Evidence map›Paper›PMID 36496380›Full record

ArticleRespiratory research2022

Gut microbiota modulates bleomycin-induced acute lung injury response in mice.

Young Me Yoon, Cara L Hrusch, Na Fei, Gabriel M Barrón, Kathleen A M Mills, Maile K Hollinger, Tania E Velez, Vanessa A Leone, Eugene B Chang, Anne I Sperling

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Gut microbiota associate with disease severity and survival in idiopathic pulmonary fibrosis.American journal of respiratory and critical care medicine · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Frontiers in microbiology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The lung microbiome in interstitial lung disease.Breathe (Sheffield, England) · 2025
    Review
  13. Article
  14. Article
  15. Reply to FujimotoAmerican journal of respiratory and critical care medicine · 2024
    Article
  16. Article
  17. Cell-free hemoglobin triggers macrophage cytokine production via TLR4 and MyD88.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  18. Article
  19. Review
  20. 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

10 authors at 2 institutions in 1 country.

Young Me YoonCommittee on Immunology, University of Chicago, Chicago, IL, USA.
Cara L HruschSection of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Na FeiSection of Gastroenterology, Department of Medicine, University of Chicago, Chicago, IL, USA.
Gabriel M BarrónSection of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Kathleen A M MillsSection of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Maile K HollingerCommittee on Immunology, University of Chicago, Chicago, IL, USA.
Tania E VelezSection of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
Vanessa A LeoneSection of Gastroenterology, Department of Medicine, University of Chicago, Chicago, IL, USA.
Eugene B ChangSection of Gastroenterology, Department of Medicine, University of Chicago, Chicago, IL, USA.
Anne I SperlingSection of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA. anne.sperling@virginia.edu.
University of Chicago · USUniversity of Virginia · US

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 1990 to 2025
$29.8M
RESEARCH TRAINING IN RESPIRATORY BIOLOGYT32HL007605 · NHLBI · UNIVERSITY OF CHICAGO · PI Yun Fang, Gokhan M. Mutlu · 1985 to 2026
$18.1M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
University of Chicago Initiative for Maximizing Student Development (IMSD) - Renewal 01R25GM109439 · NIGMS · UNIVERSITY OF CHICAGO · PI SCHWARTZ, NANCY B · 2014 to 2023
$5.7M
Microbial effects on Acute Lung InjuryR21AI142360 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2019 to 2020
$446k
The Role of IL-5 in Lung InjuryR21AI149416 · NIAID · UNIVERSITY OF CHICAGO · PI MUTLU, GOKHAN M., SPERLING, ANNE I. · 2020 to 2021
$446k
NHLBI NIH HHS T32 HL007605NIAID NIH HHS R21 AI142360NIAID NIH HHS R21 AI149416NIAID NIH HHS T32 AI007090NIDDK NIH HHS P30 DK042086NIGMS NIH HHS R25 GM109439NIH HHS 2T32HL007605NIH HHS 5R21AI142360NIH HHS T32AI007090
6 · The paper itself

Abstract

backgroundAirway instillation of bleomycin (BLM) in mice is a widely used, yet challenging, model for acute lung injury (ALI) with high variability in treatment scheme and animal outcomes among investigators. Whether the gut microbiota plays any role in the outcome of BLM-induced lung injury is currently unknown.

methodsIntratracheal instillation of BLM into C57BL/6 mice was performed. Fecal microbiomes were analyzed by 16s rRNA amplicon and metagenomic sequencing. Germ-free mice conventionalization and fecal microbiota transfer between SPF mice were performed to determine dominant commensal species that are associated with more severe BLM response. Further, lungs and gut draining lymph nodes of the mice were analyzed by flow cytometry to define immunophenotypes associated with the BLM-sensitive microbiome.

resultsMice from two SPF barrier facilities at the University of Chicago exhibited significantly different mortality and weight loss during BLM-induced lung injury. Conventionalizing germ-free mice with SPF microbiota from two different housing facilities recapitulated the respective donors' response to BLM. Fecal microbiota transfer from the facility where the mice had worse mortality into the mice in the facility with more survival rendered recipient mice more susceptible to BLM-induced weight loss in a dominant negative manner. BLM-sensitive phenotype was associated with the presence of Helicobacter and Desulfovibrio in the gut, decreased Th17-neutrophil axis during steady state, and augmented lung neutrophil accumulation during the acute phase of the injury response.

conclusionThe composition of gut microbiota has significant impact on BLM-induced wasting and death suggesting a role of the lung-gut axis in lung injury.

Indexed as

Acute Lung InjuryBleomycinAnimalsLungMiceMice, Inbred C57BLRNA, Ribosomal, 16SWeight LossBleomycinRNA, Ribosomal, 16S

Identifiers

PMID36496380
PMCPMC9741526
OpenAlexW4311673275

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.