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A transgenic tool to assess Anopheles mating competitiveness in the field

BACKGROUND: Malaria parasites, transmitted by the bite of an anopheline mosquito, pose an immense public health burden on many tropical and subtropical regions. The most important malaria vectors in sub-Saharan Africa are mosquitoes of the Anopheles gambiae complex including An. gambiae (sensu stric...

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Autores principales: Smidler, Andrea L., Scott, Sean N., Mameli, Enzo, Shaw, W. Robert, Catteruccia, Flaminia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304768/
https://www.ncbi.nlm.nih.gov/pubmed/30583744
http://dx.doi.org/10.1186/s13071-018-3218-5
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author Smidler, Andrea L.
Scott, Sean N.
Mameli, Enzo
Shaw, W. Robert
Catteruccia, Flaminia
author_facet Smidler, Andrea L.
Scott, Sean N.
Mameli, Enzo
Shaw, W. Robert
Catteruccia, Flaminia
author_sort Smidler, Andrea L.
collection PubMed
description BACKGROUND: Malaria parasites, transmitted by the bite of an anopheline mosquito, pose an immense public health burden on many tropical and subtropical regions. The most important malaria vectors in sub-Saharan Africa are mosquitoes of the Anopheles gambiae complex including An. gambiae (sensu stricto). Given the increasing rates of insecticide resistance in these mosquitoes, alternative control strategies based on the release of genetically modified males are being evaluated to stop transmission by these disease vectors. These strategies rely on the mating competitiveness of release males, however currently there is no method to determine male mating success without sacrificing the female. Interestingly, unlike other insects, during mating An. gambiae males transfer their male accessory glands (MAGs) seminal secretions as a coagulated mating plug which is deposited in the female atrium. RESULTS: Here we exploit this male reproductive feature and validate the use of a MAG-specific promoter to fluorescently label the mating plug and visualize the occurrence of insemination in vivo. We used the promoter region of the major mating plug protein, Plugin, to control the expression of a Plugin-tdTomato (PluTo) fusion protein, hypothesizing that this fusion protein could be incorporated into the plug for sexual transfer to the female. Anopheles gambiae PluTo transgenic males showed strong red fluorescence specifically in the MAGs and with a pattern closely matching endogenous Plugin expression. Moreover, the fusion protein was integrated into the mating plug and transferred to the female atrium during mating where it could be visualized microscopically in vivo without sacrificing the female. PluTo males were equally as competitive at mating as wild type males, and females mated to these males did not show any reduction in reproductive fitness. CONCLUSION: The validation of the first MAG-specific promoter in transgenic An. gambiae facilitates the live detection of successful insemination hours after copulation has occurred. This provides a valuable tool for the assessment of male mating competitiveness not only in laboratory experiments but also in semi-field and field studies aimed at testing the feasibility of releasing genetically modified mosquitoes for disease control. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3218-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-63047682019-01-02 A transgenic tool to assess Anopheles mating competitiveness in the field Smidler, Andrea L. Scott, Sean N. Mameli, Enzo Shaw, W. Robert Catteruccia, Flaminia Parasit Vectors Research BACKGROUND: Malaria parasites, transmitted by the bite of an anopheline mosquito, pose an immense public health burden on many tropical and subtropical regions. The most important malaria vectors in sub-Saharan Africa are mosquitoes of the Anopheles gambiae complex including An. gambiae (sensu stricto). Given the increasing rates of insecticide resistance in these mosquitoes, alternative control strategies based on the release of genetically modified males are being evaluated to stop transmission by these disease vectors. These strategies rely on the mating competitiveness of release males, however currently there is no method to determine male mating success without sacrificing the female. Interestingly, unlike other insects, during mating An. gambiae males transfer their male accessory glands (MAGs) seminal secretions as a coagulated mating plug which is deposited in the female atrium. RESULTS: Here we exploit this male reproductive feature and validate the use of a MAG-specific promoter to fluorescently label the mating plug and visualize the occurrence of insemination in vivo. We used the promoter region of the major mating plug protein, Plugin, to control the expression of a Plugin-tdTomato (PluTo) fusion protein, hypothesizing that this fusion protein could be incorporated into the plug for sexual transfer to the female. Anopheles gambiae PluTo transgenic males showed strong red fluorescence specifically in the MAGs and with a pattern closely matching endogenous Plugin expression. Moreover, the fusion protein was integrated into the mating plug and transferred to the female atrium during mating where it could be visualized microscopically in vivo without sacrificing the female. PluTo males were equally as competitive at mating as wild type males, and females mated to these males did not show any reduction in reproductive fitness. CONCLUSION: The validation of the first MAG-specific promoter in transgenic An. gambiae facilitates the live detection of successful insemination hours after copulation has occurred. This provides a valuable tool for the assessment of male mating competitiveness not only in laboratory experiments but also in semi-field and field studies aimed at testing the feasibility of releasing genetically modified mosquitoes for disease control. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3218-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-24 /pmc/articles/PMC6304768/ /pubmed/30583744 http://dx.doi.org/10.1186/s13071-018-3218-5 Text en © The Author(s). 2018 Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution IGO License (https://creativecommons.org/licenses/by/3.0/igo/) which permits unrestricted use, distribution, and reproduction in any medium, provided appropriate credit to the original author(s) and the source is given.
spellingShingle Research
Smidler, Andrea L.
Scott, Sean N.
Mameli, Enzo
Shaw, W. Robert
Catteruccia, Flaminia
A transgenic tool to assess Anopheles mating competitiveness in the field
title A transgenic tool to assess Anopheles mating competitiveness in the field
title_full A transgenic tool to assess Anopheles mating competitiveness in the field
title_fullStr A transgenic tool to assess Anopheles mating competitiveness in the field
title_full_unstemmed A transgenic tool to assess Anopheles mating competitiveness in the field
title_short A transgenic tool to assess Anopheles mating competitiveness in the field
title_sort transgenic tool to assess anopheles mating competitiveness in the field
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304768/
https://www.ncbi.nlm.nih.gov/pubmed/30583744
http://dx.doi.org/10.1186/s13071-018-3218-5
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