Cargando…
Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis
Bacterial metabolism is fundamental to survival and pathogenesis. We explore how Mycobacterium tuberculosis utilises amino acids as nitrogen sources, using a combination of bacterial physiology and stable isotope tracing coupled to mass spectrometry metabolomics methods. Our results define core prop...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361586/ https://www.ncbi.nlm.nih.gov/pubmed/30702426 http://dx.doi.org/10.7554/eLife.41129 |
_version_ | 1783392705344176128 |
---|---|
author | Agapova, Aleksandra Serafini, Agnese Petridis, Michael Hunt, Debbie M Garza-Garcia, Acely Sohaskey, Charles D de Carvalho, Luiz Pedro Sório |
author_facet | Agapova, Aleksandra Serafini, Agnese Petridis, Michael Hunt, Debbie M Garza-Garcia, Acely Sohaskey, Charles D de Carvalho, Luiz Pedro Sório |
author_sort | Agapova, Aleksandra |
collection | PubMed |
description | Bacterial metabolism is fundamental to survival and pathogenesis. We explore how Mycobacterium tuberculosis utilises amino acids as nitrogen sources, using a combination of bacterial physiology and stable isotope tracing coupled to mass spectrometry metabolomics methods. Our results define core properties of the nitrogen metabolic network from M. tuberculosis, such as: (i) the lack of homeostatic control of certain amino acid pool sizes; (ii) similar rates of utilisation of different amino acids as sole nitrogen sources; (iii) improved nitrogen utilisation from amino acids compared to ammonium; and (iv) co-metabolism of nitrogen sources. Finally, we discover that alanine dehydrogenase is involved in ammonium assimilation in M. tuberculosis, in addition to its essential role in alanine utilisation as a nitrogen source. This study represents the first in-depth analysis of nitrogen source utilisation by M. tuberculosis and reveals a flexible metabolic network with characteristics that are likely a product of evolution in the human host. |
format | Online Article Text |
id | pubmed-6361586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63615862019-02-06 Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis Agapova, Aleksandra Serafini, Agnese Petridis, Michael Hunt, Debbie M Garza-Garcia, Acely Sohaskey, Charles D de Carvalho, Luiz Pedro Sório eLife Microbiology and Infectious Disease Bacterial metabolism is fundamental to survival and pathogenesis. We explore how Mycobacterium tuberculosis utilises amino acids as nitrogen sources, using a combination of bacterial physiology and stable isotope tracing coupled to mass spectrometry metabolomics methods. Our results define core properties of the nitrogen metabolic network from M. tuberculosis, such as: (i) the lack of homeostatic control of certain amino acid pool sizes; (ii) similar rates of utilisation of different amino acids as sole nitrogen sources; (iii) improved nitrogen utilisation from amino acids compared to ammonium; and (iv) co-metabolism of nitrogen sources. Finally, we discover that alanine dehydrogenase is involved in ammonium assimilation in M. tuberculosis, in addition to its essential role in alanine utilisation as a nitrogen source. This study represents the first in-depth analysis of nitrogen source utilisation by M. tuberculosis and reveals a flexible metabolic network with characteristics that are likely a product of evolution in the human host. eLife Sciences Publications, Ltd 2019-01-31 /pmc/articles/PMC6361586/ /pubmed/30702426 http://dx.doi.org/10.7554/eLife.41129 Text en © 2019, Agapova et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Agapova, Aleksandra Serafini, Agnese Petridis, Michael Hunt, Debbie M Garza-Garcia, Acely Sohaskey, Charles D de Carvalho, Luiz Pedro Sório Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title | Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title_full | Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title_fullStr | Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title_full_unstemmed | Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title_short | Flexible nitrogen utilisation by the metabolic generalist pathogen Mycobacterium tuberculosis |
title_sort | flexible nitrogen utilisation by the metabolic generalist pathogen mycobacterium tuberculosis |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361586/ https://www.ncbi.nlm.nih.gov/pubmed/30702426 http://dx.doi.org/10.7554/eLife.41129 |
work_keys_str_mv | AT agapovaaleksandra flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT serafiniagnese flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT petridismichael flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT huntdebbiem flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT garzagarciaacely flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT sohaskeycharlesd flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis AT decarvalholuizpedrosorio flexiblenitrogenutilisationbythemetabolicgeneralistpathogenmycobacteriumtuberculosis |