Infertility resulting from transgenic I-Ppol male Anopheles gambiae in large cage trials
Objectives: Anopheles gambiae is the primary vector of malaria in sub-Saharan Africa and is a potential target of genetic control programs. We determined the capacity of male A. gambiae created by germline transformation to introduce infertility into stable age-distribution populations. We also dete...
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Published in: | Pathogens and global health Vol. 106; no. 1; pp. 20 - 31 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London
Maney
01-03-2012
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Subjects: | |
Online Access: | Get full text |
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Summary: | Objectives: Anopheles gambiae is the primary vector of malaria in sub-Saharan Africa and is a potential target of genetic control programs. We determined the capacity of male A. gambiae created by germline transformation to introduce infertility into stable age-distribution populations. We also determined effects of the transgenes on life history. Methods: Stable age-distribution populations of A. gambiae mosquitoes were established in large indoor cages. Male mosquitoes carrying an I-Ppol homing endonuclease gene were introduced at x 5 and x 10 release rates where they competed with target male mosquitoes for matings. Similar trials were conducted in small cages with an additional x 1 release level. Results: Infertility was successfully introduced into all target populations. In supporting experiments, complete female infertility was observed in all strains and species of the A. gambiae complex to which transgenic males were mated. Life history experiments demonstrated that reductions in I-Ppol male vigor exist in the form of reduced adult male emergence, longevity and competitiveness. Discussion: A. gambiae I-Ppol males are capable of introducing high levels of infertility in target populations in indoor cage trials. This was accomplished despite losses of vigor resulting from the HEG transgene. These results motivate further trials of sexually I-Ppol A. gambiae in outdoor cage and field trials. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2047-7724 2047-7732 |
DOI: | 10.1179/2047773212Y.0000000003 |