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About:
Development of a duplex reverse transcription recombinase-aided amplification assay for respiratory syncytial virus incorporating an internal control
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covidontheweb.inria.fr
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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
Development of a duplex reverse transcription recombinase-aided amplification assay for respiratory syncytial virus incorporating an internal control
Creator
Zhang, Yi
Ma, Xuejun
Fan, Tao
Wang, Ruihuan
Li, Lixin
Li, Xinna
Pan, Jing
Qi, Juju
Shen, Xinxin
Song, Guowei
Song, ·
Cn, Maxj@ivdc
Fan, ·
Shen, ·
Source
Medline; PMC
abstract
Human respiratory syncytial virus (RSV) is a common viral pathogen that causes lower respiratory tract infections in infants and children globally. In this study, we developed a duplex reverse transcription recombinase-aided amplification (duplex-rtRAA) assay containing an internal control in a single closed tube for the detection of human RSV. The internal control in the amplification effectively eliminated false-negative results and ensured the accuracy of the duplex-rtRAA system. We first developed and evaluated a universal singleplex-rtRAA assay for RSV. The sensitivity of this assay for RSV was determined as 4.4 copies per reaction, and the specificity was 100%. Next, a duplex-rtRAA assay with an internal control was established. The sensitivity of the duplex-rtRAA assay approached 5.0 copies per reaction, and no cross-reaction with other common respiratory viruses was observed. The two detection methods (singleplex-rtRAA and duplex-rtRAA) developed in this study were used to test 278 clinical specimens, and the results showed absolute consistency with RSV RT-qPCR analysis, demonstrating 100% diagnostic sensitivity and specificity. These data indicate that the duplex-rtRAA has great potential for the rapid detection of RSV with a high sensitivity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00705-019-04230-z) contains supplementary material, which is available to authorized users.
has issue date
2019-05-03
(
xsd:dateTime
)
bibo:doi
10.1007/s00705-019-04230-z
bibo:pmid
31053978
has license
no-cc
sha1sum (hex)
6ca3f120df064f4cf573e1d8d60ee81cd1ed68e7
schema:url
https://doi.org/10.1007/s00705-019-04230-z
resource representing a document's title
Development of a duplex reverse transcription recombinase-aided amplification assay for respiratory syncytial virus incorporating an internal control
has PubMed Central identifier
PMC7086889
has PubMed identifier
31053978
schema:publication
Arch Virol
resource representing a document's body
covid:6ca3f120df064f4cf573e1d8d60ee81cd1ed68e7#body_text
is
schema:about
of
named entity 'assay'
named entity 'RSV'
named entity 'sensitivity'
named entity 'absolute'
named entity 'developed'
named entity 'sensitivity'
named entity 'internal control'
named entity 'internal control'
named entity 'Development'
named entity 'ESTABLISHED'
named entity 'ACCURACY'
named entity 'GLOBALLY'
named entity '100%'
named entity 'ELIMINATED'
named entity 'IS A'
named entity 'RESULTS'
named entity 'A COMMON'
named entity 'OBSERVED'
named entity 'CLOSED'
named entity 'COMMON'
named entity 'INTERNAL'
named entity 'ASSAY'
named entity 'SPECIMENS'
named entity 'CONTROL'
named entity 'DEVELOPMENT'
named entity 'RECOMBINASE'
named entity 'REVERSE TRANSCRIPTION'
named entity 'AMPLIFICATION'
named entity 'RESPIRATORY SYNCYTIAL VIRUS'
named entity 'RSV'
named entity 'ASSAY'
named entity 'CONTROL'
named entity 'UNIVERSAL'
named entity 'NEGATIVE RESULTS'
named entity 'ANALYSIS'
named entity 'GREAT'
named entity 'RECOMBINASE'
named entity 'STUDY'
named entity 'DETERMINED'
named entity 'SINGLE'
named entity 'INFANTS'
named entity 'SENSITIVITY'
named entity 'RAPID'
named entity 'SYSTEM'
named entity 'REACTION'
named entity 'RT-QPCR'
named entity 'CLINICAL'
named entity 'DUPLEX'
named entity 'SENSITIVITY AND SPECIFICITY'
named entity 'RESPIRATORY VIRUSES'
named entity 'THESE'
named entity 'DETECTION'
named entity 'TO TEST'
named entity '4.4'
named entity 'FALSE'
named entity 'AMPLIFICATION'
named entity 'CHILDREN'
named entity 'HUMAN RESPIRATORY SYNCYTIAL VIRUS'
named entity 'EVALUATED'
named entity 'CAUSES'
named entity 'TUBE'
named entity 'DETECTION METHODS'
named entity 'USED'
named entity 'SPECIFICITY'
named entity 'CONTAINING'
named entity 'POTENTIAL'
named entity 'INTERNAL'
named entity 'COPIES'
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