Abstract
Purpose
Antibiotic resistance is widespread throughout the world and represents a serious health concern. There is an urgent need for the development of novel tools for rapidly distinguishing antibiotic resistant bacteria from susceptible strains. Previous work has demonstrated that differences in antimicrobial susceptibility can be reflected in differences in the profile of volatile organic compounds (VOCs) produced by dissimilar strains. The aim of this study was to investigate the effect of the presence of cephalosporin antibiotics on the VOC profile of extended spectrum beta-lactamase (ESBL) and non-ESBL producing strains of Escherichia coli.
Material and methods
In this study, VOCs from strains of Escherichia coli positive and negative for the most commonly encountered ESBL, CTX-M in the presence of cephalosporin antibiotics were assessed using solid-phase microextraction (SPME) coupled with a combined gas chromatography-mass spectrometry/metal oxide sensor (GC-MS/MOS) system.
Results
Our proof-of-concept study allowed for distinguishing CTX-M positive and negative bacteria within 2 h after the addition of antibiotics. One MOS signal (RT: 22.6) showed a statistically significant three-way interaction (p = 0.033) in addition to significant two-way interactions for culture and additive (p = 0.046) plus time and additive (p = 0.020). There were also significant effects observed for time (p = 0.009), culture (p = 0.030) and additive (p = 0.028). No effects were observed in the MS data.
Conclusions
The results of our study showed the potential of VOC analysis using SPME combined with a GC-MS/MOS system for the early detection of CTX-M-producing, antibiotic-resistant E. coli, responsible for urinary tract infections (UTIs).
Antibiotic resistance is widespread throughout the world and represents a serious health concern. There is an urgent need for the development of novel tools for rapidly distinguishing antibiotic resistant bacteria from susceptible strains. Previous work has demonstrated that differences in antimicrobial susceptibility can be reflected in differences in the profile of volatile organic compounds (VOCs) produced by dissimilar strains. The aim of this study was to investigate the effect of the presence of cephalosporin antibiotics on the VOC profile of extended spectrum beta-lactamase (ESBL) and non-ESBL producing strains of Escherichia coli.
Material and methods
In this study, VOCs from strains of Escherichia coli positive and negative for the most commonly encountered ESBL, CTX-M in the presence of cephalosporin antibiotics were assessed using solid-phase microextraction (SPME) coupled with a combined gas chromatography-mass spectrometry/metal oxide sensor (GC-MS/MOS) system.
Results
Our proof-of-concept study allowed for distinguishing CTX-M positive and negative bacteria within 2 h after the addition of antibiotics. One MOS signal (RT: 22.6) showed a statistically significant three-way interaction (p = 0.033) in addition to significant two-way interactions for culture and additive (p = 0.046) plus time and additive (p = 0.020). There were also significant effects observed for time (p = 0.009), culture (p = 0.030) and additive (p = 0.028). No effects were observed in the MS data.
Conclusions
The results of our study showed the potential of VOC analysis using SPME combined with a GC-MS/MOS system for the early detection of CTX-M-producing, antibiotic-resistant E. coli, responsible for urinary tract infections (UTIs).
Original language | English |
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Pages (from-to) | 1-9 |
Number of pages | 9 |
Journal | Advances in Medical Sciences |
Volume | 67 |
Issue number | 1 |
Early online date | 22 Sep 2021 |
DOIs | |
Publication status | Published - 1 Mar 2022 |
Bibliographical note
Funding Information:This research was funded by the National Institute for Health Research (NIHR) Research Capability Funding (RCF) , Avon Primary Care Research Collaborative.
Publisher Copyright:
© 2021 Medical University of Bialystok
Keywords
- Volatile organic compounds
- gas chromatography-mass spectrometry
- metal-oxide sensor
- antibiotic resistance
- urinary tract infection