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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Main Authors: Yuan Hou, Xue-Li Wang, Tusar T Saha, Sourav Roy, Bo Zhao, Alexander S Raikhel, Zhen Zou
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4497655?pdf=render
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author Yuan Hou
Xue-Li Wang
Tusar T Saha
Sourav Roy
Bo Zhao
Alexander S Raikhel
Zhen Zou
author_facet Yuan Hou
Xue-Li Wang
Tusar T Saha
Sourav Roy
Bo Zhao
Alexander S Raikhel
Zhen Zou
author_sort Yuan Hou
collection DOAJ
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 doaj.art-2621b2b1fdc54ec8836efa42cdef1fa62022-12-21T18:42:24ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-07-01117e100530910.1371/journal.pgen.1005309Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction.Yuan HouXue-Li WangTusar T SahaSourav RoyBo ZhaoAlexander S RaikhelZhen ZouHematophagous 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.http://europepmc.org/articles/PMC4497655?pdf=render
spellingShingle Yuan Hou
Xue-Li Wang
Tusar T Saha
Sourav Roy
Bo Zhao
Alexander S Raikhel
Zhen Zou
Temporal Coordination of Carbohydrate Metabolism during Mosquito Reproduction.
PLoS Genetics
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
url http://europepmc.org/articles/PMC4497655?pdf=render
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AT alexandersraikhel temporalcoordinationofcarbohydratemetabolismduringmosquitoreproduction
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