A novel murine model for evaluating bovine papillomavirus prophylactics/therapeutics for equine sarcoid-like tumours
Author(s) -
Lies Bogaert,
Andrew W. Woodham,
Diane M. Da Silva,
Ann Martens,
Evelyne Meyer,
W. Martin Kast
Publication year - 2015
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.000212
Subject(s) - bovine papillomavirus , virology , venezuelan equine encephalitis virus , biology , fibroblast , transfection , virus , cell culture , papillomaviridae , replicon , cancer research , cancer , cervical cancer , encephalitis , plasmid , gene , genome , biochemistry , genetics
Equine sarcoids are highly recurrent bovine papillomavirus (BPV)-induced fibroblastic neoplasms that are the most common skin tumours in horses. In order to facilitate the study of potential equine sarcoid prophylactics or therapeutics, which can be a slow and costly process in equines, a murine model for BPV-1 protein-expressing equine sarcoid-like tumours was developed in mice through stable transfection of BPV-1 E5 and E6 in a murine fibroblast tumour cell line (K-BALB). Like equine sarcoids, these murine tumour cells (BPV-KB) were of fibroblast origin, were tumorigenic and expressed BPV-1 proteins. As an initial investigation of the preclinical potential of this tumour model for equine sarcoids prophylactics, mice were immunized with BPV-1 E5E6 Venezuelan equine encephalitis virus replicon particles, prior to BPV-KB challenge, which resulted in an increased tumour-free period compared with controls, indicating that the BPV-KB murine model may be a valuable preclinical alternative to equine clinical trials.
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