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Aerosol and nasal transmission of chronic wasting disease in cervidized mice

Little is known regarding the potential risk posed by aerosolized prions. Chronic wasting disease (CWD) is transmitted horizontally, almost surely by mucosal exposure, and CWD prions are present in saliva and urine of infected animals. However, whether CWD may be transmissible by the aerosol or nasa...

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Detalles Bibliográficos
Autores principales: Denkers, Nathaniel D., Seelig, Davis M., Telling, Glenn C., Hoover, Edward A.
Formato: Texto
Lenguaje:English
Publicado: Society for General Microbiology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888164/
https://www.ncbi.nlm.nih.gov/pubmed/20164261
http://dx.doi.org/10.1099/vir.0.017335-0
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author Denkers, Nathaniel D.
Seelig, Davis M.
Telling, Glenn C.
Hoover, Edward A.
author_facet Denkers, Nathaniel D.
Seelig, Davis M.
Telling, Glenn C.
Hoover, Edward A.
author_sort Denkers, Nathaniel D.
collection PubMed
description Little is known regarding the potential risk posed by aerosolized prions. Chronic wasting disease (CWD) is transmitted horizontally, almost surely by mucosal exposure, and CWD prions are present in saliva and urine of infected animals. However, whether CWD may be transmissible by the aerosol or nasal route is not known. To address this question, FVB mice transgenetically expressing the normal cervid PrP(C) protein [Tg(cerPrP) mice] were exposed to CWD prions by either nose-only aerosol exposure or by drop-wise instillation into the nostrils. Mice were monitored for signs of disease for up to 755 days post-inoculation (p.i.) and by examination of tissues for lesions and PrP(CWD) after necropsy. In particular, nasal mucosa, vomeronasal organ, lungs, lymphoid tissue and the brain were assessed for PrP(CWD) by Western blotting and immunohistochemistry. Six of seven aerosol-exposed Tg(cerPrP) mice developed clinical signs of neurological dysfunction mandating euthanasia between 411 and 749 days p.i. In all these mice, CWD infection was confirmed by detection of spongiform lesions and PrP(CWD) in the brain. Two of nine intranasally inoculated Tg(cerPrP) mice also developed transmissible spongiform encephalopathy associated with PrP(CWD) between 417 and 755 days p.i. No evidence of PrP(CWD) was detected in CWD-inoculated Tg(cerPrP) mice examined at pre-terminal time points. These results demonstrate that CWD can be transmitted by aerosol (as well as nasal) exposure and suggest that exposure via the respiratory system merits consideration for prion disease transmission and biosafety.
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spelling pubmed-28881642011-06-13 Aerosol and nasal transmission of chronic wasting disease in cervidized mice Denkers, Nathaniel D. Seelig, Davis M. Telling, Glenn C. Hoover, Edward A. J Gen Virol Other Agents Little is known regarding the potential risk posed by aerosolized prions. Chronic wasting disease (CWD) is transmitted horizontally, almost surely by mucosal exposure, and CWD prions are present in saliva and urine of infected animals. However, whether CWD may be transmissible by the aerosol or nasal route is not known. To address this question, FVB mice transgenetically expressing the normal cervid PrP(C) protein [Tg(cerPrP) mice] were exposed to CWD prions by either nose-only aerosol exposure or by drop-wise instillation into the nostrils. Mice were monitored for signs of disease for up to 755 days post-inoculation (p.i.) and by examination of tissues for lesions and PrP(CWD) after necropsy. In particular, nasal mucosa, vomeronasal organ, lungs, lymphoid tissue and the brain were assessed for PrP(CWD) by Western blotting and immunohistochemistry. Six of seven aerosol-exposed Tg(cerPrP) mice developed clinical signs of neurological dysfunction mandating euthanasia between 411 and 749 days p.i. In all these mice, CWD infection was confirmed by detection of spongiform lesions and PrP(CWD) in the brain. Two of nine intranasally inoculated Tg(cerPrP) mice also developed transmissible spongiform encephalopathy associated with PrP(CWD) between 417 and 755 days p.i. No evidence of PrP(CWD) was detected in CWD-inoculated Tg(cerPrP) mice examined at pre-terminal time points. These results demonstrate that CWD can be transmitted by aerosol (as well as nasal) exposure and suggest that exposure via the respiratory system merits consideration for prion disease transmission and biosafety. Society for General Microbiology 2010-06 /pmc/articles/PMC2888164/ /pubmed/20164261 http://dx.doi.org/10.1099/vir.0.017335-0 Text en Copyright © 2010, SGM
spellingShingle Other Agents
Denkers, Nathaniel D.
Seelig, Davis M.
Telling, Glenn C.
Hoover, Edward A.
Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title_full Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title_fullStr Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title_full_unstemmed Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title_short Aerosol and nasal transmission of chronic wasting disease in cervidized mice
title_sort aerosol and nasal transmission of chronic wasting disease in cervidized mice
topic Other Agents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888164/
https://www.ncbi.nlm.nih.gov/pubmed/20164261
http://dx.doi.org/10.1099/vir.0.017335-0
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