Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)

<p>Abstract</p> <p>Background</p> <p>Venezuelan equine encephalitis virus (VEEV) belongs to the Alphavirus group. Several species of this family are also pathogenic to humans and are recognized as potential agents of biological warfare and terrorism. The objective of th...

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Main Authors: Hust Michael, Marschall Hans-Jürgen, Schirrmann Thomas, Rülker Torsten, Nacke Christoph, Hülseweh Birgit, Kirsch Martina, Dübel Stefan
Format: Article
Language:English
Published: BMC 2008-09-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/8/66
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spelling doaj-9341e6ca02dd431ebcc19ecc655d829c2020-11-25T03:39:22ZengBMCBMC Biotechnology1472-67502008-09-01816610.1186/1472-6750-8-66Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)Hust MichaelMarschall Hans-JürgenSchirrmann ThomasRülker TorstenNacke ChristophHülseweh BirgitKirsch MartinaDübel Stefan<p>Abstract</p> <p>Background</p> <p>Venezuelan equine encephalitis virus (VEEV) belongs to the Alphavirus group. Several species of this family are also pathogenic to humans and are recognized as potential agents of biological warfare and terrorism. The objective of this work was the generation of recombinant antibodies for the detection of VEEV after a potential bioterrorism assault or an natural outbreak of VEEV.</p> <p>Results</p> <p>In this work, human anti-VEEV single chain Fragments variable (scFv) were isolated for the first time from a human naïve antibody gene library using optimized selection processes. In total eleven different scFvs were identified and their immunological specificity was assessed. The specific detection of the VEEV strains TC83, H12/93 and 230 by the selected antibody fragments was proved. Active as well as formalin inactivated virus particles were recognized by the selected antibody fragments which could be also used for Western blot analysis of VEEV proteins and immunohistochemistry of VEEV infected cells. The anti-VEEV scFv phage clones did not show any cross-reactivity with Alphavirus species of the Western equine encephalitis virus (WEEV) and Eastern equine encephalitis virus (EEEV) antigenic complex, nor did they react with Chikungunya virus (CHIKV), if they were used as detection reagent.</p> <p>Conclusion</p> <p>For the first time, this study describes the selection of antibodies against a human pathogenic virus from a human naïve scFv antibody gene library using complete, active virus particles as antigen. The broad and sensitive applicability of scFv-presenting phage for the immunological detection and diagnosis of Alphavirus species was demonstrated. The selected antibody fragments will improve the fast identification of VEEV in case of a biological warfare or terroristic attack or a natural outbreak.</p> http://www.biomedcentral.com/1472-6750/8/66
collection DOAJ
language English
format Article
sources DOAJ
author Hust Michael
Marschall Hans-Jürgen
Schirrmann Thomas
Rülker Torsten
Nacke Christoph
Hülseweh Birgit
Kirsch Martina
Dübel Stefan
spellingShingle Hust Michael
Marschall Hans-Jürgen
Schirrmann Thomas
Rülker Torsten
Nacke Christoph
Hülseweh Birgit
Kirsch Martina
Dübel Stefan
Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
BMC Biotechnology
author_facet Hust Michael
Marschall Hans-Jürgen
Schirrmann Thomas
Rülker Torsten
Nacke Christoph
Hülseweh Birgit
Kirsch Martina
Dübel Stefan
author_sort Hust Michael
title Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
title_short Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
title_full Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
title_fullStr Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
title_full_unstemmed Development of human antibody fragments using antibody phage display for the detection and diagnosis of Venezuelan equine encephalitis virus (VEEV)
title_sort development of human antibody fragments using antibody phage display for the detection and diagnosis of venezuelan equine encephalitis virus (veev)
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2008-09-01
description <p>Abstract</p> <p>Background</p> <p>Venezuelan equine encephalitis virus (VEEV) belongs to the Alphavirus group. Several species of this family are also pathogenic to humans and are recognized as potential agents of biological warfare and terrorism. The objective of this work was the generation of recombinant antibodies for the detection of VEEV after a potential bioterrorism assault or an natural outbreak of VEEV.</p> <p>Results</p> <p>In this work, human anti-VEEV single chain Fragments variable (scFv) were isolated for the first time from a human naïve antibody gene library using optimized selection processes. In total eleven different scFvs were identified and their immunological specificity was assessed. The specific detection of the VEEV strains TC83, H12/93 and 230 by the selected antibody fragments was proved. Active as well as formalin inactivated virus particles were recognized by the selected antibody fragments which could be also used for Western blot analysis of VEEV proteins and immunohistochemistry of VEEV infected cells. The anti-VEEV scFv phage clones did not show any cross-reactivity with Alphavirus species of the Western equine encephalitis virus (WEEV) and Eastern equine encephalitis virus (EEEV) antigenic complex, nor did they react with Chikungunya virus (CHIKV), if they were used as detection reagent.</p> <p>Conclusion</p> <p>For the first time, this study describes the selection of antibodies against a human pathogenic virus from a human naïve scFv antibody gene library using complete, active virus particles as antigen. The broad and sensitive applicability of scFv-presenting phage for the immunological detection and diagnosis of Alphavirus species was demonstrated. The selected antibody fragments will improve the fast identification of VEEV in case of a biological warfare or terroristic attack or a natural outbreak.</p>
url http://www.biomedcentral.com/1472-6750/8/66
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