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A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish

Stable mutualism between a host and its resident bacteria requires a moderated immune response to control bacterial population size without eliciting excessive inflammation that could harm both partners. Little is known about the specific molecular mechanisms utilized by bacterial mutualists to temp...

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Autores principales: Rolig, Annah S, Sweeney, Emily Goers, Kaye, Lila E, DeSantis, Michael D, Perkins, Arden, Banse, Allison V, Hamilton, M Kristina, Guillemin, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219842/
https://www.ncbi.nlm.nih.gov/pubmed/30398151
http://dx.doi.org/10.7554/eLife.37172
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author Rolig, Annah S
Sweeney, Emily Goers
Kaye, Lila E
DeSantis, Michael D
Perkins, Arden
Banse, Allison V
Hamilton, M Kristina
Guillemin, Karen
author_facet Rolig, Annah S
Sweeney, Emily Goers
Kaye, Lila E
DeSantis, Michael D
Perkins, Arden
Banse, Allison V
Hamilton, M Kristina
Guillemin, Karen
author_sort Rolig, Annah S
collection PubMed
description Stable mutualism between a host and its resident bacteria requires a moderated immune response to control bacterial population size without eliciting excessive inflammation that could harm both partners. Little is known about the specific molecular mechanisms utilized by bacterial mutualists to temper their hosts’ responses and protect themselves from aggressive immune attack. Using a gnotobiotic larval zebrafish model, we identified an Aeromonas secreted immunomodulatory protein, AimA. AimA is required during colonization to prevent intestinal inflammation that simultaneously compromises both bacterial and host survival. Administration of exogenous AimA prevents excessive intestinal neutrophil accumulation and protects against septic shock in models of both bacterially and chemically induced intestinal inflammation. We determined the molecular structure of AimA, which revealed two related calycin-like domains with structural similarity to the mammalian immune modulatory protein, lipocalin-2. As a secreted bacterial protein required by both partners for optimal fitness, AimA is an exemplar bacterial mutualism factor.
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spelling pubmed-62198422018-11-09 A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish Rolig, Annah S Sweeney, Emily Goers Kaye, Lila E DeSantis, Michael D Perkins, Arden Banse, Allison V Hamilton, M Kristina Guillemin, Karen eLife Immunology and Inflammation Stable mutualism between a host and its resident bacteria requires a moderated immune response to control bacterial population size without eliciting excessive inflammation that could harm both partners. Little is known about the specific molecular mechanisms utilized by bacterial mutualists to temper their hosts’ responses and protect themselves from aggressive immune attack. Using a gnotobiotic larval zebrafish model, we identified an Aeromonas secreted immunomodulatory protein, AimA. AimA is required during colonization to prevent intestinal inflammation that simultaneously compromises both bacterial and host survival. Administration of exogenous AimA prevents excessive intestinal neutrophil accumulation and protects against septic shock in models of both bacterially and chemically induced intestinal inflammation. We determined the molecular structure of AimA, which revealed two related calycin-like domains with structural similarity to the mammalian immune modulatory protein, lipocalin-2. As a secreted bacterial protein required by both partners for optimal fitness, AimA is an exemplar bacterial mutualism factor. eLife Sciences Publications, Ltd 2018-11-06 /pmc/articles/PMC6219842/ /pubmed/30398151 http://dx.doi.org/10.7554/eLife.37172 Text en © 2018, Rolig et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Immunology and Inflammation
Rolig, Annah S
Sweeney, Emily Goers
Kaye, Lila E
DeSantis, Michael D
Perkins, Arden
Banse, Allison V
Hamilton, M Kristina
Guillemin, Karen
A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title_full A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title_fullStr A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title_full_unstemmed A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title_short A bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
title_sort bacterial immunomodulatory protein with lipocalin-like domains facilitates host–bacteria mutualism in larval zebrafish
topic Immunology and Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219842/
https://www.ncbi.nlm.nih.gov/pubmed/30398151
http://dx.doi.org/10.7554/eLife.37172
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