scholarly journals Tissue-Specific Biochemical Differences Between Chronic Wasting Disease Prions Isolated From Free Ranging, White-Tailed Deer (Odocoileus virginianus)

2021 ◽  
Author(s):  
Kaitlyn Wagner ◽  
Robyn Pierce ◽  
Elizabeth Gordon ◽  
Jennifer R Ballard ◽  
Julie A Moreno ◽  
...  
Keyword(s):  
Lymph Node ◽  
Neurodegenerative Disease ◽  
World Wide ◽  
Chronic Wasting Disease ◽  
Strain Differences ◽  
Wasting Disease ◽  
Prion Strains ◽  
Future Work ◽  
Free Ranging ◽  
The Brain

Chronic wasting disease is an invariably fatal prion disease affecting cervid species world-wide. Prions can manifest as distinct strains that can influence disease pathology and transmission. CWD is profoundly lymphotropic and most infected cervids likely shed peripheral prions replicated in lymphoid organs. However, CWD is a neurodegenerative disease and most research on prion strains has focused on neurogenic prions. Thus, a knowledge gap exists comparing prions in the brain to prions in the lymph node. In this study we compared prions from the obex and lymph node of naturally exposed white-tailed deer to identify potential biochemical strain differences. Here, we report biochemical evidence of strain differences between the brain and lymph node from these animals. Future work should examine the biological and zoonotic impact of these biochemical differences and examine more cervids from multiple locations to see if these differences are conserved across species and locations.

scholarly journals Cervid Prion Protein Polymorphisms: Role in Chronic Wasting Disease Pathogenesis

2021 ◽  
Vol 22 (5) ◽  
pp. 2271
Author(s):  
Maria Immaculata Arifin ◽  
Samia Hannaoui ◽  
Sheng Chun Chang ◽  
Simrika Thapa ◽  
Hermann M. Schatzl ◽  
...  
Keyword(s):  
Prion Protein ◽  
Chronic Wasting Disease ◽  
In Vivo Studies ◽  
Wasting Disease ◽  
Endogenous Factors ◽  
Prion Strains ◽  
Free Ranging

Chronic wasting disease (CWD) is a prion disease found in both free-ranging and farmed cervids. Susceptibility of these animals to CWD is governed by various exogenous and endogenous factors. Past studies have demonstrated that polymorphisms within the prion protein (PrP) sequence itself affect an animal’s susceptibility to CWD. PrP polymorphisms can modulate CWD pathogenesis in two ways: the ability of the endogenous prion protein (PrPC) to convert into infectious prions (PrPSc) or it can give rise to novel prion strains. In vivo studies in susceptible cervids, complemented by studies in transgenic mice expressing the corresponding cervid PrP sequence, show that each polymorphism has distinct effects on both PrPC and PrPSc. It is not entirely clear how these polymorphisms are responsible for these effects, but in vitro studies suggest they play a role in modifying PrP epitopes crucial for PrPC to PrPSc conversion and determining PrPC stability. PrP polymorphisms are unique to one or two cervid species and most confer a certain degree of reduced susceptibility to CWD. However, to date, there are no reports of polymorphic cervid PrP alleles providing absolute resistance to CWD. Studies on polymorphisms have focused on those found in CWD-endemic areas, with the hope that understanding the role of an animal’s genetics in CWD can help to predict, contain, or prevent transmission of CWD.

scholarly journals Comparison of Chronic Wasting Disease Detection Methods and Procedures: implications for free-ranging white-tailed deer (Odocoileus virginianus) surveillance and management

2021 ◽  
Author(s):  
Marc D Schwabenlander ◽  
Gage R Rowden ◽  
Manci Li ◽  
Kelsie LaSharr ◽  
Erik C Hildebrand ◽  
...  
Keyword(s):  
Lymph Node ◽  
North America ◽  
Lymph Nodes ◽  
Odocoileus Virginianus ◽  
Chronic Wasting Disease ◽  
Enzyme Linked Immunosorbent Assay ◽  
Lymphoid Tissues ◽  
Sample Type ◽  
Wasting Disease ◽  
Free Ranging

Throughout North America, chronic wasting disease (CWD) has emerged as perhaps the greatest threat to wild cervid populations, including white-tailed deer (Odocoileus virginianus). White-tailed deer are the most sought after big game species across North America with populations of various subspecies in nearly all Canadian provinces, the contiguous USA, and Mexico. Documented CWD cases have dramatically increased across the white-tailed deer range since the mid-1990s, including in Minnesota. CWD surveillance in free-ranging white-tailed deer and other cervid populations mainly depends upon immunodetection methods (e.g., immunohistochemistry [IHC] and enzyme-linked immunosorbent assay [ELISA]) on medial retropharyngeal lymph nodes and obex. More recent technologies centered on prion protein amplification methods of detection have shown promise as more sensitive and rapid CWD diagnostic tools. Here, we used blinded samples to test the efficacy of real time quaking-induced conversion (RT-QuIC) in comparison to ELISA and IHC for screening tissues, blood, and feces collected in 2019 from white-tailed deer in southeastern Minnesota, where CWD has been routinely detected since 2016. Our results support previous findings that RT-QuIC is a more sensitive tool for CWD detection than current antibody-based methods. Additionally, a CWD testing protocol that includes multiple lymphoid tissues (medial retropharyngeal lymph node, parotid lymph node, and palatine tonsil) per animal may effectively identify a greater number of CWD detections in a white-tailed deer population than a single sample type (i.e., medial retropharyngeal lymph nodes). These results reveal that the variability of CWD pathogenesis, sampling protocol, and testing platform must be considered for the effective detection and management of CWD throughout North America.

scholarly journals Studies in bank voles reveal strain differences between chronic wasting disease prions from Norway and North America

2020 ◽  
Vol 117 (49) ◽  
pp. 31417-31426 ◽  
Author(s):  
Romolo Nonno ◽  
Michele A. Di Bari ◽  
Laura Pirisinu ◽  
Claudia D’Agostino ◽  
Ilaria Vanni ◽  
...  
Keyword(s):  
North America ◽  
North American ◽  
Rangifer Tarandus ◽  
Chronic Wasting Disease ◽  
Strain Differences ◽  
Myodes Glareolus ◽  
Wasting Disease ◽  
Proximate Cause ◽  
Bank Voles ◽  
Regional Deposition

Chronic wasting disease (CWD) is a relentless epidemic disorder caused by infectious prions that threatens the survival of cervid populations and raises increasing public health concerns in North America. In Europe, CWD was detected for the first time in wild Norwegian reindeer (Rangifer tarandus) and moose (Alces alces) in 2016. In this study, we aimed at comparing the strain properties of CWD prions derived from different cervid species in Norway and North America. Using a classical strain typing approach involving transmission and adaptation to bank voles (Myodes glareolus), we found that prions causing CWD in Norway induced incubation times, neuropathology, regional deposition of misfolded prion protein aggregates in the brain, and size of their protease-resistant core, different from those that characterize North American CWD. These findings show that CWD prion strains affecting Norwegian cervids are distinct from those found in North America, implying that the highly contagious North American CWD prions are not the proximate cause of the newly discovered Norwegian CWD cases. In addition, Norwegian CWD isolates showed an unexpected strain variability, with reindeer and moose being caused by different CWD strains. Our findings shed light on the origin of emergent European CWD, have significant implications for understanding the nature and the ecology of CWD in Europe, and highlight the need to assess the zoonotic potential of the new CWD strains detected in Europe.

Differentially expressed genes in the brain of TgElk mice with chronic wasting disease

2016 ◽  
Vol 40 (4) ◽  
pp. 120-126
Author(s):  
Hyo-Jin Kim ◽  
◽  
In Soon Roh ◽  
Min-Jeong Kim ◽  
Dong-Seob Tark ◽  
...  
Keyword(s):  
Differentially Expressed Genes ◽  
Chronic Wasting Disease ◽  
Differentially Expressed ◽  
Wasting Disease ◽  
The Brain

scholarly journals EPIZOOTIOLOGY OF CHRONIC WASTING DISEASE IN FREE-RANGING CERVIDS IN COLORADO AND WYOMING

2000 ◽  
Vol 36 (4) ◽  
pp. 676-690 ◽  
Author(s):  
Michael W. Miller ◽  
Elizabeth S. Williams ◽  
Craig W. McCarty ◽  
Terry R. Spraker ◽  
Terry J. Kreeger ◽  
...  
Keyword(s):  
Chronic Wasting Disease ◽  
Wasting Disease ◽  
Free Ranging

EFFICACY OF ANTEMORTEM RECTAL BIOPSIES TO DIAGNOSE AND ESTIMATE PREVALENCE OF CHRONIC WASTING DISEASE IN FREE-RANGING COW ELK (CERVUS ELAPHUS NELSONI)

2013 ◽  
Vol 49 (2) ◽  
pp. 270-278 ◽  
Author(s):  
Ryan J. Monello ◽  
Jenny G. Powers ◽  
N. Thompson Hobbs ◽  
Terry R. Spraker ◽  
Katherine I. O’Rourke ◽  
...  
Keyword(s):  
Cervus Elaphus ◽  
Chronic Wasting Disease ◽  
Wasting Disease ◽  
Cervus Elaphus Nelsoni ◽  
Rectal Biopsies ◽  
Estimate Prevalence ◽  
Free Ranging

scholarly journals PrP genotypes of free-ranging wapiti (Cervus elaphus nelsoni) with chronic wasting disease

2008 ◽  
Vol 89 (5) ◽  
pp. 1324-1328 ◽  
Author(s):  
Matteo Perucchini ◽  
Karen Griffin ◽  
Michael W. Miller ◽  
Wilfred Goldmann
Keyword(s):  
Cervus Elaphus ◽  
Gene Sequence ◽  
Chronic Wasting Disease ◽  
Wasting Disease ◽  
Susceptibility To Infection ◽  
Cervus Elaphus Nelsoni ◽  
Naturally Occurring ◽  
Genotype Frequencies ◽  
The Family ◽  
Free Ranging

Variation in PrP prion gene sequence appears to modulate susceptibility to chronic wasting disease (CWD), a naturally occurring prion disease affecting four North American species of the family Cervidae. Wapiti (Cervus elaphus nelsoni) PrP is polymorphic at codon 132 [methionine (M) or leucine (L)]. We genotyped 171 samples, collected between 2002 and 2005 from CWD-infected and uninfected wapiti from three free-ranging populations in Colorado, USA, to study influences of PrP polymorphisms on CWD susceptibility further. Overall genotype frequencies for 124 apparently uninfected animals were 65.3 % MM132, 32.3 % ML132 and 2.4 % LL132; for 47 CWD-infected animals, these frequencies were 70.2 % MM132, 27.7 % ML132 and 2.1 % LL132. Surprisingly, our data revealed that, among recent (approx. 2002–2005) CWD cases detected in free-ranging Colorado wapiti, the three PrP codon 132 genotypes were represented in proportion to their abundance in sampled populations (P≥0.24) and all three genotypes showed equivalent susceptibility to infection.

scholarly journals PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease

1999 ◽  
Vol 80 (10) ◽  
pp. 2765-2679 ◽  
Author(s):  
K. I. O’Rourke ◽  
T. E. Besser ◽  
M. W. Miller ◽  
T. F. Cline ◽  
T. R. Spraker ◽  
...  
Keyword(s):  
Cervus Elaphus ◽  
Chronic Wasting Disease ◽  
Rocky Mountain ◽  
Transmissible Spongiform Encephalopathies ◽  
Spongiform Encephalopathy ◽  
Wasting Disease ◽  
Jakob Disease ◽  
Rocky Mountain Elk ◽  
Free Ranging ◽  
Prp Gene

The PrP gene encodes the putative causative agent of the transmissible spongiform encephalopathies (TSEs), a heterogeneous group of fatal, neurodegenerative disorders including human Creutzfeldt–Jakob disease, bovine spongiform encephalopathy, ovine scrapie and chronic wasting disease (CWD) of North American deer and elk. Polymorphisms in the PrP gene are associated with variations in relative susceptibility, pathological lesion patterns, incubation times and clinical course of TSEs of humans, mice and sheep. Sequence analysis of the PrP gene from Rocky Mountain elk showed only one amino acid change (Met to Leu at cervid codon 132). Homozygosity for Met at the corresponding polymorphic site (Met to Val) in humans (human codon 129) predisposes exposed individuals to some forms of Creutzfeldt–Jakob disease. In this study, Rocky Mountain elk homozygous for PrP codon 132 Met were over-represented in both free- ranging and farm-raised CWD-affected elk when compared to unaffected control groups.

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