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Related Experiment Video

Updated: Sep 10, 2025

High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions
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Stacking ensemble learning models diagnose pulmonary infections using host transcriptome data from

Tian Zhang1,2, Ying Deng1, Wentao Wang3

  • 1Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, People's Republic of China.

Scientific Reports
|August 20, 2025
PubMed
Summary
This summary is machine-generated.

Diagnosing severe pulmonary infections is difficult. This study developed a rapid, inexpensive gene expression test that accurately identifies infection status and type, similar to slower sequencing methods.

Keywords:
Machine learning modelsMetatranscriptomic sequencingPatients in severe conditionPrompt diagnosisPulmonary infections

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Area of Science:

  • * Medical Diagnostics
  • * Computational Biology
  • * Infectious Diseases

Background:

  • * Prompt diagnosis of pulmonary infections in critically ill patients is challenging due to limitations in current diagnostic methods.
  • * Metatranscriptomic sequencing is powerful but often lacks the timeliness required for clinical settings.
  • * Rapid and cost-effective diagnostic tools are crucial for managing severe infections.

Purpose of the Study:

  • * To develop a rapid and inexpensive adjunctive diagnostic strategy for pulmonary infections in severe patients.
  • * To identify host gene expression signatures associated with different infection types.
  • * To create accurate machine learning-based diagnostic models using limited gene expression data.

Main Methods:

  • * Metatranscriptomic sequencing of bronchoalveolar lavage fluid (BALF) from critically ill patients.
  • * Screening of characteristic host genes by comparing infected versus non-infected patient data.
  • * Construction of ensemble machine learning models (including Lasso regression) using identified gene signatures.

Main Results:

  • * Machine learning models achieved high accuracy in distinguishing infection from non-infection (AUC=0.984), bacterial infection (AUC=0.98), and viral infection (AUC=0.98) during cross-validation.
  • * Test cohorts showed consistent accuracy, discerning infection status (AUC=0.865) and type (viral: AUC=0.934, bacterial: AUC=0.871).
  • * The developed diagnostic strategy demonstrated accuracy comparable to metatranscriptomic sequencing.

Conclusions:

  • * A rapid, cost-effective diagnostic strategy using host gene expression signatures was developed.
  • * The method enables timely identification of infection status and type in pulmonary infections.
  • * This approach serves as a valuable adjunctive tool for clinical decision-making in severe cases.