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Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis
Skin immunity protects animals from airborne pathogen infection. Unlike mammals, arthropods, including insects, undergo periodic ecdysis to grow and develop. Newly molted insects emerge with unsclerotized thin cuticles but successfully escape pathogenic infections during the post-molt period. Here w...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671992/ https://www.ncbi.nlm.nih.gov/pubmed/29163517 http://dx.doi.org/10.3389/fimmu.2017.01445 |
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author | Zhang, Jie Huang, Wuren Yuan, Chuanfei Lu, Yuzhen Yang, Bing Wang, Cheng-Yuan Zhang, Peng Dobens, Leonard Zou, Zhen Wang, Chengshu Ling, Erjun |
author_facet | Zhang, Jie Huang, Wuren Yuan, Chuanfei Lu, Yuzhen Yang, Bing Wang, Cheng-Yuan Zhang, Peng Dobens, Leonard Zou, Zhen Wang, Chengshu Ling, Erjun |
author_sort | Zhang, Jie |
collection | PubMed |
description | Skin immunity protects animals from airborne pathogen infection. Unlike mammals, arthropods, including insects, undergo periodic ecdysis to grow and develop. Newly molted insects emerge with unsclerotized thin cuticles but successfully escape pathogenic infections during the post-molt period. Here we show that prophenoloxidases (PPOs) in molting fluids remain bioactive on the integument and impede fungal infection after ecdysis. We found that the purified plasma PPOs or recombinant PPOs could effectively bind to fungal spores (conidia) by targeting the cell wall components chitin and β-1,3-glucan. Pretreatment of the spores of the fungal pathogen Beauveria bassiana with PPOs increased spore hydrophilicity and reduced spore adhesion activity, resulting in a significant decrease in virulence as compared with mock infection. We also identified a spore-secreted protease BPS8, a member of peptidase S8 family of protease that degrade PPOs at high levels to benefit fungal infection, but which at lower doses activate PPOs to inhibit spore germination after melanization. These data indicate that insects have evolved a distinct strategy of ex vivo immunity to survive pathogen infections after ecdysis using PPOs in molting fluids retained on the underdeveloped and tender integument of newly molted insects for protection against airborne fungal infection. |
format | Online Article Text |
id | pubmed-5671992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56719922017-11-21 Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis Zhang, Jie Huang, Wuren Yuan, Chuanfei Lu, Yuzhen Yang, Bing Wang, Cheng-Yuan Zhang, Peng Dobens, Leonard Zou, Zhen Wang, Chengshu Ling, Erjun Front Immunol Immunology Skin immunity protects animals from airborne pathogen infection. Unlike mammals, arthropods, including insects, undergo periodic ecdysis to grow and develop. Newly molted insects emerge with unsclerotized thin cuticles but successfully escape pathogenic infections during the post-molt period. Here we show that prophenoloxidases (PPOs) in molting fluids remain bioactive on the integument and impede fungal infection after ecdysis. We found that the purified plasma PPOs or recombinant PPOs could effectively bind to fungal spores (conidia) by targeting the cell wall components chitin and β-1,3-glucan. Pretreatment of the spores of the fungal pathogen Beauveria bassiana with PPOs increased spore hydrophilicity and reduced spore adhesion activity, resulting in a significant decrease in virulence as compared with mock infection. We also identified a spore-secreted protease BPS8, a member of peptidase S8 family of protease that degrade PPOs at high levels to benefit fungal infection, but which at lower doses activate PPOs to inhibit spore germination after melanization. These data indicate that insects have evolved a distinct strategy of ex vivo immunity to survive pathogen infections after ecdysis using PPOs in molting fluids retained on the underdeveloped and tender integument of newly molted insects for protection against airborne fungal infection. Frontiers Media S.A. 2017-11-01 /pmc/articles/PMC5671992/ /pubmed/29163517 http://dx.doi.org/10.3389/fimmu.2017.01445 Text en Copyright © 2017 Zhang, Huang, Yuan, Lu, Yang, Wang, Zhang, Dobens, Zou, Wang and Ling. 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 Zhang, Jie Huang, Wuren Yuan, Chuanfei Lu, Yuzhen Yang, Bing Wang, Cheng-Yuan Zhang, Peng Dobens, Leonard Zou, Zhen Wang, Chengshu Ling, Erjun Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title | Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title_full | Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title_fullStr | Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title_full_unstemmed | Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title_short | Prophenoloxidase-Mediated Ex Vivo Immunity to Delay Fungal Infection after Insect Ecdysis |
title_sort | prophenoloxidase-mediated ex vivo immunity to delay fungal infection after insect ecdysis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671992/ https://www.ncbi.nlm.nih.gov/pubmed/29163517 http://dx.doi.org/10.3389/fimmu.2017.01445 |
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