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Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression

BACKGROUND: Plasmodium development in the mosquito is crucial for malaria transmission and depends on the parasite's interaction with a variety of cell types and specific mosquito factors that have both positive and negative effects on infection. Whereas the defensive response of the mosquito c...

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Autores principales: Abrantes, Patrícia, Dimopoulos, George, Grosso, Ana Rita, do Rosário, Virgílio E., Silveira, Henrique
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2432468/
https://www.ncbi.nlm.nih.gov/pubmed/18596975
http://dx.doi.org/10.1371/journal.pone.0002587
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author Abrantes, Patrícia
Dimopoulos, George
Grosso, Ana Rita
do Rosário, Virgílio E.
Silveira, Henrique
author_facet Abrantes, Patrícia
Dimopoulos, George
Grosso, Ana Rita
do Rosário, Virgílio E.
Silveira, Henrique
author_sort Abrantes, Patrícia
collection PubMed
description BACKGROUND: Plasmodium development in the mosquito is crucial for malaria transmission and depends on the parasite's interaction with a variety of cell types and specific mosquito factors that have both positive and negative effects on infection. Whereas the defensive response of the mosquito contributes to a decrease in parasite numbers during these stages, some components of the blood meal are known to favor infection, potentiating the risk of increased transmission. The presence of the antimalarial drug chloroquine in the mosquito's blood meal has been associated with an increase in Plasmodium infectivity for the mosquito, which is possibly caused by chloroquine interfering with the capacity of the mosquito to defend against the infection. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we report a detailed survey of the Anopheles gambiae genes that are differentially regulated by the presence of chloroquine in the blood meal, using an A. gambiae cDNA microarray. The effect of chloroquine on transcript abundance was evaluated separately for non-infected and Plasmodium berghei-infected mosquitoes. Chloroquine was found to affect the abundance of transcripts that encode proteins involved in a variety of processes, including immunity, apoptosis, cytoskeleton and the response to oxidative stress. This pattern of differential gene expression may explain the weakened mosquito defense response which accounts for the increased infectivity observed in chloroquine-treated mosquitoes. CONCLUSIONS/SIGNIFICANCE: The results of the present study suggest that chloroquine can interfere with several putative mosquito mechanisms of defense against Plasmodium at the level of gene expression and highlight the need for a better understanding of the impacts of antimalarial agents on parasite transmission.
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spelling pubmed-24324682008-07-02 Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression Abrantes, Patrícia Dimopoulos, George Grosso, Ana Rita do Rosário, Virgílio E. Silveira, Henrique PLoS One Research Article BACKGROUND: Plasmodium development in the mosquito is crucial for malaria transmission and depends on the parasite's interaction with a variety of cell types and specific mosquito factors that have both positive and negative effects on infection. Whereas the defensive response of the mosquito contributes to a decrease in parasite numbers during these stages, some components of the blood meal are known to favor infection, potentiating the risk of increased transmission. The presence of the antimalarial drug chloroquine in the mosquito's blood meal has been associated with an increase in Plasmodium infectivity for the mosquito, which is possibly caused by chloroquine interfering with the capacity of the mosquito to defend against the infection. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we report a detailed survey of the Anopheles gambiae genes that are differentially regulated by the presence of chloroquine in the blood meal, using an A. gambiae cDNA microarray. The effect of chloroquine on transcript abundance was evaluated separately for non-infected and Plasmodium berghei-infected mosquitoes. Chloroquine was found to affect the abundance of transcripts that encode proteins involved in a variety of processes, including immunity, apoptosis, cytoskeleton and the response to oxidative stress. This pattern of differential gene expression may explain the weakened mosquito defense response which accounts for the increased infectivity observed in chloroquine-treated mosquitoes. CONCLUSIONS/SIGNIFICANCE: The results of the present study suggest that chloroquine can interfere with several putative mosquito mechanisms of defense against Plasmodium at the level of gene expression and highlight the need for a better understanding of the impacts of antimalarial agents on parasite transmission. Public Library of Science 2008-07-02 /pmc/articles/PMC2432468/ /pubmed/18596975 http://dx.doi.org/10.1371/journal.pone.0002587 Text en Abrantes 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
Abrantes, Patrícia
Dimopoulos, George
Grosso, Ana Rita
do Rosário, Virgílio E.
Silveira, Henrique
Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title_full Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title_fullStr Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title_full_unstemmed Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title_short Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression
title_sort chloroquine mediated modulation of anopheles gambiae gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2432468/
https://www.ncbi.nlm.nih.gov/pubmed/18596975
http://dx.doi.org/10.1371/journal.pone.0002587
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