TY - JOUR
T1 - Comparison of protection levels against pseudorabies virus infection of transgenic mice expressing a soluble form of porcine nectin-1/HveC and vaccinated mice
AU - Ono, Etsuro
AU - Tomioka, Yukiko
AU - Taharaguchi, Satoshi
AU - Cherel, Pierre
N1 - Funding Information:
This work was supported by Grants-in-Aid for Scientific Research (B)(2) and (C)(2) from The Ministry of Education, Culture, Sports, Science and Technology, Japan.
PY - 2006/5/31
Y1 - 2006/5/31
N2 - We recently generated transgenic mice expressing a soluble form of porcine nectin-1 (PHveCIg) showing remarkable resistance to pseudorabies virus (PRV) infection. Nectin-1, also known as herpesvirus entry mediator C (HveC), is an alphaherpesvirus receptor that binds to virion glycoprotein D (gD). In order to evaluate the level of resistance to PRV infection induced by the expression of PHveCIg in the transgenic mice, the protective effects of vaccinated and transgenic mice were directly compared. Mice were immunized with a live vaccine, through intraperitoneal injection of PRV strain Begonia (an attenuated vaccine strain deleted for gE and thymidine kinase genes) at 4 weeks before challenge. The vaccinated and transgenic mice were challenged with 10LD50, 20LD50 or 50LD50 of PRV strainYS-81 via intranasal route. In the vaccinated mice, no protection was observed in the challenges with 20LD50 and 50LD50. Only two out of six vaccinated mice survived in the challenge with 10LD50. In contrast, four transgenic mouse lines showed significant resistance to PRV infection, although the survival rates varied in the challenge with each viral dose. These results demonstrate clearly the high potential of transgenic strategy in control of pseudorabies.
AB - We recently generated transgenic mice expressing a soluble form of porcine nectin-1 (PHveCIg) showing remarkable resistance to pseudorabies virus (PRV) infection. Nectin-1, also known as herpesvirus entry mediator C (HveC), is an alphaherpesvirus receptor that binds to virion glycoprotein D (gD). In order to evaluate the level of resistance to PRV infection induced by the expression of PHveCIg in the transgenic mice, the protective effects of vaccinated and transgenic mice were directly compared. Mice were immunized with a live vaccine, through intraperitoneal injection of PRV strain Begonia (an attenuated vaccine strain deleted for gE and thymidine kinase genes) at 4 weeks before challenge. The vaccinated and transgenic mice were challenged with 10LD50, 20LD50 or 50LD50 of PRV strainYS-81 via intranasal route. In the vaccinated mice, no protection was observed in the challenges with 20LD50 and 50LD50. Only two out of six vaccinated mice survived in the challenge with 10LD50. In contrast, four transgenic mouse lines showed significant resistance to PRV infection, although the survival rates varied in the challenge with each viral dose. These results demonstrate clearly the high potential of transgenic strategy in control of pseudorabies.
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U2 - 10.1016/j.vetmic.2005.12.011
DO - 10.1016/j.vetmic.2005.12.011
M3 - Article
C2 - 16427216
AN - SCOPUS:33646469711
SN - 0378-1135
VL - 114
SP - 327
EP - 330
JO - Veterinary Microbiology
JF - Veterinary Microbiology
IS - 3-4
ER -