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About:
Evaluation of two singleplex reverse transcription-Insulated isothermal PCR tests and a duplex real-time RT-PCR test for the detection of porcine epidemic diarrhea virus and porcine deltacoronavirus
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Evaluation of two singleplex reverse transcription-Insulated isothermal PCR tests and a duplex real-time RT-PCR test for the detection of porcine epidemic diarrhea virus and porcine deltacoronavirus
Creator
Chen, Qi
Zhang, Yan
Gauger, Phillip
Harmon, Karen
Zhang, Jianqiang
Tsai, Yun-Long
Lee, Pei-Yu
Chang, Hsiao-Fen
Chiang, Cheng-Jen
Li, Fu-Chun
Shen, Yu-Han
Wang, Thomas
Source
Elsevier; Medline; PMC
abstract
Abstract Recent outbreaks of porcine epidemic diarrhea virus (PEDV) and porcine deltacoronavirus (PDCoV) in multiple countries have caused significant economic losses and remain a serious challenge to the swine industry. Rapid diagnosis is critical for the implementation of efficient control strategies before and during PEDV and PDCoV outbreaks. Insulated isothermal PCR (iiPCR) on the portable POCKITâ„¢ device is user friendly for on-site pathogen detection. In the present study, a singleplex PEDV RT-iiPCR, a singleplex PDCoV RT-iiPCR, and a duplex PEDV/PDCoV real-time RT-PCR (rRT-PCR) commercial reagents targeting the M gene were compared to an N gene-based PEDV rRT-PCR and an M gene-based PDCoV rRT-PCR that were previously published and used as reference PCRs. All PCR assays were highly specific and did not cross react with other porcine enteric pathogens. Analytical sensitivities of the PEDV RT-iiPCR, PDCoV RT-iiPCR and duplex PEDV/PDCoV rRT-PCR were determined using in vitro transcribed RNA as well as viral RNA extracted from ten-fold serial dilutions of PEDV and PDCoV cell culture isolates. Performance of each PCR assay was further evaluated using 170 clinical samples (86 fecal swabs, 24 feces, 19 intestines, and 41 oral fluids). Compared to the reference PEDV rRT-PCR, the sensitivity, specificity and accuracy of the PEDV RT-iiPCR were 97.73%, 98.78%, and 98.24%, respectively, and those of the duplex PEDV/PDCoV rRT-PCR were 98.86%, 96.34%, and 97.65%, respectively. Compared to the reference PDCoV rRT-PCR, the sensitivity, specificity and accuracy of the PDCoV RT-iiPCR were 100%, 100%, and 100%, respectively, and those of the PEDV/PDCoV duplex rRT-PCR were 96.34%, 100%, and 98.24%, respectively. Overall, all three new PCR assays were comparable to the reference rRT-PCRs for detection of PEDV and/or PDCoV. The PEDV and PDCoV RT-iiPCRs are potentially useful tools for on-site detection and the duplex PEDV/PDCoV rRT-PCR provides a convenient method to simultaneously detect the two viruses and differentiate PEDV from PDCoV.
has issue date
2016-08-31
(
xsd:dateTime
)
bibo:doi
10.1016/j.jviromet.2016.03.016
bibo:pmid
27060624
has license
els-covid
sha1sum (hex)
c58715798b7ae050186df99882c4f62fd73c2916
schema:url
https://doi.org/10.1016/j.jviromet.2016.03.016
resource representing a document's title
Evaluation of two singleplex reverse transcription-Insulated isothermal PCR tests and a duplex real-time RT-PCR test for the detection of porcine epidemic diarrhea virus and porcine deltacoronavirus
has PubMed Central identifier
PMC7113669
has PubMed identifier
27060624
schema:publication
Journal of Virological Methods
resource representing a document's body
covid:c58715798b7ae050186df99882c4f62fd73c2916#body_text
is
schema:about
of
named entity 'compared'
named entity 'diagnosis'
named entity 'DETECTION'
covid:arg/c58715798b7ae050186df99882c4f62fd73c2916
named entity 'DUPLEX'
named entity 'M GENE'
named entity 'USER'
named entity 'NEW'
named entity 'TEST'
named entity 'SAMPLES'
named entity 'RAPID DIAGNOSIS'
named entity 'METHOD'
named entity 'PRESENT'
named entity 'REAL-TIME RT-PCR'
named entity 'FECES'
named entity 'IMPLEMENTATION'
named entity 'IN VITRO'
named entity 'DEVICE'
named entity 'SPECIFICITY'
named entity 'TARGETING'
named entity 'CROSS'
named entity 'EXTRACTED'
named entity 'EFFICIENT'
named entity 'SIMULTANEOUSLY'
named entity 'REAGENTS'
named entity 'CONVENIENT'
named entity 'VIRUSES'
named entity 'STRATEGIES'
named entity 'OF EACH'
named entity 'PATHOGEN DETECTION'
named entity 'TOOLS'
named entity 'DID'
named entity 'FLUIDS'
named entity 'COUNTRIES'
named entity 'COMPARED'
named entity 'PCR ASSAY'
named entity 'ACCURACY'
named entity 'OVERALL'
named entity 'HAVE'
named entity 'PCR'
named entity 'CAUSED'
named entity 'USING'
named entity 'PROVIDES'
named entity 'PORCINE DELTACORONAVIRUS'
named entity 'REAL-TIME RT-PCR'
named entity 'FRIENDLY'
named entity 'PORTABLE'
named entity 'EVALUATED'
named entity 'CHALLENGE'
named entity 'ISOLATES'
named entity 'FECAL'
named entity 'TESTS'
named entity 'PORCINE EPIDEMIC DIARRHEA VIRUS'
named entity 'PCR'
named entity 'DETECTION'
named entity 'ANALYTICAL'
named entity 'DUPLEX'
named entity 'CELL CULTURE'
named entity 'ORAL'
named entity 'ENTERIC'
named entity 'HIGHLY'
named entity 'OUTBREAKS'
named entity 'SITE'
named entity 'REVERSE TRANSCRIPTION'
named entity 'EVALUATION'
named entity 'PORCINE DELTACORONAVIRUS'
named entity 'INTESTINES'
named entity '170'
named entity 'PERFORMANCE'
named entity 'CONTROL'
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