Comparing Rearing Efficiency and Competitiveness of Sterile Male Strains Produced by Genetic, Transgenic or Symbiont-based Technologies

Closed for proposals

Project Type

Coordinated Research Project

Project Code

D42016

CRP

2046

Approved Date

29 May 2014

Start Date

6 February 2015

Expected End Date

6 February 2020

Completed Date

20 May 2020

Description

The application of the Sterile Insect Technique (SIT) in area-wide integrated pest management (AW-IPM) programmes continues to increase in response to requests from Member States. However, programme efficiency can still be considerably enhanced when certain components of the technology are improved, such as the strains used to mass-produce sterile males, which are the key component of SIT programmes. They can be produced by classical and modern biotechnology approaches and strains producing such males are now available for key insect pests. The pests targeted for SIT applications include species of agricultural, veterinary and medical importance such as the Mexican fruit fly, the oriental fruit fly, the codling moth, the pink bollworm, the screwworm as well as disease transmitting mosquitoes. This CRP will focus on comparing the performance of strains developed or improved by classical genetic, transgenic and symbiont-based approaches to a level where a decision can be made as to their suitability to produce high-quality sterile males for use in large scale SIT programmes. Major beneficiaries will be operational AW-IPM programmes in MS that apply the SIT against these major insect pests. By the end of the CRP several strains, including strains for new target species, producing high quality sterile males will be available with the following tangible benefits for pest control programmes in MS using SIT: 1.) As only the males are needed for the SIT, the production, handling and release costs can be reduced significantly if sexing strains are used.2.) The efficacy, sustainability and the cost of SIT programmes depends on the performance of released sterile males. The availability of strains producing high quality sterile males will increase the efficiency and will decrease the cost of SIT programmes. 3.) A considerable proportion of the cost of SIT programmes is used for monitoring sterile insects in the field and therefore a stable, fail proof genetic marking system for the released flies will reduce costs considerably.4.) Male-only releases are several-fold more efficient than releases of both sexes and are mandatory for disease transmitting insect species such as mosquitoes. Consequently, when the genetic sexing technology is available, SIT programmes are significantly more efficient, safe and cost effective.5.) As horizontal transfer phenomena are of major ecological concern, strains producing males by transgenic or symbiont-based approaches for SIT applications will be assessed.

Objectives

To compare the performance of sterile males produced by classical genetic, transgenic or symbiont-based technologies to address the increasing demand for environment-friendly and sustainable integrated pest management approaches for insect pests of agricultural, veterinary or public health importance.

Specific objectives

7.1) To comparatively evaluate the performance of sterile males produced by classical genetic, transgenic or symbiont-based technologies

7.2) To refine, if necessary, existing technologies and/or adopt new ones for the development and application of strains for the control of agricultural pests and disease vectors

7.3) To assess potential genetic instability and/or horizontal transfer phenomena towards the use of strains developed by classical genetic, transgenic or symbiont-based approaches for SIT applications

Impact

The successful implementation of this CRP resulted into the following: (a) classical GSS were developed for first time for two new target species, Anastrepha fraterculus sp. 1 and Aedes aegypti while significant progress has been achieved for the development of sexing strains for Bactrocera tryoni, Drosophila suzukii and Aedes albopictus; (b) Novel and/or refined strains were developed for Ceratitis capitata, Anastrepha ludens, Cochliomyia hominivorax, Aedes aegypti and Aedes albopictus; (c) strains produced by all three technological platforms were evaluated under mass rearing conditions and in four cases also in the field [the agricultural pest Anastrepha ludens (classical GSS Tap-7 refreshed and GUA 10), the livestock pest Cochliomyia hominivorax (transgenic FL12-56) and human disease vector Aedes albopictus (symbiont-based HC)] and (d) more than thirty strains of five agricultural pest species (Anastrepha fraterculus sp. 1, Anastrepha ludens, Bactrocera dorsalis, Ceratitis capitata, Zeugodacus cucurbitae), one livestock pest species (Cochliomyia hominivorax) and two human disease vectors (Aedes albopictus and Aedes aegypti), produced by all three technological platforms, were assessed in respect to their genetic stability while a transgenic strain was also assessed in respect to its potential involvement in horizontal gene transfer phenomena. No evidence of genetic instability or horizontal gene transfer phenomena were detected.

Relevance

The results of this CRP project will be very useful for ongoing and future field projects. For example: (a) the new GSS of Ceratitis capitata, V8 FDF, is to be tested in a mass rearing facility with the the potential to replace the currently used strain V8 strain; (b) the new GSS of Anastrepha ludens, GUA 10, is to be tested in a mass rearing facility with the the potential to replace the currently used Tap-7 strain; (c) GSS were developed for first time for Anastrepha fraterculus sp. 1 and Aedes aegypti which could be useful for future field projects. All new strains developed are ready to be transferred to Member States through Technical Cooperation projects. In addition, new knowledge produced in the frame of this CRP, for example the gene responsible for determining the male sex in several tephritid pest species, could result in a new and generic framework for the development of novel GSS in the future.

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