Summary of Study ST001426
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000978. The data can be accessed directly via it's Project DOI: 10.21228/M88Q44 This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.
Study ID | ST001426 |
Study Title | Dependence of the Staphylococcal Volatilome Composition on Microbial Nutrition |
Study Type | Untargeted MS |
Study Summary | Introduction: In vitro cultivation of staphylococci is fundamental to both clinical and research microbiology, and selection of growth medium will substantially influence staph growth rates, genetic integrity, pathogenicity, and metabolic capacity. Few studies, to-date, have investigated how the differences in rich media can influence the volatilome of cultivated bacteria. Objectives: The objective of this study was to determine the influence of rich media composition on the chemical characteristics of the volatilomes of Staphylococcus aureus and S. epidermidis. Methods: S. aureus (ATCC 12600) and S. epidermidis (ATCC 12228) were cultured in triplicate in four rich complex media (BHI, LB, MHB, and TSB), and the volatile metabolites produced by each culture were analyzed using headspace solid-phase microextraction combined with comprehensive two-dimensional gas chromatography – time-of-flight mass spectrometry (HS-SPME-GC×GC-TOFMS). Results: When comparing the chemical compositions of the staph volatilomes produced in each medium, we observed few differences when the presence versus absence of volatiles were compared. However, when the relative abundances of volatiles were included in the analyses, we observed that culturing staph in media containing free glucose (BHI and TSB) resulted in volatilomes dominated by acids and esters (67%). The low-glucose media (LB and MHB) produced ketones in greatest relative abundances, but the volatilome compositions in these two media were highly dissimilar. Conclusion: The staphylococcal volatilome is strongly influenced by the nutritional composition of the growth medium, especially the availability of free glucose, which is much more evident when the relative abundances of the volatiles are analyzed, compared to the presence versus absence. |
Institute | Arizona State University |
Department | School of Life Sciences |
Laboratory | Heather D. Bean Lab |
Last Name | Bean, Ph.D. |
First Name | Heather |
Address | PO Box 874501 Tempe, AZ 85287 |
heather.d.bean@asu.edu | |
Phone | 4807273395 |
Submit Date | 2020-07-13 |
Study Comments | Staphylococcus aureus (ATCC 12600) and Stpahylococcus epidermidis (ATCC 12228) grown in four complex media |
Publications | Jenkins, C. L., H. D. Bean (2020). Influence of media on the differentiation of Staphylococcus spp. by volatile compounds. Journal of breath research 14, 016007 doi:10.1088/1752-7163/ab3e9d |
Raw Data Available | Yes |
Raw Data File Type(s) | smp |
Analysis Type Detail | GC-MS |
Release Date | 2020-07-30 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000978 |
Project DOI: | doi: 10.21228/M88Q44 |
Project Title: | Influence of growth medium on the volatilomes of Pseudomonas spp. and Staphylococcus spp. |
Project Type: | Untargeted MS |
Project Summary: | Pseudomonas aeruginosa and Staphylococcus aureus are the predominant opportunistic lung pathogens persons with CF [2017 CF Foundation Annual Report] and are leading causes of respiratory failure and mortality [Malhotra, et al. Clin Microbiol Rev, 2019]. Currently, sputum culture remains the standard of care for lung infection detection, but sputum production is on the decline due to improvements in CF therapies. To fill this diagnostic gap, we are working toward the development of breath tests for lung infections by characterizing the volatile metabolome (or “volatilome”) of P. aeruginosa and S. aureus. In this study, we explored the influence of growth medium on the volatilomes of two strains of P. aeruginosa (PAO1 and PA14) and S. aureus, as well as two other species from the same genera, S. epidermidis and P. chlororaphis. We hypothesized that the volatilomes would be influenced by the growth medium, but that biological differences between these species and strains would dominate the volatilomes and facilitate identification. |
Institute: | Arizona State University |
Department: | School of Life Sciences |
Laboratory: | Heather D. Bean Lab |
Last Name: | Bean, Ph.D. |
First Name: | Heather |
Address: | PO Box 874501 Tempe, AZ 85287 |
Email: | heather.d.bean@asu.edu |
Phone: | 480-727-3395 |
Publications: | Jenkins, C. L., H. D. Bean (2020). Influence of media on the differentiation of Staphylococcus spp. by volatile compounds. Journal of breath research 14, 016007 doi:10.1088/1752-7163/ab3e9d |
Subject:
Subject ID: | SU001500 |
Subject Type: | Bacteria |
Subject Species: | Staphylococcus epidermidis |
Taxonomy ID: | 1282 |
Genotype Strain: | ATCC 12600; ATCC 12228 |
Cell Biosource Or Supplier: | ATCC |
Cell Strain Details: | ATCC 12600; ATCC 12228 |
Species Group: | Bacteria |
Factors:
Subject type: Bacteria; Subject species: Staphylococcus epidermidis (Factor headings shown in green)
mb_sample_id | local_sample_id | Treatment | Culture Medium |
---|---|---|---|
SA120056 | MediaBlank2_BHI_1 | BLANK | BHI |
SA120057 | MediaBlank2_BHI_3 | BLANK | BHI |
SA120058 | MediaBlank2_BHI_2 | BLANK | BHI |
SA120059 | MediaBlank1_BHI_1 | BLANK | BHI |
SA120060 | MediaBlank1_BHI_2 | BLANK | BHI |
SA120061 | MediaBlank1_BHI_3 | BLANK | BHI |
SA120062 | MediaBlank2_LB_1 | BLANK | LB_LENNOX |
SA120063 | MediaBlank2_LB_2 | BLANK | LB_LENNOX |
SA120064 | MediaBlank2_LB_3 | BLANK | LB_LENNOX |
SA120065 | MediaBlank1_LB_1 | BLANK | LB_LENNOX |
SA120066 | MediaBlank1_LB_2 | BLANK | LB_LENNOX |
SA120067 | MediaBlank1_LB_3 | BLANK | LB_LENNOX |
SA120068 | MediaBlank1_MH_1 | BLANK | MUELLER-HINTON |
SA120069 | MediaBlank2_MH_1 | BLANK | MUELLER-HINTON |
SA120070 | MediaBlank1_MH_2 | BLANK | MUELLER-HINTON |
SA120071 | MediaBlank1_MH_3 | BLANK | MUELLER-HINTON |
SA120072 | MediaBlank2_MH_3 | BLANK | MUELLER-HINTON |
SA120073 | MediaBlank2_MH_2 | BLANK | MUELLER-HINTON |
SA120074 | MediaBlank1_TSB_3 | BLANK | TSB |
SA120075 | MediaBlank1_TSB_2 | BLANK | TSB |
SA120076 | MediaBlank1_TSB_1 | BLANK | TSB |
SA120077 | KIMix_2 | Chemical Standards | none |
SA120078 | KIMix_1 | Chemical Standards | none |
SA120079 | KIMix_3 | Chemical Standards | none |
SA120080 | Pcl_BHI_2 | MEDIUM | BHI |
SA120081 | Pcl_BHI_1 | MEDIUM | BHI |
SA120082 | PA01_BHI_1 | MEDIUM | BHI |
SA120083 | Staphau_BHI_1 | MEDIUM | BHI |
SA120084 | Staphau_BHI_2 | MEDIUM | BHI |
SA120085 | Staphep_BHI_2 | MEDIUM | BHI |
SA120086 | Staphep_BHI_3 | MEDIUM | BHI |
SA120087 | Staphau_BHI_3 | MEDIUM | BHI |
SA120088 | PA01_BHI_2 | MEDIUM | BHI |
SA120089 | Pcl_BHI_3 | MEDIUM | BHI |
SA120090 | Staphep_BHI_1 | MEDIUM | BHI |
SA120091 | PA01_BHI_3 | MEDIUM | BHI |
SA120092 | PA14_BHI_1 | MEDIUM | BHI |
SA120093 | PA14_BHI_3 | MEDIUM | BHI |
SA120094 | PA14_BHI_2 | MEDIUM | BHI |
SA120095 | Staphep_LB_2 | MEDIUM | LB_LENNOX |
SA120096 | Staphep_LB_3 | MEDIUM | LB_LENNOX |
SA120097 | Staphau_LB_3 | MEDIUM | LB_LENNOX |
SA120098 | Staphau_LB_2 | MEDIUM | LB_LENNOX |
SA120099 | Staphau_LB_1 | MEDIUM | LB_LENNOX |
SA120100 | PA14_LB_3 | MEDIUM | LB_LENNOX |
SA120101 | Pcl_LB_3 | MEDIUM | LB_LENNOX |
SA120102 | PA14_LB_1 | MEDIUM | LB_LENNOX |
SA120103 | PA01_LB_3 | MEDIUM | LB_LENNOX |
SA120104 | PA14_LB_2 | MEDIUM | LB_LENNOX |
SA120105 | PA01_LB_2 | MEDIUM | LB_LENNOX |
SA120106 | Pcl_LB_1 | MEDIUM | LB_LENNOX |
SA120107 | Staphep_LB_1 | MEDIUM | LB_LENNOX |
SA120108 | Pcl_LB_2 | MEDIUM | LB_LENNOX |
SA120109 | PA01_LB_1 | MEDIUM | LB_LENNOX |
SA120110 | Staphep_MH_1 | MEDIUM | MUELLER-HINTON |
SA120111 | Staphep_MH_3 | MEDIUM | MUELLER-HINTON |
SA120112 | Staphep_MH_2 | MEDIUM | MUELLER-HINTON |
SA120113 | PA14_MH_3 | MEDIUM | MUELLER-HINTON |
SA120114 | PA14_MH_1 | MEDIUM | MUELLER-HINTON |
SA120115 | Pcl_MH_1 | MEDIUM | MUELLER-HINTON |
SA120116 | PA01_MH_3 | MEDIUM | MUELLER-HINTON |
SA120117 | PA01_MH_2 | MEDIUM | MUELLER-HINTON |
SA120118 | PA01_MH_1 | MEDIUM | MUELLER-HINTON |
SA120119 | Pcl_MH_2 | MEDIUM | MUELLER-HINTON |
SA120120 | PA14_MH_2 | MEDIUM | MUELLER-HINTON |
SA120121 | Pcl_MH_3 | MEDIUM | MUELLER-HINTON |
SA120122 | Staphau_MH_2 | MEDIUM | MUELLER-HINTON |
SA120123 | Staphau_MH_1 | MEDIUM | MUELLER-HINTON |
SA120124 | Staphau_MH_3 | MEDIUM | MUELLER-HINTON |
SA120125 | Staphau_TSB_2 | MEDIUM | TSB |
SA120126 | Staphau_TSB_1 | MEDIUM | TSB |
SA120127 | Staphep_TSB_3 | MEDIUM | TSB |
SA120128 | Staphep_TSB_2 | MEDIUM | TSB |
SA120129 | Staphep_TSB_1 | MEDIUM | TSB |
SA120130 | Staphau_TSB_3 | MEDIUM | TSB |
SA120131 | Vial-Blank_1 | Vial Blank | none |
SA120132 | VIAL_BLANK_1 | Vial Blank | none |
Showing results 1 to 77 of 77 |
Collection:
Collection ID: | CO001495 |
Collection Summary: | Staphylococcus aureus (ATCC 12600) and Staphylococcus epidermidis (ATCC 12228) were cultured in four filter-sterilized complex media for metabolomics analysis: Brain Heart Infusion broth (BHI; Bacto); lysogeny broth Lennox (LB; Fisher Scientific); Mueller Hinton broth (MHB; Difco); and Tryptic Soy broth (TSB; Bacto). Each species was prepared in biological triplicate. Uninoculated media control blanks were prepared in six replicates for BHI, LB, and MHB, and in triplicate for TSB, following the same procedures as the bacterial samples and processed in parallel. Samples were transferred to capped GC vials and stored at -20 °C for approximately two weeks prior to GC×GC-TOFMS analysis. |
Collection Protocol Filename: | CLJenkins_Collection_Protocol_Metadata.txt |
Sample Type: | Bacterial cells |
Collection Frequency: | Once, at the completion of 24 hour aerobic incubation at 37 C with orbital shaking |
Treatment:
Treatment ID: | TR001515 |
Treatment Summary: | Two ATCC strains of staphylococci were grown in four different filter-sterilized complex media under identical conditions. Please see the Collection Protocol for details. |
Cell Media: | BHI Broth, LB Lennox, Mueller Hinton Broth, Tryptic Soy Broth |
Sample Preparation:
Sampleprep ID: | SP001508 |
Sampleprep Summary: | No sample preparation was required due to sampling via Head-Space Solid-phase microextraction by autosampler robot. |
Sampleprep Protocol Filename: | CLJenkins_MS__Methods.pdf |
Combined analysis:
Analysis ID | AN002384 |
---|---|
Analysis type | MS |
Chromatography type | GC |
Chromatography system | Agilent 7890B |
Column | Multidimensional configuration |
MS Type | EI |
MS instrument type | GC x GC-TOF |
MS instrument name | Leco Pegasus 4D GCxGC TOF |
Ion Mode | POSITIVE |
Units | peak area |
Chromatography:
Chromatography ID: | CH001751 |
Chromatography Summary: | Comprehensive two-dimensional gas chromatography with multi-dimensional column configuration |
Instrument Name: | Agilent 7890B |
Column Name: | Multidimensional configuration |
Chromatography Type: | GC |
MS:
MS ID: | MS002226 |
Analysis ID: | AN002384 |
Instrument Name: | Leco Pegasus 4D GCxGC TOF |
Instrument Type: | GC x GC-TOF |
MS Type: | EI |
MS Comments: | none |
Ion Mode: | POSITIVE |