C A Rees1, F A Franchina2, K V Nordick3, P J Kim3, J E Hill1,2. 1. Geisel School of Medicine at Dartmouth, Hanover, NH, USA. 2. Thayer School of Engineering at Dartmouth, Hanover, NH, USA. 3. Dartmouth College, Hanover, NH, USA.
Abstract
AIMS: The purpose of this study was to identify the volatile molecules produced by the pathogenic Gram-negative bacterium Klebsiella pneumoniae (ATCC 13883) during in vitro growth using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS). METHODS AND RESULTS: Klebsiella pneumoniae ATCC 13883 was incubated in lysogeny broth to mid-exponential and stationary growth phases. Headspace volatile molecules from culture supernatants were concentrated using solid-phase microextraction (SPME) and analysed via GC×GC-TOFMS. Ninety-two K. pneumoniae-associated volatile molecules were detected, of which 78 (85%) were detected at both phases of growth and 14 (15%) were detected at either mid-exponential or stationary growth phases. CONCLUSIONS: This study has increased the total number of reported K. pneumoniae-associated volatile molecules from 77 to 150, demonstrating the sensitivity and resolution achieved by employing GC×GC-TOFMS for the analysis of bacterial headspace volatiles. SIGNIFICANCE AND IMPACT OF THE STUDY: This study represents an early-stage comprehensive volatile metabolomic analysis of an opportunistic bacterial pathogen. Characterizing the volatile molecules produced by K. pneumoniae during in vitro growth could provide us with a better understanding of this organisms' metabolism, an area that has not been extensively studied to date.
AIMS: The purpose of this study was to identify the volatile molecules produced by the pathogenic Gram-negative bacterium Klebsiella pneumoniae (ATCC 13883) during in vitro growth using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS). METHODS AND RESULTS:Klebsiella pneumoniaeATCC 13883 was incubated in lysogeny broth to mid-exponential and stationary growth phases. Headspace volatile molecules from culture supernatants were concentrated using solid-phase microextraction (SPME) and analysed via GC×GC-TOFMS. Ninety-two K. pneumoniae-associated volatile molecules were detected, of which 78 (85%) were detected at both phases of growth and 14 (15%) were detected at either mid-exponential or stationary growth phases. CONCLUSIONS: This study has increased the total number of reported K. pneumoniae-associated volatile molecules from 77 to 150, demonstrating the sensitivity and resolution achieved by employing GC×GC-TOFMS for the analysis of bacterial headspace volatiles. SIGNIFICANCE AND IMPACT OF THE STUDY: This study represents an early-stage comprehensive volatile metabolomic analysis of an opportunistic bacterial pathogen. Characterizing the volatile molecules produced by K. pneumoniae during in vitro growth could provide us with a better understanding of this organisms' metabolism, an area that has not been extensively studied to date.
Authors: Christiaan A Rees; Alison Burklund; Pierre-Hugues Stefanuto; Joseph D Schwartzman; Jane E Hill Journal: J Breath Res Date: 2018-01-03 Impact factor: 3.262
Authors: Christiaan A Rees; Pierre-Hugues Stefanuto; Sarah R Beattie; Katherine M Bultman; Robert A Cramer; Jane E Hill Journal: J Breath Res Date: 2017-08-21 Impact factor: 3.262
Authors: Giorgia Purcaro; Pierre-Hugues Stefanuto; Flavio A Franchina; Marco Beccaria; Wendy F Wieland-Alter; Peter F Wright; Jane E Hill Journal: Anal Chim Acta Date: 2018-03-30 Impact factor: 6.558
Authors: Christiaan A Rees; Katherine V Nordick; Flavio A Franchina; Alexa E Lewis; Elizabeth B Hirsch; Jane E Hill Journal: Metabolomics Date: 2017-01-12 Impact factor: 4.290
Authors: Christiaan A Rees; Mavra Nasir; Agnieszka Smolinska; Alexa E Lewis; Katherine R Kane; Shannon E Kossmann; Orkan Sezer; Paola C Zucchi; Yohei Doi; Elizabeth B Hirsch; Jane E Hill Journal: Sci Rep Date: 2018-09-05 Impact factor: 4.379