The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32

The role of the cytoskeleton, actin, and microtubules were examined during the process of Japanese encephalitis (JEV) infection in a human neuroblastoma cell line, IMR32. Cytochalasin D and nocodazole were used to depolymerise the cellular actin and microtubules, respectively, in order to study the...

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Main Author: Henry Sum, Magdline Sia
Format: Article
Language:English
Published: Hidawi Publishing Coperation 2015
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Online Access:http://ir.unimas.my/id/eprint/10572/1/Magdline%20Sia.pdf
http://ir.unimas.my/id/eprint/10572/
http://www.hindawi.com/journals/bmri/2015/695283/
http://dx.doi.org/10.1155/2015/695283
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spelling my.unimas.ir.105722022-01-26T08:14:20Z http://ir.unimas.my/id/eprint/10572/ The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32 Henry Sum, Magdline Sia Q Science (General) QR Microbiology QR180 Immunology QR355 Virology R Medicine (General) The role of the cytoskeleton, actin, and microtubules were examined during the process of Japanese encephalitis (JEV) infection in a human neuroblastoma cell line, IMR32. Cytochalasin D and nocodazole were used to depolymerise the cellular actin and microtubules, respectively, in order to study the effect of JEV infection in the cell. This study shows that depolymerisation of the actin cytoskeleton at early process of infection inhibits JEV infection in the cell; however infection was not inhibited when depolymerisation occurred at the later stage of infection.The microtubules, on the other hand, are required at 2 points in infection. The antigen production in the cells was inhibited when the infected cells were treated at time up to 2 hours after inoculation and there was no significant effect at later times, while the viable virus released continued to be affected until 10 hours after inoculation. In conclusion, infection of JEV in IMR32 cells required actin to facilitate early process in infection and the microtubular network is utilised as the transport system to the virus replication site and the release of mature virus. Hidawi Publishing Coperation 2015 Article PeerReviewed text en http://ir.unimas.my/id/eprint/10572/1/Magdline%20Sia.pdf Henry Sum, Magdline Sia (2015) The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32. BioMed Research International, 2015. pp. 1-8. ISSN 695283 http://www.hindawi.com/journals/bmri/2015/695283/ http://dx.doi.org/10.1155/2015/695283
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic Q Science (General)
QR Microbiology
QR180 Immunology
QR355 Virology
R Medicine (General)
spellingShingle Q Science (General)
QR Microbiology
QR180 Immunology
QR355 Virology
R Medicine (General)
Henry Sum, Magdline Sia
The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
description The role of the cytoskeleton, actin, and microtubules were examined during the process of Japanese encephalitis (JEV) infection in a human neuroblastoma cell line, IMR32. Cytochalasin D and nocodazole were used to depolymerise the cellular actin and microtubules, respectively, in order to study the effect of JEV infection in the cell. This study shows that depolymerisation of the actin cytoskeleton at early process of infection inhibits JEV infection in the cell; however infection was not inhibited when depolymerisation occurred at the later stage of infection.The microtubules, on the other hand, are required at 2 points in infection. The antigen production in the cells was inhibited when the infected cells were treated at time up to 2 hours after inoculation and there was no significant effect at later times, while the viable virus released continued to be affected until 10 hours after inoculation. In conclusion, infection of JEV in IMR32 cells required actin to facilitate early process in infection and the microtubular network is utilised as the transport system to the virus replication site and the release of mature virus.
format Article
author Henry Sum, Magdline Sia
author_facet Henry Sum, Magdline Sia
author_sort Henry Sum, Magdline Sia
title The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
title_short The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
title_full The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
title_fullStr The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
title_full_unstemmed The Involvement of Microtubules and Actin during the Infection of Japanese Encephalitis Virus in Neuroblastoma Cell Line, IMR32
title_sort involvement of microtubules and actin during the infection of japanese encephalitis virus in neuroblastoma cell line, imr32
publisher Hidawi Publishing Coperation
publishDate 2015
url http://ir.unimas.my/id/eprint/10572/1/Magdline%20Sia.pdf
http://ir.unimas.my/id/eprint/10572/
http://www.hindawi.com/journals/bmri/2015/695283/
http://dx.doi.org/10.1155/2015/695283
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