Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>

<p>Abstract</p> <p>Background</p> <p>Antigens for Hantavirus serological tests have been produced using DNA recombinant technology for more than twenty years. Several different strategies have been used for that purpose. All of them avoid the risks and difficulties invo...

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Main Authors: Wolff Jose LC, Figueiredo Luiz TM, Ribeiro Bergmann M, Moreli Marcos L, Machado Aline RSR, Machado Alex M
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/8/1/218
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spelling doaj-50fbdd148967492480e09274d92bec922020-11-24T22:30:23ZengBMCVirology Journal1743-422X2011-05-018121810.1186/1743-422X-8-218Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>Wolff Jose LCFigueiredo Luiz TMRibeiro Bergmann MMoreli Marcos LMachado Aline RSRMachado Alex M<p>Abstract</p> <p>Background</p> <p>Antigens for Hantavirus serological tests have been produced using DNA recombinant technology for more than twenty years. Several different strategies have been used for that purpose. All of them avoid the risks and difficulties involved in multiplying Hantavirus in the laboratory. In Brazil, the Araraquara virus is one of the main causes of Hantavirus Cardio-Pulmonary Syndrome (HCPS).</p> <p>Methods</p> <p>In this investigation, we report the expression of the N protein of the Araraquara Hantavirus in a Baculovirus Expression System, the use of this protein in IgM and IgG ELISA and comparison with the same antigen generated in <it>E. coli</it>.</p> <p>Results</p> <p>The protein obtained, and purified in a nickel column, was effectively recognized by antibodies from confirmed HCPS patients. Comparison of the baculovirus generated antigen with the N protein produced in <it>E. coli </it>showed that both were equally effective in terms of sensitivity and specificity.</p> <p>Conclusions</p> <p>Our results therefore indicate that either of these proteins can be used in serological tests in Brazil.</p> http://www.virologyj.com/content/8/1/218
collection DOAJ
language English
format Article
sources DOAJ
author Wolff Jose LC
Figueiredo Luiz TM
Ribeiro Bergmann M
Moreli Marcos L
Machado Aline RSR
Machado Alex M
spellingShingle Wolff Jose LC
Figueiredo Luiz TM
Ribeiro Bergmann M
Moreli Marcos L
Machado Aline RSR
Machado Alex M
Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
Virology Journal
author_facet Wolff Jose LC
Figueiredo Luiz TM
Ribeiro Bergmann M
Moreli Marcos L
Machado Aline RSR
Machado Alex M
author_sort Wolff Jose LC
title Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
title_short Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
title_full Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
title_fullStr Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
title_full_unstemmed Expression of recombinant Araraquara Hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>Escherichia coli</it>
title_sort expression of recombinant araraquara hantavirus nucleoprotein in insect cells and its use as an antigen for immunodetection compared to the same antigen expressed in <it>escherichia coli</it>
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-05-01
description <p>Abstract</p> <p>Background</p> <p>Antigens for Hantavirus serological tests have been produced using DNA recombinant technology for more than twenty years. Several different strategies have been used for that purpose. All of them avoid the risks and difficulties involved in multiplying Hantavirus in the laboratory. In Brazil, the Araraquara virus is one of the main causes of Hantavirus Cardio-Pulmonary Syndrome (HCPS).</p> <p>Methods</p> <p>In this investigation, we report the expression of the N protein of the Araraquara Hantavirus in a Baculovirus Expression System, the use of this protein in IgM and IgG ELISA and comparison with the same antigen generated in <it>E. coli</it>.</p> <p>Results</p> <p>The protein obtained, and purified in a nickel column, was effectively recognized by antibodies from confirmed HCPS patients. Comparison of the baculovirus generated antigen with the N protein produced in <it>E. coli </it>showed that both were equally effective in terms of sensitivity and specificity.</p> <p>Conclusions</p> <p>Our results therefore indicate that either of these proteins can be used in serological tests in Brazil.</p>
url http://www.virologyj.com/content/8/1/218
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