Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance
The Burkholderia cepacia complex (Bcc) is a collection of closely related, genetically distinct, ecologically diverse species known to cause life-threatening infections in cystic fibrosis (CF) patients. By virtue of a flexible genomic structure and diverse metabolic activity, Bcc bacteria employ a w...
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doaj-789230ad165c4c5884b73da61501ea502020-11-24T23:58:41ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2015-07-01610.3389/fmicb.2015.00668122836Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistanceDouglas Gordon Storey0Hans J. Vogel1Nusrat Sharmeen Shommu2University of CalgaryUniversity of CalgaryUniversity of CalgaryThe Burkholderia cepacia complex (Bcc) is a collection of closely related, genetically distinct, ecologically diverse species known to cause life-threatening infections in cystic fibrosis (CF) patients. By virtue of a flexible genomic structure and diverse metabolic activity, Bcc bacteria employ a wide array of virulence factors for pathogenesis in CF patients and have developed resistance to most of the commonly used antibiotics. However, the mechanism of pathogenesis and antibiotic resistance is still not fully understood. This mini review discusses the established and potential virulence determinants of Bcc and some of the contemporary strategies including transcriptomics and proteomics used to identify these traits. We also propose the application of metabolic profiling, a cost-effective modern-day approach to achieve new insights.http://journal.frontiersin.org/Journal/10.3389/fmicb.2015.00668/fullBurkholderia cepacia complexCystic FibrosisMetabolomicsVirulenceantibiotic resistance |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Douglas Gordon Storey Hans J. Vogel Nusrat Sharmeen Shommu |
spellingShingle |
Douglas Gordon Storey Hans J. Vogel Nusrat Sharmeen Shommu Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance Frontiers in Microbiology Burkholderia cepacia complex Cystic Fibrosis Metabolomics Virulence antibiotic resistance |
author_facet |
Douglas Gordon Storey Hans J. Vogel Nusrat Sharmeen Shommu |
author_sort |
Douglas Gordon Storey |
title |
Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance |
title_short |
Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance |
title_full |
Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance |
title_fullStr |
Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance |
title_full_unstemmed |
Potential of metabolomics to reveal Burkholderia cepacia complex pathogenesis and antibiotic resistance |
title_sort |
potential of metabolomics to reveal burkholderia cepacia complex pathogenesis and antibiotic resistance |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Microbiology |
issn |
1664-302X |
publishDate |
2015-07-01 |
description |
The Burkholderia cepacia complex (Bcc) is a collection of closely related, genetically distinct, ecologically diverse species known to cause life-threatening infections in cystic fibrosis (CF) patients. By virtue of a flexible genomic structure and diverse metabolic activity, Bcc bacteria employ a wide array of virulence factors for pathogenesis in CF patients and have developed resistance to most of the commonly used antibiotics. However, the mechanism of pathogenesis and antibiotic resistance is still not fully understood. This mini review discusses the established and potential virulence determinants of Bcc and some of the contemporary strategies including transcriptomics and proteomics used to identify these traits. We also propose the application of metabolic profiling, a cost-effective modern-day approach to achieve new insights. |
topic |
Burkholderia cepacia complex Cystic Fibrosis Metabolomics Virulence antibiotic resistance |
url |
http://journal.frontiersin.org/Journal/10.3389/fmicb.2015.00668/full |
work_keys_str_mv |
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