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Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression

Analysis of the PRNP gene in cervids naturally infected with chronic wasting disease (CWD) suggested that PRNP polymorphisms affect the susceptibility of deer to infection. To test this effect, we orally inoculated 12 white-tailed deer with CWD agent. Three different PRNP alleles, wild-type (wt; glu...

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Autores principales: Johnson, Chad J., Herbst, Allen, Duque-Velasquez, Camilo, Vanderloo, Joshua P., Bochsler, Phil, Chappell, Rick, McKenzie, Debbie
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060816/
https://www.ncbi.nlm.nih.gov/pubmed/21445256
http://dx.doi.org/10.1371/journal.pone.0017450
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author Johnson, Chad J.
Herbst, Allen
Duque-Velasquez, Camilo
Vanderloo, Joshua P.
Bochsler, Phil
Chappell, Rick
McKenzie, Debbie
author_facet Johnson, Chad J.
Herbst, Allen
Duque-Velasquez, Camilo
Vanderloo, Joshua P.
Bochsler, Phil
Chappell, Rick
McKenzie, Debbie
author_sort Johnson, Chad J.
collection PubMed
description Analysis of the PRNP gene in cervids naturally infected with chronic wasting disease (CWD) suggested that PRNP polymorphisms affect the susceptibility of deer to infection. To test this effect, we orally inoculated 12 white-tailed deer with CWD agent. Three different PRNP alleles, wild-type (wt; glutamine at amino acid 95 and glycine at 96), Q95H (glutamine to histidine at amino acid position 95) and G96S (glycine to serine at position 96) were represented in the study cohort with 5 wt/wt, 3 wt/G96S, and 1 each wt/Q95H and Q95H/G96S. Two animals were lost to follow-up due to intercurrent disease. The inoculum was prepared from Wisconsin hunter-harvested homozygous wt/wt animals. All infected deer presented with clinical signs of CWD; the orally infected wt/wt had an average survival period of 693 days post inoculation (dpi) and G96S/wt deer had an average survival period of 956 dpi. The Q95H/wt and Q95H/G96S deer succumbed to CWD at 1,508 and 1,596 dpi respectively. These data show that polymorphisms in the PRNP gene affect CWD incubation period. Deer heterozygous for the PRNP alleles had extended incubation periods with the Q95H allele having the greatest effect.
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spelling pubmed-30608162011-03-28 Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression Johnson, Chad J. Herbst, Allen Duque-Velasquez, Camilo Vanderloo, Joshua P. Bochsler, Phil Chappell, Rick McKenzie, Debbie PLoS One Research Article Analysis of the PRNP gene in cervids naturally infected with chronic wasting disease (CWD) suggested that PRNP polymorphisms affect the susceptibility of deer to infection. To test this effect, we orally inoculated 12 white-tailed deer with CWD agent. Three different PRNP alleles, wild-type (wt; glutamine at amino acid 95 and glycine at 96), Q95H (glutamine to histidine at amino acid position 95) and G96S (glycine to serine at position 96) were represented in the study cohort with 5 wt/wt, 3 wt/G96S, and 1 each wt/Q95H and Q95H/G96S. Two animals were lost to follow-up due to intercurrent disease. The inoculum was prepared from Wisconsin hunter-harvested homozygous wt/wt animals. All infected deer presented with clinical signs of CWD; the orally infected wt/wt had an average survival period of 693 days post inoculation (dpi) and G96S/wt deer had an average survival period of 956 dpi. The Q95H/wt and Q95H/G96S deer succumbed to CWD at 1,508 and 1,596 dpi respectively. These data show that polymorphisms in the PRNP gene affect CWD incubation period. Deer heterozygous for the PRNP alleles had extended incubation periods with the Q95H allele having the greatest effect. Public Library of Science 2011-03-18 /pmc/articles/PMC3060816/ /pubmed/21445256 http://dx.doi.org/10.1371/journal.pone.0017450 Text en Johnson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Johnson, Chad J.
Herbst, Allen
Duque-Velasquez, Camilo
Vanderloo, Joshua P.
Bochsler, Phil
Chappell, Rick
McKenzie, Debbie
Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title_full Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title_fullStr Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title_full_unstemmed Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title_short Prion Protein Polymorphisms Affect Chronic Wasting Disease Progression
title_sort prion protein polymorphisms affect chronic wasting disease progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060816/
https://www.ncbi.nlm.nih.gov/pubmed/21445256
http://dx.doi.org/10.1371/journal.pone.0017450
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