Inga Dry
Alcelaphine herpesvirus 1 glycoprotein B: recombinant expression and antibody recognition
Dry, Inga; Todd, Helen; Deane, David; Percival, Ann; Mclean, Kevin; Inglis, Neil F.; Manson, Erin D. T.; Haig, David M.; Nayuni, Shilpa; Hutt-Fletcher, Lindsey M.; Grant, Dawn M.; Bartley, Kathryn; Stewart, James P.; Russell, George C.
Authors
Helen Todd
David Deane
Ann Percival
Kevin Mclean
Neil F. Inglis
Erin D. T. Manson
David M. Haig
Shilpa Nayuni
Lindsey M. Hutt-Fletcher
Dawn M. Grant
Kathryn Bartley
James P. Stewart
George C. Russell
Contributors
I Dry
Researcher
H Todd
Researcher
D Deane
Researcher
A Percival
Researcher
K Mclean
Researcher
NF Inglis
Researcher
ED Manson
Researcher
DM Haig
Researcher
S Nayuni
Researcher
LM Hutt-Fletcher
Researcher
DM Grant
Researcher
K Bartley
Researcher
JP Stewart
Researcher
GC. Russell
Researcher
Abstract
The gammaherpesvirus alcelaphine herpesvirus 1 (AlHV-1) causes fatal malignant catarrhal fever (MCF) in susceptible species including cattle, but infects its reservoir host, wildebeest, without causing disease. Pathology in cattle may be influenced by virus-host cell interactions mediated by the virus glycoproteins. Cloning and expression of a haemagglutinin-tagged version of the AlHV-1 glycoprotein B (gB) was used to demonstrate that the AlHV-1-specific monoclonal antibody 12B5 recognised gB and that gB was the main component of the gp115 complex of AlHV-1, a glycoprotein complex of five components identified on the surface of AlHV-1 by immunoprecipitation and radiolabelling. Analysis of AlHV-1 virus particles showed that the native form of gB was detected by mAb 12B5 as a band of about 70 kDa, whilst recombinant gB expressed by transfected HEK293T cells appeared to be subject to additional cleavage and incomplete post-translational processing. Antibody 12B5 recognised an epitope on the N-terminal furin-cleaved fragment of gB on AlHV-1 virus particles. It could be used to detect recombinant and virus-expressed gB on western blots and on the surface of infected cells by flow cytometry, whilst recombinant gB was detected on the surface of transfected cells by immunofluorescence. Recombinant gB has potential as an antigen for ELISA detection of MCF virus infection and as a candidate vaccine antigen.
Citation
Dry, I., Todd, H., Deane, D., Percival, A., Mclean, K., Inglis, N. F., …Russell, G. C. (2016). Alcelaphine herpesvirus 1 glycoprotein B: recombinant expression and antibody recognition. Archives of Virology, 161(3), 613-619. https://doi.org/10.1007/s00705-015-2701-y
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 22, 2015 |
Online Publication Date | Dec 9, 2015 |
Publication Date | 2016-03 |
Deposit Date | Dec 4, 2018 |
Journal | Archives of Virology |
Print ISSN | 0304-8608 |
Electronic ISSN | 1432-8798 |
Publisher | Springer Verlag |
Peer Reviewed | Peer Reviewed |
Volume | 161 |
Issue | 3 |
Pages | 613-619 |
DOI | https://doi.org/10.1007/s00705-015-2701-y |
Keywords | HEK293T Cell Malignant Catarrhal Fever Transfected HEK293T Cell Furin Cleavage Monoclonal Antibody 12B5 |
Public URL | https://nottingham-repository.worktribe.com/output/1362380 |
Publisher URL | https://link.springer.com/article/10.1007%2Fs00705-015-2701-y |
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