Calcium: a central player in Cryptococcus biology

IF 5.7 2区 生物学 Q1 MYCOLOGY Fungal Biology Reviews Pub Date : 2021-06-01 DOI:10.1016/j.fbr.2021.03.004
Eamim D. Squizani , Júlia C.V. Reuwsaat , Heryk Motta , Andrea Tavanti , Livia Kmetzsch
{"title":"Calcium: a central player in Cryptococcus biology","authors":"Eamim D. Squizani ,&nbsp;Júlia C.V. Reuwsaat ,&nbsp;Heryk Motta ,&nbsp;Andrea Tavanti ,&nbsp;Livia Kmetzsch","doi":"10.1016/j.fbr.2021.03.004","DOIUrl":null,"url":null,"abstract":"<div><p><span>Adaptation to the host environment is crucial for fungal pathogenesis. Calcium (Ca</span><sup>2+</sup><span>) signals are essential for fungal cells<span> to respond rapidly to stress stimuli. In eukaryotic cells, Ca</span></span><sup>2+</sup> is the main intracellular secondary messenger and regulates a myriad of processes, including the cellular fitness of the fungal pathogen <span><em>Cryptococcus neoformans</em></span>. In this minireview, we highlight the main cryptococcal processes regulated by Ca<sup>2+</sup><span>. Moreover, we underline all the characterized proteins responsible for intracellular calcium homeostasis in this yeast, such as Ca</span><sup>2+</sup><span> transporters and binding proteins. These elements, in general, are essential for </span><em>C. neoformans’</em><span> growth and adaptation to the host environment, as well as to virulence mechanisms. We also revisit the specific traits of the calcineurin<span> signaling pathway in </span></span><em>C. neoformans</em>, which is the major pathway regulated by calcium and is crucial for yeast pathogenesis, adaptation, and growth at 37 °C. Notably, several Ca<sup>2+</sup>-related functions are highly conserved throughout fungal cells. Moreover, <em>C. neoformans</em> exhibits exclusive, significant features that are required for disease progression, thus attracting attention as feasible targets for antifungal drug development. Collectively, all the available data related to Ca<sup>2+</sup> processes clarify the complex role that Ca<sup>2+</sup><span> plays within cryptococcal cells, participating in host adaptation, transmigration, antifungal resistance, cell growth, and more.</span></p></div>","PeriodicalId":12563,"journal":{"name":"Fungal Biology Reviews","volume":"36 ","pages":"Pages 27-41"},"PeriodicalIF":5.7000,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.fbr.2021.03.004","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Biology Reviews","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1749461321000130","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 2

Abstract

Adaptation to the host environment is crucial for fungal pathogenesis. Calcium (Ca2+) signals are essential for fungal cells to respond rapidly to stress stimuli. In eukaryotic cells, Ca2+ is the main intracellular secondary messenger and regulates a myriad of processes, including the cellular fitness of the fungal pathogen Cryptococcus neoformans. In this minireview, we highlight the main cryptococcal processes regulated by Ca2+. Moreover, we underline all the characterized proteins responsible for intracellular calcium homeostasis in this yeast, such as Ca2+ transporters and binding proteins. These elements, in general, are essential for C. neoformans’ growth and adaptation to the host environment, as well as to virulence mechanisms. We also revisit the specific traits of the calcineurin signaling pathway in C. neoformans, which is the major pathway regulated by calcium and is crucial for yeast pathogenesis, adaptation, and growth at 37 °C. Notably, several Ca2+-related functions are highly conserved throughout fungal cells. Moreover, C. neoformans exhibits exclusive, significant features that are required for disease progression, thus attracting attention as feasible targets for antifungal drug development. Collectively, all the available data related to Ca2+ processes clarify the complex role that Ca2+ plays within cryptococcal cells, participating in host adaptation, transmigration, antifungal resistance, cell growth, and more.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
钙:隐球菌生物学的核心角色
对宿主环境的适应是真菌发病的关键。钙(Ca2+)信号是真菌细胞对应激刺激快速反应所必需的。在真核细胞中,Ca2+是主要的细胞内次级信使,并调节无数的过程,包括真菌病原体新隐球菌的细胞适应性。在这篇综述中,我们强调了Ca2+调节的主要隐球菌过程。此外,我们强调了在这种酵母中负责细胞内钙稳态的所有特征蛋白,如Ca2+转运蛋白和结合蛋白。总的来说,这些元素对于新生芽孢杆菌的生长和对宿主环境的适应以及毒力机制都是必不可少的。我们还回顾了C. neoformmans中钙调神经磷酸酶信号通路的具体特征,钙调神经磷酸酶信号通路是钙调节的主要途径,对酵母在37℃下的发病、适应和生长至关重要。值得注意的是,一些Ca2+相关功能在真菌细胞中高度保守。此外,新型C. neformmans表现出疾病进展所需的独特、重要特征,因此作为抗真菌药物开发的可行靶点引起了人们的关注。总的来说,所有与Ca2+过程相关的可用数据阐明了Ca2+在隐球菌细胞中发挥的复杂作用,参与宿主适应、转运、抗真菌抗性、细胞生长等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
10.60
自引率
0.00%
发文量
36
期刊介绍: Fungal Biology Reviews is an international reviews journal, owned by the British Mycological Society. Its objective is to provide a forum for high quality review articles within fungal biology. It covers all fields of fungal biology, whether fundamental or applied, including fungal diversity, ecology, evolution, physiology and ecophysiology, biochemistry, genetics and molecular biology, cell biology, interactions (symbiosis, pathogenesis etc), environmental aspects, biotechnology and taxonomy. It considers aspects of all organisms historically or recently recognized as fungi, including lichen-fungi, microsporidia, oomycetes, slime moulds, stramenopiles, and yeasts.
期刊最新文献
Editorial Board Lichen hydration, moisture dynamics and climate change: A synthesis of established methods and potential new directions Modes of action and inhibitory activity of Trichoderma species on potato and tomato pathogenic Phytophthora infestans: A review Editorial: Opening a new year with updated guidelines, a new cover, and thought-provoking insights in fungal biology Understanding cargo sorting and interactive effects of membrane vesicles in fungal phytopathogens: Current knowledge and research gaps
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1