Evidence map›Paper›PMID 21777560›Full record

ArticleThe American journal of pathology2011

Chronic wasting disease prion trafficking via the autonomic nervous system.

Davis M Seelig, Gary L Mason, Glenn C Telling, Edward A Hoover

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. The ecology of chronic wasting disease in wildlife.Biological reviews of the Cambridge Philosophical Society · 2020
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Emerging roles for enteric glia in gastrointestinal disorders.The Journal of clinical investigation · 2015
    Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Davis M SeeligDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA.
Gary L Mason
Glenn C Telling
Edward A Hoover
Colorado State University · US

Funding

BIOMEDICAL RESEARCH TRAINING FOR VETERINARIANST32RR007072 · NCRR · COLORADO STATE UNIVERSITY-FORT COLLINS · PI HOOVER, EDWARD ARTHUR · 2002 to 2011
$2.6M
U.S. BASED COLLABORATION IN EMERGING VIRAL AND PRION DISEASES-N01AI025491 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · 2003 to 2003
–
NCRR NIH HHS T32 RR007072NCRR NIH HHS T32-RR07072NIAID NIH HHS N01 AI025491
6 · The paper itself

Abstract

Chronic wasting disease (CWD) is a fatal spongiform encephalopathy that is efficiently transmitted among members of the mammalian family Cervidae, including deer, elk, and moose. Typical of prion diseases, CWD is characterized by the conversion of the native protease-sensitive protein PrP(C) to a protease-resistant isoform, denoted PrP(RES). In native species, spread of the disease likely results from the ingestion of prion-containing excreta, including urine, saliva, or feces. Although cervid prion protein-expressing transgenic [Tg(CerPrP)] mice have been shown to be effective surrogates of natural CWD, uncertainties remain regarding the mechanisms by which CWD prions traffic in vivo, including the manner by which CWD prions traffic from the gastrointestinal tract to the central nervous system. We used elk prion protein-expressing transgenic [Tg(CerPrP-E)] mice, infected by three different routes of inoculation, and tissue-based IHC to elucidate that centripetal and centrifugal CWD prion transit pathways involve cells and fibers of the autonomic nervous systems, including the enteric nervous system and central autonomic network. Moreover, we identified CWD PrP(RES) associated with the cell bodies and processes of enteric glial cells within the enteric nervous system of CWD-infected Tg(CerPrP-E) mice. The present findings demonstrate the importance of the peripheral and central autonomic networks in CWD neuroinvasion and neuropathogenesis and suggest that enteroglial cells may facilitate the shedding of prions via the intestinal tract.

Indexed as

AnimalsAutonomic Nervous SystemBrainFemaleInjections, IntraperitonealInjections, IntravenousIntestinal MucosaMaleMiceMice, TransgenicNeurogliaPrionsProtein TransportWasting Disease, ChronicPrions

Identifiers

PMID21777560
PMCPMC3157164
OpenAlexW1975100390

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.