| Literature DB >> 29405697 |
Renuka Sriram1, Jinny Sun1, Javier Villanueva-Meyer1, Christopher Mutch1, Justin De Los Santos1, Jason Peters2, David E Korenchan1, Kiel Neumann3, Mark Van Criekinge1, John Kurhanewicz1, Oren Rosenberg4, David Wilson1, Michael A Ohliger1,5.
Abstract
The differentiation of bacterial infection from other causes of inflammation is difficult in clinical practice and is critical where patient outcomes rely heavily on early interventions. In addition to physical exam and laboratory markers, several imaging modalities are frequently employed, but these techniques generally target the host immune response, rather than the living microorganisms themselves. Here, we describe a method to detect bacteria-specific metabolism using hyperpolarized (HP) 13C magnetic resonance spectroscopy. This technology allows visualization of the real-time conversion of enriched 13C substrates to their metabolic products, identified by their distinct chemical shifts. We have identified the rapid metabolism of HP [2-13C]pyruvate to [1-13C]acetate as a metabolic signature of common bacterial pathogens. We demonstrate this conversion in representative Gram-negative and Gram-positive bacteria, namely, Escherichia coli and Staphylococcus aureus, and its absence in key mammalian cell types. Furthermore, this conversion was successfully modulated in three mutant strains, corresponding to deletions of relevant enzymes.Entities:
Keywords: acetate; bacterial metabolism; dynamic nuclear polarization (DNP); hyperpolarized 13C nuclear magnetic resonance (MR); pyruvate
Mesh:
Substances:
Year: 2018 PMID: 29405697 PMCID: PMC6008482 DOI: 10.1021/acsinfecdis.7b00234
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084