Cargando…

Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti

Blood-feeding mosquitoes are exposed to high levels of heme, the product of hemoglobin degradation. Heme is a pro-oxidant that influences a variety of cellular processes. We performed a global analysis of heme-regulated Aedes aegypti (yellow fever mosquito) transcriptional changes to better understa...

Descripción completa

Detalles Bibliográficos
Autores principales: Bottino-Rojas, Vanessa, Talyuli, Octávio A. C., Jupatanakul, Natapong, Sim, Shuzhen, Dimopoulos, George, Venancio, Thiago M., Bahia, Ana C., Sorgine, Marcos H., Oliveira, Pedro L., Paiva-Silva, Gabriela O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537099/
https://www.ncbi.nlm.nih.gov/pubmed/26275150
http://dx.doi.org/10.1371/journal.pone.0135985
_version_ 1782385847138516992
author Bottino-Rojas, Vanessa
Talyuli, Octávio A. C.
Jupatanakul, Natapong
Sim, Shuzhen
Dimopoulos, George
Venancio, Thiago M.
Bahia, Ana C.
Sorgine, Marcos H.
Oliveira, Pedro L.
Paiva-Silva, Gabriela O.
author_facet Bottino-Rojas, Vanessa
Talyuli, Octávio A. C.
Jupatanakul, Natapong
Sim, Shuzhen
Dimopoulos, George
Venancio, Thiago M.
Bahia, Ana C.
Sorgine, Marcos H.
Oliveira, Pedro L.
Paiva-Silva, Gabriela O.
author_sort Bottino-Rojas, Vanessa
collection PubMed
description Blood-feeding mosquitoes are exposed to high levels of heme, the product of hemoglobin degradation. Heme is a pro-oxidant that influences a variety of cellular processes. We performed a global analysis of heme-regulated Aedes aegypti (yellow fever mosquito) transcriptional changes to better understand influence on mosquito physiology at the molecular level. We observed an iron- and reactive oxygen species (ROS)-independent signaling induced by heme that comprised genes related to redox metabolism. By modulating the abundance of these transcripts, heme possibly acts as a danger signaling molecule. Furthermore, heme triggered critical changes in the expression of energy metabolism and immune response genes, altering the susceptibility towards bacteria and dengue virus. These findings seem to have implications on the adaptation of mosquitoes to hematophagy and consequently on their ability to transmit diseases. Altogether, these results may also contribute to the understanding of heme cell biology in eukaryotic cells.
format Online
Article
Text
id pubmed-4537099
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-45370992015-08-20 Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti Bottino-Rojas, Vanessa Talyuli, Octávio A. C. Jupatanakul, Natapong Sim, Shuzhen Dimopoulos, George Venancio, Thiago M. Bahia, Ana C. Sorgine, Marcos H. Oliveira, Pedro L. Paiva-Silva, Gabriela O. PLoS One Research Article Blood-feeding mosquitoes are exposed to high levels of heme, the product of hemoglobin degradation. Heme is a pro-oxidant that influences a variety of cellular processes. We performed a global analysis of heme-regulated Aedes aegypti (yellow fever mosquito) transcriptional changes to better understand influence on mosquito physiology at the molecular level. We observed an iron- and reactive oxygen species (ROS)-independent signaling induced by heme that comprised genes related to redox metabolism. By modulating the abundance of these transcripts, heme possibly acts as a danger signaling molecule. Furthermore, heme triggered critical changes in the expression of energy metabolism and immune response genes, altering the susceptibility towards bacteria and dengue virus. These findings seem to have implications on the adaptation of mosquitoes to hematophagy and consequently on their ability to transmit diseases. Altogether, these results may also contribute to the understanding of heme cell biology in eukaryotic cells. Public Library of Science 2015-08-14 /pmc/articles/PMC4537099/ /pubmed/26275150 http://dx.doi.org/10.1371/journal.pone.0135985 Text en © 2015 Bottino-Rojas et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bottino-Rojas, Vanessa
Talyuli, Octávio A. C.
Jupatanakul, Natapong
Sim, Shuzhen
Dimopoulos, George
Venancio, Thiago M.
Bahia, Ana C.
Sorgine, Marcos H.
Oliveira, Pedro L.
Paiva-Silva, Gabriela O.
Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title_full Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title_fullStr Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title_full_unstemmed Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title_short Heme Signaling Impacts Global Gene Expression, Immunity and Dengue Virus Infectivity in Aedes aegypti
title_sort heme signaling impacts global gene expression, immunity and dengue virus infectivity in aedes aegypti
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537099/
https://www.ncbi.nlm.nih.gov/pubmed/26275150
http://dx.doi.org/10.1371/journal.pone.0135985
work_keys_str_mv AT bottinorojasvanessa hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT talyulioctavioac hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT jupatanakulnatapong hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT simshuzhen hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT dimopoulosgeorge hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT venanciothiagom hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT bahiaanac hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT sorginemarcosh hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT oliveirapedrol hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti
AT paivasilvagabrielao hemesignalingimpactsglobalgeneexpressionimmunityanddenguevirusinfectivityinaedesaegypti