The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model

There are conflicting data on the relationship between the level of secreted NS1 (sNS1), viremia, and disease severity upon dengue virus (DENV) infection in the clinical setting, and therefore, we examined this relationship in the widely accepted AG129 mouse model. Because of the failure of a routin...

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Main Authors: Watanabe, Satoru, Tan, Kah Hin, Rathore, Abhay P. S., Rozen-Gagnon, Kathryn, Shuai, Wang, Ruedl, Christiane, Vasudevan, Subhash G.
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2013
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Online Access:https://hdl.handle.net/10356/97639
http://hdl.handle.net/10220/11196
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-976392022-02-16T16:28:54Z The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model Watanabe, Satoru Tan, Kah Hin Rathore, Abhay P. S. Rozen-Gagnon, Kathryn Shuai, Wang Ruedl, Christiane Vasudevan, Subhash G. School of Biological Sciences DRNTU::Science::Biological sciences There are conflicting data on the relationship between the level of secreted NS1 (sNS1), viremia, and disease severity upon dengue virus (DENV) infection in the clinical setting, and therefore, we examined this relationship in the widely accepted AG129 mouse model. Because of the failure of a routinely used NS1 detection kit to detect sNS1 of the mouse-adapted DENV2 strain, we screened 15 previously undescribed NS1 monoclonal antibodies and developed a robust capture enzyme-linked immunosorbent assay (ELISA) with detection sensitivity at the low nanogram level (0.2 ng/ml) using recombinant baculovirus-expressed sNS1 as well as sNS1 that was immunoaffinity purified from the various DENV2 strains employed in this study. Using this test, we demonstrated that increased viremia paralleled severe pathologies; however, sNS1 level did not correlate with viremia or severity. Furthermore, among the DENV2 strains that were tested, the level of NS1 secretion did not correspond to virus replication rate in vitro, at the cellular level. Together, our data indicate that the magnitude of NS1 secretion appears to be strain dependent and does not correlate with viral virulence in the AG129 mouse model. 2013-07-11T04:33:26Z 2019-12-06T19:44:50Z 2013-07-11T04:33:26Z 2019-12-06T19:44:50Z 2012 2012 Journal Article Watanabe, S., Tan, K. H., Rathore, A. P. S., Rozen-Gagnon, K., Shuai, W., Ruedl, C., et al. (2012). The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model. Journal of Virology, 86(10), 5508-5514. https://hdl.handle.net/10356/97639 http://hdl.handle.net/10220/11196 10.1128/JVI.07081-11 22419801 en Journal of virology © 2012 American Society of Microbiology.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences
spellingShingle DRNTU::Science::Biological sciences
Watanabe, Satoru
Tan, Kah Hin
Rathore, Abhay P. S.
Rozen-Gagnon, Kathryn
Shuai, Wang
Ruedl, Christiane
Vasudevan, Subhash G.
The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
description There are conflicting data on the relationship between the level of secreted NS1 (sNS1), viremia, and disease severity upon dengue virus (DENV) infection in the clinical setting, and therefore, we examined this relationship in the widely accepted AG129 mouse model. Because of the failure of a routinely used NS1 detection kit to detect sNS1 of the mouse-adapted DENV2 strain, we screened 15 previously undescribed NS1 monoclonal antibodies and developed a robust capture enzyme-linked immunosorbent assay (ELISA) with detection sensitivity at the low nanogram level (0.2 ng/ml) using recombinant baculovirus-expressed sNS1 as well as sNS1 that was immunoaffinity purified from the various DENV2 strains employed in this study. Using this test, we demonstrated that increased viremia paralleled severe pathologies; however, sNS1 level did not correlate with viremia or severity. Furthermore, among the DENV2 strains that were tested, the level of NS1 secretion did not correspond to virus replication rate in vitro, at the cellular level. Together, our data indicate that the magnitude of NS1 secretion appears to be strain dependent and does not correlate with viral virulence in the AG129 mouse model.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Watanabe, Satoru
Tan, Kah Hin
Rathore, Abhay P. S.
Rozen-Gagnon, Kathryn
Shuai, Wang
Ruedl, Christiane
Vasudevan, Subhash G.
format Article
author Watanabe, Satoru
Tan, Kah Hin
Rathore, Abhay P. S.
Rozen-Gagnon, Kathryn
Shuai, Wang
Ruedl, Christiane
Vasudevan, Subhash G.
author_sort Watanabe, Satoru
title The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
title_short The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
title_full The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
title_fullStr The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
title_full_unstemmed The magnitude of dengue virus NS1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
title_sort magnitude of dengue virus ns1 protein secretion is strain dependent and does not correlate with severe pathologies in the mouse infection model
publishDate 2013
url https://hdl.handle.net/10356/97639
http://hdl.handle.net/10220/11196
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