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...

Descripción completa

Detalles Bibliográficos
Autores principales: Borghi, Monica, Puccetti, Matteo, Pariano, Marilena, Renga, Giorgia, Stincardini, Claudia, Ricci, Maurizio, Giovagnoli, Stefano, Costantini, Claudio, Romani, Luigina
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