Breath metabolome of mice infected with Pseudomonas aeruginosa.
Breath
Comprehensive gas chromatography-time-of-flight mass spectrometer (GC×GC ToF MS)
Pseudomonas aeruginosa
Volatile organic compounds (VOCs)
Journal
Metabolomics : Official journal of the Metabolomic Society
ISSN: 1573-3890
Titre abrégé: Metabolomics
Pays: United States
ID NLM: 101274889
Informations de publication
Date de publication:
07 01 2019
07 01 2019
Historique:
received:
27
07
2018
accepted:
10
12
2018
entrez:
5
3
2019
pubmed:
5
3
2019
medline:
24
3
2020
Statut:
epublish
Résumé
The measurement of specific volatile organic compounds in breath has been proposed as a potential diagnostic for a variety of diseases. The most well-studied bacterial lung infection in the breath field is that caused by Pseudomonas aeruginosa. To determine a discriminatory core of molecules in the "breath-print" of mice during a lung infection with four strains of P. aeruginosa (PAO1, PA14, PAK, PA7). Furthermore, we attempted to extrapolate a strain-specific "breath-print" signature to investigate the possibility of recapitulating the genetic phylogenetic groups (Stewart et al. Pathog Dis 71(1), 20-25, 2014. https://doi.org/10.1111/2049-632X.12107 ). Breath was collected into a Tedlar bag and shortly after drawn into a thermal desorption tube. The latter was then analyzed into a comprehensive multidimensional gas chromatography coupled with a time-of-flight mass spectrometer. Random forest algorithm was used for selecting the most discriminatory features and creating a prediction model. Three hundred and one molecules were significantly different between animals infected with P. aeruginosa, and those given a sham infection (PBS) or inoculated with UV-killed P. aeruginosa. Of those, nine metabolites could be used to discriminate between the three groups with an accuracy of 81%. Hierarchical clustering showed that the signature from breath was due to a specific response to live bacteria instead of a generic infection response. Furthermore, we identified ten additional volatile metabolites that could differentiate mice infected with different strains of P. aeruginosa. A phylogram generated from the ten metabolites showed that PAO1 and PA7 were the most distinct group, while PAK and PA14 were interspersed between the former two groups. To the best of our knowledge, this is the first study to report on a 'core' murine breath print, as well as, strain level differences between the compounds in breath. We provide identifications (by running commercially available analytical standards) to five breath compounds that are predictive of P. aeruginosa infection.
Identifiants
pubmed: 30830447
doi: 10.1007/s11306-018-1461-6
pii: 10.1007/s11306-018-1461-6
pmc: PMC6537093
mid: NIHMS1010447
doi:
Substances chimiques
Volatile Organic Compounds
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
10Subventions
Organisme : NLM NIH HHS
ID : T32 LM012204
Pays : United States
Références
J Allergy Clin Immunol. 2004 Nov;114(5):1241-56
pubmed: 15536442
Lancet. 1994 Jan 15;343(8890):133-5
pubmed: 7904001
Environ Microbiol. 2010 Jun;12(6):1734-47
pubmed: 20553553
J Breath Res. 2014 Jun;8(2):027105
pubmed: 24713999
Sci Rep. 2018 Jan 16;8(1):826
pubmed: 29339749
J Heart Lung Transplant. 2004 Jun;23(6):701-8
pubmed: 15366430
Nat Rev Mol Cell Biol. 2012 Mar 22;13(4):263-9
pubmed: 22436749
Chem Soc Rev. 2014 Mar 7;43(5):1423-49
pubmed: 24305596
J Breath Res. 2018 Feb 07;12(2):026008
pubmed: 29219122
Clin Microbiol Rev. 2013 Jul;26(3):462-75
pubmed: 23824368
Aliment Pharmacol Ther. 2004 Nov 15;20(10):1001-17
pubmed: 15569102
Eur Respir J. 2015 Jan;45(1):181-90
pubmed: 25323243
Pathog Dis. 2014 Jun;71(1):20-5
pubmed: 24167005
J Breath Res. 2013 Mar;7(1):016003
pubmed: 23307645
J Breath Res. 2013 Sep;7(3):037106
pubmed: 23867706
J Breath Res. 2016 Nov 21;10(4):047102
pubmed: 27869104
Front Microbiol. 2015 Oct 06;6:1056
pubmed: 26500617
Respir Res. 2012 Oct 02;13:87
pubmed: 23031195
Science. 1995 Jun 30;268(5219):1899-902
pubmed: 7604262
Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14339-44
pubmed: 14617778
Microbes Infect. 2000 Jul;2(9):1051-60
pubmed: 10967285
PLoS One. 2010 Jan 22;5(1):e8842
pubmed: 20107499
J Appl Microbiol. 2012 Sep;113(3):701-13
pubmed: 22726261
J Virol. 1968 Mar;2(3):208-13
pubmed: 4986905
Pediatr Res. 2010 Jul;68(1):75-80
pubmed: 20351658
J Appl Physiol (1985). 2013 Jun;114(11):1544-9
pubmed: 23519230