Evidence map›Paper›PMID 24651568›Full record

ArticlePLoS neglected tropical diseases2014

Development of a prototype lateral flow immunoassay (LFI) for the rapid diagnosis of melioidosis.

Raymond L Houghton, Dana E Reed, Mark A Hubbard, Michael J Dillon, Hongjing Chen, Bart J Currie, Mark Mayo, Derek S Sarovich, Vanessa Theobald, Direk Limmathurotsakul and 8 more

Registry-linked trialOpen access · goldAbstract readEvaluation Study
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03578133 (A Cross-sectional Study Investigating the Causes of Pneumonia in Two Community Clinics in Two Yangon Townships, Myanmar), which is not on this map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
7.1field-weighted citation impact, top 2% 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.

NCT03578133 completednot on this mapstarted 2018, after this paper: background citation

A Cross-sectional Study Investigating the Causes of Pneumonia in Two Community Clinics in Two Yangon Townships, Myanmar

TypeobservationalSponsorMyanmar Oxford Clinical Research UnitRan2018 to 2019Enrolled300ConditionsMelioidosis PneumoniaArmsInBios® Active Melioidosis DetectTM-Lateral Flow Assay
3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 141 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Laboratory diagnosis of melioidosis.PLoS neglected tropical diseases · 2025
    Review
  7. Stability assessment of whole cell ELISA for Burkholderia pseudomallei antibodies detection.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Identification ofMicrobiology spectrum · 2024
    Article
  15. Burkholderia pseudomallei and melioidosis.Nature reviews. Microbiology · 2024
    Review
  16. Article
  17. Phylogenetic and phenotypic characterization ofFrontiers in microbiology · 2024
    Article
  18. Review
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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

18 authors at 10 institutions in 4 countries.

Raymond L HoughtonInBios International, Inc., Seattle, Washington, United States of America.
Dana E ReedDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Mark A HubbardDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Michael J DillonDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Hongjing ChenInBios International, Inc., Seattle, Washington, United States of America.
Bart J CurrieMenzies School of Health Research and Northern Territory Clinical School, Royal Darwin Hospital, Darwin, Northern Territory, Australia.
Mark MayoMenzies School of Health Research and Northern Territory Clinical School, Royal Darwin Hospital, Darwin, Northern Territory, Australia.
Derek S SarovichMenzies School of Health Research and Northern Territory Clinical School, Royal Darwin Hospital, Darwin, Northern Territory, Australia.
Vanessa TheobaldMenzies School of Health Research and Northern Territory Clinical School, Royal Darwin Hospital, Darwin, Northern Territory, Australia.
Direk LimmathurotsakulDepartment of Tropical Hygiene, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Gumphol WongsuvanDepartment of Clinical Pathology, Sappasithiprasong Hospital, Ubon Ratchathani, Thailand.
Narisara ChantratitaDepartment of Microbiology and Immunology, and Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Sharon J PeacockMahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Department of Microbiology and Immunology, Mahidol University, Bangkok, Thailand, and Department of Medicine, Cambridge University, Addenbrooke's Hospital, Cambridge, United Kingdom.
Alex R HoffmasterBacterial Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Brea DuvalBacterial Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Paul J BrettDepartment of Microbiology and Immunology, University of South Alabama, Mobile, Alabama, United States of America.
Mary N BurtnickDepartment of Microbiology and Immunology, University of South Alabama, Mobile, Alabama, United States of America.
David P AucoinDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
University of Nevada, Reno · USMenzies School of Health Research · AUInBios International (United States) · USNational Center for Emerging and Zoonotic Infectious Diseases · USUniversity of South Alabama · USAddenbrooke's Hospital · GBMahidol Oxford Tropical Medicine Research Unit · THMahidol University · THRoyal Darwin Hospital · AUSappasithiprasong Hospital · TH

Funding

Vaccines and Diagnostics TrialsU54AI065359 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI BARBOUR, ALAN G. · 2005 to 2013
$88.8M
Antigen Detection assay for the Diagnosis of MelioidosisR42AI102482 · NIAID · INBIOS INTERNATIONAL, INC. · PI AUCOIN, DAVID P, RAYCHAUDHURI, SYAMAL X · 2014 to 2016
$2.0M
Antigen Detection Assay for the Diagnosis of MelioidosisR41AI102482 · NIAID · INBIOS INTERNATIONAL, INC. · PI AUCOIN, DAVID P, HOUGHTON, RAYMOND · 2012 to 2013
$599k
NIAID NIH HHS 1R41AI102482NIAID NIH HHS R41 AI102482NIAID NIH HHS R42 AI102482NIAID NIH HHS U54 AI065359NIAID NIH HHS U54AI065359
6 · The paper itself

Abstract

Burkholderia pseudomallei is a soil-dwelling bacterium and the causative agent of melioidosis. Isolation of B. pseudomallei from clinical samples is the "gold standard" for the diagnosis of melioidosis; results can take 3-7 days to produce. Alternatively, antibody-based tests have low specificity due to a high percentage of seropositive individuals in endemic areas. There is a clear need to develop a rapid point-of-care antigen detection assay for the diagnosis of melioidosis. Previously, we employed In vivo Microbial Antigen Discovery (InMAD) to identify potential B. pseudomallei diagnostic biomarkers. The B. pseudomallei capsular polysaccharide (CPS) and numerous protein antigens were identified as potential candidates. Here, we describe the development of a diagnostic immunoassay based on the detection of CPS. Following production of a CPS-specific monoclonal antibody (mAb), an antigen-capture immunoassay was developed to determine the concentration of CPS within a panel of melioidosis patient serum and urine samples. The same mAb was used to produce a prototype Active Melioidosis Detect Lateral Flow Immunoassay (AMD LFI); the limit of detection of the LFI for CPS is comparable to the antigen-capture immunoassay (∼0.2 ng/ml). The analytical reactivity (inclusivity) of the AMD LFI was 98.7% (76/77) when tested against a large panel of B. pseudomallei isolates. Analytical specificity (cross-reactivity) testing determined that 97.2% of B. pseudomallei near neighbor species (35/36) were not reactive. The non-reactive B. pseudomallei strain and the reactive near neighbor strain can be explained through genetic sequence analysis. Importantly, we show the AMD LFI is capable of detecting CPS in a variety of patient samples. The LFI is currently being evaluated in Thailand and Australia; the focus is to optimize and validate testing procedures on melioidosis patient samples prior to initiation of a large, multisite pre-clinical evaluation.

Indexed as

Point-of-Care SystemsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialAustraliaBurkholderia pseudomalleiChromatography, AffinityHumansMelioidosisPolysaccharides, BacterialSensitivity and SpecificityThailandAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialPolysaccharides, Bacterial

Identifiers

PMID24651568
PMCPMC3961207
OpenAlexW2076635087

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Registered trials

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.