Evidence map›Paper›PMID 42788689›Full record

ArticleThe Journal of antimicrobial chemotherapy2026

Potential clinical implications due to essential differences in antimicrobial susceptibility profiles of actinomycetoma causative agents of the Actinomadura, Nocardia and Streptomyces genera towards commonly used anti-actinomycetoma drugs.

Rihab A H Mohammed, Andrew K Watson, Mickey Konings, Katarzyna Mickiewicz, Ahmed H Fahal, Alexandro Bonifaz, Doudou Sow, Jeff Errington, Michiel L Bexkens, Wendy W J van de Sande

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Rihab A H MohammedErasmus MC, Department of Medical Microbiology and Infectious Diseases, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0002-3552-669X
Andrew K WatsonCentre for Bacterial Cell Biology, Bioscience Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-3389-515X
Mickey KoningsErasmus MC, Department of Medical Microbiology and Infectious Diseases, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0003-3983-4304
Katarzyna MickiewiczCentre for Bacterial Cell Biology, Bioscience Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-9109-2120
Ahmed H FahalMycetoma Research Centre, University of Khartoum, Khartoum, Sudan.ORCID 0000-0003-4922-7321
Alexandro BonifazHospital General de México Dr Eduardo Liceaga: Ciudad de Mexico, Mexico City, Mexico.ORCID 0000-0003-2045-3317
Doudou SowDepartment of Parasitology-Mycology, UFR Sciences de La Santé, Université Gaston Berger, Saint Louis, Senegal.ORCID 0000-0002-0560-2372
Jeff ErringtonCentre for Bacterial Cell Biology, Bioscience Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-6977-9388
Michiel L BexkensErasmus MC, Department of Medical Microbiology and Infectious Diseases, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0002-2740-7797
Wendy W J van de SandeErasmus MC, Department of Medical Microbiology and Infectious Diseases, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0002-8652-8783

Funding

Diorapthe Foundation
6 · The paper itself

Abstract

backgroundActinomycetoma is a neglected tropical disease characterized by large tumorous lesions. It is caused by actinomycetes belonging to the genera Actinomadura, Nocardia and Streptomyces. Despite the differences between these genera and species, all actinomycetoma cases are treated with the same antibiotics. It is currently not known if the actinomycetoma causative agents have similar susceptibility patterns against these antibiotics. We therefore set out to determine the MICs for the most common causative agents against commonly used antibiotics. MATERIALS AND

methodsWe used the standard in vitro susceptibility method from the CLSI to assess the antimicrobial susceptibility of 94 actinomycete isolates belonging to the Actinomadura, Nocardia and Streptomyces genera and associated with actinomycetoma against 12 antibiotics. The molecular basis behind the reduced susceptibility was further explored using the genomes of the isolates.

resultsAll isolates were highly susceptible to linezolid (100%), amikacin (98.9%) and trimethoprim/sulfamethoxazole (87.2%). For amoxicillin/clavulanate and rifampicin, species-dependent susceptibility was noted. We found that 55% of Actinomadura madurae isolates, 61.5% of Nocardia brasiliensis isolates and 100% of Streptomyces somaliensis and Streptomyces sudanensis were susceptible to amoxicillin/clavulanate. All A. madurae, Actinomadura pelletieri and N. brasiliensis isolates were resistant to rifampicin, whereas all S. somaliensis and S. sudanensis isolates were susceptible. This was most likely due to amino acid differences in the RpoB gene.

conclusionsClear differences in antimicrobial susceptibility patterns were noted for the different actinomycetoma causative agents, indicating that actinomycetoma treatment should be tailored to the causative agent.

Indexed as

ActinomaduraAnti-Bacterial AgentsMycetomaNocardiaStreptomycesHumansMicrobial Sensitivity TestsAnti-Bacterial Agents

Identifiers

PMID42788689
PMCPMC13613230

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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.