TY - JOUR
T1 - Wounding prior to challenge substantially improves infectivity of cottontail rabbit papillomavirus and allows for standardization of infection
AU - Cladel, Nancy M.
AU - Hu, Jiafen
AU - Balogh, Karla
AU - Mejia, Andres
AU - Christensen, Neil D.
N1 - Funding Information:
This work was supported by NCI grant CA47622 and NIAID grant AI15435 (Utah State University; subcontract to Penn State University, College of Medicine), and the Jake Gittlen Memorial Golf Tournament.
PY - 2008/3
Y1 - 2008/3
N2 - The cottontail rabbit papillomavirus (CRPV)/rabbit model has proved useful for the investigation of prophylactic and therapeutic vaccines and for the study of the pathogenesis of papillomavirus infection. It is currently the only animal model in which the entire viral program can be recapitulated, including progression to cancer. CRPV DNA is infectious in domestic rabbits and therefore mutants can be studied without the need to generate corresponding viruses. Although the CRPV animal model is used widely in various laboratories, no optimized or standardized method is used for creating CRPV viral and especially DNA infections. These different methods have made it difficult for investigators to compare results from laboratory to laboratory. A simple and highly efficient method is reported here; it has been refined based on previous methodology for the production of CRPV infections from both virus and plasmid DNA. This method can be adapted easily by other investigators in the field. The resulting standardization will aid in the evaluation of data from different laboratories.
AB - The cottontail rabbit papillomavirus (CRPV)/rabbit model has proved useful for the investigation of prophylactic and therapeutic vaccines and for the study of the pathogenesis of papillomavirus infection. It is currently the only animal model in which the entire viral program can be recapitulated, including progression to cancer. CRPV DNA is infectious in domestic rabbits and therefore mutants can be studied without the need to generate corresponding viruses. Although the CRPV animal model is used widely in various laboratories, no optimized or standardized method is used for creating CRPV viral and especially DNA infections. These different methods have made it difficult for investigators to compare results from laboratory to laboratory. A simple and highly efficient method is reported here; it has been refined based on previous methodology for the production of CRPV infections from both virus and plasmid DNA. This method can be adapted easily by other investigators in the field. The resulting standardization will aid in the evaluation of data from different laboratories.
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U2 - 10.1016/j.jviromet.2007.10.005
DO - 10.1016/j.jviromet.2007.10.005
M3 - Article
C2 - 18061687
AN - SCOPUS:39049149358
SN - 0166-0934
VL - 148
SP - 34
EP - 39
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 1-2
ER -