Evidence map›Paper›PMID 27685162›Full record

ArticleJournal of visualized experiments : JoVE2016

Developing a Salivary Antibody Multiplex Immunoassay to Measure Human Exposure to Environmental Pathogens.

Swinburne A J Augustine, Tarsha N Eason, Kaneatra J Simmons, Clarissa L Curioso, Shannon M Griffin, Malini K D Ramudit, Trevor R Plunkett

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Rapid Salivary IgG Antibody Screening for Hepatitis A.Journal of clinical microbiology · 2020
    Article
  6. Article
  7. Observational
  8. Potable Water Reuse: What Are the Microbiological Risks?Current environmental health reports · 2018
    Review
  9. 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 3 institutions in 1 country.

Swinburne A J AugustineNational Exposure Research Laboratory, U.S. Environmental Protection Agency; Augustine.Swinburne@epa.gov.
Tarsha N EasonNational Risk Management Research Laboratory, U.S. Environmental Protection Agency.
Kaneatra J SimmonsNational Exposure Research Laboratory, U.S. Environmental Protection Agency.
Clarissa L CuriosoOak Ridge Institute for Science and Education.
Shannon M GriffinNational Exposure Research Laboratory, U.S. Environmental Protection Agency.
Malini K D RamuditNational Exposure Research Laboratory, U.S. Environmental Protection Agency.
Trevor R PlunkettDepartment of Biological Sciences, McMicken College of Arts and Sciences, University of Cincinnati.
Environmental Protection Agency · USOak Ridge Institute for Science and EducationUniversity of Cincinnati · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The etiology and impacts of human exposure to environmental pathogens are of major concern worldwide and, thus, the ability to assess exposure and infections using cost effective, high-throughput approaches would be indispensable. This manuscript describes the development and analysis of a bead-based multiplex immunoassay capable of measuring the presence of antibodies in human saliva to multiple pathogens simultaneously. Saliva is particularly attractive in this application because it is noninvasive, cheaper and easier to collect than serum. Antigens from environmental pathogens were coupled to carboxylated microspheres (beads) and used to measure antibodies in very small volumes of human saliva samples using a bead-based, solution-phase assay. Beads were coupled with antigens from Campylobacter jejuni, Helicobacter pylori, Toxoplasma gondii, noroviruses (G I.1 and G II.4) and hepatitis A virus. To ensure that the antigens were sufficiently coupled to the beads, coupling was confirmed using species-specific, animal-derived primary capture antibodies, followed by incubation with biotinylated anti-species secondary detection antibodies and streptavidin-R-phycoerythrin reporter (SAPE). As a control to measure non-specific binding, one bead set was treated identically to the others except it was not coupled to any antigen. The antigen-coupled and control beads were then incubated with prospectively-collected human saliva samples, measured on a high throughput analyzer based on the principles of flow cytometry, and the presence of antibodies to each antigen was measured in Median Fluorescence Intensity units (MFI). This multiplex immunoassay has a number of advantages, including more data with less sample; reduced costs and labor; and the ability to customize the assay to many targets of interest. Results indicate that the salivary multiplex immunoassay may be capable of identifying previous exposures and infections, which can be especially useful in surveillance studies involving large human populations.

Indexed as

AnimalsAntibodiesAntigens, BacterialAntigens, ViralEnvironmental ExposureEnvironmental MicrobiologyHelicobacter pyloriHumansImmunoassayImmunologic TestsMicrospheresNorovirusSalivaToxoplasmaAntibodiesAntigens, BacterialAntigens, Viral

Identifiers

PMID27685162
PMCPMC5092007
OpenAlexW2520464402

What OpenQuestion holds

Textmetadata
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.