Evidence map›Paper›PMID 29202739›Full record

Observational studyBMC pulmonary medicine2017

The lung microbiome in patients with pneumocystosis.

J Kehrmann, B Veckollari, D Schmidt, O Schildgen, V Schildgen, N Wagner, M Zeschnigk, L Klein-Hitpass, O Witzke, J Buer and 1 more

Abstract readObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. iScience · 2025
    Article
  2. Pathogens (Basel, Switzerland) · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Aspergillus fumigatus and Aspergillosis in 2019.Clinical microbiology reviews · 2019
    Review
  9. Article
  10. Article
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

11 authors.

J KehrmannInstitute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45122, Essen, Germany. jan.kehrmann@uk-essen.de.
B VeckollariInstitute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45122, Essen, Germany.
D SchmidtInstitute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45122, Essen, Germany.
O SchildgenInstitute of Pathology, Kliniken der Stadt Köln gGmbH, Hospital of the University of Witten/Herdecke, Cologne, Germany.
V SchildgenInstitute of Pathology, Kliniken der Stadt Köln gGmbH, Hospital of the University of Witten/Herdecke, Cologne, Germany.
N WagnerInstitute of Human Genetics, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.
M ZeschnigkInstitute of Human Genetics, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.
L Klein-HitpassBiochip Laboratory, Institute for Cell Biology-Tumor Research, University of Duisburg-Essen, Essen, Germany.
O WitzkeDepartment of Infectious Diseases, University of Duisburg-Essen, Essen, Germany.
J BuerInstitute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45122, Essen, Germany.
J SteinmannInstitute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45122, Essen, Germany. joerg.steinmann@uk-essen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backroundPneumocystis jirovecii pneumonia (PCP) is an opportunistic fungal infection that is associated with a high morbidity and mortality in immunocompromised individuals. In this study, we analysed the microbiome of the lower respiratory tract from critically ill intensive care unit patients with and without pneumocystosis.

methodsBroncho-alveolar fluids from 65 intubated and mechanically ventilated intensive care unit patients (34 PCP+ and 31 PCP- patients) were collected. Sequence analysis of bacterial 16S rRNA gene V3/V4 regions was performed to study the composition of the respiratory microbiome using the Illumina MiSeq platform.

resultsDifferences in the microbial composition detected between PCP+ and PCP- patients were not statistically significant on class, order, family and genus level. In addition, alpha and beta diversity metrics did not reveal significant differences between PCP+ and PCP- patients. The composition of the lung microbiota was highly variable between PCP+ patients and comparable in its variety with the microbiota composition of the heterogeneous collective of PCP- patients.

conclusionsThe lower respiratory tract microbiome in patients with pneumocystosis does not appear to be determined by a specific microbial composition or to be dominated by a single bacterial species.

Indexed as

MicrobiotaAdolescentAdultAgedAged, 80 and overBronchoalveolar Lavage FluidCase-Control StudiesFemaleHumansIntensive Care UnitsIntubation, IntratrachealLungMaleMiddle AgedPneumonia, PneumocystisRespiration, ArtificialRNA, Ribosomal, 16SPneumocystis jiroveciiPneumocystosisPulmonary microbiome

Identifiers

PMID29202739
PMCPMC5715545

What OpenQuestion holds

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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.