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Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1
L-amino acid oxidases (LAAO) are flavoproteins that catalyze the oxidative deamination of L-amino acids to a keto-acid along with the production of H(2)O(2) and ammonia. Interleukin 4 induced gene 1 (IL4I1) is a secreted LAAO expressed by macrophages and dendritic cells stimulated by microbial deriv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552961/ https://www.ncbi.nlm.nih.gov/pubmed/23355881 http://dx.doi.org/10.1371/journal.pone.0054589 |
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author | Puiffe, Marie-Line Lachaise, Isabelle Molinier-Frenkel, Valérie Castellano, Flavia |
author_facet | Puiffe, Marie-Line Lachaise, Isabelle Molinier-Frenkel, Valérie Castellano, Flavia |
author_sort | Puiffe, Marie-Line |
collection | PubMed |
description | L-amino acid oxidases (LAAO) are flavoproteins that catalyze the oxidative deamination of L-amino acids to a keto-acid along with the production of H(2)O(2) and ammonia. Interleukin 4 induced gene 1 (IL4I1) is a secreted LAAO expressed by macrophages and dendritic cells stimulated by microbial derived products or interferons, which is endowed with immunoregulatory properties. It is the first LAAO described in mammalian innate immune cells. In this work, we show that this enzyme blocks the in vitro and in vivo growth of Gram negative and Gram positive bacteria. This antibiotic effect is primarily mediated by H(2)O(2) production but is amplified by basification of the medium due to the accumulation of ammonia. The depletion of phenylalanine (the primary amino acid catabolized by IL4I1) may also participate in the in vivo inhibition of staphylococci growth. Thus, IL4I1 plays a distinct role compared to other antibacterial enzymes produced by mononuclear phagocytes. |
format | Online Article Text |
id | pubmed-3552961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35529612013-01-25 Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 Puiffe, Marie-Line Lachaise, Isabelle Molinier-Frenkel, Valérie Castellano, Flavia PLoS One Research Article L-amino acid oxidases (LAAO) are flavoproteins that catalyze the oxidative deamination of L-amino acids to a keto-acid along with the production of H(2)O(2) and ammonia. Interleukin 4 induced gene 1 (IL4I1) is a secreted LAAO expressed by macrophages and dendritic cells stimulated by microbial derived products or interferons, which is endowed with immunoregulatory properties. It is the first LAAO described in mammalian innate immune cells. In this work, we show that this enzyme blocks the in vitro and in vivo growth of Gram negative and Gram positive bacteria. This antibiotic effect is primarily mediated by H(2)O(2) production but is amplified by basification of the medium due to the accumulation of ammonia. The depletion of phenylalanine (the primary amino acid catabolized by IL4I1) may also participate in the in vivo inhibition of staphylococci growth. Thus, IL4I1 plays a distinct role compared to other antibacterial enzymes produced by mononuclear phagocytes. Public Library of Science 2013-01-23 /pmc/articles/PMC3552961/ /pubmed/23355881 http://dx.doi.org/10.1371/journal.pone.0054589 Text en © 2013 Puiffe 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Puiffe, Marie-Line Lachaise, Isabelle Molinier-Frenkel, Valérie Castellano, Flavia Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title | Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title_full | Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title_fullStr | Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title_full_unstemmed | Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title_short | Antibacterial Properties of the Mammalian L-Amino Acid Oxidase IL4I1 |
title_sort | antibacterial properties of the mammalian l-amino acid oxidase il4i1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552961/ https://www.ncbi.nlm.nih.gov/pubmed/23355881 http://dx.doi.org/10.1371/journal.pone.0054589 |
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