Faeces from infected animals have been suggested as a potential source of contamination and transmission of prion diseases in the environment. This work describes the development of a procedure for the detection of PrP(res) in stools which is based on a detergent-based extraction and immunoprecipitation (IP). The procedure was evaluated by analyzing TSE-spiked sheep and mice faeces, and proved to be specific for PrP(res) with sensitivities of 5-10 microg of infected brain tissue. In order to analyze the shedding of prions, we studied stools from orally inoculated mice over 4-days post-inoculation and also stools from terminally sick scrapie-infected mice. PrP(res) was only detected in stools shortly after the oral ingestion of TSE agents. T...
Scrapie and chronic wasting disease are contagious prion diseases affecting sheep and cervids, respe...
Transgenic mouse lines expressing different levels of the bovine prion protein gene (boPrP(C)) were ...
AbstractA hallmark of prion diseases is the accumulation of an abnormally folded prion protein, deno...
Faeces from infected animals have been suggested as a potential source of contamination and transmis...
Classical scrapie is a naturally transmitted prion disease of sheep and goats. Contaminated environm...
Prions are largely contained within the nervous and lymphoid tissue of transmissible spongiform ence...
Shedding of prions via faeces may be involved in the transmission of contagious prion diseases. Her...
Shedding of prions via faeces may be involved in the transmission of contagious prion diseases. Here...
Abstract – Shedding of prions via faeces may be involved in the transmission of contagious prion dis...
Environmental contamination is considered a potential mechanism of transmission of prion diseases. S...
<div><p>The transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of fatal ...
Scrapie and chronic wasting disease are contagious prion diseases affecting sheep and cervids, respe...
Cellular prion protein (PrPC) is expressed ubiquitously on the normal cell surfaces of nerve cells, ...
The transmissible spongiform encephalopathies (TSEs) are caused by infectious agents whose structure...
Horizontal transmission of prion diseases through the environment represents a considerable concern....
Scrapie and chronic wasting disease are contagious prion diseases affecting sheep and cervids, respe...
Transgenic mouse lines expressing different levels of the bovine prion protein gene (boPrP(C)) were ...
AbstractA hallmark of prion diseases is the accumulation of an abnormally folded prion protein, deno...
Faeces from infected animals have been suggested as a potential source of contamination and transmis...
Classical scrapie is a naturally transmitted prion disease of sheep and goats. Contaminated environm...
Prions are largely contained within the nervous and lymphoid tissue of transmissible spongiform ence...
Shedding of prions via faeces may be involved in the transmission of contagious prion diseases. Her...
Shedding of prions via faeces may be involved in the transmission of contagious prion diseases. Here...
Abstract – Shedding of prions via faeces may be involved in the transmission of contagious prion dis...
Environmental contamination is considered a potential mechanism of transmission of prion diseases. S...
<div><p>The transmissible spongiform encephalopathies (TSEs) or prion diseases are a group of fatal ...
Scrapie and chronic wasting disease are contagious prion diseases affecting sheep and cervids, respe...
Cellular prion protein (PrPC) is expressed ubiquitously on the normal cell surfaces of nerve cells, ...
The transmissible spongiform encephalopathies (TSEs) are caused by infectious agents whose structure...
Horizontal transmission of prion diseases through the environment represents a considerable concern....
Scrapie and chronic wasting disease are contagious prion diseases affecting sheep and cervids, respe...
Transgenic mouse lines expressing different levels of the bovine prion protein gene (boPrP(C)) were ...
AbstractA hallmark of prion diseases is the accumulation of an abnormally folded prion protein, deno...