Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.

Heme crystallization as hemozoin represents the dominant mechanism of heme disposal in blood feeding triatomine insect vectors of the Chagas disease. The absence of drugs or vaccine for the Chagas disease causative agent, the parasite Trypanosoma cruzi, makes the control of vector population the bes...

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Main Authors: Caroline M Ferreira, Renata Stiebler, Francis M Saraiva, Guilherme C Lechuga, Ana Beatriz Walter-Nuno, Saulo C Bourguignon, Marcelo S Gonzalez, Patrícia Azambuja, Ana Caroline P Gandara, Rubem F S Menna-Barreto, Gabriela O Paiva-Silva, Marcia C Paes, Marcus F Oliveira
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-07-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC6084092?pdf=render
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spelling doaj-7e262eabe1d44f248dba27615638d89d2020-11-25T01:21:40ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352018-07-01127e000666110.1371/journal.pntd.0006661Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.Caroline M FerreiraRenata StieblerFrancis M SaraivaGuilherme C LechugaAna Beatriz Walter-NunoSaulo C BourguignonMarcelo S GonzalezPatrícia AzambujaAna Caroline P GandaraRubem F S Menna-BarretoGabriela O Paiva-SilvaMarcia C PaesMarcus F OliveiraHeme crystallization as hemozoin represents the dominant mechanism of heme disposal in blood feeding triatomine insect vectors of the Chagas disease. The absence of drugs or vaccine for the Chagas disease causative agent, the parasite Trypanosoma cruzi, makes the control of vector population the best available strategy to limit disease spread. Although heme and redox homeostasis regulation is critical for both triatomine insects and T. cruzi, the physiological relevance of hemozoin for these organisms remains unknown. Here, we demonstrate that selective blockage of heme crystallization in vivo by the antimalarial drug quinidine, caused systemic heme overload and redox imbalance in distinct insect tissues, assessed by spectrophotometry and fluorescence microscopy. Quinidine treatment activated compensatory defensive heme-scavenging mechanisms to cope with excessive heme, as revealed by biochemical hemolymph analyses, and fat body gene expression. Importantly, egg production, oviposition, and total T. cruzi parasite counts in R. prolixus were significantly reduced by quinidine treatment. These effects were reverted by oral supplementation with the major insect antioxidant urate. Altogether, these data underscore the importance of heme crystallization as the main redox regulator for triatomine vectors, indicating the dual role of hemozoin as a protective mechanism to allow insect fertility, and T. cruzi life-cycle. Thus, targeting heme crystallization in insect vectors represents an innovative way for Chagas disease control, by reducing simultaneously triatomine reproduction and T. cruzi transmission.http://europepmc.org/articles/PMC6084092?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Caroline M Ferreira
Renata Stiebler
Francis M Saraiva
Guilherme C Lechuga
Ana Beatriz Walter-Nuno
Saulo C Bourguignon
Marcelo S Gonzalez
Patrícia Azambuja
Ana Caroline P Gandara
Rubem F S Menna-Barreto
Gabriela O Paiva-Silva
Marcia C Paes
Marcus F Oliveira
spellingShingle Caroline M Ferreira
Renata Stiebler
Francis M Saraiva
Guilherme C Lechuga
Ana Beatriz Walter-Nuno
Saulo C Bourguignon
Marcelo S Gonzalez
Patrícia Azambuja
Ana Caroline P Gandara
Rubem F S Menna-Barreto
Gabriela O Paiva-Silva
Marcia C Paes
Marcus F Oliveira
Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
PLoS Neglected Tropical Diseases
author_facet Caroline M Ferreira
Renata Stiebler
Francis M Saraiva
Guilherme C Lechuga
Ana Beatriz Walter-Nuno
Saulo C Bourguignon
Marcelo S Gonzalez
Patrícia Azambuja
Ana Caroline P Gandara
Rubem F S Menna-Barreto
Gabriela O Paiva-Silva
Marcia C Paes
Marcus F Oliveira
author_sort Caroline M Ferreira
title Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
title_short Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
title_full Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
title_fullStr Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
title_full_unstemmed Heme crystallization in a Chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
title_sort heme crystallization in a chagas disease vector acts as a redox-protective mechanism to allow insect reproduction and parasite infection.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2018-07-01
description Heme crystallization as hemozoin represents the dominant mechanism of heme disposal in blood feeding triatomine insect vectors of the Chagas disease. The absence of drugs or vaccine for the Chagas disease causative agent, the parasite Trypanosoma cruzi, makes the control of vector population the best available strategy to limit disease spread. Although heme and redox homeostasis regulation is critical for both triatomine insects and T. cruzi, the physiological relevance of hemozoin for these organisms remains unknown. Here, we demonstrate that selective blockage of heme crystallization in vivo by the antimalarial drug quinidine, caused systemic heme overload and redox imbalance in distinct insect tissues, assessed by spectrophotometry and fluorescence microscopy. Quinidine treatment activated compensatory defensive heme-scavenging mechanisms to cope with excessive heme, as revealed by biochemical hemolymph analyses, and fat body gene expression. Importantly, egg production, oviposition, and total T. cruzi parasite counts in R. prolixus were significantly reduced by quinidine treatment. These effects were reverted by oral supplementation with the major insect antioxidant urate. Altogether, these data underscore the importance of heme crystallization as the main redox regulator for triatomine vectors, indicating the dual role of hemozoin as a protective mechanism to allow insect fertility, and T. cruzi life-cycle. Thus, targeting heme crystallization in insect vectors represents an innovative way for Chagas disease control, by reducing simultaneously triatomine reproduction and T. cruzi transmission.
url http://europepmc.org/articles/PMC6084092?pdf=render
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