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Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts
Insects and mammals share evolutionary conserved innate immune responses to maintain intestinal homeostasis. We investigated whether the larvae of the greater wax moth Galleria mellonella may be used as an experimental organism to distinguish between symbiotic Bacteroides vulgatus and pathobiotic Es...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156133/ https://www.ncbi.nlm.nih.gov/pubmed/30283451 http://dx.doi.org/10.3389/fimmu.2018.02114 |
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author | Lange, Anna Schäfer, Andrea Bender, Annika Steimle, Alexander Beier, Sina Parusel, Raphael Frick, Julia-Stefanie |
author_facet | Lange, Anna Schäfer, Andrea Bender, Annika Steimle, Alexander Beier, Sina Parusel, Raphael Frick, Julia-Stefanie |
author_sort | Lange, Anna |
collection | PubMed |
description | Insects and mammals share evolutionary conserved innate immune responses to maintain intestinal homeostasis. We investigated whether the larvae of the greater wax moth Galleria mellonella may be used as an experimental organism to distinguish between symbiotic Bacteroides vulgatus and pathobiotic Escherichia coli, which are mammalian intestinal commensals. Oral application of the symbiont or pathobiont to G. mellonella resulted in clearly distinguishable innate immune responses that could be verified by analyzing similar innate immune components in mice in vivo and in vitro. The differential innate immune responses were initiated by the recognition of bacterial components via pattern recognition receptors. The pathobiont detection resulted in increased expression of reactive oxygen and nitrogen species related genes as well as antimicrobial peptide gene expression. In contrast, the treatment/application with symbiotic bacteria led to weakened immune responses in both mammalian and insect models. As symbionts and pathobionts play a crucial role in development of inflammatory bowel diseases, we hence suggest G. mellonella as a future replacement organism in inflammatory bowel disease research. |
format | Online Article Text |
id | pubmed-6156133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61561332018-10-03 Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts Lange, Anna Schäfer, Andrea Bender, Annika Steimle, Alexander Beier, Sina Parusel, Raphael Frick, Julia-Stefanie Front Immunol Immunology Insects and mammals share evolutionary conserved innate immune responses to maintain intestinal homeostasis. We investigated whether the larvae of the greater wax moth Galleria mellonella may be used as an experimental organism to distinguish between symbiotic Bacteroides vulgatus and pathobiotic Escherichia coli, which are mammalian intestinal commensals. Oral application of the symbiont or pathobiont to G. mellonella resulted in clearly distinguishable innate immune responses that could be verified by analyzing similar innate immune components in mice in vivo and in vitro. The differential innate immune responses were initiated by the recognition of bacterial components via pattern recognition receptors. The pathobiont detection resulted in increased expression of reactive oxygen and nitrogen species related genes as well as antimicrobial peptide gene expression. In contrast, the treatment/application with symbiotic bacteria led to weakened immune responses in both mammalian and insect models. As symbionts and pathobionts play a crucial role in development of inflammatory bowel diseases, we hence suggest G. mellonella as a future replacement organism in inflammatory bowel disease research. Frontiers Media S.A. 2018-09-19 /pmc/articles/PMC6156133/ /pubmed/30283451 http://dx.doi.org/10.3389/fimmu.2018.02114 Text en Copyright © 2018 Lange, Schäfer, Bender, Steimle, Beier, Parusel and Frick. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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 | Immunology Lange, Anna Schäfer, Andrea Bender, Annika Steimle, Alexander Beier, Sina Parusel, Raphael Frick, Julia-Stefanie Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title | Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title_full | Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title_fullStr | Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title_full_unstemmed | Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title_short | Galleria mellonella: A Novel Invertebrate Model to Distinguish Intestinal Symbionts From Pathobionts |
title_sort | galleria mellonella: a novel invertebrate model to distinguish intestinal symbionts from pathobionts |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156133/ https://www.ncbi.nlm.nih.gov/pubmed/30283451 http://dx.doi.org/10.3389/fimmu.2018.02114 |
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