Evidence map›Paper›PMID 42709887›Full record

ArticlePLoS neglected tropical diseases2026

A qPCR identification scheme to detect the most common causative agents of actinomycetoma in Africa.

Andrew K Watson, Sahar Bakhiet, Emmanuel E Siddig, Carole Pab Minlekib, Rihab Mohammed, Willemien Zandijk, Mickey Konings, Ahmed H Fahal, Maguette Faye, Katarzyna Mickiewicz and 4 more

Abstract read
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

14 authors.

Andrew K WatsonCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Sahar BakhietErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.
Emmanuel E SiddigErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.
Carole Pab MinlekibCentre de Recherche sur les maladies Tropicales Négligées, UFR Sciences de la Santé, Université Gaston Berger, Saint-Louis, Senegal.
Rihab MohammedErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.
Willemien ZandijkErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.
Mickey KoningsErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.
Ahmed H FahalMycetoma Research Centre, University of Khartoum, Khartoum, Sudan.
Maguette FayeCentre de Recherche sur les maladies Tropicales Négligées, UFR Sciences de la Santé, Université Gaston Berger, Saint-Louis, Senegal.
Katarzyna MickiewiczCentre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Fatehmeh Mazraati TajabadiSydney Institute for Infectious Diseases, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Doudou SowCentre de Recherche sur les maladies Tropicales Négligées, UFR Sciences de la Santé, Université Gaston Berger, Saint-Louis, Senegal.
Jeffrey ErringtonMycetoma Research Centre, University of Khartoum, Khartoum, Sudan.
Wendy W J van de SandeErasmusMC, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-8652-8783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycetoma is a neglected tropical disease characterized by mutilating tumorous lesions in the subcutaneous tissue. The causative agents are found embedded in granules called grains. Mycetoma is either caused by bacteria (actinomycetoma) or fungi (eumycetoma). To initiate the appropriate treatment, it is important to identify the causative agent rapidly and molecular identification for eumycetoma revolutionized the time to identification. For actinomycetoma this was not possible yet. Here we developed a multiplex qPCR identification scheme for the most common causative agents of actinomycetoma in Africa. Whole genome sequencing was used to identify species-specific gene families for Actinomadura madurae, Actinomadura pelletieri, Streptomyces somaliensis and Streptomyces sudanensis. qPCR primers and probes were developed on these species and validated against DNA isolated from mycetoma strains and grains. Each probe was unique with no cross-reactivity with other tested species. The limit of detection ranged from 0.000013 to 0.00067 ng bacterial DNA. When the qPCRs were validated against 28 grain samples, all fungal grains remained negative and 11 out of 12 Actinomadura grains were correctly identified. This resulted in a sensitivity of 85.7% for the A. pelletieri probe and a specificity of 100%. For the A. madurae probe, a sensitivity and specificity of 100% was obtained. The actinomycetoma qPCR developed in this study can be used to identify the most common causative agents of actinomycetoma in Africa.

Indexed as

ActinomaduraMultiplex Polymerase Chain ReactionMycetomaReal-Time Polymerase Chain ReactionStreptomycesAfricaDNA, BacterialDNA PrimersHumansSensitivity and SpecificityWhole Genome SequencingDNA, BacterialDNA Primers

Identifiers

PMID42709887
PMCPMC13577489

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.