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Characterization of monoclonal antibodies against hantavirus nucleocapsid protein and their use for immunohistochemistry on rodent and human samples

Authors :
Kestutis Sasnauskas
Paula Padula
Rafael A. Medina
Rasa Petraityte-Burneikiene
Alma Gedvilaite
Rainer G. Ulrich
Indre Kucinskaite-Kodze
Marc Mertens
Ausra Razanskiene
Aurelija Zvirbliene
Jonas Schmidt-Chanasit
Brian Hjelle
Source :
Arch Virol, Archives of Virology, 2011, 156(3), 443-456., Sistema de Gestión del Conocimiento ANLIS MALBRÁN, Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán", instacron:ANLIS
Publication Year :
2010
Publisher :
Springer Science and Business Media LLC, 2010.

Abstract

Monoclonal antibodies are important tools for various applications in hantavirus diagnostics. Recently, we generated Puumala virus (PUUV)-reactive monoclonal antibodies (mAbs) by immunisation of mice with chimeric polyomavirus-derived virus-like particles (VLPs) harbouring the 120-amino-acid-long amino-terminal region of the PUUV nucleocapsid (N) protein. Here, we describe the generation of two mAbs by co-immunisation of mice with hexahistidine-tagged full-length N proteins of Sin Nombre virus (SNV) and Andes virus (ANDV), their characterization by different immunoassays and comparison with the previously generated mAbs raised against a segment of PUUV N protein inserted into VLPs. All of the mAbs reacted strongly in ELISA and western blot tests with the antigens used for immunization and cross-reacted to varying extents with N proteins of other hantaviruses. All mAbs raised against a segment of the PUUV N protein presented on chimeric VLPs and both mAbs raised against the full-length AND/SNV N protein reacted with Vero cells infected with different hantaviruses. The reactivity of mAbs with native viral nucleocapsids was also confirmed by their reactivity in immunohistochemistry assays with kidney tissue specimens from experimentally SNV-infected rodents and human heart tissue specimens from hantavirus cardiopulmonary syndrome patients. Therefore, the described mAbs represent useful tools for the immunodetection of hantavirus infection. Fil: Kucinskaite-Kodze, Indre. Vilnius University. Institute of Biotechnology; Lituania. Fil: Petraityte-Burneikiene, Rasa. Vilnius University. Institute of Biotechnology; Lituania. Fil: Zvirbliene, Aurelija. Vilnius University. Institute of Biotechnology; Lituania. Fil: Hjelle, Brian. University of New Mexico School of Medicine. Department of Pathology; Estados Unidos. Fil: Medina, Rafael A. University of New Mexico School of Medicine. Department of Pathology; Estados Unidos. Fil: Gedvilaite, Alma. Vilnius University. Institute of Biotechnology; Lituania. Fil: Razanskiene, Ausra. Vilnius University. Institute of Biotechnology; Lituania. Fil: Schmidt-Chanasit, Jonas. Federal Research Institute for Animal Health. Institute of Epidemiology; Alemania. Fil: Mertens, Marc. Federal Research Institute for Animal Health. Institute of Epidemiology; Alemania. Fil: Padula, Paula. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Virología; Argentina. Fil: Sasnauskas, Kestutis. Vilnius University. Institute of Biotechnology; Lituania. Fil: Ulrich, Rainer G. Federal Research Institute for Animal Health. Institute of Epidemiology; Alemania.

Details

ISSN :
14328798 and 03048608
Volume :
156
Database :
OpenAIRE
Journal :
Archives of Virology
Accession number :
edsair.doi.dedup.....a85ca8d84769b1ad30c9a1897487013b
Full Text :
https://doi.org/10.1007/s00705-010-0879-6