Evidence map›Paper›PMID 42719862›Full record

ArticleInfection and drug resistance2026

Gut-Lung Axis Microbiome Dysbiosis and Cross-Domain Network Analysis in Bronchiectasis Complicated by Invasive Pulmonary Aspergillosis.

Wei Zhao, Chunlai Feng, Yilei Zhang, Linlin Wang

Abstract read
In one paragraph

Article in Infection and drug resistance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

4 authors.

Wei ZhaoDepartment of Respiratory and Critical Care Medicine, The Third Affiliated Hospital of Soochow University, Changzhou, People's Republic of China.
Chunlai FengDepartment of Respiratory and Critical Care Medicine, The Third Affiliated Hospital of Soochow University, Changzhou, People's Republic of China.
Yilei ZhangDepartment of Respiratory and Critical Care Medicine, The Third Affiliated Hospital of Soochow University, Changzhou, People's Republic of China.
Linlin WangDepartment of Medicine, Dinfectome Inc, Nanjing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To explore the clinical significance of pulmonary and gut microbiota in patients with bronchiectasis (BE) with invasive pulmonary aspergillosis (BE-IPA). By analyzing cross-domain microbial networks, we aimed to elucidate the bidirectional interaction mechanisms of the gut-lung axis, provide a theoretical basis for clinical diagnosis, and to identify potential candidate biomarkers and inform future mechanistic studies from a microbiomic perspective. Patients and Methods: We retrospectively examined 78 patients with BE, divided into BE without IPA (n = 37) and BE-IPA (n = 41) groups. Bronchoalveolar lavage fluid and anal swabs were collected. Metagenomic next-generation sequencing was used to analyze microbiota diversity, species composition, and metabolic pathways between the groups. Clinical data were evaluated for correlations with specific taxa, and a cross-domain microbial co-occurrence network was constructed. Results: Compared to the BE group, the BE-IPA group exhibited significant differences in pulmonary microbiota β-diversity ( Conclusion: The pulmonary microbiota in the BE-IPA group showed a fungal-bacterial symbiotic network centered on

Indexed as

bronchiectasis with invasive pulmonary aspergillosisgut–lung axisgut microbiotalung microbiotametagenomic next-generation sequencing

Identifiers

PMID42719862
PMCPMC13557177

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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.