Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells

Despite the availability of an effective vaccine, Japanese encephalitis remains a significant cause of morbidity and mortality in many parts of Asia. Japanese encephalitis is caused by the Japanese encephalitis virus (JEV), a mosquito transmitted flavivirus. Many of the details of the virus replicat...

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Main Authors: Chanida Fongsaran, Narumon Phaonakrop, Sittiruk Roytrakul, Chutima Thepparit, Atichat Kuadkitkan, Smith, Duncan R.
Other Authors: Mahidol University. Institute of Molecular Biosciences
Format: Article
Language:English
Published: 2015
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/1842
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spelling th-mahidol.18422023-04-12T15:26:03Z Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells Chanida Fongsaran Narumon Phaonakrop Sittiruk Roytrakul Chutima Thepparit Atichat Kuadkitkan Smith, Duncan R. Mahidol University. Institute of Molecular Biosciences Mahidol University. Center for Emerging and Neglected Infectious Diseases Voltage Dependent Anion Channel Redistributed during Japanese Encephalitis Virus Infection of Insect Cells Virus Infection Open Access article Despite the availability of an effective vaccine, Japanese encephalitis remains a significant cause of morbidity and mortality in many parts of Asia. Japanese encephalitis is caused by the Japanese encephalitis virus (JEV), a mosquito transmitted flavivirus. Many of the details of the virus replication cycle in mosquito cells remain unknown. This study sought to determine whether GRP78, a well-characterized flavivirus E protein interacting protein, interacted with JEV E protein in insect cells, and whether this interaction was mediated at the cell surface. GRP78 was shown to interact with JEV E protein by coimmunoprecipitation, and was additionally shown to interact with voltage dependent anion protein (VDAC) through the same methodology. Antibody inhibition experiments showed that neither GRP78 nor VDAC played a role in JEV internalization to insect cells. Interestingly, VDAC was shown to be significantly relocalized in response to JEV infection, and significant levels of colocalization between VDAC and GRP78 and VDAC and ribosomal L28 protein were seen in JEV infected but not uninfected cells. This is the first report of relocalization of VDAC in response to JEV infection and suggests that this may be a part of the JEV replication strategy in insect cells. 2015-03-21T03:46:17Z 2017-04-25T03:40:57Z 2015-03-21T03:46:17Z 2017-04-25T03:40:57Z 2015-03-21 2014 Article The Scientific World Journal. 2014, ID 976015 10.1155/2014/976015 https://repository.li.mahidol.ac.th/handle/123456789/1842 eng Mahidol University application/pdf
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
language English
topic Voltage Dependent
Anion Channel
Redistributed during
Japanese Encephalitis
Virus Infection of Insect Cells
Virus Infection
Open Access article
spellingShingle Voltage Dependent
Anion Channel
Redistributed during
Japanese Encephalitis
Virus Infection of Insect Cells
Virus Infection
Open Access article
Chanida Fongsaran
Narumon Phaonakrop
Sittiruk Roytrakul
Chutima Thepparit
Atichat Kuadkitkan
Smith, Duncan R.
Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
description Despite the availability of an effective vaccine, Japanese encephalitis remains a significant cause of morbidity and mortality in many parts of Asia. Japanese encephalitis is caused by the Japanese encephalitis virus (JEV), a mosquito transmitted flavivirus. Many of the details of the virus replication cycle in mosquito cells remain unknown. This study sought to determine whether GRP78, a well-characterized flavivirus E protein interacting protein, interacted with JEV E protein in insect cells, and whether this interaction was mediated at the cell surface. GRP78 was shown to interact with JEV E protein by coimmunoprecipitation, and was additionally shown to interact with voltage dependent anion protein (VDAC) through the same methodology. Antibody inhibition experiments showed that neither GRP78 nor VDAC played a role in JEV internalization to insect cells. Interestingly, VDAC was shown to be significantly relocalized in response to JEV infection, and significant levels of colocalization between VDAC and GRP78 and VDAC and ribosomal L28 protein were seen in JEV infected but not uninfected cells. This is the first report of relocalization of VDAC in response to JEV infection and suggests that this may be a part of the JEV replication strategy in insect cells.
author2 Mahidol University. Institute of Molecular Biosciences
author_facet Mahidol University. Institute of Molecular Biosciences
Chanida Fongsaran
Narumon Phaonakrop
Sittiruk Roytrakul
Chutima Thepparit
Atichat Kuadkitkan
Smith, Duncan R.
format Article
author Chanida Fongsaran
Narumon Phaonakrop
Sittiruk Roytrakul
Chutima Thepparit
Atichat Kuadkitkan
Smith, Duncan R.
author_sort Chanida Fongsaran
title Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
title_short Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
title_full Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
title_fullStr Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
title_full_unstemmed Voltage dependent anion channel is redistributed during Japanese encephalitis virus infection of insect cells
title_sort voltage dependent anion channel is redistributed during japanese encephalitis virus infection of insect cells
publishDate 2015
url https://repository.li.mahidol.ac.th/handle/123456789/1842
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