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Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon

Zika virus (ZIKV) is a global public health emergency due to its association with microcephaly, Guillain-Barré syndrome, neuropathy, and myelitis in children and adults. A total of 87 countries have had evidence of autochthonous mosquito-borne transmission of ZIKV, distributed across four continents...

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Autores principales: Martins, Michele, Ramos, Luis Felipe Costa, Murillo, Jimmy Rodriguez, Torres, André, de Carvalho, Stephanie Serafim, Domont, Gilberto Barbosa, de Oliveira, Danielle Maria Perpétua, Mesquita, Rafael Dias, Nogueira, Fábio César Sousa, Maciel-de-Freitas, Rafael, Junqueira, Magno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947915/
https://www.ncbi.nlm.nih.gov/pubmed/33716790
http://dx.doi.org/10.3389/fphys.2021.642237
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author Martins, Michele
Ramos, Luis Felipe Costa
Murillo, Jimmy Rodriguez
Torres, André
de Carvalho, Stephanie Serafim
Domont, Gilberto Barbosa
de Oliveira, Danielle Maria Perpétua
Mesquita, Rafael Dias
Nogueira, Fábio César Sousa
Maciel-de-Freitas, Rafael
Junqueira, Magno
author_facet Martins, Michele
Ramos, Luis Felipe Costa
Murillo, Jimmy Rodriguez
Torres, André
de Carvalho, Stephanie Serafim
Domont, Gilberto Barbosa
de Oliveira, Danielle Maria Perpétua
Mesquita, Rafael Dias
Nogueira, Fábio César Sousa
Maciel-de-Freitas, Rafael
Junqueira, Magno
author_sort Martins, Michele
collection PubMed
description Zika virus (ZIKV) is a global public health emergency due to its association with microcephaly, Guillain-Barré syndrome, neuropathy, and myelitis in children and adults. A total of 87 countries have had evidence of autochthonous mosquito-borne transmission of ZIKV, distributed across four continents, and no antivirus therapy or vaccines are available. Therefore, several strategies have been developed to target the main mosquito vector, Aedes aegypti, to reduce the burden of different arboviruses. Among such strategies, the use of the maternally-inherited endosymbiont Wolbachia pipientis has been applied successfully to reduce virus susceptibility and decrease transmission. However, the mechanisms by which Wolbachia orchestrate resistance to ZIKV infection remain to be elucidated. In this study, we apply isobaric labeling quantitative mass spectrometry (MS)-based proteomics to quantify proteins and identify pathways altered during ZIKV infection; Wolbachia infection; co-infection with Wolbachia/ZIKV in the A. aegypti heads and salivary glands. We show that Wolbachia regulates proteins involved in reactive oxygen species production, regulates humoral immune response, and antioxidant production. The reduction of ZIKV polyprotein in the presence of Wolbachia in mosquitoes was determined by MS and corroborates the idea that Wolbachia helps to block ZIKV infections in A. aegypti. The present study offers a rich resource of data that may help to elucidate mechanisms by which Wolbachia orchestrate resistance to ZIKV infection in A. aegypti, and represents a step further on the development of new targeted methods to detect and quantify ZIKV and Wolbachia directly in complex tissues.
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spelling pubmed-79479152021-03-12 Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon Martins, Michele Ramos, Luis Felipe Costa Murillo, Jimmy Rodriguez Torres, André de Carvalho, Stephanie Serafim Domont, Gilberto Barbosa de Oliveira, Danielle Maria Perpétua Mesquita, Rafael Dias Nogueira, Fábio César Sousa Maciel-de-Freitas, Rafael Junqueira, Magno Front Physiol Physiology Zika virus (ZIKV) is a global public health emergency due to its association with microcephaly, Guillain-Barré syndrome, neuropathy, and myelitis in children and adults. A total of 87 countries have had evidence of autochthonous mosquito-borne transmission of ZIKV, distributed across four continents, and no antivirus therapy or vaccines are available. Therefore, several strategies have been developed to target the main mosquito vector, Aedes aegypti, to reduce the burden of different arboviruses. Among such strategies, the use of the maternally-inherited endosymbiont Wolbachia pipientis has been applied successfully to reduce virus susceptibility and decrease transmission. However, the mechanisms by which Wolbachia orchestrate resistance to ZIKV infection remain to be elucidated. In this study, we apply isobaric labeling quantitative mass spectrometry (MS)-based proteomics to quantify proteins and identify pathways altered during ZIKV infection; Wolbachia infection; co-infection with Wolbachia/ZIKV in the A. aegypti heads and salivary glands. We show that Wolbachia regulates proteins involved in reactive oxygen species production, regulates humoral immune response, and antioxidant production. The reduction of ZIKV polyprotein in the presence of Wolbachia in mosquitoes was determined by MS and corroborates the idea that Wolbachia helps to block ZIKV infections in A. aegypti. The present study offers a rich resource of data that may help to elucidate mechanisms by which Wolbachia orchestrate resistance to ZIKV infection in A. aegypti, and represents a step further on the development of new targeted methods to detect and quantify ZIKV and Wolbachia directly in complex tissues. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7947915/ /pubmed/33716790 http://dx.doi.org/10.3389/fphys.2021.642237 Text en Copyright © 2021 Martins, Ramos, Murillo, Torres, de Carvalho, Domont, de Oliveira, Mesquita, Nogueira, Maciel-de-Freitas and Junqueira. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Martins, Michele
Ramos, Luis Felipe Costa
Murillo, Jimmy Rodriguez
Torres, André
de Carvalho, Stephanie Serafim
Domont, Gilberto Barbosa
de Oliveira, Danielle Maria Perpétua
Mesquita, Rafael Dias
Nogueira, Fábio César Sousa
Maciel-de-Freitas, Rafael
Junqueira, Magno
Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title_full Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title_fullStr Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title_full_unstemmed Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title_short Comprehensive Quantitative Proteome Analysis of Aedes aegypti Identifies Proteins and Pathways Involved in Wolbachia pipientis and Zika Virus Interference Phenomenon
title_sort comprehensive quantitative proteome analysis of aedes aegypti identifies proteins and pathways involved in wolbachia pipientis and zika virus interference phenomenon
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947915/
https://www.ncbi.nlm.nih.gov/pubmed/33716790
http://dx.doi.org/10.3389/fphys.2021.642237
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