Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis
Enterococcus faecalis is a Gram-positive, opportunistic, pathogenic bacterium that causes a significant number of antibiotic-resistant infections in hospitalized patients. The development of antibiotic resistance in hospital-associated pathogens is a formidable public health threat. In E. faecalis a...
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sg-ntu-dr.10356-834822020-09-21T11:33:23Z Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis Rashid, Rafi Cazenave-Gassiot, Amaury Gao, Iris H. Nair, Zeus J. Kumar, Jaspal K. Gao, Liang Kline, Kimberly A. Wenk, Markus R. Hancock, Lynn E. School of Biological Sciences Singapore Centre for Environmental Life Sciences Engineering Enterococcus faecalis Lipids Enterococcus faecalis is a Gram-positive, opportunistic, pathogenic bacterium that causes a significant number of antibiotic-resistant infections in hospitalized patients. The development of antibiotic resistance in hospital-associated pathogens is a formidable public health threat. In E. faecalis and other Gram-positive pathogens, correlations exist between lipid composition and antibiotic resistance. Resistance to the last-resort antibiotic daptomycin is accompanied by a decrease in phosphatidylglycerol (PG) levels, whereas multiple peptide resistance factor (MprF) converts anionic PG into cationic lysyl-PG via a trans-esterification reaction, providing resistance to cationic antimicrobial peptides. Unlike previous studies that relied on thin layer chromatography and spectrophotometry, we have performed liquid chromatography-tandem mass spectrometry (LC-MS/MS) directly on lipids extracted from E. faecalis, and quantified the phospholipids through multiple reaction monitoring (MRM). In the daptomycin-sensitive E. faecalis strain OG1RF, we have identified 17 PGs, 8 lysyl-PGs (LPGs), 23 cardiolipins (CL), 3 glycerophospho-diglucosyl-diacylglycerols (GPDGDAG), 5 diglucosyl-diacylglycerols (DGDAG), 3 diacylglycerols (DAGs), and 4 triacylglycerols (TAGs). We have quantified PG and shown that PG levels vary during growth of E. faecalis in vitro. We also show that two daptomycin-resistant (DapR) strains of E. faecalis have substantially lower levels of PG and LPG levels. Since LPG levels in these strains are lower, daptomycin resistance is likely due to the reduction in PG. This lipidome map is the first comprehensive analysis of membrane phospholipids and glycolipids in the important human pathogen E. faecalis, for which antimicrobial resistance and altered lipid homeostasis have been intimately linked. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Published version 2017-06-08T08:36:16Z 2019-12-06T15:23:56Z 2017-06-08T08:36:16Z 2019-12-06T15:23:56Z 2017 Journal Article Rashid, R., Cazenave-Gassiot, A., Gao, I. H., Nair, Z. J., Kumar, J. K., Gao, L., et al. (2017). Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis. PLOS ONE, 12(4), e0175886-. 1932-6203 https://hdl.handle.net/10356/83482 http://hdl.handle.net/10220/42630 10.1371/journal.pone.0175886 en PLOS ONE © 2017 Rashid et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 20 p. application/pdf |
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Enterococcus faecalis Lipids Rashid, Rafi Cazenave-Gassiot, Amaury Gao, Iris H. Nair, Zeus J. Kumar, Jaspal K. Gao, Liang Kline, Kimberly A. Wenk, Markus R. Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
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Enterococcus faecalis is a Gram-positive, opportunistic, pathogenic bacterium that causes a significant number of antibiotic-resistant infections in hospitalized patients. The development of antibiotic resistance in hospital-associated pathogens is a formidable public health threat. In E. faecalis and other Gram-positive pathogens, correlations exist between lipid composition and antibiotic resistance. Resistance to the last-resort antibiotic daptomycin is accompanied by a decrease in phosphatidylglycerol (PG) levels, whereas multiple peptide resistance factor (MprF) converts anionic PG into cationic lysyl-PG via a trans-esterification reaction, providing resistance to cationic antimicrobial peptides. Unlike previous studies that relied on thin layer chromatography and spectrophotometry, we have performed liquid chromatography-tandem mass spectrometry (LC-MS/MS) directly on lipids extracted from E. faecalis, and quantified the phospholipids through multiple reaction monitoring (MRM). In the daptomycin-sensitive E. faecalis strain OG1RF, we have identified 17 PGs, 8 lysyl-PGs (LPGs), 23 cardiolipins (CL), 3 glycerophospho-diglucosyl-diacylglycerols (GPDGDAG), 5 diglucosyl-diacylglycerols (DGDAG), 3 diacylglycerols (DAGs), and 4 triacylglycerols (TAGs). We have quantified PG and shown that PG levels vary during growth of E. faecalis in vitro. We also show that two daptomycin-resistant (DapR) strains of E. faecalis have substantially lower levels of PG and LPG levels. Since LPG levels in these strains are lower, daptomycin resistance is likely due to the reduction in PG. This lipidome map is the first comprehensive analysis of membrane phospholipids and glycolipids in the important human pathogen E. faecalis, for which antimicrobial resistance and altered lipid homeostasis have been intimately linked. |
author2 |
Hancock, Lynn E. |
author_facet |
Hancock, Lynn E. Rashid, Rafi Cazenave-Gassiot, Amaury Gao, Iris H. Nair, Zeus J. Kumar, Jaspal K. Gao, Liang Kline, Kimberly A. Wenk, Markus R. |
format |
Article |
author |
Rashid, Rafi Cazenave-Gassiot, Amaury Gao, Iris H. Nair, Zeus J. Kumar, Jaspal K. Gao, Liang Kline, Kimberly A. Wenk, Markus R. |
author_sort |
Rashid, Rafi |
title |
Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
title_short |
Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
title_full |
Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
title_fullStr |
Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
title_full_unstemmed |
Comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen Enterococcus faecalis |
title_sort |
comprehensive analysis of phospholipids and glycolipids in the opportunistic pathogen enterococcus faecalis |
publishDate |
2017 |
url |
https://hdl.handle.net/10356/83482 http://hdl.handle.net/10220/42630 |
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1681057406324310016 |