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The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features
The triatomine bug Rhodnius prolixus is a main vector of Chagas disease, which affects several million people, mostly in Latin-America. Host searching, pheromone communication, and microclimatic preferences are aspects of its behaviour that depend on multimodal sensory inputs. The molecular bases of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216343/ https://www.ncbi.nlm.nih.gov/pubmed/28059141 http://dx.doi.org/10.1038/srep40049 |
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author | Latorre-Estivalis, Jose Manuel Robertson, Hugh M. Walden, Kimberly K. O. Ruiz, Jerônimo Gonçalves, Leilane Oliveira Guarneri, Alessandra A. Lorenzo, Marcelo Gustavo |
author_facet | Latorre-Estivalis, Jose Manuel Robertson, Hugh M. Walden, Kimberly K. O. Ruiz, Jerônimo Gonçalves, Leilane Oliveira Guarneri, Alessandra A. Lorenzo, Marcelo Gustavo |
author_sort | Latorre-Estivalis, Jose Manuel |
collection | PubMed |
description | The triatomine bug Rhodnius prolixus is a main vector of Chagas disease, which affects several million people, mostly in Latin-America. Host searching, pheromone communication, and microclimatic preferences are aspects of its behaviour that depend on multimodal sensory inputs. The molecular bases of these sensory processes are largely unknown. The expression levels of genes transcribed in antennae were compared between 5(th) instar larvae, and female and male adults by means of RNA-Seq. The antennae of R. prolixus showed increased expression of several chemosensory-related genes in imaginal bugs, while both sexes had similar expression patterns for most target genes. Few cases suggest involvement of target genes in sexually dimorphic functions. Most odorant and ionotropic receptor genes seemed to be expressed in all libraries. OBPs and CSPs showed very high expression levels. Other sensory-related genes such as TRPs, PPKs and mechanoreceptors had consistent levels of expression in all libraries. Our study characterises most of the sensory gene repertoire of these insects, opening an avenue for functional genetics studies. The increase in expression of chemosensory genes suggests an enhanced role in adult bugs. This knowledge allows developing new behaviour interfering strategies, increasing the options for translational research in the vector control field. |
format | Online Article Text |
id | pubmed-5216343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52163432017-01-09 The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features Latorre-Estivalis, Jose Manuel Robertson, Hugh M. Walden, Kimberly K. O. Ruiz, Jerônimo Gonçalves, Leilane Oliveira Guarneri, Alessandra A. Lorenzo, Marcelo Gustavo Sci Rep Article The triatomine bug Rhodnius prolixus is a main vector of Chagas disease, which affects several million people, mostly in Latin-America. Host searching, pheromone communication, and microclimatic preferences are aspects of its behaviour that depend on multimodal sensory inputs. The molecular bases of these sensory processes are largely unknown. The expression levels of genes transcribed in antennae were compared between 5(th) instar larvae, and female and male adults by means of RNA-Seq. The antennae of R. prolixus showed increased expression of several chemosensory-related genes in imaginal bugs, while both sexes had similar expression patterns for most target genes. Few cases suggest involvement of target genes in sexually dimorphic functions. Most odorant and ionotropic receptor genes seemed to be expressed in all libraries. OBPs and CSPs showed very high expression levels. Other sensory-related genes such as TRPs, PPKs and mechanoreceptors had consistent levels of expression in all libraries. Our study characterises most of the sensory gene repertoire of these insects, opening an avenue for functional genetics studies. The increase in expression of chemosensory genes suggests an enhanced role in adult bugs. This knowledge allows developing new behaviour interfering strategies, increasing the options for translational research in the vector control field. Nature Publishing Group 2017-01-06 /pmc/articles/PMC5216343/ /pubmed/28059141 http://dx.doi.org/10.1038/srep40049 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Latorre-Estivalis, Jose Manuel Robertson, Hugh M. Walden, Kimberly K. O. Ruiz, Jerônimo Gonçalves, Leilane Oliveira Guarneri, Alessandra A. Lorenzo, Marcelo Gustavo The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title | The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title_full | The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title_fullStr | The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title_full_unstemmed | The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title_short | The molecular sensory machinery of a Chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
title_sort | molecular sensory machinery of a chagas disease vector: expression changes through imaginal moult and sexually dimorphic features |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216343/ https://www.ncbi.nlm.nih.gov/pubmed/28059141 http://dx.doi.org/10.1038/srep40049 |
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