Evidence map›Paper›PMID 35460243›Full record

ArticleLaboratory medicine2022

Multiplex Microsphere PCR (mmPCR) Allows Simultaneous Gram Typing, Detection of Fungal DNA, and Antibiotic Resistance Genes.

Daniel J Browne, Fang Liang, Kate H Gartlan, Patrick N A Harris, Geoffrey R Hill, Simon R Corrie, Kate A Markey

Open access · hybridAbstract read
In one paragraph

Article in Laboratory medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 60% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Daniel J BrowneDivision of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.ORCID 0000-0003-1840-8904
Fang LiangDivision of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kate H GartlanDivision of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Patrick N A HarrisFaculty of Medicine, UQ Centre for Clinical Research, University of Queensland, Royal Brisbane and Women's Hospital, Brisbane, Australia.ORCID 0000-0002-2895-0345
Geoffrey R HillDivision of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Simon R CorrieDepartment of Chemical Engineering, ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Monash and QLD Nodes, Monash University, Clayton, Australia.
Kate A MarkeyDivision of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUMemorial Sloan Kettering Cancer Center · USMonash University · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748Prestige Research Training ProgramQueensland Health Junior Clinical Research Fellowship
6 · The paper itself

Abstract

objectiveTo show the high analytical specificity of our multiplex microsphere polymerase chain reaction (mmPCR) method, which offers the simultaneous detection of both general (eg, Gram type) and specific (eg, Pseudomonas species) clinically relevant genetic targets in a single modular multiplex reaction. MATERIALS AND

methodsIsolated gDNA of 16S/rRNA Sanger-sequenced and Basic Local Alignment Tool-identified bacterial and fungal isolates were selectively amplified in a custom 10-plex Luminex MagPlex-TAG microsphere-based mmPCR assay. The signal/noise ratio for each reaction was calculated from flow cytometry standard data collected on a BD LSR Fortessa II flow cytometer. Data were normalized to the no-template negative control and the signal maximum. The analytical specificity of the assay was compared to single-plex SYBR chemistry quantitative PCR.

resultsBoth general and specific primer sets were functional in the 10-plex mmPCR. The general Gram typing and pan-fungal primers correctly identified all bacterial and fungal isolates, respectively. The species-specific and antibiotic resistance-specific primers correctly identified the species- and resistance-carrying isolates, respectively. Low-level cross-reactive signals were present in some reactions with high signal/noise primer ratios.

conclusionWe found that mmPCR can simultaneously detect specific and general clinically relevant genetic targets in multiplex. These results serve as a proof-of-concept advance that highlights the potential of high multiplex mmPCR diagnostics in clinical practice. Further development of specimen-specific DNA extraction techniques is required for sensitivity testing.

Indexed as

Anti-Bacterial AgentsMultiplex Polymerase Chain ReactionDNA, FungalDNA PrimersDrug Resistance, MicrobialHumansMicrospheresSensitivity and SpecificityAnti-Bacterial AgentsDNA, FungalDNA Primersanalytical specificityantibiotic resistance testingflow cytometryfungiGram typingMagPlex-TAG microspheresmultiplex PCR

Identifiers

PMID35460243
PMCPMC9435484
OpenAlexW4213422463

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.