Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.

Mosquitoes transmit a number of diseases in animals and humans, including Dengue, Chikungunya and Zika viruses that affect millions of people each year. Controlling the disease-transmitting mosquitoes has proven to be a successful strategy to reduce the viruses transmission. Polyamines are required...

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Main Authors: Huai Guan, Maoying Wang, Chenghong Liao, Jing Liang, Prajwalini Mehere, Meiling Tian, Hairong Liu, Howard Robinson, Jianyong Li, Qian Han
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5858766?pdf=render
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spelling doaj-e04ab0f774e146f594634851b4b2c63b2020-11-24T21:09:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019449910.1371/journal.pone.0194499Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.Huai GuanMaoying WangChenghong LiaoJing LiangPrajwalini MehereMeiling TianHairong LiuHoward RobinsonJianyong LiQian HanMosquitoes transmit a number of diseases in animals and humans, including Dengue, Chikungunya and Zika viruses that affect millions of people each year. Controlling the disease-transmitting mosquitoes has proven to be a successful strategy to reduce the viruses transmission. Polyamines are required for the life cycle of the RNA viruses, Chikungunya virus and Zika virus, and a depletion of spermidine and spermine in the host via induction of spermine N-acetyltransferase restricts their replication. Spermine N-acetyltransferase is a key catabolic enzyme in the polyamine pathway, however there is no information of the enzyme identification in any insects. Aliphatic polyamines play a fundamental role in tissue growth and development in organisms. They are acetylated by spermidine/spermine N1-acetyltransferase (SAT). In this study we provided a molecular and biochemical identification of SAT from Aedes aegypti mosquitoes. Screening of purified recombinant proteins against polyamines established that aaNAT5b, named previously based on sequence similarity with identified aaNAT1 in insects, is active to spermine and spermidine. A crystal structure was determined and used in molecular docking in this study. Key residues were identified to be involved in spermine binding using molecular docking and simulation. In addition, SAT transcript was down regulated by blood feeding using a real time PCR test. Based on its substrate profile and transcriptional levels after blood feeding, together with previous reports for polyamines required in arboviruses replication, SAT might be potentially used as a target to control arboviruses with human interference.http://europepmc.org/articles/PMC5858766?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Huai Guan
Maoying Wang
Chenghong Liao
Jing Liang
Prajwalini Mehere
Meiling Tian
Hairong Liu
Howard Robinson
Jianyong Li
Qian Han
spellingShingle Huai Guan
Maoying Wang
Chenghong Liao
Jing Liang
Prajwalini Mehere
Meiling Tian
Hairong Liu
Howard Robinson
Jianyong Li
Qian Han
Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
PLoS ONE
author_facet Huai Guan
Maoying Wang
Chenghong Liao
Jing Liang
Prajwalini Mehere
Meiling Tian
Hairong Liu
Howard Robinson
Jianyong Li
Qian Han
author_sort Huai Guan
title Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
title_short Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
title_full Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
title_fullStr Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
title_full_unstemmed Identification of aaNAT5b as a spermine N-acetyltransferase in the mosquito, Aedes aegypti.
title_sort identification of aanat5b as a spermine n-acetyltransferase in the mosquito, aedes aegypti.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Mosquitoes transmit a number of diseases in animals and humans, including Dengue, Chikungunya and Zika viruses that affect millions of people each year. Controlling the disease-transmitting mosquitoes has proven to be a successful strategy to reduce the viruses transmission. Polyamines are required for the life cycle of the RNA viruses, Chikungunya virus and Zika virus, and a depletion of spermidine and spermine in the host via induction of spermine N-acetyltransferase restricts their replication. Spermine N-acetyltransferase is a key catabolic enzyme in the polyamine pathway, however there is no information of the enzyme identification in any insects. Aliphatic polyamines play a fundamental role in tissue growth and development in organisms. They are acetylated by spermidine/spermine N1-acetyltransferase (SAT). In this study we provided a molecular and biochemical identification of SAT from Aedes aegypti mosquitoes. Screening of purified recombinant proteins against polyamines established that aaNAT5b, named previously based on sequence similarity with identified aaNAT1 in insects, is active to spermine and spermidine. A crystal structure was determined and used in molecular docking in this study. Key residues were identified to be involved in spermine binding using molecular docking and simulation. In addition, SAT transcript was down regulated by blood feeding using a real time PCR test. Based on its substrate profile and transcriptional levels after blood feeding, together with previous reports for polyamines required in arboviruses replication, SAT might be potentially used as a target to control arboviruses with human interference.
url http://europepmc.org/articles/PMC5858766?pdf=render
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