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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...

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Autores principales: Zhang, Jie, Huang, Wuren, Yuan, Chuanfei, Lu, Yuzhen, Yang, Bing, Wang, Cheng-Yuan, Zhang, Peng, Dobens, Leonard, Zou, Zhen, Wang, Chengshu, Ling, Erjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
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.
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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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