Evidence map›Paper›PMID 39962513›Full record

ArticleAnnals of clinical microbiology and antimicrobials2025

Diagnostics, resistance and clinical relevance of non-tuberculous mycobacteria unidentified at the species level by line probe assays: a bi-national study.

Matúš Dohál, Nils Wetzstein, Michaela Hromádková, Simona Mäsiarová, Erik M Rasmussen, Peter Kunč, Mária Škereňová, Igor Porvazník, Ivan Solovič, Stefan Niemann and 4 more

Abstract read
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Frontiers in tuberculosis · 2025
    Review
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.

Matúš DohálBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University, Bratislava, Slovakia. matus.dohal@uniba.sk.
Nils WetzsteinMolecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
Michaela HromádkováNational Institute of Public Health, Prague, Czech Republic.
Simona MäsiarováDepartment of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University, Bratislava, Slovakia.
Erik M RasmussenInternational Reference Laboratory of Mycobacteriology, Statens Serum Institut, Copenhagen, Denmark.
Peter KunčClinic of Pediatric Respiratory Diseases and Tuberculosis, National Institute of Pediatric Tuberculosis and Respiratory Diseases, Dolny Smokovec, Jessenius Faculty of Medicine in Martin, Comenius University, Bratislava, Slovakia.
Mária ŠkereňováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University, Bratislava, Slovakia.
Igor PorvazníkNational Institute of Tuberculosis Lung Diseases and Thoracic Surgery, Vyšné Hágy, Slovakia.
Ivan SolovičNational Institute of Tuberculosis Lung Diseases and Thoracic Surgery, Vyšné Hágy, Slovakia.
Stefan NiemannMolecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.
Jarmila HnilicováDepartment of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
Juraj MokrýDepartment of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University, Bratislava, Slovakia.
Věra Dvořáková *National Institute of Public Health, Prague, Czech Republic. vera.dvorakova@szu.cz.
Margo Diricks *Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany.

Funding

Agentúra na Podporu Výskumu a Vývoja 18-0084Czech Science Foundation 23-05622SDeutsche Forschungsgemeinschaft 2167Grant of Ministry of Health, Czech Republic 75010330Vedecká Grantová Agentúra MŠVVaŠ SR a SAV 1/0093/22
6 · The paper itself

Abstract

objectivesWhile the reported incidence of non-tuberculous mycobacterial (NTM) infections is increasing, the true prevalence remains uncertain due to limitations in diagnostics and surveillance. The emergence of rare and novel species underscores the need for characterization to improve surveillance, detection, and management.

methodsWe performed whole-genome sequencing (WGS) and/or targeted deep-sequencing using the Deeplex Myc-TB assay on all NTM isolates collected in Slovakia and the Czech Republic between the years 2019 to 2023 that were unidentifiable at the species level by the routine diagnostic line probe assays (LPA) GenoType CM/AS and NTM-DR. Minimal inhibitory concentrations against amikacin, ciprofloxacin, moxifloxacin, clarithromycin, and linezolid were determined, and clinical data were collected.

resultsTwenty-eight cultures from different patients were included, of which 9 (32.1%) met the clinically relevant NTM disease criteria. The majority of those had pulmonary involvement, while two children presented with lymphadenitis. Antimycobacterial resistance rates were low. In total, 15 different NTM species were identified, predominantly rare NTM like M. neoaurum, M. kumamotonense and M. arupense. Notably, clinically relevant M. chimaera variants were also identified with WGS and Deeplex-Myc TB, which, unlike other M. chimaera strains, appeared to be undetectable by LPA assays. Deeplex detected four mixed infections that were missed by WGS analysis. In contrast, WGS identified two novel species, M. celatum and M. branderi, which were not detected by Deeplex-Myc TB. Importantly, one of these novel species strains was associated with clinically relevant pulmonary disease. DISCUSSION: Our study demonstrates the clinical relevance of uncommon NTM and the effectiveness of targeted deep-sequencing combined with WGS in identifying rare and novel NTM species.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialMycobacterium Infections, NontuberculousNontuberculous MycobacteriaAdolescentAdultAgedChildChild, PreschoolClinical RelevanceCzech RepublicFemaleHumansInfantMaleMicrobial Sensitivity TestsAnti-Bacterial AgentsDiagnosticsNon-tuberculous mycobacteriaNovel speciesTargeted next-generation sequencingWhole-genome sequencing

Identifiers

PMID39962513
PMCPMC11834575

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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.