Cargando…

The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores

Higher fungi can rapidly produce large numbers of spores suitable for aerial dispersal. The efficiency of the dispersal and spore resilience to abiotic stresses correlate with their hydrophobicity provided by the unique amphiphilic and superior surface-active proteins–hydrophobins (HFBs)–that self-a...

Descripción completa

Detalles Bibliográficos
Autores principales: Cai, Feng, Zhao, Zheng, Gao, Renwei, Chen, Peijie, Ding, Mingyue, Jiang, Siqi, Fu, Zhifei, Xu, Pingyong, Chenthamara, Komal, Shen, Qirong, Bayram Akcapinar, Günseli, Druzhinina, Irina S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635391/
https://www.ncbi.nlm.nih.gov/pubmed/34788288
http://dx.doi.org/10.1371/journal.pgen.1009924
_version_ 1784608293555011584
author Cai, Feng
Zhao, Zheng
Gao, Renwei
Chen, Peijie
Ding, Mingyue
Jiang, Siqi
Fu, Zhifei
Xu, Pingyong
Chenthamara, Komal
Shen, Qirong
Bayram Akcapinar, Günseli
Druzhinina, Irina S.
author_facet Cai, Feng
Zhao, Zheng
Gao, Renwei
Chen, Peijie
Ding, Mingyue
Jiang, Siqi
Fu, Zhifei
Xu, Pingyong
Chenthamara, Komal
Shen, Qirong
Bayram Akcapinar, Günseli
Druzhinina, Irina S.
author_sort Cai, Feng
collection PubMed
description Higher fungi can rapidly produce large numbers of spores suitable for aerial dispersal. The efficiency of the dispersal and spore resilience to abiotic stresses correlate with their hydrophobicity provided by the unique amphiphilic and superior surface-active proteins–hydrophobins (HFBs)–that self-assemble at hydrophobic/hydrophilic interfaces and thus modulate surface properties. Using the HFB-enriched mold Trichoderma (Hypocreales, Ascomycota) and the HFB-free yeast Pichia pastoris (Saccharomycetales, Ascomycota), we revealed that the rapid release of HFBs by aerial hyphae shortly prior to conidiation is associated with their intracellular accumulation in vacuoles and/or lipid-enriched organelles. The occasional internalization of the latter organelles in vacuoles can provide the hydrophobic/hydrophilic interface for the assembly of HFB layers and thus result in the formation of HFB-enriched vesicles and vacuolar multicisternal structures (VMSs) putatively lined up by HFBs. These HFB-enriched vesicles and VMSs can become fused in large tonoplast-like organelles or move to the periplasm for secretion. The tonoplast-like structures can contribute to the maintenance of turgor pressure in aerial hyphae supporting the erection of sporogenic structures (e.g., conidiophores) and provide intracellular force to squeeze out HFB-enriched vesicles and VMSs from the periplasm through the cell wall. We also show that the secretion of HFBs occurs prior to the conidiation and reveal that the even spore coating of HFBs deposited in the extracellular matrix requires microscopic water droplets that can be either guttated by the hyphae or obtained from the environment. Furthermore, we demonstrate that at least one HFB, HFB4 in T. guizhouense, is produced and secreted by wetted spores. We show that this protein possibly controls spore dormancy and contributes to the water sensing mechanism required for the detection of germination conditions. Thus, intracellular HFBs have a range of pleiotropic functions in aerial hyphae and spores and are essential for fungal development and fitness.
format Online
Article
Text
id pubmed-8635391
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-86353912021-12-02 The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores Cai, Feng Zhao, Zheng Gao, Renwei Chen, Peijie Ding, Mingyue Jiang, Siqi Fu, Zhifei Xu, Pingyong Chenthamara, Komal Shen, Qirong Bayram Akcapinar, Günseli Druzhinina, Irina S. PLoS Genet Research Article Higher fungi can rapidly produce large numbers of spores suitable for aerial dispersal. The efficiency of the dispersal and spore resilience to abiotic stresses correlate with their hydrophobicity provided by the unique amphiphilic and superior surface-active proteins–hydrophobins (HFBs)–that self-assemble at hydrophobic/hydrophilic interfaces and thus modulate surface properties. Using the HFB-enriched mold Trichoderma (Hypocreales, Ascomycota) and the HFB-free yeast Pichia pastoris (Saccharomycetales, Ascomycota), we revealed that the rapid release of HFBs by aerial hyphae shortly prior to conidiation is associated with their intracellular accumulation in vacuoles and/or lipid-enriched organelles. The occasional internalization of the latter organelles in vacuoles can provide the hydrophobic/hydrophilic interface for the assembly of HFB layers and thus result in the formation of HFB-enriched vesicles and vacuolar multicisternal structures (VMSs) putatively lined up by HFBs. These HFB-enriched vesicles and VMSs can become fused in large tonoplast-like organelles or move to the periplasm for secretion. The tonoplast-like structures can contribute to the maintenance of turgor pressure in aerial hyphae supporting the erection of sporogenic structures (e.g., conidiophores) and provide intracellular force to squeeze out HFB-enriched vesicles and VMSs from the periplasm through the cell wall. We also show that the secretion of HFBs occurs prior to the conidiation and reveal that the even spore coating of HFBs deposited in the extracellular matrix requires microscopic water droplets that can be either guttated by the hyphae or obtained from the environment. Furthermore, we demonstrate that at least one HFB, HFB4 in T. guizhouense, is produced and secreted by wetted spores. We show that this protein possibly controls spore dormancy and contributes to the water sensing mechanism required for the detection of germination conditions. Thus, intracellular HFBs have a range of pleiotropic functions in aerial hyphae and spores and are essential for fungal development and fitness. Public Library of Science 2021-11-17 /pmc/articles/PMC8635391/ /pubmed/34788288 http://dx.doi.org/10.1371/journal.pgen.1009924 Text en © 2021 Cai et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cai, Feng
Zhao, Zheng
Gao, Renwei
Chen, Peijie
Ding, Mingyue
Jiang, Siqi
Fu, Zhifei
Xu, Pingyong
Chenthamara, Komal
Shen, Qirong
Bayram Akcapinar, Günseli
Druzhinina, Irina S.
The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title_full The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title_fullStr The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title_full_unstemmed The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title_short The pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
title_sort pleiotropic functions of intracellular hydrophobins in aerial hyphae and fungal spores
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635391/
https://www.ncbi.nlm.nih.gov/pubmed/34788288
http://dx.doi.org/10.1371/journal.pgen.1009924
work_keys_str_mv AT caifeng thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT zhaozheng thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT gaorenwei thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT chenpeijie thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT dingmingyue thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT jiangsiqi thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT fuzhifei thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT xupingyong thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT chenthamarakomal thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT shenqirong thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT bayramakcapinargunseli thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT druzhininairinas thepleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT caifeng pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT zhaozheng pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT gaorenwei pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT chenpeijie pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT dingmingyue pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT jiangsiqi pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT fuzhifei pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT xupingyong pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT chenthamarakomal pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT shenqirong pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT bayramakcapinargunseli pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores
AT druzhininairinas pleiotropicfunctionsofintracellularhydrophobinsinaerialhyphaeandfungalspores