Evidence map›Paper›PMID 42406856›Full record

ArticlePLoS neglected tropical diseases2026

Development and international multicenter evaluation of a second-generation immunochromatography test for the serological diagnosis of melioidosis.

Hasyanee Binmaeil, Thanakon Bunsong, Koukeo Phommasone, Matthew T Robinson, Manivanh Vongsouvath, Elizabeth A Ashley, Enoka Corea, Trung Thanh Trinh, Shirley Yi Fen Hii, Rohaidah Hashim and 12 more

Abstract readMulticenter StudyEvaluation Study
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Hasyanee BinmaeilDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Thanakon BunsongDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Koukeo PhommasoneLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Matthew T RobinsonLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Manivanh VongsouvathLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Elizabeth A AshleyLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Enoka CoreaDepartment of Medical Microbiology and Immunology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Trung Thanh TrinhVNU-Institute of Microbiology and Biotechnology, Vietnam National University, Hanoi, Vietnam.
Shirley Yi Fen HiiBacteriology Unit, Infectious Diseases Research Centre, Institute for Medical Research, National Institutes of Health, Selangor, Malaysia.
Rohaidah HashimBacteriology Unit, Infectious Diseases Research Centre, Institute for Medical Research, National Institutes of Health, Selangor, Malaysia.
Habib Abdul Hakim EsaBacteriology Unit, Infectious Diseases Research Centre, Institute for Medical Research, National Institutes of Health, Selangor, Malaysia.
Tonnii SiaDepartment of Medicine, Miri Hospital, Miri, Malaysia.
Yuwana PodinInstitute of Health and Community Medicine, Universiti Malaysia Sarawak, Sarawak, Malaysia.
Robert NortonPathology Queensland Townsville, Townsville University Hospital, Townsville, Queensland, Australia.
Sophie CunninghamPathology Queensland Townsville, Townsville University Hospital, Townsville, Queensland, Australia.
Jamal I-Ching SamDepartment of Medical Microbiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Christina YekInternational Center of Excellence in Research, U.S. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Phnom Penh, Cambodia.
Ella M MeumannGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
Bart J CurrieGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
Mary N BurtnickDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Paul J BrettDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Narisara ChantratitaDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-3906-7379

Funding

Wellcome Trust
6 · The paper itself

Abstract

Melioidosis is a life-threatening infectious disease caused by Burkholderia pseudomallei. Early and accurate diagnosis is critical for timely treatment and improved outcomes. Although highly endemic in tropical regions, it remains underdiagnosed due to limitations of current diagnostic methods. Bacterial culture, the diagnostic gold standard, is time-consuming, prone to misidentified species, requires specialized laboratory facilities, and has low sensitivity. The indirect hemagglutination assay is also unreliable due to poor sensitivity and specificity. We developed a second-generation immunochromatography test (Hcp1-ICT) to detect anti-Hcp1 IgG antibodies against hemolysin co-regulated protein 1 of B. pseudomallei and evaluated its diagnostic performance in an international multi-center study. A total of 1,838 stored serum samples from 601 culture-proven melioidosis patients, 598 healthy individuals and 639 patients with non-melioidosis infections in Thailand, Lao PDR, Vietnam, Malaysia, Sri Lanka, Cambodia, and Australia were analyzed for diagnosis of melioidosis. The sensitivities in Thailand, Lao PDR, Vietnam, Malaysia, Sri Lanka, Cambodia, and Australia were 92%, 77%, 76%, 80%, 74%, 90%, and 48%, respectively. The specificities with healthy donor samples were 96%, 79%, 98%, 100%, 100%, 87%, and 100%, while the specificities for cases with samples from other infections other than melioidosis were 97%, 87%, 98%, 98%, 100%, 90%, and 94%, respectively. These findings indicate that the Hcp1-ICT is a promising point-of-care tool for serodiagnosis of melioidosis. However, its variable performance across regions underscores the need for prospective validation locally in various regions to optimize its diagnostic utility and facilitate implementation in both referral centers and resource-limited settings.

Indexed as

Antibodies, BacterialBurkholderia pseudomalleiChromatography, AffinityMelioidosisSerologic TestsBacterial ProteinsFemaleHumansImmunoglobulin GRapid Diagnostic TestsSensitivity and SpecificityVirulence FactorsAntibodies, BacterialBacterial ProteinsHcp1 protein, Burkholderia pseudomalleiImmunoglobulin GVirulence Factors

Identifiers

PMID42406856
PMCPMC13379097

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Registered trials

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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.