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Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate
Detection of pathogens by all living organisms is the primary step needed to implement a coherent and efficient immune response. This implies a mediation by different soluble and/or membrane-anchored proteins related to innate immune receptors called PRRs (pattern-recognition receptors) to trigger i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633686/ https://www.ncbi.nlm.nih.gov/pubmed/29051762 http://dx.doi.org/10.3389/fimmu.2017.01249 |
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author | Tetreau, Guillaume Pinaud, Silvain Portet, Anaïs Galinier, Richard Gourbal, Benjamin Duval, David |
author_facet | Tetreau, Guillaume Pinaud, Silvain Portet, Anaïs Galinier, Richard Gourbal, Benjamin Duval, David |
author_sort | Tetreau, Guillaume |
collection | PubMed |
description | Detection of pathogens by all living organisms is the primary step needed to implement a coherent and efficient immune response. This implies a mediation by different soluble and/or membrane-anchored proteins related to innate immune receptors called PRRs (pattern-recognition receptors) to trigger immune signaling pathways. In most invertebrates, their roles have been inferred by analogy to those already characterized in vertebrate homologs. Despite the induction of their gene expression upon challenge and the presence of structural domains associated with the detection of pathogen-associated molecular patterns in their sequence, their exact role in the induction of immune response and their binding capacity still remain to be demonstrated. To this purpose, we developed a fast interactome approach, usable on any host–pathogen couple, to identify soluble proteins capable of directly or indirectly detecting the presence of pathogens. To investigate the molecular basis of immune recognition specificity, different pathogens (Gram-positive bacterium, Micrococcus luteus; Gram-negative, Escherichia coli; yeast, Saccharomyces cerevisiae; and metazoan parasites, Echinostoma caproni or Schistosoma mansoni) were exposed to hemocyte-free hemolymph from the gastropod Biomphalaria glabrata. Twenty-three different proteins bound to pathogens were identified and grouped into three different categories based on their primary function. Each pathogen was recognized by a specific but overlapping set of circulating proteins in mollusk’s hemolymph. While known PRRs such as C-type lectins were identified, other proteins not known to be primarily involved in pathogen recognition were found, including actin, tubulin, collagen, and hemoglobin. Confocal microscopy and specific fluorescent labeling revealed that extracellular actin present in snail hemolymph was able to bind to yeasts and induce their clotting, a preliminary step for their elimination by the snail immune system. Aerolysin-like proteins (named biomphalysins) were the only ones involved in the recognition of all the five pathogens tested, suggesting a sentinel role of these horizontally acquired toxins. These findings highlight the diversity and complexity of a highly specific innate immune sensing system. It paves the way for the use of such approach on a wide range of host–pathogen systems to provide new insights into the specificity and diversity of immune recognition by innate immune systems. |
format | Online Article Text |
id | pubmed-5633686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56336862017-10-19 Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate Tetreau, Guillaume Pinaud, Silvain Portet, Anaïs Galinier, Richard Gourbal, Benjamin Duval, David Front Immunol Immunology Detection of pathogens by all living organisms is the primary step needed to implement a coherent and efficient immune response. This implies a mediation by different soluble and/or membrane-anchored proteins related to innate immune receptors called PRRs (pattern-recognition receptors) to trigger immune signaling pathways. In most invertebrates, their roles have been inferred by analogy to those already characterized in vertebrate homologs. Despite the induction of their gene expression upon challenge and the presence of structural domains associated with the detection of pathogen-associated molecular patterns in their sequence, their exact role in the induction of immune response and their binding capacity still remain to be demonstrated. To this purpose, we developed a fast interactome approach, usable on any host–pathogen couple, to identify soluble proteins capable of directly or indirectly detecting the presence of pathogens. To investigate the molecular basis of immune recognition specificity, different pathogens (Gram-positive bacterium, Micrococcus luteus; Gram-negative, Escherichia coli; yeast, Saccharomyces cerevisiae; and metazoan parasites, Echinostoma caproni or Schistosoma mansoni) were exposed to hemocyte-free hemolymph from the gastropod Biomphalaria glabrata. Twenty-three different proteins bound to pathogens were identified and grouped into three different categories based on their primary function. Each pathogen was recognized by a specific but overlapping set of circulating proteins in mollusk’s hemolymph. While known PRRs such as C-type lectins were identified, other proteins not known to be primarily involved in pathogen recognition were found, including actin, tubulin, collagen, and hemoglobin. Confocal microscopy and specific fluorescent labeling revealed that extracellular actin present in snail hemolymph was able to bind to yeasts and induce their clotting, a preliminary step for their elimination by the snail immune system. Aerolysin-like proteins (named biomphalysins) were the only ones involved in the recognition of all the five pathogens tested, suggesting a sentinel role of these horizontally acquired toxins. These findings highlight the diversity and complexity of a highly specific innate immune sensing system. It paves the way for the use of such approach on a wide range of host–pathogen systems to provide new insights into the specificity and diversity of immune recognition by innate immune systems. Frontiers Media S.A. 2017-10-05 /pmc/articles/PMC5633686/ /pubmed/29051762 http://dx.doi.org/10.3389/fimmu.2017.01249 Text en Copyright © 2017 Tetreau, Pinaud, Portet, Galinier, Gourbal and Duval. 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) or licensor 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 Tetreau, Guillaume Pinaud, Silvain Portet, Anaïs Galinier, Richard Gourbal, Benjamin Duval, David Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title | Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title_full | Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title_fullStr | Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title_full_unstemmed | Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title_short | Specific Pathogen Recognition by Multiple Innate Immune Sensors in an Invertebrate |
title_sort | specific pathogen recognition by multiple innate immune sensors in an invertebrate |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633686/ https://www.ncbi.nlm.nih.gov/pubmed/29051762 http://dx.doi.org/10.3389/fimmu.2017.01249 |
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