Detailed Information on Publication Record
2021
A broadly cross-reactive monoclonal antibody against hepatitis E virus capsid antigen
KUBÍČKOVÁ, Barbara, Joerg A. SCHENK, Franziska RAMM, Kornelija MARKUSKIENE, Jochen REETZ et. al.Basic information
Original name
A broadly cross-reactive monoclonal antibody against hepatitis E virus capsid antigen
Authors
KUBÍČKOVÁ, Barbara (276 Germany, guarantor, belonging to the institution), Joerg A. SCHENK (276 Germany), Franziska RAMM (276 Germany), Kornelija MARKUSKIENE (276 Germany), Jochen REETZ (276 Germany), Paul DREMSEK (276 Germany), Paulius Lukas TAMOSIUNAS (440 Lithuania), Laima CEPULYTE (440 Lithuania), Hoai Anh TRINH (276 Germany), Johannes SCHOLZ (276 Germany), Henry MEMCZAK (276 Germany), Marc HOVESTAEDT (276 Germany), Rene RYLL (276 Germany), Rasa PETRAITYTE-BURNEIKIENE (440 Lithuania), Victor M. CORMAN (276 Germany), Anika ANDERSSON (276 Germany), Dietmar BECHER (276 Germany), Martin H. GROSCHUP (276 Germany), Stefan KUBICK (276 Germany), Frank SELLRIE (276 Germany), Reimar JOHNE (276 Germany) and Rainer G. ULRICH (276 Germany)
Edition
Applied Microbiology and Biotechnology, NEW YORK, SPRINGER, 2021, 0175-7598
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30405 Medical biotechnology related ethics
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.560
RIV identification code
RIV/00216224:14310/21:00122250
Organization unit
Faculty of Science
UT WoS
000661794700001
Keywords in English
Hepatitis E virus; HEV-1; HEV-2; HEV-3; HEV-4; HEV-7; ratHEV; batHEV; cvHEV; Monoclonal antibody; Cross-reactivity; Cell-free synthesis
Tags
Tags
International impact, Reviewed
Změněno: 4/9/2021 21:09, Mgr. Michaela Hylsová, Ph.D.
Abstract
V originále
To generate a hepatitis E virus (HEV) genotype 3 (HEV-3)-specific monoclonal antibody (mAb), the Escherichia coli-expressed carboxy-terminal part of its capsid protein was used to immunise BALB/c mice. The immunisation resulted in the induction of HEV-specific antibodies of high titre. The mAb G117-AA4 of IgG1 isotype was obtained showing a strong reactivity with the homologous E. coli, but also yeast-expressed capsid protein of HEV-3. The mAb strongly cross-reacted with ratHEV capsid protein derivatives produced in both expression systems and weaker with an E. coli-expressed batHEV capsid protein fragment. In addition, the mAb reacted with capsid protein derivatives of genotypes HEV-2 and HEV-4 and common vole hepatitis E virus (cvHEV), produced by the cell-free synthesis in Chinese hamster ovary (CHO) and Spodoptera frugiperda (Sf21) cell lysates. Western blot and line blot reactivity of the mAb with capsid protein derivatives of HEV-1 to HEV-4, cvHEV, ratHEV and batHEV suggested a linear epitope. Use of truncated derivatives of ratHEV capsid protein in ELISA, Western blot, and a Pepscan analysis allowed to map the epitope within a partially surface-exposed region with the amino acid sequence LYTSV. The mAb was also shown to bind to human patient-derived HEV-3 from infected cell culture and to hare HEV-3 and camel HEV-7 capsid proteins from transfected cells by immunofluorescence assay. The novel mAb may serve as a useful tool for further investigations on the pathogenesis of HEV infections and might be used for diagnostic purposes.