Abstract
Infections with Chlamydia pneumoniae cause several respiratory diseases, such as community-acquired pneumonia, bronchitis or sinusitis. Here, we present an integrated non-targeted metabolomics analysis applying ultra-high-resolution mass spectrometry and ultra-performance liquid chromatography mass spectrometry to determine metabolite alterations in C. pneumoniae-infected HEp-2 cells. Most important permutations are elaborated using uni- and multivariate statistical analysis, logD retention time regression and mass defect-based network analysis. Classes of metabolites showing high variations upon infection are lipids, carbohydrates and amino acids. Moreover, we observed several non-annotated compounds as predominantly abundant after infection, which are promising biomarker candidates for drug-target and diagnostic research.
| Original language | English |
|---|---|
| Journal | Analytical and Bioanalytical Chemistry |
| Volume | 405 |
| Issue number | 15 |
| Pages (from-to) | 5119-5131 |
| Number of pages | 13 |
| ISSN | 1618-2642 |
| DOIs | |
| Publication status | Published - 01.06.2013 |
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)