11], and non-sex-specific lethality strains may provide a means for genetic sterility that eliminates the need for male irradiation [12]. Given that the SIT control strategy bases its efficacy on the mating competition of released males with wild males, alternatives to the debilitating effects of irradiation is a high priority

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