Evidence map›Paper›PMID 40893175›Full record

ArticleHealth information science and systems2025

Identification and applications of disease-associated differential human and bacterial proteins with metaproteomic evidence.

Jamie Canderan, Moses Stamboulian, Yuzhen Ye

Abstract read
In one paragraph

Article in Health information science and systems, 2025. 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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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

3 authors.

Jamie CanderanLuddy School of Informatics, Computing, and Engineering, Indiana University, Bloomington, IN 47408 USA.ORCID 0000-0002-3079-8856
Moses StamboulianLuddy School of Informatics, Computing, and Engineering, Indiana University, Bloomington, IN 47408 USA.
Yuzhen YeLuddy School of Informatics, Computing, and Engineering, Indiana University, Bloomington, IN 47408 USA.

Funding

Subtractive assembly approaches for inferring disease-associated microbial genes and pathways from microbiome sequencing dataR01AI143254 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI YE, YUZHEN · 2019 to 2023
$1.1M
NIAID NIH HHS R01 AI143254
6 · The paper itself

Abstract

The gut microbiome plays a fundamental role in human health and disease. Individual variations in the microbiome and the corresponding functional implications are key considerations to enhance precision health and medicine. Metaproteomics has recently revealed protein expression that might be associated with human health and disease. Existing studies focused on either human proteins or bacterial proteins that can be identified from (meta)proteomics data sets, but not both. In this study, we examined the feasibility of identifying both human and bacterial proteins that are differentially expressed between healthy and diseased individuals from metaproteomics data sets. We further evaluated different strategies of using identified peptides and proteins for building predictive models. By leveraging existing metaproteomics data sets and a tool that we have developed for metaproteomics data analysis (MetaProD), we were able to derive both human and bacterial differentially expressed proteins that could serve as potential biomarkers for all diseases we studied. We also built predictive models using identified peptides and proteins as features for prediction of human diseases. Our results showed peptide-based identifications over protein-based ones often produce the most accurate models and that feature selection can offer improvements. Prediction accuracy could be further improved, in some cases, by including bacterial identifications, but missing data in bacterial identifications remains problematic.

Identifiers

PMID40893175
PMCPMC12397042

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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.