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Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis

Haemophilus influenzae is a host adapted human pathogen known to contribute to a variety of acute and chronic diseases of the upper and lower respiratory tract as well as the middle ear. At the sites of infection as well as during growth as a commensal the environmental conditions encountered by H....

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Autores principales: Othman, Dk Seti Maimonah Pg, Schirra, Horst, McEwan, Alastair G., Kappler, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941224/
https://www.ncbi.nlm.nih.gov/pubmed/24624122
http://dx.doi.org/10.3389/fmicb.2014.00069
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author Othman, Dk Seti Maimonah Pg
Schirra, Horst
McEwan, Alastair G.
Kappler, Ulrike
author_facet Othman, Dk Seti Maimonah Pg
Schirra, Horst
McEwan, Alastair G.
Kappler, Ulrike
author_sort Othman, Dk Seti Maimonah Pg
collection PubMed
description Haemophilus influenzae is a host adapted human pathogen known to contribute to a variety of acute and chronic diseases of the upper and lower respiratory tract as well as the middle ear. At the sites of infection as well as during growth as a commensal the environmental conditions encountered by H. influenzae will vary significantly, especially in terms of oxygen availability, however, the mechanisms by which the bacteria can adapt their metabolism to cope with such changes have not been studied in detail. Using targeted metabolomics the spectrum of metabolites produced during growth of H. influenzae on glucose in RPMI-based medium was found to change from acetate as the main product during aerobic growth to formate as the major product during anaerobic growth. This change in end-product is likely caused by a switch in the major route of pyruvate degradation. Neither lactate nor succinate or fumarate were major products of H. influenzae growth under any condition studied. Gene expression studies and enzyme activity data revealed that despite an identical genetic makeup and very similar metabolite production profiles, H. influenzae strain Rd appeared to favor glucose degradation via the pentose phosphate pathway, while strain 2019, a clinical isolate, showed higher expression of enzymes involved in glycolysis. Components of the respiratory chain were most highly expressed during microaerophilic and anaerobic growth in both strains, but again clear differences existed in the expression of genes associated e.g., with NADH oxidation, nitrate and nitrite reduction in the two strains studied. Together our results indicate that H. influenzae uses a specialized type of metabolism that could be termed “respiration assisted fermentation” where the respiratory chain likely serves to alleviate redox imbalances caused by incomplete glucose oxidation, and at the same time provides a means of converting a variety of compounds including nitrite and nitrate that arise as part of the host defence mechanisms.
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spelling pubmed-39412242014-03-12 Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis Othman, Dk Seti Maimonah Pg Schirra, Horst McEwan, Alastair G. Kappler, Ulrike Front Microbiol Microbiology Haemophilus influenzae is a host adapted human pathogen known to contribute to a variety of acute and chronic diseases of the upper and lower respiratory tract as well as the middle ear. At the sites of infection as well as during growth as a commensal the environmental conditions encountered by H. influenzae will vary significantly, especially in terms of oxygen availability, however, the mechanisms by which the bacteria can adapt their metabolism to cope with such changes have not been studied in detail. Using targeted metabolomics the spectrum of metabolites produced during growth of H. influenzae on glucose in RPMI-based medium was found to change from acetate as the main product during aerobic growth to formate as the major product during anaerobic growth. This change in end-product is likely caused by a switch in the major route of pyruvate degradation. Neither lactate nor succinate or fumarate were major products of H. influenzae growth under any condition studied. Gene expression studies and enzyme activity data revealed that despite an identical genetic makeup and very similar metabolite production profiles, H. influenzae strain Rd appeared to favor glucose degradation via the pentose phosphate pathway, while strain 2019, a clinical isolate, showed higher expression of enzymes involved in glycolysis. Components of the respiratory chain were most highly expressed during microaerophilic and anaerobic growth in both strains, but again clear differences existed in the expression of genes associated e.g., with NADH oxidation, nitrate and nitrite reduction in the two strains studied. Together our results indicate that H. influenzae uses a specialized type of metabolism that could be termed “respiration assisted fermentation” where the respiratory chain likely serves to alleviate redox imbalances caused by incomplete glucose oxidation, and at the same time provides a means of converting a variety of compounds including nitrite and nitrate that arise as part of the host defence mechanisms. Frontiers Media S.A. 2014-03-04 /pmc/articles/PMC3941224/ /pubmed/24624122 http://dx.doi.org/10.3389/fmicb.2014.00069 Text en Copyright © 2014 Othman, Schirra, McEwan and Kappler. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Othman, Dk Seti Maimonah Pg
Schirra, Horst
McEwan, Alastair G.
Kappler, Ulrike
Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title_full Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title_fullStr Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title_full_unstemmed Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title_short Metabolic versatility in Haemophilus influenzae: a metabolomic and genomic analysis
title_sort metabolic versatility in haemophilus influenzae: a metabolomic and genomic analysis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941224/
https://www.ncbi.nlm.nih.gov/pubmed/24624122
http://dx.doi.org/10.3389/fmicb.2014.00069
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