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PlexProbes enhance qPCR multiplexing by discriminating multiple targets in each fluorescent channel

The probe technology described in this paper facilitates detection and discrimination of multiple targets in a single fluorescent channel during PCR. This provides a strategy for doubling the number of targets that can be analysed simultaneously on existing PCR instruments. These probes are referred...

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Published in:PloS one 2022-03, Vol.17 (3), p.e0263329-e0263329
Main Authors: Hasick, Nicole, Kim, Ryung Rae, Xu, Yin, Bone, Simon, Lawrence, Andrea, Gibbs, Claire, Danckert, Nathan, Todd, Alison
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container_title PloS one
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creator Hasick, Nicole
Kim, Ryung Rae
Xu, Yin
Bone, Simon
Lawrence, Andrea
Gibbs, Claire
Danckert, Nathan
Todd, Alison
description The probe technology described in this paper facilitates detection and discrimination of multiple targets in a single fluorescent channel during PCR. This provides a strategy for doubling the number of targets that can be analysed simultaneously on existing PCR instruments. These probes are referred to as PlexProbes and produce fluorescence that can be switched 'on' or 'off' in the presence of target by manipulating the temperature. During PCR, fluorescence can be measured at multiple temperatures allowing discrimination of specific targets at defined temperatures. In a single fluorescent channel, a model duplex assay allowed either real-time or endpoint detection of Chlamydia trachomatis (CT) at 52°C and end-point detection of Neisseria gonorrhoeae (GC) at 74°C. Using this model system, as few as 40 copies of each specific target could be detected as single infection or co-infection, regardless of the presence or absence of the other target. A PlexProbe prototype assay for sexually transmitted infections (PP-STI) which simultaneously enables detection and differentiation of six targets using only three fluorescent channels was then constructed and evaluated. The PP-STI assay detects GC (2 gene targets), CT, Mycoplasma genitalium (MG), Trichomonas vaginalis (TV) and an internal control (IC). To evaluate assay performance, a panel of archived clinical samples (n = 337) were analysed using PP-STI and results compared to those obtained with a commercially available diagnostic assay. The overall agreement between results obtained with the PP-STI assay and the reference test was greater than 99.5%. PlexProbes offer a method of detecting more targets from a single diagnostic test, empowering physicians to make evidence-based treatment decisions while conserving time, labour, sample volume and reagent costs.
doi_str_mv 10.1371/journal.pone.0263329
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1932-6203
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subjects Assaying
Biochemical assays
Biology and Life Sciences
Chlamydia Infections - diagnosis
Chlamydia trachomatis - genetics
Diagnostic systems
Discrimination
Engineering and Technology
Fluorescence
Gonorrhea - diagnosis
Humans
Infections
Medical diagnosis
Medicine and Health Sciences
Methods
Molecular diagnostic techniques
Multiplexing
Mycoplasma genitalium - genetics
Mycoplasma Infections - diagnosis
Neisseria gonorrhoeae - genetics
Pathogens
Performance evaluation
Physicians
Polymerase chain reaction
Reagents
Real-Time Polymerase Chain Reaction
Research and Analysis Methods
Sexually transmitted diseases
Sexually Transmitted Diseases - diagnosis
STD
Target detection
Trichomonas vaginalis - genetics
title PlexProbes enhance qPCR multiplexing by discriminating multiple targets in each fluorescent channel
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T10%3A14%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PlexProbes%20enhance%20qPCR%20multiplexing%20by%20discriminating%20multiple%20targets%20in%20each%20fluorescent%20channel&rft.jtitle=PloS%20one&rft.au=Hasick,%20Nicole&rft.date=2022-03-09&rft.volume=17&rft.issue=3&rft.spage=e0263329&rft.epage=e0263329&rft.pages=e0263329-e0263329&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0263329&rft_dat=%3Cgale_plos_%3EA696221683%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c6079-6fb47be79dd07cf9ab509c0667c0a6a21edce65a367acc74cb8e5753b9a738ae3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2637572214&rft_id=info:pmid/35263349&rft_galeid=A696221683&rfr_iscdi=true