Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
06 Feb 2019
Historique:
received: 25 05 2018
accepted: 03 01 2019
entrez: 8 2 2019
pubmed: 8 2 2019
medline: 20 2 2019
Statut: epublish

Résumé

Novel transgenic mosquito control methods require progressively more realistic evaluation. The goal of this study was to determine the effect of a transgene that causes a male-bias sex ratio on Anopheles gambiae target populations in large insectary cages. Life history characteristics of Anopheles gambiae wild type and Ag(PMB)1 (aka The frequency of transgenic mosquitoes in target populations reached an average of 0.44 ± 0.02 and 0.56 ± 0.02 after 6 weeks in the 1:1 and in the 3:1 release ratio treatments (transgenic male:wild male) respectively. Transgenic males caused sex-ratio distortion of 73% and 80% males in the 1:1 and 3:1 treatments, respectively. The number of eggs laid in the transgenic treatments declined as the experiment progressed, with a steeper decline in the 3:1 than in the 1:1 releases. The results of the experiment are partially consistent with predictions of the model; effect size and variability did not conform to the model in two out of three trials, effect size was over-estimated by the model and variability was greater than anticipated, possibly because of sampling effects in restocking. The model estimating the effects of hypothetical releases on the mosquito population of a West African village demonstrated that releases could significantly reduce the number of females in the wild population. The interval of releases is not expected to have a strong effect. The biological data produced to parameterize the model, the model itself, and the results of the experiments are components of a system to evaluate and predict the performance of transgenic mosquitoes. Together these suggest that the Ag(PMB)1 strain has the potential to be useful for reversible population suppression while this novel field develops.

Sections du résumé

BACKGROUND BACKGROUND
Novel transgenic mosquito control methods require progressively more realistic evaluation. The goal of this study was to determine the effect of a transgene that causes a male-bias sex ratio on Anopheles gambiae target populations in large insectary cages.
METHODS METHODS
Life history characteristics of Anopheles gambiae wild type and Ag(PMB)1 (aka
RESULTS RESULTS
The frequency of transgenic mosquitoes in target populations reached an average of 0.44 ± 0.02 and 0.56 ± 0.02 after 6 weeks in the 1:1 and in the 3:1 release ratio treatments (transgenic male:wild male) respectively. Transgenic males caused sex-ratio distortion of 73% and 80% males in the 1:1 and 3:1 treatments, respectively. The number of eggs laid in the transgenic treatments declined as the experiment progressed, with a steeper decline in the 3:1 than in the 1:1 releases. The results of the experiment are partially consistent with predictions of the model; effect size and variability did not conform to the model in two out of three trials, effect size was over-estimated by the model and variability was greater than anticipated, possibly because of sampling effects in restocking. The model estimating the effects of hypothetical releases on the mosquito population of a West African village demonstrated that releases could significantly reduce the number of females in the wild population. The interval of releases is not expected to have a strong effect.
CONCLUSIONS CONCLUSIONS
The biological data produced to parameterize the model, the model itself, and the results of the experiments are components of a system to evaluate and predict the performance of transgenic mosquitoes. Together these suggest that the Ag(PMB)1 strain has the potential to be useful for reversible population suppression while this novel field develops.

Identifiants

pubmed: 30728060
doi: 10.1186/s13071-019-3289-y
pii: 10.1186/s13071-019-3289-y
pmc: PMC6366042
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

70

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Auteurs

Luca Facchinelli (L)

Department of Experimental Medicine, University of Perugia, Perugia, Italy.
Present address: Department of Vector Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK.

Ace R North (AR)

Department of Zoology, University of Oxford, New Radcliffe House, Woodstock Road, Oxford, OX2 6GG, UK.

C Matilda Collins (CM)

Centre for Environmental Policy, Imperial College London, 16-18 Princes Gardens, London, SW7 1NE, UK.

Miriam Menichelli (M)

Polo di Genomica Genetica e Biologia, Via mazzieri 3, 05100, Terni, Italy.

Tania Persampieri (T)

Polo di Genomica Genetica e Biologia, Via mazzieri 3, 05100, Terni, Italy.

Alessandro Bucci (A)

Polo di Genomica Genetica e Biologia, Via mazzieri 3, 05100, Terni, Italy.

Roberta Spaccapelo (R)

Department of Experimental Medicine, University of Perugia, 06132, Perugia, Italy.

Andrea Crisanti (A)

Department of Life Sciences, Imperial College London, Sir Alexander Fleming Building Imperial College Road South Kensington, London, SW7 2AZ, UK.

Mark Q Benedict (MQ)

Centers for Disease Control and Prevention (CDC), 1600 Clifton Road, Atlanta, GA, 30329, USA. mqbenedict@yahoo.com.

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Classifications MeSH