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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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 |
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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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