NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes

碩士 === 國防醫學院 === 微生物及免疫學研究所 === 99 === Dengue virus (DENV) is a member of the mosquito-borne flaviviruses and causes dengue fever or more severe dengue hemorrhagic fever or shock syndrome diseases over the world and caused approximately 25,000 deaths with 25 to 100 million new infections per year....

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Main Authors: Chen, Chung-Chen, 陳宗鉦
Other Authors: Lin, Chang-Chi
Format: Others
Language:zh-TW
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/07307297344387931851
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spelling ndltd-TW-099NDMC03800062015-10-28T04:07:08Z http://ndltd.ncl.edu.tw/handle/07307297344387931851 NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes 登革熱病毒一二三四型NS3蛋白與蚊子JAK-STAT作用之研究 Chen, Chung-Chen 陳宗鉦 碩士 國防醫學院 微生物及免疫學研究所 99 Dengue virus (DENV) is a member of the mosquito-borne flaviviruses and causes dengue fever or more severe dengue hemorrhagic fever or shock syndrome diseases over the world and caused approximately 25,000 deaths with 25 to 100 million new infections per year. The mosquitoes Aedes aegypti as well as Aedes albopictus are major vectors to transmit dengue virus to humans. Endemic dengue infection occurs periodically in Taiwan with imported cases from other tropic regions followed by outbreaks of abundant endogenous cases in southern Taiwan, where more Aedes aegypti mosquitoes are breeding, while few endogenous infection in other northern region due to absent of Aedes aegypti. In the past study, C6/36 and CCL125 mosquito cell lines infected with DENVs revealed a decreased tyrosine phosphorylation and DNA binding activity of AaSTAT and AegSTAT, respectively. And in our study, we have found that the NS3 of JEV- also a member of the mosquito-borne flaviviruses- is interacted with AaSTAT by immunoprecipitation. we have constructed the DENV type1~4 N-terminal histidine (6XHis) fusion protein comprising the NS3 full protein (residues 1 to 618) linked via a flexible glycine linker (Gly4-Ser-Gly4) to an NS2B hydrophilic domain (residues 51 to 94) in pRSET expression vector. The proteins were produced in BL21 (DE3) pLys S induction by IPTG and purified by Ni-NTA agarose (Qiagen). To evaluate DENV NS3 inhibiting mosquito STAT activities, TNT (Promega) products of STAT and STAT fusion with Jak1 domain from Aedes aegypti and Aedes albopictus were put together with the purified NS2B51-94-Glycine linker-NS3 protein in vitro for enzyme activity assay. These mixtures would further to test the disturbance of NS3 protein on the DNA probe binding activity of STAT-Jak1 TNT product by EMSA examination. This experiment might provide more specific molecular events that the DENV counteract host innate immunity in mosquito, and provide an avenue to further about test the anti-dengue drug development on whole NS3 molecule not just on the N-terminal protease part of NS3. Lin, Chang-Chi 林昌棋 2011 學位論文 ; thesis 67 zh-TW
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description 碩士 === 國防醫學院 === 微生物及免疫學研究所 === 99 === Dengue virus (DENV) is a member of the mosquito-borne flaviviruses and causes dengue fever or more severe dengue hemorrhagic fever or shock syndrome diseases over the world and caused approximately 25,000 deaths with 25 to 100 million new infections per year. The mosquitoes Aedes aegypti as well as Aedes albopictus are major vectors to transmit dengue virus to humans. Endemic dengue infection occurs periodically in Taiwan with imported cases from other tropic regions followed by outbreaks of abundant endogenous cases in southern Taiwan, where more Aedes aegypti mosquitoes are breeding, while few endogenous infection in other northern region due to absent of Aedes aegypti. In the past study, C6/36 and CCL125 mosquito cell lines infected with DENVs revealed a decreased tyrosine phosphorylation and DNA binding activity of AaSTAT and AegSTAT, respectively. And in our study, we have found that the NS3 of JEV- also a member of the mosquito-borne flaviviruses- is interacted with AaSTAT by immunoprecipitation. we have constructed the DENV type1~4 N-terminal histidine (6XHis) fusion protein comprising the NS3 full protein (residues 1 to 618) linked via a flexible glycine linker (Gly4-Ser-Gly4) to an NS2B hydrophilic domain (residues 51 to 94) in pRSET expression vector. The proteins were produced in BL21 (DE3) pLys S induction by IPTG and purified by Ni-NTA agarose (Qiagen). To evaluate DENV NS3 inhibiting mosquito STAT activities, TNT (Promega) products of STAT and STAT fusion with Jak1 domain from Aedes aegypti and Aedes albopictus were put together with the purified NS2B51-94-Glycine linker-NS3 protein in vitro for enzyme activity assay. These mixtures would further to test the disturbance of NS3 protein on the DNA probe binding activity of STAT-Jak1 TNT product by EMSA examination. This experiment might provide more specific molecular events that the DENV counteract host innate immunity in mosquito, and provide an avenue to further about test the anti-dengue drug development on whole NS3 molecule not just on the N-terminal protease part of NS3.
author2 Lin, Chang-Chi
author_facet Lin, Chang-Chi
Chen, Chung-Chen
陳宗鉦
author Chen, Chung-Chen
陳宗鉦
spellingShingle Chen, Chung-Chen
陳宗鉦
NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
author_sort Chen, Chung-Chen
title NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
title_short NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
title_full NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
title_fullStr NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
title_full_unstemmed NS3 proteins from dengue four serotypes interacts with JAK-STAT pathway in mosquitoes
title_sort ns3 proteins from dengue four serotypes interacts with jak-stat pathway in mosquitoes
publishDate 2011
url http://ndltd.ncl.edu.tw/handle/07307297344387931851
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