Christopher J. Johnson, PhD (Former Employee)
Science and Products
Filter Total Items: 20
Red-backed vole brain promotes highly efficient in vitro amplification of abnormal prion protein from macaque and human brains infected with variant Creutzfeldt-Jakob disease agent. Red-backed vole brain promotes highly efficient in vitro amplification of abnormal prion protein from macaque and human brains infected with variant Creutzfeldt-Jakob disease agent.
Rapid antemortem tests to detect individuals with transmissible spongiform encephalopathies (TSE) would contribute to public health. We investigated a technique known as protein misfolding cyclic amplification (PMCA) to amplify abnormal prion protein (PrPTSE) from highly diluted variant Creutzfeldt-Jakob disease (vCJD)-infected human and macaque brain homogenates, seeking to improve the...
Authors
Julie Nemecek, Nabanita Nag, Christina M. Carlson, Jay R. Schneider, Dennis M. Heisey, Christopher J. Johnson, David M. Asher, Luisa Gregori
Prion protein degradation by lichens of the genus Cladonia Prion protein degradation by lichens of the genus Cladonia
It has recently been discovered that lichens contain a serine protease capable of degrading the pathogenic prion protein, the etiological agent of prion diseases such as sheep scrapie and cervid chronic wasting disease. Limited methods are available to degrade or inactivate prion disease agents, especially in the environment, and lichens or their serine protease could prove important for
Authors
James P. Bennett, Cynthia M. Rodriguez, Christopher J. Johnson
Lichens: Unexpected anti-prion agents? Lichens: Unexpected anti-prion agents?
The prion diseases sheep scrapie and cervid chronic wasting disease are transmitted, in part, via an environmental reservoir of infectivity; prions released from infected animals persist in the environment and can cause disease years later. Central to controlling disease transmission is the identification of methods capable of inactivating these agents on the landscape. We have found...
Authors
Cynthia M. Rodriguez, James P. Bennett, Christopher J. Johnson
Alteration of the chronic wasting disease species barrier by in vitro prion amplification Alteration of the chronic wasting disease species barrier by in vitro prion amplification
Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) of cervids now detected in 19 states of the United States, three Canadian provinces, and South Korea. Whether noncervid species can be infected by CWD and thereby serve as reservoirs for the infection is not known. To investigate this issue, we previously used serial protein misfolding cyclic amplification...
Authors
Timothy D. Kurt, Davis M. Seelig, Jay R. Schneider, Christopher J. Johnson, Glenn C. Telling, Dennis M. Heisey, Edward A. Hoover
Degradation of the disease-associated prion protein by a serine protease from lichens. Degradation of the disease-associated prion protein by a serine protease from lichens.
The disease-associated prion protein (PrPTSE), the probable etiological agent of the transmissible spongiform encephalopathies (TSEs), is resistant to degradation and can persist in the environment. Lichens, mutualistic symbioses containing fungi, algae, bacteria and occasionally cyanobacteria, are ubiquitous in the environment and have evolved unique biological activities allowing their...
Authors
Christopher J. Johnson, James P. Bennett, S.M. Biro, J. C. Duque-Velasquez, Cynthia M. Rodriguez, R. A. Bessen, Tonie E. Rocke
Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmission Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmission
Ingestion of prion-contaminated materials is postulated to be a primary route of prion disease transmission. Binding of prions to soil (micro)particles dramatically enhances peroral disease transmission relative to unbound prions, and it was hypothesized that micrometer-sized particles present in other consumed materials may affect prion disease transmission via the oral route of...
Authors
Christopher J. Johnson, Debbie McKenzie, Joel A. Pedersen, Judd M. Aiken
Modeling routes of chronic wasting disease transmission: Environmental prion persistence promotes deer population decline and extinction Modeling routes of chronic wasting disease transmission: Environmental prion persistence promotes deer population decline and extinction
Chronic wasting disease (CWD) is a fatal disease of deer, elk, and moose transmitted through direct, animal-to-animal contact, and indirectly, via environmental contamination. Considerable attention has been paid to modeling direct transmission, but despite the fact that CWD prions can remain infectious in the environment for years, relatively little information exists about the...
Authors
Emily S. Almberg, Paul C. Cross, Christopher J. Johnson, Dennis M. Heisey, Bryan J. Richards
Modeling survival: application of the Andersen-Gill model to Yellowstone grizzly bears Modeling survival: application of the Andersen-Gill model to Yellowstone grizzly bears
Wildlife ecologists often use the Kaplan-Meier procedure or Cox proportional hazards model to estimate survival rates, distributions, and magnitude of risk factors. The Andersen-Gill formulation (A-G) of the Cox proportional hazards model has seen limited application to mark-resight data but has a number of advantages, including the ability to accommodate left-censored data, time-varying
Authors
Christopher J. Johnson, Mark S. Boyce, Charles C. Schwartz, Mark A. Haroldson
Science and Products
Filter Total Items: 20
Red-backed vole brain promotes highly efficient in vitro amplification of abnormal prion protein from macaque and human brains infected with variant Creutzfeldt-Jakob disease agent. Red-backed vole brain promotes highly efficient in vitro amplification of abnormal prion protein from macaque and human brains infected with variant Creutzfeldt-Jakob disease agent.
Rapid antemortem tests to detect individuals with transmissible spongiform encephalopathies (TSE) would contribute to public health. We investigated a technique known as protein misfolding cyclic amplification (PMCA) to amplify abnormal prion protein (PrPTSE) from highly diluted variant Creutzfeldt-Jakob disease (vCJD)-infected human and macaque brain homogenates, seeking to improve the...
Authors
Julie Nemecek, Nabanita Nag, Christina M. Carlson, Jay R. Schneider, Dennis M. Heisey, Christopher J. Johnson, David M. Asher, Luisa Gregori
Prion protein degradation by lichens of the genus Cladonia Prion protein degradation by lichens of the genus Cladonia
It has recently been discovered that lichens contain a serine protease capable of degrading the pathogenic prion protein, the etiological agent of prion diseases such as sheep scrapie and cervid chronic wasting disease. Limited methods are available to degrade or inactivate prion disease agents, especially in the environment, and lichens or their serine protease could prove important for
Authors
James P. Bennett, Cynthia M. Rodriguez, Christopher J. Johnson
Lichens: Unexpected anti-prion agents? Lichens: Unexpected anti-prion agents?
The prion diseases sheep scrapie and cervid chronic wasting disease are transmitted, in part, via an environmental reservoir of infectivity; prions released from infected animals persist in the environment and can cause disease years later. Central to controlling disease transmission is the identification of methods capable of inactivating these agents on the landscape. We have found...
Authors
Cynthia M. Rodriguez, James P. Bennett, Christopher J. Johnson
Alteration of the chronic wasting disease species barrier by in vitro prion amplification Alteration of the chronic wasting disease species barrier by in vitro prion amplification
Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) of cervids now detected in 19 states of the United States, three Canadian provinces, and South Korea. Whether noncervid species can be infected by CWD and thereby serve as reservoirs for the infection is not known. To investigate this issue, we previously used serial protein misfolding cyclic amplification...
Authors
Timothy D. Kurt, Davis M. Seelig, Jay R. Schneider, Christopher J. Johnson, Glenn C. Telling, Dennis M. Heisey, Edward A. Hoover
Degradation of the disease-associated prion protein by a serine protease from lichens. Degradation of the disease-associated prion protein by a serine protease from lichens.
The disease-associated prion protein (PrPTSE), the probable etiological agent of the transmissible spongiform encephalopathies (TSEs), is resistant to degradation and can persist in the environment. Lichens, mutualistic symbioses containing fungi, algae, bacteria and occasionally cyanobacteria, are ubiquitous in the environment and have evolved unique biological activities allowing their...
Authors
Christopher J. Johnson, James P. Bennett, S.M. Biro, J. C. Duque-Velasquez, Cynthia M. Rodriguez, R. A. Bessen, Tonie E. Rocke
Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmission Meat and bone meal and mineral feed additives may increase the risk of oral prion disease transmission
Ingestion of prion-contaminated materials is postulated to be a primary route of prion disease transmission. Binding of prions to soil (micro)particles dramatically enhances peroral disease transmission relative to unbound prions, and it was hypothesized that micrometer-sized particles present in other consumed materials may affect prion disease transmission via the oral route of...
Authors
Christopher J. Johnson, Debbie McKenzie, Joel A. Pedersen, Judd M. Aiken
Modeling routes of chronic wasting disease transmission: Environmental prion persistence promotes deer population decline and extinction Modeling routes of chronic wasting disease transmission: Environmental prion persistence promotes deer population decline and extinction
Chronic wasting disease (CWD) is a fatal disease of deer, elk, and moose transmitted through direct, animal-to-animal contact, and indirectly, via environmental contamination. Considerable attention has been paid to modeling direct transmission, but despite the fact that CWD prions can remain infectious in the environment for years, relatively little information exists about the...
Authors
Emily S. Almberg, Paul C. Cross, Christopher J. Johnson, Dennis M. Heisey, Bryan J. Richards
Modeling survival: application of the Andersen-Gill model to Yellowstone grizzly bears Modeling survival: application of the Andersen-Gill model to Yellowstone grizzly bears
Wildlife ecologists often use the Kaplan-Meier procedure or Cox proportional hazards model to estimate survival rates, distributions, and magnitude of risk factors. The Andersen-Gill formulation (A-G) of the Cox proportional hazards model has seen limited application to mark-resight data but has a number of advantages, including the ability to accommodate left-censored data, time-varying
Authors
Christopher J. Johnson, Mark S. Boyce, Charles C. Schwartz, Mark A. Haroldson