Evidence map›Paper›PMID 42533315›Full record

ArticleBMC microbiology2026

Targeting nontuberculous mycobacteria with phages: optimization of in vitro host range assays.

Tobias Weirauch, Eva Brügger, Kai Litzius, Maria J G T Vehreschild, Silvia M Würstle, Simone C Lieberknecht-Jouy

Abstract read
In one paragraph

Article in BMC microbiology, 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

6 authors.

Tobias WeirauchDepartment II of Internal Medicine, Infectious Diseases, Goethe University Frankfurt, University Hospital Frankfurt, Frankfurt Am Main, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany. weirauch@med.uni-frankfurt.de.ORCID 0000-0003-3739-9601
Eva BrüggerDepartment II of Internal Medicine, Infectious Diseases, Goethe University Frankfurt, University Hospital Frankfurt, Frankfurt Am Main, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Kai LitziusExperimental Physics V, Center for Electronic Correlations and Magnetism, University of Augsburg, Augsburg, Germany.
Maria J G T VehreschildDepartment II of Internal Medicine, Infectious Diseases, Goethe University Frankfurt, University Hospital Frankfurt, Frankfurt Am Main, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Silvia M WürstleDepartment II of Internal Medicine, Infectious Diseases, Goethe University Frankfurt, University Hospital Frankfurt, Frankfurt Am Main, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Simone C Lieberknecht-JouyDepartment II of Internal Medicine, Infectious Diseases, Goethe University Frankfurt, University Hospital Frankfurt, Frankfurt Am Main, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical implementation of mycobacteriophages is hampered by the lack of standardized in vitro methods and inconsistent host range results, limiting reliable assessment of their therapeutic potential. Nontuberculous mycobacterial (NTM) infections are frequently difficult to treat, emphasizing the urgent need for alternative or adjunctive strategies to antibiotics. To facilitate reproducible translational research, a detailed and systematic understanding of in vitro assay conditions is essential. Here, we comprehensively evaluated commonly used liquid and solid media for their suitability in supporting growth of multiple NTM strains and subsequent phage application. We compared bacterial growth kinetics, aggregation tendencies, and the efficiency of phage-induced lysis, including plaque formation, across three liquid media and corresponding solid agars. Our results demonstrate that Middlebrook-based media and agar consistently support robust NTM growth, reduce bacterial clumping, and enable reproducible detection of phage activity, outperforming TSB-based alternatives despite higher cost and labor requirements. These findings provide a standardized framework for in vitro NTM cultivation and phage testing, which is critical for reliable evaluation of host range, infection dynamics, and the development of mycobacteriophage-based therapies.

Indexed as

Host SpecificityMycobacteriophagesNontuberculous MycobacteriaCulture MediaHumansMycobacterium Infections, NontuberculousCulture MediaCultivation comparisonHost range testingMycobacteriophagesNontuberculous mycobacteriaPhage assay

Identifiers

PMID42533315
PMCPMC13422341

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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.