Evidence map›Paper›PMID 42297837›Full record

ArticleNPJ biofilms and microbiomes2026

The human lung microbiome progressively diminishes in the distal alveolar regions.

Pauline Potratz, Antje Häder, Laura Kursawe, Judith Kikhney, Nikolaus Gaßler, Thurid Lauf, Lukáš Radosa, Tim Sandhaus, Patrick von Samson, Xiuqiang Chen and 7 more

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 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

17 authors.

Pauline PotratzInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany.
Antje HäderInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany.
Laura KursaweUniversity of Leipzig Medical Center, Institute of Medical Microbiology and Virology, Leipzig, Germany.
Judith KikhneyUniversity of Leipzig Medical Center, Institute of Medical Microbiology and Virology, Leipzig, Germany.
Nikolaus GaßlerSection of Pathology, Institute of Forensic Medicine, Jena University Hospital, Jena, Germany.
Thurid LaufInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany.
Lukáš RadosaInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany.
Tim SandhausKlinik für Herz-und Thoraxchirurgie, Jena, Germany.
Patrick von SamsonKlinik für Herz-und Thoraxchirurgie, Jena, Germany.
Xiuqiang ChenMicrobiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (HKI), Jena, Germany.
Lu WangMicrobiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (HKI), Jena, Germany.
Axel A BrakhageDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute (HKI), Jena, Germany.
Annette MoterUniversity of Leipzig Medical Center, Institute of Medical Microbiology and Virology, Leipzig, Germany.
Gianni PanagiotouMicrobiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (HKI), Jena, Germany.
Torsten DoenstKlinik für Herz-und Thoraxchirurgie, Jena, Germany.
Stefanie Deinhardt-EmmerInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany. Stefanie.deinhardt-emmer@med.uni-jena.de.
Bettina LöfflerInstitute of Medical Microbiology, Jena University Hospital, Jena, Germany. Bettina.loeffler@med.uni-jena.de.

Funding

Bundesministerium für Bildung und Forschung 13N15745Deutsche Forschungsgemeinschaft SFB 1278/2 "PolyTarget" D02DFG SFB 1278/2 "PolyTarget" B02
6 · The paper itself

Abstract

Extensive investigations with sequencing methods demonstrate a large and diverse microbiome even in profound areas of the lung. However, there is still substantial lack of cultivation-based evidence and of the viability of the resident microorganisms. We collected human tissue specimens obtained from various regions during lung transplantations and from operations in distal alveolar areas. We characterized the samples by histology and applied sequencing, culture and imaging methods. Sequencing data detected the following trends in the composition of the microbiome: (i) From proximal to distal samples we observed a bacterial shift from Staphylococci, Streptococci and Corynebacteria towards preferentially anaerobically growing bacteria; (ii) we found large variations between individual patients regarding the detected bacterial genera. Culture and imaging methods revealed almost no viable microorganism in the distal alveolar regions in these patients. Bacterial signals detected by sequencing in the lung are likely due to very low numbers of bacteria and/or their remnants.

Indexed as

BacteriaLungMicrobiotaPulmonary AlveoliHumansRNA, Ribosomal, 16SSequence Analysis, DNARNA, Ribosomal, 16S

Identifiers

PMID42297837
PMCPMC13287667

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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.