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Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction

Hematophagous mosquitoes serve as vectors of multiple devastating human diseases, and many unique physiological features contribute to the incredible evolutionary success of these insects. These functions place high-energy demands on a reproducing female mosquito, and carbohydrate metabolism (CM) mu...

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Autores principales: Hou, Yuan, Wang, Xue-Li, Saha, Tusar T., Roy, Sourav, Zhao, Bo, Raikhel, Alexander S., Zou, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4497655/
https://www.ncbi.nlm.nih.gov/pubmed/26158648
http://dx.doi.org/10.1371/journal.pgen.1005309
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author Hou, Yuan
Wang, Xue-Li
Saha, Tusar T.
Roy, Sourav
Zhao, Bo
Raikhel, Alexander S.
Zou, Zhen
author_facet Hou, Yuan
Wang, Xue-Li
Saha, Tusar T.
Roy, Sourav
Zhao, Bo
Raikhel, Alexander S.
Zou, Zhen
author_sort Hou, Yuan
collection PubMed
description Hematophagous mosquitoes serve as vectors of multiple devastating human diseases, and many unique physiological features contribute to the incredible evolutionary success of these insects. These functions place high-energy demands on a reproducing female mosquito, and carbohydrate metabolism (CM) must be synchronized with these needs. Functional analysis of metabolic gene profiling showed that major CM pathways, including glycolysis, glycogen and sugar metabolism, and citrate cycle, are dramatically repressed at post eclosion (PE) stage in mosquito fat body followed by a sharply increase at post-blood meal (PBM) stage, which were also verified by Real-time RT-PCR. Consistent to the change of transcript and protein level of CM genes, the level of glycogen, glucose and trehalose and other secondary metabolites are also periodically accumulated and degraded during the reproductive cycle respectively. Levels of triacylglycerols (TAG), which represent another important energy storage form in the mosquito fat body, followed a similar tendency. On the other hand, ATP, which is generated by catabolism of these secondary metabolites, showed an opposite trend. Additionally, we used RNA interference studies for the juvenile hormone and ecdysone receptors, Met and EcR, coupled with transcriptomics and metabolomics analyses to show that these hormone receptors function as major regulatory switches coordinating CM with the differing energy requirements of the female mosquito throughout its reproductive cycle. Our study demonstrates how, by metabolic reprogramming, a multicellular organism adapts to drastic and rapid functional changes.
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spelling pubmed-44976552015-07-14 Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction Hou, Yuan Wang, Xue-Li Saha, Tusar T. Roy, Sourav Zhao, Bo Raikhel, Alexander S. Zou, Zhen PLoS Genet Research Article Hematophagous mosquitoes serve as vectors of multiple devastating human diseases, and many unique physiological features contribute to the incredible evolutionary success of these insects. These functions place high-energy demands on a reproducing female mosquito, and carbohydrate metabolism (CM) must be synchronized with these needs. Functional analysis of metabolic gene profiling showed that major CM pathways, including glycolysis, glycogen and sugar metabolism, and citrate cycle, are dramatically repressed at post eclosion (PE) stage in mosquito fat body followed by a sharply increase at post-blood meal (PBM) stage, which were also verified by Real-time RT-PCR. Consistent to the change of transcript and protein level of CM genes, the level of glycogen, glucose and trehalose and other secondary metabolites are also periodically accumulated and degraded during the reproductive cycle respectively. Levels of triacylglycerols (TAG), which represent another important energy storage form in the mosquito fat body, followed a similar tendency. On the other hand, ATP, which is generated by catabolism of these secondary metabolites, showed an opposite trend. Additionally, we used RNA interference studies for the juvenile hormone and ecdysone receptors, Met and EcR, coupled with transcriptomics and metabolomics analyses to show that these hormone receptors function as major regulatory switches coordinating CM with the differing energy requirements of the female mosquito throughout its reproductive cycle. Our study demonstrates how, by metabolic reprogramming, a multicellular organism adapts to drastic and rapid functional changes. Public Library of Science 2015-07-09 /pmc/articles/PMC4497655/ /pubmed/26158648 http://dx.doi.org/10.1371/journal.pgen.1005309 Text en © 2015 Hou 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
Hou, Yuan
Wang, Xue-Li
Saha, Tusar T.
Roy, Sourav
Zhao, Bo
Raikhel, Alexander S.
Zou, Zhen
Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title_full Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title_fullStr Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title_full_unstemmed Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title_short Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction
title_sort temporal coordination of carbohydrate metabolism during mosquito reproduction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4497655/
https://www.ncbi.nlm.nih.gov/pubmed/26158648
http://dx.doi.org/10.1371/journal.pgen.1005309
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