Microbiota in septic lungs using extracellular vesicle proteomics in bronchoalveolar lavage fluid 3180

Abstract Description Heterogeneous pulmonary sepsis has an unacceptably high mortality rate of up to 48% in severe patients, characterized by inflammation, lung tissue injury, and hypoxia. Identification of pathogenic microbes is essential for practicing personalized medicine with specific and effective therapies. To mitigate the effects of long-term storage on protein stability, we extracted extracellular vesicles and generated a proteomics dataset by performing LC-MS/MS to analyze EV peptides. The proteomics data was analyzed using R. Different taxonomy, functional annotation, Shannon index, and correlations to clinical variables were observed between various stages of the diseases. AUC identified potential microbial proteins as diagnostic biomarkers. Our study suggests that extracellular vesicle (EV) proteomics is an effective strategy for analyzing long-term stored liquid biopsies. Microbial EV proteins can serve as biomarkers and can be utilized for the identification of druggable targets. Funding Sources Supported by NIH/HL134828. Topic Categories Translational and Interventional Immunology (TI)

Authors

Institutions

Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.1009
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Microbiota in septic lungs using extracellular vesicle proteomics in bronchoalveolar lavage fluid 3180

Meng Qiao, Hong‐Long Ji, Nan Miles Xi, Xuan Guo et al.
The Journal of Immunology
Extracellular vesicles in disease
article

Microbiota in septic lungs using extracellular vesicle proteomics in bronchoalveolar lavage fluid 3180

Meng Qiao, Hong‐Long Ji, Nan Miles Xi, Xuan Guo, Shaoguang Feng, Runzhen Zhao
article en

Abstract

Abstract Description Heterogeneous pulmonary sepsis has an unacceptably high mortality rate of up to 48% in severe patients, characterized by inflammation, lung tissue injury, and hypoxia. Identification of pathogenic microbes is essential for practicing personalized medicine with specific and effective therapies. To mitigate the effects of long-term storage on protein stability, we extracted extracellular vesicles and generated a proteomics dataset by performing LC-MS/MS to analyze EV peptides. The proteomics data was analyzed using R. Different taxonomy, functional annotation, Shannon index, and correlations to clinical variables were observed between various stages of the diseases. AUC identified potential microbial proteins as diagnostic biomarkers. Our study suggests that extracellular vesicle (EV) proteomics is an effective strategy for analyzing long-term stored liquid biopsies. Microbial EV proteins can serve as biomarkers and can be utilized for the identification of druggable targets. Funding Sources Supported by NIH/HL134828. Topic Categories Translational and Interventional Immunology (TI)

The Journal of ImmunologyVol. 214(Supplement_1)
Loyola University Chicago (US)
National Institutes of Health
Openalex Percentile: Top 68%
Extracellular vesicles in disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.