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Similar Neural Pathways Control Foraging in Mosquitoes and Worms

Female Aedes aegypti mosquitoes bite human hosts to obtain a blood meal and, in the process, act as vectors for many disease-causing viruses, including the dengue, chikungunya, yellow fever, and Zika viruses. After a complete meal, the female mosquitoes lose attraction to their hosts for several day...

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Detalles Bibliográficos
Autores principales: Singh, Jogender, Aballay, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495376/
https://www.ncbi.nlm.nih.gov/pubmed/31040241
http://dx.doi.org/10.1128/mBio.00656-19
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author Singh, Jogender
Aballay, Alejandro
author_facet Singh, Jogender
Aballay, Alejandro
author_sort Singh, Jogender
collection PubMed
description Female Aedes aegypti mosquitoes bite human hosts to obtain a blood meal and, in the process, act as vectors for many disease-causing viruses, including the dengue, chikungunya, yellow fever, and Zika viruses. After a complete meal, the female mosquitoes lose attraction to their hosts for several days. New research shows that pharmacological activation of neuropeptide Y-like receptor (NPYLR) signaling elicits host aversion in female mosquitoes. This behavior of mosquitoes shows remarkable similarities to a bacterial-aversion behavior of the nematode Caenorhabditis elegans. Feeding on pathogenic bacteria causes bloating of the gut in C. elegans that leads to activation of NPYLR signaling and bacterial aversion. Several studies suggest that this newly discovered mechanism underlying foraging may be conserved across a large number of species. A better understanding of the regulation of NPYLR signaling pathways could provide molecular targets for the control of eating behaviors in different animals, including human-disease vectors.
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spelling pubmed-64953762019-05-03 Similar Neural Pathways Control Foraging in Mosquitoes and Worms Singh, Jogender Aballay, Alejandro mBio Perspective Female Aedes aegypti mosquitoes bite human hosts to obtain a blood meal and, in the process, act as vectors for many disease-causing viruses, including the dengue, chikungunya, yellow fever, and Zika viruses. After a complete meal, the female mosquitoes lose attraction to their hosts for several days. New research shows that pharmacological activation of neuropeptide Y-like receptor (NPYLR) signaling elicits host aversion in female mosquitoes. This behavior of mosquitoes shows remarkable similarities to a bacterial-aversion behavior of the nematode Caenorhabditis elegans. Feeding on pathogenic bacteria causes bloating of the gut in C. elegans that leads to activation of NPYLR signaling and bacterial aversion. Several studies suggest that this newly discovered mechanism underlying foraging may be conserved across a large number of species. A better understanding of the regulation of NPYLR signaling pathways could provide molecular targets for the control of eating behaviors in different animals, including human-disease vectors. American Society for Microbiology 2019-04-30 /pmc/articles/PMC6495376/ /pubmed/31040241 http://dx.doi.org/10.1128/mBio.00656-19 Text en Copyright © 2019 Singh and Aballay. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Perspective
Singh, Jogender
Aballay, Alejandro
Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title_full Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title_fullStr Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title_full_unstemmed Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title_short Similar Neural Pathways Control Foraging in Mosquitoes and Worms
title_sort similar neural pathways control foraging in mosquitoes and worms
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495376/
https://www.ncbi.nlm.nih.gov/pubmed/31040241
http://dx.doi.org/10.1128/mBio.00656-19
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