MétaCan
Menu
Back to cohort
Record W2116197112 · doi:10.1177/104063870001200116

Diagnostic Performance of a Reverse Transcription-Polymerase Chain Reaction Test for Porcine Reproductive and Respiratory Syndrome Virus

2000· article· en· W2116197112 on OpenAlexaboutno aff
Elizabeth A. Wagstrom, Kyoung‐Jin Yoon, Carolyn Cook, Jeffrey J. Zimmerman

Bibliographic record

VenueJournal of Veterinary Diagnostic Investigation · 2000
Typearticle
Languageen
FieldAgricultural and Biological Sciences
TopicAnimal Virus Infections Studies
Canadian institutionsnot available
Fundersnot available
KeywordsReverse transcription polymerase chain reactionPolymerase chain reactionVirologyReverse transcriptaseBiologyPorcine reproductive and respiratory syndrome virusRespiratory systemVirusReal-time polymerase chain reactionMedicineGeneMessenger RNAGeneticsAnatomy

Abstract

fetched live from OpenAlex

Porcine reproductive and respiratory syndrome (PRRS) virus first appeared in swine in Canada in the late 1970s, in the United States in the mid 1980s, and in Europe in 1990.23 Since that time, PRRS virus infection has become endemic in most pork-producing areas of the world. Although infection is frequently subclinical, PRRS virus plays a significant role in swine health, as reflected in the number of cases submitted to veterinary diagnostic laboratories located in swine-dense areas. For instance, in 1998 the Iowa State University Veterinary Diagnostic Laboratory (ISU-VDL) performed 90,608 serologic tests for the detection of PRRS virus antibody (J. Zimmerman, personal communication), and among diagnostic cases involving swine, 83% of samples (5,026/6,023) submitted for virus isolation included a request for isolation of PRRS virus (K.-J. Yoon, personal communication). Economically, PRRS is generally perceived to be the most significant infectious disease of swine in North America. Over the last several years, the economic impact of PRRS virus on swine production has stimulated a substantial investment of research resources into the search for effective disease control strategies. The development of accurate and rapid diagnostic assays has been an essential part of this effort. Numerous procedures have been developed and implemented for the diagnosis of PRRS, including serum antibody assays, virus isolation techniques, and antigen detection and visualization in tissues by immunohistochemistry or immunofluorescence microscopy.24 In addition, a number of polymerase chain reaction (PCR) assays and in situ hybridization techniques have been developed for the detection of PRRS virus RNA in clinical specimens, including serum, semen, and tissues.4,9–12,16,17 The transfer of PCR technology into the diagnostic setting has been of particular interest to diagnosticians and swine practitioners. Generally, PCR is considered to offer distinct advantages over other techniques, including faster availability of results, higher diagnostic sensitivity, and higher diagnostic specificity. At the present time, however, documentation of the specific diagnostic performance characteristics of PCR assays is sparse. Here, we report observations on the diagnostic performance of a PCR assay for the detection of PRRS virus. The original intent of this research was to use a reverse transcription-nested PCR (RT-nPCR) to detect PRRS virus genomic material in field samples collected from 20 commercial swine herds. Field samples (n 5 756) were submit-

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.003
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.923
Threshold uncertainty score0.363

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.038
GPT teacher head0.244
Teacher spread0.207 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations16
Published2000
Admission routes1
Has abstractyes

Explore more

Same venueJournal of Veterinary Diagnostic InvestigationSame topicAnimal Virus Infections StudiesFrench-language works237,207