TY - JOUR
T1 - Mucosal immunization with an attenuated Salmonella vaccine partially protects white-tailed deer from chronic wasting disease
AU - Goñi, Fernando
AU - Mathiason, Candace K.
AU - Yim, Lucia
AU - Wong, Kinlung
AU - Hayes-Klug, Jeanette
AU - Nalls, Amy
AU - Peyser, Daniel
AU - Estevez, Veronica
AU - Denkers, Nathaniel
AU - Xu, Jinfeng
AU - Osborn, David A.
AU - Miller, Karl V.
AU - Warren, Robert J.
AU - Brown, David R.
AU - Chabalgoity, Jose A.
AU - Hoover, Edward A.
AU - Wisniewski, Thomas
PY - 2015/1
Y1 - 2015/1
N2 - Prion disease is a unique category of illness, affecting both animals and humans, in which the underlying pathogenesis is related to a conformational change of a normal, self-protein called PrPC (C for cellular) to a pathological and infectious conformer known as PrPSc (Sc for scrapie). Bovine spongiform encephalopathy (BSE), a prion disease believed to have arisen from feeding cattle with prion contaminated meat and bone meal products, crossed the species barrier to infect humans. Chronic wasting disease (CWD) infects large numbers of deer and elk, with the potential to infect humans. Currently no prionosis has an effective treatment. Previously, we have demonstrated we could prevent transmission of prions in a proportion of susceptible mice with a mucosal vaccine. In the current study, white-tailed deer were orally inoculated with attenuated Salmonella expressing PrP, while control deer were orally inoculated with vehicle attenuated Salmonella. Once a mucosal response was established, the vaccinated animals were boosted orally and locally by application of polymerized recombinant PrP onto the tonsils and rectal mucosa. The vaccinated and control animals were then challenged orally with CWD-infected brain homogenate. Three years post CWD oral challenge all control deer developed clinical CWD (median survival 602 days), while among the vaccinated there was a significant prolongation of the incubation period (median survival 909 days; p=0.012 by Weibull regression analysis) and one deer has remained CWD free both clinically and by RAMALT and tonsil biopsies. This negative vaccinate has the highest titers of IgA in saliva and systemic IgG against PrP. Western blots showed that immunoglobulins from this vaccinate react to PrPCWD. We document the first partially successful vaccination for a prion disease in a species naturally at risk.
AB - Prion disease is a unique category of illness, affecting both animals and humans, in which the underlying pathogenesis is related to a conformational change of a normal, self-protein called PrPC (C for cellular) to a pathological and infectious conformer known as PrPSc (Sc for scrapie). Bovine spongiform encephalopathy (BSE), a prion disease believed to have arisen from feeding cattle with prion contaminated meat and bone meal products, crossed the species barrier to infect humans. Chronic wasting disease (CWD) infects large numbers of deer and elk, with the potential to infect humans. Currently no prionosis has an effective treatment. Previously, we have demonstrated we could prevent transmission of prions in a proportion of susceptible mice with a mucosal vaccine. In the current study, white-tailed deer were orally inoculated with attenuated Salmonella expressing PrP, while control deer were orally inoculated with vehicle attenuated Salmonella. Once a mucosal response was established, the vaccinated animals were boosted orally and locally by application of polymerized recombinant PrP onto the tonsils and rectal mucosa. The vaccinated and control animals were then challenged orally with CWD-infected brain homogenate. Three years post CWD oral challenge all control deer developed clinical CWD (median survival 602 days), while among the vaccinated there was a significant prolongation of the incubation period (median survival 909 days; p=0.012 by Weibull regression analysis) and one deer has remained CWD free both clinically and by RAMALT and tonsil biopsies. This negative vaccinate has the highest titers of IgA in saliva and systemic IgG against PrP. Western blots showed that immunoglobulins from this vaccinate react to PrPCWD. We document the first partially successful vaccination for a prion disease in a species naturally at risk.
KW - Bovine spongiform encephalopathy
KW - Chronic wasting disease
KW - Immunization
KW - Mucosal vaccination
KW - Prion protein
KW - Salmonella vaccine strain
KW - White-tailed deer
UR - http://www.scopus.com/inward/record.url?scp=84921318133&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1016/j.vaccine.2014.11.035
U2 - 10.1016/j.vaccine.2014.11.035
DO - 10.1016/j.vaccine.2014.11.035
M3 - Article
AN - SCOPUS:84921318133
SN - 0264-410X
VL - 33
SP - 726
EP - 733
JO - Vaccine
JF - Vaccine
IS - 5
ER -