Evidence map›Paper›PMID 29746561›Full record

ArticlePloS one2018

Monitoring food pathogens: Novel instrumentation for cassette PCR testing.

Darin Hunt, Curtis Figley, Dammika P Manage, Jana Lauzon, Rachel Figley, Linda M Pilarski, Lynn M McMullen, Patrick M Pilarski

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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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

8 authors at 1 institution in 1 country.

Darin HuntCBF Systems Inc., College Plaza, Edmonton, AB, Canada.
Curtis FigleyCBF Systems Inc., College Plaza, Edmonton, AB, Canada.
Dammika P ManageDepartment of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, AB, Canada.ORCID 0000-0002-9681-6674
Jana LauzonDepartment of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, AB, Canada.
Rachel FigleyCBF Systems Inc., College Plaza, Edmonton, AB, Canada.
Linda M PilarskiDepartment of Oncology, University of Alberta and Cross Cancer Institute, Edmonton, AB, Canada.
Lynn M McMullenDepartment of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB, Canada.
Patrick M PilarskiDivision of Physical Medicine & Rehabilitation, Department of Medicine, University of Alberta, 5-005 Katz Group Centre for Pharmacy and Health Research, Edmonton, AB, Canada.
University of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this manuscript, we report the design and development of a fast, reliable instrument to run gel-based cassette polymerase chain reactions (PCR). Here termed the GelCycler Mark II, our instrument is a miniaturized molecular testing system that is fast, low cost and sensitive. Cassette PCR utilizes capillary reaction units that carry all reagents needed for PCR, including primers and Taq polymerase, except the sample, which is loaded at the time of testing. Cassette PCR carries out real time quantitative PCR followed by melt curve analysis (MCA) to verify amplicon identity at the expected melt temperature (Tm). The cassette PCR technology is well developed, particularly for detecting pathogens, and has been rigorously validated for detecting pathogenic Escherichia coli in meat samples. However, the work has been hindered by the lack of a robust and stable instrument to carry out the PCR, which requires fast and accurate temperature regulation, improved light delivery and fluorescent recording, and faster PCR reactions that maintain a high sensitivity of detection. Here, we report design and testing of a new instrument to address these shortcomings and to enable standardized testing by cassette PCR and commercial manufacture of a robust and accurate instrument that can be mass produced to deliver consistent performance. As a corollary to our new instrument development, we also report the use of an improved design approach using a machined aluminum cassette to meet the new instrument standards, prevent any light bleed across different trenches in each cassette, and allow testing of a larger number of samples for more targets in a single run. The GelCycler Mark II can detect and report E. coli contamination in 41 minutes. Sample positives are defined in as having a melt curve comparable to the internal positive control, with peak height exceeding that of the internal negative control. In a fractional analysis, as little as 1 bacterium per capillary reaction unit is directly detectable, with no enrichment step, in 35 cycles of PCR/MCA, in a total time of 53 minutes, making this instrument and technology among the very best for speed and sensitivity in screening food for pathogenic contamination.

Indexed as

Escherichia coliFood AnalysisFood MicrobiologyHumansMeatPolymerase Chain Reaction

Identifiers

PMID29746561
PMCPMC5945031
OpenAlexW2799537656

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.