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“Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus”
Low levels of reactive oxygen species (ROS) are now recognized as essential players in cell signaling. Here, we studied the role of two conserved enzymes involved in redox regulation that play a critical role in the control of ROS in the digestive physiology of a blood-sucking insect, the kissing bu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947236/ https://www.ncbi.nlm.nih.gov/pubmed/33716782 http://dx.doi.org/10.3389/fphys.2021.633093 |
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author | Gandara, Ana Caroline P. Dias, Felipe A. de Lemos, Paula C. Stiebler, Renata Bombaça, Ana Cristina S. Menna-Barreto, Rubem Oliveira, Pedro L. |
author_facet | Gandara, Ana Caroline P. Dias, Felipe A. de Lemos, Paula C. Stiebler, Renata Bombaça, Ana Cristina S. Menna-Barreto, Rubem Oliveira, Pedro L. |
author_sort | Gandara, Ana Caroline P. |
collection | PubMed |
description | Low levels of reactive oxygen species (ROS) are now recognized as essential players in cell signaling. Here, we studied the role of two conserved enzymes involved in redox regulation that play a critical role in the control of ROS in the digestive physiology of a blood-sucking insect, the kissing bug Rhodnius prolixus. RNAi-mediated silencing of RpNOX5 and RpXDH induced early mortality in adult females after a blood meal. Recently, a role for RpNOX5 in gut motility was reported, and here, we show that midgut peristalsis is also under the control of RpXDH. Together with impaired peristalsis, silencing either genes impaired egg production and hemoglobin digestion, and decreased hemolymph urate titers. Ultrastructurally, the silencing of RpNOX5 or RpXDH affected midgut cells, changing the cells of blood-fed insects to a phenotype resembling the cells of unfed insects, suggesting that these genes work together in the control of blood digestion. Injection of either allopurinol (an XDH inhibitor) or uricase recapitulated the gene silencing effects, suggesting that urate itself is involved in the control of blood digestion. The silencing of each of these genes influenced the expression of the other gene in a complex way both in the unfed state and after a blood meal, revealing signaling crosstalk between them that influences redox metabolism and nitrogen excretion and plays a central role in the control of digestive physiology. |
format | Online Article Text |
id | pubmed-7947236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79472362021-03-12 “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” Gandara, Ana Caroline P. Dias, Felipe A. de Lemos, Paula C. Stiebler, Renata Bombaça, Ana Cristina S. Menna-Barreto, Rubem Oliveira, Pedro L. Front Physiol Physiology Low levels of reactive oxygen species (ROS) are now recognized as essential players in cell signaling. Here, we studied the role of two conserved enzymes involved in redox regulation that play a critical role in the control of ROS in the digestive physiology of a blood-sucking insect, the kissing bug Rhodnius prolixus. RNAi-mediated silencing of RpNOX5 and RpXDH induced early mortality in adult females after a blood meal. Recently, a role for RpNOX5 in gut motility was reported, and here, we show that midgut peristalsis is also under the control of RpXDH. Together with impaired peristalsis, silencing either genes impaired egg production and hemoglobin digestion, and decreased hemolymph urate titers. Ultrastructurally, the silencing of RpNOX5 or RpXDH affected midgut cells, changing the cells of blood-fed insects to a phenotype resembling the cells of unfed insects, suggesting that these genes work together in the control of blood digestion. Injection of either allopurinol (an XDH inhibitor) or uricase recapitulated the gene silencing effects, suggesting that urate itself is involved in the control of blood digestion. The silencing of each of these genes influenced the expression of the other gene in a complex way both in the unfed state and after a blood meal, revealing signaling crosstalk between them that influences redox metabolism and nitrogen excretion and plays a central role in the control of digestive physiology. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7947236/ /pubmed/33716782 http://dx.doi.org/10.3389/fphys.2021.633093 Text en Copyright © 2021 Gandara, Dias, de Lemos, Stiebler, Bombaça, Menna-Barreto and Oliveira. 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 Gandara, Ana Caroline P. Dias, Felipe A. de Lemos, Paula C. Stiebler, Renata Bombaça, Ana Cristina S. Menna-Barreto, Rubem Oliveira, Pedro L. “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title | “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title_full | “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title_fullStr | “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title_full_unstemmed | “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title_short | “Urate and NOX5 Control Blood Digestion in the Hematophagous Insect Rhodnius prolixus” |
title_sort | “urate and nox5 control blood digestion in the hematophagous insect rhodnius prolixus” |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947236/ https://www.ncbi.nlm.nih.gov/pubmed/33716782 http://dx.doi.org/10.3389/fphys.2021.633093 |
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