Multiplex Solid-Phase Real-Time Polymerase Chain Reaction without DNA Extraction: A Rapid Intraoperative Diagnosis Using Microvolumes.


Journal

Ophthalmology
ISSN: 1549-4713
Titre abrégé: Ophthalmology
Pays: United States
ID NLM: 7802443

Informations de publication

Date de publication:
05 2021
Historique:
received: 24 05 2020
revised: 17 08 2020
accepted: 22 09 2020
pubmed: 29 9 2020
medline: 9 10 2021
entrez: 28 9 2020
Statut: ppublish

Résumé

Current polymerase chain reaction (PCR) methods for the diagnosis of infections are time consuming and require large sample volume and skilled technicians. We developed a novel, easy-to-use, and rapid (processing time, 1 minute; total time, 33 minutes) multiplex real-time PCR test (Direct Strip PCR) that did not require DNA extraction to detect 9 pathogens that could cause uveitis in 20-μl samples. Multicenter prospective evaluation of a diagnostic PCR test. A total of 511 participants (patients with infectious uveitis and controls) were examined at 18 institutes worldwide. After validation, intraocular fluid samples were subjected to etiologic or exclusive diagnosis, including intraoperative rapid diagnosis. The concordance and correlations between Direct Strip PCR and quantitative PCR (qPCR) results. Direct Strip PCR exhibited rapid detection, good repeatability and specificity, long storage stability, and detection ability equal to that of qPCR. It also showed low interinstitutional variability compared with qPCR, even when PCR beginners used various real-time PCR machines. The Direct Strip PCR for 9 pathogens exhibited high concordance against the qPCR (positive concordance rate, 98.8%-100%; negative concordance rate, 99.8%-100%; κ coefficient, 0.969-1.000; P < 0.001-0.031). Additionally, results obtained using Direct Strip PCR and qPCR were highly correlated (ρ = 0.748; P < 0.001). This assay was used for rapid intraoperative diagnosis. The Direct Strip PCR test may improve the prognosis of various infectious diseases because it facilitates rapid etiologic evaluation at the first hospital visit and can be used for intraoperative diagnosis.

Identifiants

pubmed: 32987046
pii: S0161-6420(20)30933-7
doi: 10.1016/j.ophtha.2020.09.028
pii:
doi:

Substances chimiques

DNA Primers 0
DNA, Protozoan 0
DNA, Viral 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

729-739

Informations de copyright

Copyright © 2020 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

Auteurs

Satoko Nakano (S)

Department of Ophthalmology, Oita University, Yufu, Japan.

Yasuhiro Tomaru (Y)

Center for Stem Cell and Regenerative Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

Toshiaki Kubota (T)

Department of Ophthalmology, Oita University, Yufu, Japan.

Hiroshi Takase (H)

Department of Ophthalmology & Visual Science, Tokyo Medical and Dental University, Tokyo, Japan.

Manabu Mochizuki (M)

Department of Ophthalmology & Visual Science, Tokyo Medical and Dental University, Tokyo, Japan; Miyata Eye Hospital, Miyakonojo, Japan.

Norio Shimizu (N)

Center for Stem Cell and Regenerative Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

Sunao Sugita (S)

Department of Ophthalmology, Kobe City Eye Hospital, Kobe, Japan; Laboratory for Retinal Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan. Electronic address: sunao.sugita@riken.jp.

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Classifications MeSH