Cargando…
Tryptophan as a Central Hub for Host/Microbial Symbiosis
Amino acid catabolism occurs during inflammation and regulates innate and adaptive immunity. The role of commensal bacteria in amino acid catabolism and the production of metabolites able to regulate the development and function of the innate immune system is increasingly being recognized. Therefore...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225782/ https://www.ncbi.nlm.nih.gov/pubmed/32435131 http://dx.doi.org/10.1177/1178646920919755 |
_version_ | 1783534139566194688 |
---|---|
author | Borghi, Monica Puccetti, Matteo Pariano, Marilena Renga, Giorgia Stincardini, Claudia Ricci, Maurizio Giovagnoli, Stefano Costantini, Claudio Romani, Luigina |
author_facet | Borghi, Monica Puccetti, Matteo Pariano, Marilena Renga, Giorgia Stincardini, Claudia Ricci, Maurizio Giovagnoli, Stefano Costantini, Claudio Romani, Luigina |
author_sort | Borghi, Monica |
collection | PubMed |
description | Amino acid catabolism occurs during inflammation and regulates innate and adaptive immunity. The role of commensal bacteria in amino acid catabolism and the production of metabolites able to regulate the development and function of the innate immune system is increasingly being recognized. Therefore, commensal bacteria are key players in the maintenance of immune homeostasis. However, the intestinal microbiota also contributes to susceptibility and response to infectious diseases. This is self-evident for fungal infections known to occur as a consequence of weakened immune system and broad-spectrum antibiotic use or abuse. Thus, diseases caused by opportunistic fungi can no longer be viewed as dependent only on a weakened host but also on a disrupted microbiota. Based on these premises, the present review focuses on the role of amino acid metabolic pathways in the dialogue between the mammalian host and its microbiota and the potential implications in fungal commensalism and infectivity. |
format | Online Article Text |
id | pubmed-7225782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72257822020-05-20 Tryptophan as a Central Hub for Host/Microbial Symbiosis Borghi, Monica Puccetti, Matteo Pariano, Marilena Renga, Giorgia Stincardini, Claudia Ricci, Maurizio Giovagnoli, Stefano Costantini, Claudio Romani, Luigina Int J Tryptophan Res Review Amino acid catabolism occurs during inflammation and regulates innate and adaptive immunity. The role of commensal bacteria in amino acid catabolism and the production of metabolites able to regulate the development and function of the innate immune system is increasingly being recognized. Therefore, commensal bacteria are key players in the maintenance of immune homeostasis. However, the intestinal microbiota also contributes to susceptibility and response to infectious diseases. This is self-evident for fungal infections known to occur as a consequence of weakened immune system and broad-spectrum antibiotic use or abuse. Thus, diseases caused by opportunistic fungi can no longer be viewed as dependent only on a weakened host but also on a disrupted microbiota. Based on these premises, the present review focuses on the role of amino acid metabolic pathways in the dialogue between the mammalian host and its microbiota and the potential implications in fungal commensalism and infectivity. SAGE Publications 2020-05-11 /pmc/articles/PMC7225782/ /pubmed/32435131 http://dx.doi.org/10.1177/1178646920919755 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Borghi, Monica Puccetti, Matteo Pariano, Marilena Renga, Giorgia Stincardini, Claudia Ricci, Maurizio Giovagnoli, Stefano Costantini, Claudio Romani, Luigina Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title | Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title_full | Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title_fullStr | Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title_full_unstemmed | Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title_short | Tryptophan as a Central Hub for Host/Microbial Symbiosis |
title_sort | tryptophan as a central hub for host/microbial symbiosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225782/ https://www.ncbi.nlm.nih.gov/pubmed/32435131 http://dx.doi.org/10.1177/1178646920919755 |
work_keys_str_mv | AT borghimonica tryptophanasacentralhubforhostmicrobialsymbiosis AT puccettimatteo tryptophanasacentralhubforhostmicrobialsymbiosis AT parianomarilena tryptophanasacentralhubforhostmicrobialsymbiosis AT rengagiorgia tryptophanasacentralhubforhostmicrobialsymbiosis AT stincardiniclaudia tryptophanasacentralhubforhostmicrobialsymbiosis AT riccimaurizio tryptophanasacentralhubforhostmicrobialsymbiosis AT giovagnolistefano tryptophanasacentralhubforhostmicrobialsymbiosis AT costantiniclaudio tryptophanasacentralhubforhostmicrobialsymbiosis AT romaniluigina tryptophanasacentralhubforhostmicrobialsymbiosis |