# Alterations in nutrient availability in the lungs during Streptococcus pneumoniae-induced pneumonia

## TL;DR

This study explores how Streptococcus pneumoniae infection changes lung metabolism during pneumonia, affecting bacterial behavior and potential treatment strategies.

## Contribution

The study provides a comprehensive characterization of host and bacterial metabolic and gene expression changes across stages of pneumococcal pneumonia.

## Key findings

- Dynamic shifts in metabolites occur during pneumonia, with an initial influx followed by declines as the disease progresses.
- Glucose levels peak at early disease stages and decline later, influencing pneumococcal capsule production.
- The gene spxB shows high expression at severe pneumonia stages, indicating a shift toward mixed fermentation and hydrogen peroxide production.

## Abstract

Streptococcus pneumoniae is a leading cause of pneumonia. Importantly, the extent and impact of changes in the infected airway on bacterial nutrient availability and gene expression are not known. Utilizing untargeted UPLC-ESI-MS/MS metabolomics, we comprehensively characterized the metabolic landscape in the airway across early, mid, and severe stages of pneumococcal pneumonia. This revealed that dynamic shifts in metabolites occurred during pneumonia, with an initial influx of metabolites at the early stage, followed by declines as the disease progressed. Specific host metabolic perturbations were indicative of purine dysregulation, cellular stress, and outright tissue injury. Levels of glucose, a known modulator of pneumococcal capsule production, were highest at the early disease stage and then declined as the disease progressed, overlaying general metabolite trends. Concurrent bacterial transcriptome profiling was performed using a NanoString nCounter custom panel of 66 genes selected for their importance to metabolism, virulence, and stress response; 9% of which had disease-stage significant differences in gene expression. This analysis revealed remarkably high expression of spxB, the gene encoding pyruvate oxidase, at the severe stage of pneumonia compared to the mid-stage pneumonia, consistent with a drop in glucose levels and indicative of a shift toward mixed fermentation and the increased production of hydrogen peroxide. Our study improves our understanding of how pneumococcal infection alters the lung environment, driving profound metabolic shifts that, in turn, influence bacterial phenotypes. This detailed understanding of host-pathogen metabolic interactions offers valuable insights into novel therapeutic strategies.