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1.
Parasit Vectors ; 9: 49, 2016 Jan 28.
Artículo en Inglés | MEDLINE | ID: mdl-26818000

RESUMEN

BACKGROUND: More effective mosquito control strategies are urgently required due to the increasing prevalence of insecticide resistance. The sterile insect technique (SIT) and the release of insects carrying a dominant lethal allele (RIDL) are two proposed methods for environmentally-friendly, species-targeted population control. These methods may be more suitable for developing countries if producers reduce the cost of rearing insects. The cost of control programs could be reduced by producing all-male mosquito populations to circumvent the isolation of females before release without reducing male mating competitiveness caused by transgenes. RESULTS: An RNAi construct targeting the RNA recognition motif of the Aedes aegypti transformer-2 (tra-2) gene does not trigger female-to-male sex conversion as commonly observed among dipterous insects. Instead, homozygous insects show greater mortality among m-chromosome-bearing sperm and mm zygotes, yielding up to 100% males in the subsequent generations. The performance of transgenic males was not significantly different to wild-type males in narrow-cage competitive mating experiments. CONCLUSION: Our data provide preliminary evidence that the knockdown of Ae. aegypti tra-2 gene expression causes segregation distortion acting at the level of gametic function, which is reinforced by sex-specific zygotic lethality. This finding could promote the development of new synthetic sex distorter systems for the production of genetic sexing mosquito strains.


Asunto(s)
Aedes/fisiología , Control de Mosquitos/métodos , Aedes/genética , Animales , Animales Modificados Genéticamente , Femenino , Técnicas de Silenciamiento del Gen , Genes Dominantes/genética , Genes Letales/genética , Infertilidad/genética , Masculino , Control Biológico de Vectores , Interferencia de ARN , Reproducción , Procesos de Determinación del Sexo , Razón de Masculinidad , Conducta Sexual Animal
2.
PLoS One ; 8(5): e62711, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23690948

RESUMEN

OX513A is a transgenic strain of Aedes aegypti engineered to carry a dominant, non-sex-specific, late-acting lethal genetic system that is repressed in the presence of tetracycline. It was designed for use in a sterile-insect (SIT) pest control system called RIDL® (Release of Insects carrying a Dominant Lethal gene) by which transgenic males are released in the field to mate with wild females; in the absence of tetracycline, the progeny from such matings will not survive. We investigated the mating fitness of OX513A in the laboratory. Male OX513A were as effective as Rockefeller (ROCK) males at inducing refractoriness to further mating in wild type females and there was no reduction in their ability to inseminate multiple females. They had a lower mating success but yielded more progeny than the wild-type comparator strain (ROCK) when one male of each strain was caged with a ROCK female. Mating success and fertility of groups of 10 males-with different ratios of RIDL to ROCK-competing for five ROCK females was similar, but the median longevity of RIDL males was somewhat (18%) lower. We conclude that the fitness under laboratory conditions of OX513A males carrying a tetracycline repressible lethal gene is comparable to that of males of the wild-type comparator strain.


Asunto(s)
Aedes/genética , Aedes/fisiología , Genes Dominantes/genética , Genes Letales , Aptitud Genética/genética , Control Biológico de Vectores/métodos , Aedes/efectos de los fármacos , Animales , Animales Modificados Genéticamente , Conducta Competitiva/efectos de los fármacos , Femenino , Fertilización/efectos de los fármacos , Fertilización/genética , Aptitud Genética/efectos de los fármacos , Homocigoto , Inseminación/efectos de los fármacos , Inseminación/genética , Laboratorios , Longevidad/efectos de los fármacos , Longevidad/genética , Masculino , Oviposición/efectos de los fármacos , Oviposición/genética , Conducta Sexual Animal/efectos de los fármacos , Tetraciclina/farmacología
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