Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization

Dengue viral antigens have been demonstrated in several types of naturally infected human tissues, but little is known of whether these same tissues have detectable viral RNA. We studied tissue specimens from patients with serologically or virologically confirmed dengue infections by immunohistochem...

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Main Authors: Jessie, K., Fong, M.Y., Devi, S., Lam, S.K., Wong, K.T.
Format: Article
Language:English
Published: 2004
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Online Access:http://eprints.um.edu.my/2726/1/Localization_of_dengue_virus_in_naturally_infected_human_tissues%2C_by_immunohistochemistry_and_in_situ_hybridization.pdf
http://eprints.um.edu.my/2726/
http://jid.oxfordjournals.org/content/189/8/1411.short
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spelling my.um.eprints.27262014-10-20T02:46:41Z http://eprints.um.edu.my/2726/ Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization Jessie, K. Fong, M.Y. Devi, S. Lam, S.K. Wong, K.T. R Medicine Dengue viral antigens have been demonstrated in several types of naturally infected human tissues, but little is known of whether these same tissues have detectable viral RNA. We studied tissue specimens from patients with serologically or virologically confirmed dengue infections by immunohistochemistry (IHC) and in situ hybridization ( ISH), to localize viral antigen and RNA, respectively. IHC was performed on specimens obtained from 5 autopsies and 24 biopsies and on 20 blood-clot samples. For ISH, antisense riboprobes to the dengue E gene were applied to tissue specimens in which IHC was positive. Viral antigens were demonstrated in Kupffer and sinusoidal endothelial cells of the liver; macrophages, multinucleated cells, and reactive lymphoid cells in the spleen; macrophages and vascular endothelium in the lung; kidney tubules; and monocytes and lymphocytes in blood-clot samples. Positive-strand viral RNA was detected in the same IHC-positive cells found in the spleen and blood-clot samples. The strong, positive ISH signal in these cells indicated a high copy number of viral RNA, suggesting replication. 2004 Article PeerReviewed application/pdf en http://eprints.um.edu.my/2726/1/Localization_of_dengue_virus_in_naturally_infected_human_tissues%2C_by_immunohistochemistry_and_in_situ_hybridization.pdf Jessie, K. and Fong, M.Y. and Devi, S. and Lam, S.K. and Wong, K.T. (2004) Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization. Journal of Infectious Diseases, 189 (8). pp. 1411-1418. ISSN 0022-1899 http://jid.oxfordjournals.org/content/189/8/1411.short 10.1086/383043
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
language English
topic R Medicine
spellingShingle R Medicine
Jessie, K.
Fong, M.Y.
Devi, S.
Lam, S.K.
Wong, K.T.
Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
description Dengue viral antigens have been demonstrated in several types of naturally infected human tissues, but little is known of whether these same tissues have detectable viral RNA. We studied tissue specimens from patients with serologically or virologically confirmed dengue infections by immunohistochemistry (IHC) and in situ hybridization ( ISH), to localize viral antigen and RNA, respectively. IHC was performed on specimens obtained from 5 autopsies and 24 biopsies and on 20 blood-clot samples. For ISH, antisense riboprobes to the dengue E gene were applied to tissue specimens in which IHC was positive. Viral antigens were demonstrated in Kupffer and sinusoidal endothelial cells of the liver; macrophages, multinucleated cells, and reactive lymphoid cells in the spleen; macrophages and vascular endothelium in the lung; kidney tubules; and monocytes and lymphocytes in blood-clot samples. Positive-strand viral RNA was detected in the same IHC-positive cells found in the spleen and blood-clot samples. The strong, positive ISH signal in these cells indicated a high copy number of viral RNA, suggesting replication.
format Article
author Jessie, K.
Fong, M.Y.
Devi, S.
Lam, S.K.
Wong, K.T.
author_facet Jessie, K.
Fong, M.Y.
Devi, S.
Lam, S.K.
Wong, K.T.
author_sort Jessie, K.
title Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
title_short Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
title_full Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
title_fullStr Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
title_full_unstemmed Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
title_sort localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization
publishDate 2004
url http://eprints.um.edu.my/2726/1/Localization_of_dengue_virus_in_naturally_infected_human_tissues%2C_by_immunohistochemistry_and_in_situ_hybridization.pdf
http://eprints.um.edu.my/2726/
http://jid.oxfordjournals.org/content/189/8/1411.short
_version_ 1643686980091904000