Evidence map›Paper›PMID 29849171›Full record

ArticleScientific reports2018

A Rapid, Accurate, Single Molecule Counting Method Detects Clostridium difficile Toxin B in Stool Samples.

Sadanand Gite, Destiny Archambault, Michael P Cappillino, David Cunha, Victoria Dorich, Tatyana Shatova, Andrew Tempesta, Bruce Walsh, Jessica A Walsh, Adam Williams and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Rapid Quantification ofAnalytical chemistry · 2022
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Rapid Susceptibility Testing Methods.Clinics in laboratory medicine · 2019
    Review
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

13 authors at 2 institutions in 1 country.

Sadanand GiteFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA. sadanand@firstlightbio.com.
Destiny ArchambaultFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Michael P CappillinoFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
David CunhaFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Victoria DorichFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Tatyana ShatovaFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Andrew TempestaFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Bruce WalshFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Jessica A WalshFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Adam WilliamsFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
James E KirbyBeth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, 02215, USA.
Jayson BowersFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
Don StrausFirst Light Biosciences, 1 Oak Park Drive, Bedford, MA, 01730, USA.
First Light Diagnostics (United States) · USBeth Israel Deaconess Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a new rapid and accurate immunoassay-based technology capable of counting single target molecules using digital imaging without magnification. Using the technology, we developed a rapid test for Clostridium difficile toxin B, which is responsible for the pathology underlying potentially fatal C. difficile infections (CDI). There are currently no tests for CDI that are rapid, sensitive, and specific. The MultiPath C. difficile toxin B test images and counts complexes of target-specific magnetic and fluorescent particles that have been tethered together by toxin B molecules in minimally processed stool samples. The performance characteristics of the 30 minute test include a limit of detection of 45 pg/mL, dynamic range covering 4-5 orders of magnitude, and coefficient of variation of less than 10%. The MultiPath test detected all toxinotypes and ribotypes tested, including the one most commonly occurring in the US and EU; shows no cross reactivity with relevant bacterial species; and is robust to potential interferants commonly present in stool samples. On a training set of 320 clinical stool samples, the MultiPath C. difficile toxin B test showed 97.0% sensitivity (95% CI, 91.4-99.4%); 98.3% specificity (95% CI, 96.8-99.2%); and 98.2% accuracy (95% CI, 96.7-99.0%) compared to the cellular cytotoxicity neutralization assay (CCNA) reference method. Based on these compelling performance characteristics, we believe the MultiPath technology can address the lack of rapid, sensitive, specific, and easy-to-use diagnostic tests for C. difficile.

Indexed as

ArtifactsBacterial ProteinsBacterial ToxinsClostridioides difficileFecesHumansImmunoassayLimit of DetectionTime FactorsBacterial ProteinsBacterial ToxinstoxB protein, Clostridium difficile

Identifiers

PMID29849171
PMCPMC5976643
OpenAlexW2807145482

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.