致病性念珠菌种副性生殖的遗传和环境控制。

IF 7.8 1区 生物学 Q1 MICROBIOLOGY
Chengjun Cao, Li Tao, Tianren Hu, Haiqing Chu, Austin M Perry, Clarissa J Nobile, Guanghua Huang
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引用次数: 0

摘要

念珠菌是引起粘膜念珠菌病和危及生命的侵袭性感染的主要酵母菌病原体。大多数念珠菌物种,包括白色念珠菌,长期以来被认为是“不完美的”,因为缺乏完整的有性繁殖周期。自1999年在白色念珠菌中发现交配型位点以来,人们对这种生物以及几个系统发育密切相关的物种的有性生殖调控进行了深入的研究。性循环不仅对遗传和表型多样性的产生至关重要,而且还参与其他生物过程的调节,例如病原真菌的形态转变、生物膜发育和毒力。本文综述了致病性念珠菌的独特特征及其在生殖方面的遗传和环境调控机制。我们讨论了白色不透明切换和交配在念珠菌物种之间的关系,特别是在白色念珠菌。我们描述了在白色念珠菌和相关物种的性交配中涉及的环境因素、遗传调控因子和关键信号通路的最新发现。最后,我们讨论了几种假丝酵母物种的交配潜力和相关的调节机制,在这些物种中尚未观察到拟性生殖,并提出了一些关于拟性生殖的独特特征的开放性问题,这些问题应该在未来的研究中得到解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic and environmental control of parasexual reproduction in the pathogenic Candida species.

SUMMARYCandida species are major yeast pathogens that cause both mucosal candidiasis and life-threatening invasive infections. Most Candida species, including Candida albicans, have long been thought to be "imperfect" due to the lack of a complete sexual reproduction cycle. Since the discovery of the mating type-like locus in C. albicans in 1999, the regulation of (para)sexual reproduction has been intensively investigated in this organism as well as in several phylogenetically closely related species. The (para)sexual cycle is not only critical for the generation of genetic and phenotypic diversity but is also involved in the regulation of other biological processes, such as morphological transitions, biofilm development, and virulence in pathogenic fungi. In this review article, we focus on the unique characteristics and genetic and environmental regulatory mechanisms of parasexual reproduction in the pathogenic Candida species. We discuss the relationship between the white-opaque switching and mating in the Candida species, particularly in C. albicans. We describe recent findings on environmental factors, genetic regulators, and key signaling pathways involved in sexual mating in C. albicans and related species. Finally, we discuss the mating potential and associated regulatory machinery in several Candida species, where parasexual reproduction has not been observed and bring to light some open-ended questions regarding the unique features of parasexual reproduction that should be addressed in future studies in the field.

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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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