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About:
Panspecies molecular assays detect viral pathogens missed by real-time PCR/reverse-transcriptase PCR among pneumonia patients, Sarawak, Malaysia
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
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
title
Panspecies molecular assays detect viral pathogens missed by real-time PCR/reverse-transcriptase PCR among pneumonia patients, Sarawak, Malaysia
Creator
Gray, Gregory
Berita, Antoinette
Hii, King-Ching
Ting, Jakie
Toh, Teck-Hock
Wong, See-Chang
Wong, Toh-Mee
Lednicky, John
Blair, Patrick
Nguyen,
Bailey, Emily
Fieldhouse, Jane
Mallinson, Kerry
Galan, Diego
Than, Son
Tham, Thi
source
Medline; PMC
abstract
BACKGROUND: In a year-long pneumonia etiology study conducted June 2017 to May 2018 in Sarawak, Malaysia, 599 patients’ nasopharyngeal swab specimens were studied with real-time polymerase chain reaction (rPCR)/ reverse-transcription (rRT-PCR) assays for respiratory pathogens known to contribute to the high burden of lower respiratory tract infections. The study team sought to compare real-time assay results with panspecies conventional molecular diagnostics to compare sensitivities and learn if novel viruses had been missed. METHODS: Specimens were studied for evidence of adenovirus (AdV), enterovirus (EV) and coronavirus (CoV) with panspecies gel-based nested PCR/RT-PCR assays. Gene sequences of specimens positive by panspecies assays were sequenced and studied with the NCBI Basic Local Alignment Search Tool software. RESULTS: There was considerable discordance between real-time and conventional molecular methods. The real-time AdV assay found a positivity of 10.4%; however, the AdV panspecies assay detected a positivity of 12.4% and the conventional AdV-Hexon assay detected a positivity of 19.6%. The CoV and EV panspecies assays similarly detected more positive specimens than the real-time assays, with a positivity of 7.8% by the CoV panspecies assay versus 4.2% by rRT-PCR, and 8.0% by the EV panspecies assay versus 1.0% by rRT-PCR. We were not able to ascertain virus viability in this setting. While most discordance was likely due to assay sensitivity for previously described human viruses, two novel, possible zoonotic AdV were detected. CONCLUSIONS: The observed differences in the two modes of amplification suggest that where a problem with sensitivity is suspected, real-time assay results might be supplemented with panspecies conventional PCR/RT-PCR assays.
has issue date
2020-08-12
(
xsd:dateTime
)
bibo:doi
10.1186/s40794-020-00114-2
bibo:pmid
32817802
has license
cc-by
sha1sum (hex)
d74b784dda184bdaa4355802f7754137449cd829
schema:url
https://doi.org/10.1186/s40794-020-00114-2
resource representing a document's title
Panspecies molecular assays detect viral pathogens missed by real-time PCR/reverse-transcriptase PCR among pneumonia patients, Sarawak, Malaysia
has PubMed Central identifier
PMC7422451
has PubMed identifier
32817802
schema:publication
Trop Dis Travel Med Vaccines
resource representing a document's body
covid:d74b784dda184bdaa4355802f7754137449cd829#body_text
is
schema:about
of
named entity 'assays'
named entity 'positive'
named entity 'AdV'
named entity 'compare'
named entity 'assays'
named entity 'assays'
named entity 'assay'
named entity 'missed'
named entity 'studied'
covid:arg/d74b784dda184bdaa4355802f7754137449cd829
named entity 'human'
named entity 'specimens'
named entity 'assay'
named entity 'conventional'
named entity 'conventional'
named entity 'detected'
named entity 'assay'
named entity 'AdV'
named entity 'sequences'
named entity 'molecular'
named entity 'compare'
named entity 'assay'
named entity 'AdV'
named entity 'pneumonia'
named entity 'pathogens'
named entity 'rRT-PCR'
named entity 'Gene sequences'
named entity 'RT-PCR'
named entity 'viruses'
named entity 'RT-PCR'
named entity 'lower respiratory tract infections'
named entity 'molecular methods'
named entity 'reverse-transcriptase PCR'
named entity 'rRT-PCR'
named entity '98.8'
named entity 'Invitrogen'
named entity 'molecular methods'
named entity 'attending physician'
named entity 'rPCR'
named entity 'STATA'
named entity 'Microsoft Excel'
named entity 'nuclease'
named entity 'virus infections'
named entity 'viruses'
named entity 'cross-reactivity'
named entity 'World Health Organization'
named entity 'Malaysia'
named entity 'pathogens'
named entity 'pneumonia'
named entity 'Hilden'
named entity 'EV-D68'
named entity 'RSV'
named entity 'rPCR'
named entity 'type species'
named entity 'AdV'
named entity 'adenovirus'
named entity 'PCR'
named entity 'adenoviruses'
named entity 'AdV'
named entity 'Durham, North Carolina'
named entity 'Germany'
named entity 'infection'
named entity 'pathogens'
named entity 'Carlsbad, CA'
named entity 'gene'
named entity 'AdV'
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