Cargando…
The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi
Fungal infections, widespread throughout the world, affect a broad range of life forms, including agriculturally relevant plants, humans, and insects. In defending against fungal infections, the fruit fly Drosophila melanogaster employs the Toll pathway to induce a large number of immune peptides. S...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989431/ https://www.ncbi.nlm.nih.gov/pubmed/32038657 http://dx.doi.org/10.3389/fimmu.2020.00009 |
_version_ | 1783492396936331264 |
---|---|
author | Cohen, Lianne B. Lindsay, Scott A. Xu, Yangyang Lin, Samuel J. H. Wasserman, Steven A. |
author_facet | Cohen, Lianne B. Lindsay, Scott A. Xu, Yangyang Lin, Samuel J. H. Wasserman, Steven A. |
author_sort | Cohen, Lianne B. |
collection | PubMed |
description | Fungal infections, widespread throughout the world, affect a broad range of life forms, including agriculturally relevant plants, humans, and insects. In defending against fungal infections, the fruit fly Drosophila melanogaster employs the Toll pathway to induce a large number of immune peptides. Some have been investigated, such as the antimicrobial peptides (AMPs) and Bomanins (Boms); many, however, remain uncharacterized. Here, we examine the role in innate immunity of two related peptides, Daisho1 and Daisho2 (formerly IM4 and IM14, respectively), found in hemolymph following Toll pathway activation. By generating a CRISPR/Cas9 knockout of both genes, Δdaisho, we find that the Daisho peptides are required for defense against a subset of filamentous fungi, including Fusarium oxysporum, but not other Toll-inducible pathogens, such as Enterococcus faecalis and Candida glabrata. Analysis of null alleles and transgenes revealed that the two daisho genes are each required for defense, although their functions partially overlap. Generating and assaying a genomic epitope-tagged Daisho2 construct, we detected interaction in vitro of Daisho2 peptide in hemolymph with the hyphae of F. oxysporum. Together, these results identify the Daisho peptides as a new class of innate immune effectors with humoral activity against a select set of filamentous fungi. |
format | Online Article Text |
id | pubmed-6989431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69894312020-02-07 The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi Cohen, Lianne B. Lindsay, Scott A. Xu, Yangyang Lin, Samuel J. H. Wasserman, Steven A. Front Immunol Immunology Fungal infections, widespread throughout the world, affect a broad range of life forms, including agriculturally relevant plants, humans, and insects. In defending against fungal infections, the fruit fly Drosophila melanogaster employs the Toll pathway to induce a large number of immune peptides. Some have been investigated, such as the antimicrobial peptides (AMPs) and Bomanins (Boms); many, however, remain uncharacterized. Here, we examine the role in innate immunity of two related peptides, Daisho1 and Daisho2 (formerly IM4 and IM14, respectively), found in hemolymph following Toll pathway activation. By generating a CRISPR/Cas9 knockout of both genes, Δdaisho, we find that the Daisho peptides are required for defense against a subset of filamentous fungi, including Fusarium oxysporum, but not other Toll-inducible pathogens, such as Enterococcus faecalis and Candida glabrata. Analysis of null alleles and transgenes revealed that the two daisho genes are each required for defense, although their functions partially overlap. Generating and assaying a genomic epitope-tagged Daisho2 construct, we detected interaction in vitro of Daisho2 peptide in hemolymph with the hyphae of F. oxysporum. Together, these results identify the Daisho peptides as a new class of innate immune effectors with humoral activity against a select set of filamentous fungi. Frontiers Media S.A. 2020-01-23 /pmc/articles/PMC6989431/ /pubmed/32038657 http://dx.doi.org/10.3389/fimmu.2020.00009 Text en Copyright © 2020 Cohen, Lindsay, Xu, Lin and Wasserman. 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 Cohen, Lianne B. Lindsay, Scott A. Xu, Yangyang Lin, Samuel J. H. Wasserman, Steven A. The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title | The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title_full | The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title_fullStr | The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title_full_unstemmed | The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title_short | The Daisho Peptides Mediate Drosophila Defense Against a Subset of Filamentous Fungi |
title_sort | daisho peptides mediate drosophila defense against a subset of filamentous fungi |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989431/ https://www.ncbi.nlm.nih.gov/pubmed/32038657 http://dx.doi.org/10.3389/fimmu.2020.00009 |
work_keys_str_mv | AT cohenlianneb thedaishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT lindsayscotta thedaishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT xuyangyang thedaishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT linsamueljh thedaishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT wassermanstevena thedaishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT cohenlianneb daishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT lindsayscotta daishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT xuyangyang daishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT linsamueljh daishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi AT wassermanstevena daishopeptidesmediatedrosophiladefenseagainstasubsetoffilamentousfungi |