author_facet Lenac Roviš, Tihana
Bailer, Susanne M.
Pothineni, Venkata R.
Ouwendijk, Werner J. D.
Šimić, Hrvoje
Babić, Marina
Miklić, Karmela
Malić, Suzana
Verweij, Marieke C.
Baiker, Armin
Gonzalez, Orland
von Brunn, Albrecht
Zimmer, Ralf
Früh, Klaus
Verjans, Georges M. G. M.
Jonjić, Stipan
Haas, Jürgen
Lenac Roviš, Tihana
Bailer, Susanne M.
Pothineni, Venkata R.
Ouwendijk, Werner J. D.
Šimić, Hrvoje
Babić, Marina
Miklić, Karmela
Malić, Suzana
Verweij, Marieke C.
Baiker, Armin
Gonzalez, Orland
von Brunn, Albrecht
Zimmer, Ralf
Früh, Klaus
Verjans, Georges M. G. M.
Jonjić, Stipan
Haas, Jürgen
author Lenac Roviš, Tihana
Bailer, Susanne M.
Pothineni, Venkata R.
Ouwendijk, Werner J. D.
Šimić, Hrvoje
Babić, Marina
Miklić, Karmela
Malić, Suzana
Verweij, Marieke C.
Baiker, Armin
Gonzalez, Orland
von Brunn, Albrecht
Zimmer, Ralf
Früh, Klaus
Verjans, Georges M. G. M.
Jonjić, Stipan
Haas, Jürgen
spellingShingle Lenac Roviš, Tihana
Bailer, Susanne M.
Pothineni, Venkata R.
Ouwendijk, Werner J. D.
Šimić, Hrvoje
Babić, Marina
Miklić, Karmela
Malić, Suzana
Verweij, Marieke C.
Baiker, Armin
Gonzalez, Orland
von Brunn, Albrecht
Zimmer, Ralf
Früh, Klaus
Verjans, Georges M. G. M.
Jonjić, Stipan
Haas, Jürgen
Journal of Virology
Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
Virology
Insect Science
Immunology
Microbiology
author_sort lenac roviš, tihana
spelling Lenac Roviš, Tihana Bailer, Susanne M. Pothineni, Venkata R. Ouwendijk, Werner J. D. Šimić, Hrvoje Babić, Marina Miklić, Karmela Malić, Suzana Verweij, Marieke C. Baiker, Armin Gonzalez, Orland von Brunn, Albrecht Zimmer, Ralf Früh, Klaus Verjans, Georges M. G. M. Jonjić, Stipan Haas, Jürgen 0022-538X 1098-5514 American Society for Microbiology Virology Insect Science Immunology Microbiology http://dx.doi.org/10.1128/jvi.00407-13 <jats:title>ABSTRACT</jats:title> <jats:p> Varicella-zoster virus (VZV) is the etiological agent of chickenpox and shingles. Due to the virus's restricted host and cell type tropism and the lack of tools for VZV proteomics, it is one of the least-characterized human herpesviruses. We generated 251 monoclonal antibodies (MAbs) against 59 of the 71 (83%) currently known unique VZV proteins to characterize VZV protein expression <jats:italic>in vitro</jats:italic> and <jats:italic>in situ</jats:italic> . Using this new set of MAbs, 44 viral proteins were detected by Western blotting (WB) and indirect immunofluorescence (IF); 13 were detected by WB only, and 2 were detected by IF only. A large proportion of viral proteins was analyzed for the first time in the context of virus infection. Our study revealed the subcellular localization of 46 proteins, 14 of which were analyzed in detail by confocal microscopy. Seven viral proteins were analyzed in time course experiments and showed a cascade-like temporal gene expression pattern similar to those of other herpesviruses. Furthermore, selected MAbs tested positive on human skin lesions by using immunohistochemistry, demonstrating the wide applicability of the MAb collection. Finally, a significant portion of the VZV-specific antibodies reacted with orthologs of simian varicella virus (SVV), thus enabling the systematic analysis of varicella in a nonhuman primate model system. In summary, this study provides insight into the potential function of numerous VZV proteins and novel tools to systematically study VZV and SVV pathogenesis. </jats:p> Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection Journal of Virology
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title Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_unstemmed Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_full Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_fullStr Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_full_unstemmed Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_short Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_sort comprehensive analysis of varicella-zoster virus proteins using a new monoclonal antibody collection
topic Virology
Insect Science
Immunology
Microbiology
url http://dx.doi.org/10.1128/jvi.00407-13
publishDate 2013
physical 6943-6954
description <jats:title>ABSTRACT</jats:title> <jats:p> Varicella-zoster virus (VZV) is the etiological agent of chickenpox and shingles. Due to the virus's restricted host and cell type tropism and the lack of tools for VZV proteomics, it is one of the least-characterized human herpesviruses. We generated 251 monoclonal antibodies (MAbs) against 59 of the 71 (83%) currently known unique VZV proteins to characterize VZV protein expression <jats:italic>in vitro</jats:italic> and <jats:italic>in situ</jats:italic> . Using this new set of MAbs, 44 viral proteins were detected by Western blotting (WB) and indirect immunofluorescence (IF); 13 were detected by WB only, and 2 were detected by IF only. A large proportion of viral proteins was analyzed for the first time in the context of virus infection. Our study revealed the subcellular localization of 46 proteins, 14 of which were analyzed in detail by confocal microscopy. Seven viral proteins were analyzed in time course experiments and showed a cascade-like temporal gene expression pattern similar to those of other herpesviruses. Furthermore, selected MAbs tested positive on human skin lesions by using immunohistochemistry, demonstrating the wide applicability of the MAb collection. Finally, a significant portion of the VZV-specific antibodies reacted with orthologs of simian varicella virus (SVV), thus enabling the systematic analysis of varicella in a nonhuman primate model system. In summary, this study provides insight into the potential function of numerous VZV proteins and novel tools to systematically study VZV and SVV pathogenesis. </jats:p>
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author Lenac Roviš, Tihana, Bailer, Susanne M., Pothineni, Venkata R., Ouwendijk, Werner J. D., Šimić, Hrvoje, Babić, Marina, Miklić, Karmela, Malić, Suzana, Verweij, Marieke C., Baiker, Armin, Gonzalez, Orland, von Brunn, Albrecht, Zimmer, Ralf, Früh, Klaus, Verjans, Georges M. G. M., Jonjić, Stipan, Haas, Jürgen
author_facet Lenac Roviš, Tihana, Bailer, Susanne M., Pothineni, Venkata R., Ouwendijk, Werner J. D., Šimić, Hrvoje, Babić, Marina, Miklić, Karmela, Malić, Suzana, Verweij, Marieke C., Baiker, Armin, Gonzalez, Orland, von Brunn, Albrecht, Zimmer, Ralf, Früh, Klaus, Verjans, Georges M. G. M., Jonjić, Stipan, Haas, Jürgen, Lenac Roviš, Tihana, Bailer, Susanne M., Pothineni, Venkata R., Ouwendijk, Werner J. D., Šimić, Hrvoje, Babić, Marina, Miklić, Karmela, Malić, Suzana, Verweij, Marieke C., Baiker, Armin, Gonzalez, Orland, von Brunn, Albrecht, Zimmer, Ralf, Früh, Klaus, Verjans, Georges M. G. M., Jonjić, Stipan, Haas, Jürgen
author_sort lenac roviš, tihana
container_issue 12
container_start_page 6943
container_title Journal of Virology
container_volume 87
description <jats:title>ABSTRACT</jats:title> <jats:p> Varicella-zoster virus (VZV) is the etiological agent of chickenpox and shingles. Due to the virus's restricted host and cell type tropism and the lack of tools for VZV proteomics, it is one of the least-characterized human herpesviruses. We generated 251 monoclonal antibodies (MAbs) against 59 of the 71 (83%) currently known unique VZV proteins to characterize VZV protein expression <jats:italic>in vitro</jats:italic> and <jats:italic>in situ</jats:italic> . Using this new set of MAbs, 44 viral proteins were detected by Western blotting (WB) and indirect immunofluorescence (IF); 13 were detected by WB only, and 2 were detected by IF only. A large proportion of viral proteins was analyzed for the first time in the context of virus infection. Our study revealed the subcellular localization of 46 proteins, 14 of which were analyzed in detail by confocal microscopy. Seven viral proteins were analyzed in time course experiments and showed a cascade-like temporal gene expression pattern similar to those of other herpesviruses. Furthermore, selected MAbs tested positive on human skin lesions by using immunohistochemistry, demonstrating the wide applicability of the MAb collection. Finally, a significant portion of the VZV-specific antibodies reacted with orthologs of simian varicella virus (SVV), thus enabling the systematic analysis of varicella in a nonhuman primate model system. In summary, this study provides insight into the potential function of numerous VZV proteins and novel tools to systematically study VZV and SVV pathogenesis. </jats:p>
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spelling Lenac Roviš, Tihana Bailer, Susanne M. Pothineni, Venkata R. Ouwendijk, Werner J. D. Šimić, Hrvoje Babić, Marina Miklić, Karmela Malić, Suzana Verweij, Marieke C. Baiker, Armin Gonzalez, Orland von Brunn, Albrecht Zimmer, Ralf Früh, Klaus Verjans, Georges M. G. M. Jonjić, Stipan Haas, Jürgen 0022-538X 1098-5514 American Society for Microbiology Virology Insect Science Immunology Microbiology http://dx.doi.org/10.1128/jvi.00407-13 <jats:title>ABSTRACT</jats:title> <jats:p> Varicella-zoster virus (VZV) is the etiological agent of chickenpox and shingles. Due to the virus's restricted host and cell type tropism and the lack of tools for VZV proteomics, it is one of the least-characterized human herpesviruses. We generated 251 monoclonal antibodies (MAbs) against 59 of the 71 (83%) currently known unique VZV proteins to characterize VZV protein expression <jats:italic>in vitro</jats:italic> and <jats:italic>in situ</jats:italic> . Using this new set of MAbs, 44 viral proteins were detected by Western blotting (WB) and indirect immunofluorescence (IF); 13 were detected by WB only, and 2 were detected by IF only. A large proportion of viral proteins was analyzed for the first time in the context of virus infection. Our study revealed the subcellular localization of 46 proteins, 14 of which were analyzed in detail by confocal microscopy. Seven viral proteins were analyzed in time course experiments and showed a cascade-like temporal gene expression pattern similar to those of other herpesviruses. Furthermore, selected MAbs tested positive on human skin lesions by using immunohistochemistry, demonstrating the wide applicability of the MAb collection. Finally, a significant portion of the VZV-specific antibodies reacted with orthologs of simian varicella virus (SVV), thus enabling the systematic analysis of varicella in a nonhuman primate model system. In summary, this study provides insight into the potential function of numerous VZV proteins and novel tools to systematically study VZV and SVV pathogenesis. </jats:p> Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection Journal of Virology
spellingShingle Lenac Roviš, Tihana, Bailer, Susanne M., Pothineni, Venkata R., Ouwendijk, Werner J. D., Šimić, Hrvoje, Babić, Marina, Miklić, Karmela, Malić, Suzana, Verweij, Marieke C., Baiker, Armin, Gonzalez, Orland, von Brunn, Albrecht, Zimmer, Ralf, Früh, Klaus, Verjans, Georges M. G. M., Jonjić, Stipan, Haas, Jürgen, Journal of Virology, Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection, Virology, Insect Science, Immunology, Microbiology
title Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_full Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_fullStr Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_full_unstemmed Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_short Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
title_sort comprehensive analysis of varicella-zoster virus proteins using a new monoclonal antibody collection
title_unstemmed Comprehensive Analysis of Varicella-Zoster Virus Proteins Using a New Monoclonal Antibody Collection
topic Virology, Insect Science, Immunology, Microbiology
url http://dx.doi.org/10.1128/jvi.00407-13