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Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes
Listeria monocytogenes is a microorganism of great concern for the food industry and the cause of human foodborne disease. Therefore, novel methods of control are needed, and systems biology is one such approach to identify them. Using a combination of computational techniques and laboratory methods...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6012718/ https://www.ncbi.nlm.nih.gov/pubmed/29879172 http://dx.doi.org/10.1371/journal.pone.0198584 |
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author | Metz, Zachary P. Ding, Tong Baumler, David J. |
author_facet | Metz, Zachary P. Ding, Tong Baumler, David J. |
author_sort | Metz, Zachary P. |
collection | PubMed |
description | Listeria monocytogenes is a microorganism of great concern for the food industry and the cause of human foodborne disease. Therefore, novel methods of control are needed, and systems biology is one such approach to identify them. Using a combination of computational techniques and laboratory methods, genome-scale metabolic models (GEMs) can be created, validated, and used to simulate growth environments and discern metabolic capabilities of microbes of interest, including L. monocytogenes. The objective of the work presented here was to generate GEMs for six different strains of L. monocytogenes, and to both qualitatively and quantitatively validate these GEMs with experimental data to examine the diversity of metabolic capabilities of numerous strains from the three different serovar groups most associated with foodborne outbreaks and human disease. Following qualitative validation, 57 of the 95 carbon sources tested experimentally were present in the GEMs, and; therefore, these were the compounds from which comparisons could be drawn. Of these 57 compounds, agreement between in silico predictions and in vitro results for carbon source utilization ranged from 80.7% to 91.2% between strains. Nutrient utilization agreement between in silico predictions and in vitro results were also conducted for numerous nitrogen, phosphorous, and sulfur sources. Additionally, quantitative validation showed that the L. monocytogenes GEMs were able to generate in silico predictions for growth rate and growth yield that were strongly and significantly (p < 0.0013 and p < 0.0015, respectively) correlated with experimental results. These findings are significant because they show that these GEMs for L. monocytogenes are comparable to published GEMs of other organisms for agreement between in silico predictions and in vitro results. Therefore, as with the other GEMs, namely those for Escherichia coli, Staphylococcus aureus, Vibrio vulnificus, and Salmonella spp., they can be used to determine new methods of growth control and disease treatment. |
format | Online Article Text |
id | pubmed-6012718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60127182018-07-06 Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes Metz, Zachary P. Ding, Tong Baumler, David J. PLoS One Research Article Listeria monocytogenes is a microorganism of great concern for the food industry and the cause of human foodborne disease. Therefore, novel methods of control are needed, and systems biology is one such approach to identify them. Using a combination of computational techniques and laboratory methods, genome-scale metabolic models (GEMs) can be created, validated, and used to simulate growth environments and discern metabolic capabilities of microbes of interest, including L. monocytogenes. The objective of the work presented here was to generate GEMs for six different strains of L. monocytogenes, and to both qualitatively and quantitatively validate these GEMs with experimental data to examine the diversity of metabolic capabilities of numerous strains from the three different serovar groups most associated with foodborne outbreaks and human disease. Following qualitative validation, 57 of the 95 carbon sources tested experimentally were present in the GEMs, and; therefore, these were the compounds from which comparisons could be drawn. Of these 57 compounds, agreement between in silico predictions and in vitro results for carbon source utilization ranged from 80.7% to 91.2% between strains. Nutrient utilization agreement between in silico predictions and in vitro results were also conducted for numerous nitrogen, phosphorous, and sulfur sources. Additionally, quantitative validation showed that the L. monocytogenes GEMs were able to generate in silico predictions for growth rate and growth yield that were strongly and significantly (p < 0.0013 and p < 0.0015, respectively) correlated with experimental results. These findings are significant because they show that these GEMs for L. monocytogenes are comparable to published GEMs of other organisms for agreement between in silico predictions and in vitro results. Therefore, as with the other GEMs, namely those for Escherichia coli, Staphylococcus aureus, Vibrio vulnificus, and Salmonella spp., they can be used to determine new methods of growth control and disease treatment. Public Library of Science 2018-06-07 /pmc/articles/PMC6012718/ /pubmed/29879172 http://dx.doi.org/10.1371/journal.pone.0198584 Text en © 2018 Metz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Metz, Zachary P. Ding, Tong Baumler, David J. Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title | Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title_full | Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title_fullStr | Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title_full_unstemmed | Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title_short | Using genome-scale metabolic models to compare serovars of the foodborne pathogen Listeria monocytogenes |
title_sort | using genome-scale metabolic models to compare serovars of the foodborne pathogen listeria monocytogenes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6012718/ https://www.ncbi.nlm.nih.gov/pubmed/29879172 http://dx.doi.org/10.1371/journal.pone.0198584 |
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