A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.

The yeast-to-hypha transition is tightly associated with pathogenicity in many human pathogenic fungi, such as the model fungal pathogen Cryptococcus neoformans, which is responsible for approximately 180,000 deaths annually. In this pathogen, the yeast-to-hypha transition can be initiated by distin...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Pengjie Hu, Hao Ding, Lan Shen, Guang-Jun He, Huimin Liu, Xiuyun Tian, Changyu Tao, Xiangzheng Bai, Jingnan Liang, Cheng Jin, Xinping Xu, Ence Yang, Linqi Wang
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
Acceso en línea:https://doaj.org/article/960598d8e0284623ad635d6dda2be985
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:960598d8e0284623ad635d6dda2be985
record_format dspace
spelling oai:doaj.org-article:960598d8e0284623ad635d6dda2be9852021-12-02T20:03:32ZA unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.1553-73901553-740410.1371/journal.pgen.1009817https://doaj.org/article/960598d8e0284623ad635d6dda2be9852021-10-01T00:00:00Zhttps://doi.org/10.1371/journal.pgen.1009817https://doaj.org/toc/1553-7390https://doaj.org/toc/1553-7404The yeast-to-hypha transition is tightly associated with pathogenicity in many human pathogenic fungi, such as the model fungal pathogen Cryptococcus neoformans, which is responsible for approximately 180,000 deaths annually. In this pathogen, the yeast-to-hypha transition can be initiated by distinct stimuli: mating stimulation or glucosamine (GlcN), the monomer of cell wall chitosan. However, it remains poorly understood how the signal specificity for Cryptococcus morphological transition by disparate stimuli is ensured. Here, by integrating temporal expression signature analysis and phenome-based clustering evaluation, we demonstrate that GlcN specifically triggers a unique cellular response, which acts as a critical determinant underlying the activation of GlcN-induced filamentation (GIF). This cellular response is defined by an unusually hyperactive cell wall synthesis that is highly ATP-consuming. A novel cell surface protein Gis1 was identified as the indicator molecule for the GlcN-induced cell wall response. The Mpk1-directed cell wall pathway critically bridges global cell wall gene induction and intracellular ATP supply, ensuring the Gis1-dependent cell wall response and the stimulus specificity of GIF. We further reveal that the ability of Mpk1 to coordinate the cell wall response and GIF activation is conserved in different Cryptococcus pathogens. Phosphoproteomics-based profiling together with genetic and phenotypic analysis revealed that the Mpk1 kinase mediates the regulatory specificity of GIF through a coordinated downstream regulatory network centered on Skn7 and Crz1. Overall, our findings discover an unprecedented and conserved cell wall biosynthesis-dependent fungal differentiation commitment mechanism, which enables the signal specificity of pathogenicity-related dimorphism induced by GlcN in Cryptococcus pathogens.Pengjie HuHao DingLan ShenGuang-Jun HeHuimin LiuXiuyun TianChangyu TaoXiangzheng BaiJingnan LiangCheng JinXinping XuEnce YangLinqi WangPublic Library of Science (PLoS)articleGeneticsQH426-470ENPLoS Genetics, Vol 17, Iss 10, p e1009817 (2021)
institution DOAJ
collection DOAJ
language EN
topic Genetics
QH426-470
spellingShingle Genetics
QH426-470
Pengjie Hu
Hao Ding
Lan Shen
Guang-Jun He
Huimin Liu
Xiuyun Tian
Changyu Tao
Xiangzheng Bai
Jingnan Liang
Cheng Jin
Xinping Xu
Ence Yang
Linqi Wang
A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
description The yeast-to-hypha transition is tightly associated with pathogenicity in many human pathogenic fungi, such as the model fungal pathogen Cryptococcus neoformans, which is responsible for approximately 180,000 deaths annually. In this pathogen, the yeast-to-hypha transition can be initiated by distinct stimuli: mating stimulation or glucosamine (GlcN), the monomer of cell wall chitosan. However, it remains poorly understood how the signal specificity for Cryptococcus morphological transition by disparate stimuli is ensured. Here, by integrating temporal expression signature analysis and phenome-based clustering evaluation, we demonstrate that GlcN specifically triggers a unique cellular response, which acts as a critical determinant underlying the activation of GlcN-induced filamentation (GIF). This cellular response is defined by an unusually hyperactive cell wall synthesis that is highly ATP-consuming. A novel cell surface protein Gis1 was identified as the indicator molecule for the GlcN-induced cell wall response. The Mpk1-directed cell wall pathway critically bridges global cell wall gene induction and intracellular ATP supply, ensuring the Gis1-dependent cell wall response and the stimulus specificity of GIF. We further reveal that the ability of Mpk1 to coordinate the cell wall response and GIF activation is conserved in different Cryptococcus pathogens. Phosphoproteomics-based profiling together with genetic and phenotypic analysis revealed that the Mpk1 kinase mediates the regulatory specificity of GIF through a coordinated downstream regulatory network centered on Skn7 and Crz1. Overall, our findings discover an unprecedented and conserved cell wall biosynthesis-dependent fungal differentiation commitment mechanism, which enables the signal specificity of pathogenicity-related dimorphism induced by GlcN in Cryptococcus pathogens.
format article
author Pengjie Hu
Hao Ding
Lan Shen
Guang-Jun He
Huimin Liu
Xiuyun Tian
Changyu Tao
Xiangzheng Bai
Jingnan Liang
Cheng Jin
Xinping Xu
Ence Yang
Linqi Wang
author_facet Pengjie Hu
Hao Ding
Lan Shen
Guang-Jun He
Huimin Liu
Xiuyun Tian
Changyu Tao
Xiangzheng Bai
Jingnan Liang
Cheng Jin
Xinping Xu
Ence Yang
Linqi Wang
author_sort Pengjie Hu
title A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
title_short A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
title_full A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
title_fullStr A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
title_full_unstemmed A unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
title_sort unique cell wall synthetic response evoked by glucosamine determines pathogenicity-associated fungal cellular differentiation.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/960598d8e0284623ad635d6dda2be985
work_keys_str_mv AT pengjiehu auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT haoding auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT lanshen auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT guangjunhe auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT huiminliu auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xiuyuntian auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT changyutao auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xiangzhengbai auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT jingnanliang auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT chengjin auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xinpingxu auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT enceyang auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT linqiwang auniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT pengjiehu uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT haoding uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT lanshen uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT guangjunhe uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT huiminliu uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xiuyuntian uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT changyutao uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xiangzhengbai uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT jingnanliang uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT chengjin uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT xinpingxu uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT enceyang uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
AT linqiwang uniquecellwallsyntheticresponseevokedbyglucosaminedeterminespathogenicityassociatedfungalcellulardifferentiation
_version_ 1718375673630818304