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Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector
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: Life history character...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366042/ https://www.ncbi.nlm.nih.gov/pubmed/30728060 http://dx.doi.org/10.1186/s13071-019-3289-y |
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author | Facchinelli, Luca North, Ace R. Collins, C. Matilda Menichelli, Miriam Persampieri, Tania Bucci, Alessandro Spaccapelo, Roberta Crisanti, Andrea Benedict, Mark Q. |
author_facet | Facchinelli, Luca North, Ace R. Collins, C. Matilda Menichelli, Miriam Persampieri, Tania Bucci, Alessandro Spaccapelo, Roberta Crisanti, Andrea Benedict, Mark Q. |
author_sort | Facchinelli, Luca |
collection | PubMed |
description | 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: Life history characteristics of Anopheles gambiae wild type and Ag(PMB)1 (aka (gfp)124L-2) transgenic mosquitoes, whose progeny are 95% male, were measured in order to parameterize predictive population models. Ag(PMB)1 males were then introduced at two ratios into large insectary cages containing target wild type populations with stable age distributions and densities. The predicted proportion of females and those observed in the large cages were compared. A related model was then used to predict effects of male releases on wild mosquitoes in a west African village. 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: 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. |
format | Online Article Text |
id | pubmed-6366042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63660422019-02-15 Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector Facchinelli, Luca North, Ace R. Collins, C. Matilda Menichelli, Miriam Persampieri, Tania Bucci, Alessandro Spaccapelo, Roberta Crisanti, Andrea Benedict, Mark Q. Parasit Vectors Research 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: Life history characteristics of Anopheles gambiae wild type and Ag(PMB)1 (aka (gfp)124L-2) transgenic mosquitoes, whose progeny are 95% male, were measured in order to parameterize predictive population models. Ag(PMB)1 males were then introduced at two ratios into large insectary cages containing target wild type populations with stable age distributions and densities. The predicted proportion of females and those observed in the large cages were compared. A related model was then used to predict effects of male releases on wild mosquitoes in a west African village. 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: 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. BioMed Central 2019-02-06 /pmc/articles/PMC6366042/ /pubmed/30728060 http://dx.doi.org/10.1186/s13071-019-3289-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Facchinelli, Luca North, Ace R. Collins, C. Matilda Menichelli, Miriam Persampieri, Tania Bucci, Alessandro Spaccapelo, Roberta Crisanti, Andrea Benedict, Mark Q. Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title | Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title_full | Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title_fullStr | Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title_full_unstemmed | Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title_short | Large-cage assessment of a transgenic sex-ratio distortion strain on populations of an African malaria vector |
title_sort | large-cage assessment of a transgenic sex-ratio distortion strain on populations of an african malaria vector |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366042/ https://www.ncbi.nlm.nih.gov/pubmed/30728060 http://dx.doi.org/10.1186/s13071-019-3289-y |
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