School of Biosciences, Institute of Microbiology and Infection, University of Birmingham, Birmingham, United Kingdom.
School of Biosciences, Institute of Microbiology and Infection, University of Birmingham, Birmingham, United Kingdom.
Adv Appl Microbiol. 2018;102:117-157. doi: 10.1016/bs.aambs.2017.10.002. Epub 2017 Nov 22.
Fungi, algae, plants, protozoa, and bacteria are all known to form spores, especially hardy and ubiquitous propagation structures that are also often the infectious agents of diseases. Spores can survive for thousands of years, frozen in the permafrost (Kochkina et al., 2012), with the oldest viable spores extracted after 250 million years from salt crystals (Vreeland, Rosenzweig, & Powers, 2000). Their resistance to high levels of UV, desiccation, pressure, heat, and cold enables the survival of spores in the harshest conditions (Setlow, 2016). For example, Bacillus subtilis spores can survive and remain viable after experiencing conditions similar to those on Mars (Horneck et al., 2012). Spores are disseminated through environmental factors. Wind, water, or animal carriage allow spores to be spread ubiquitously throughout the environment. Spores will break dormancy and begin to germinate once exposed to favorable conditions. Germination is the mechanism that converts the spore from a dormant biological organism to one that grows vegetatively and is capable of either sexual or asexual reproduction. The process of germination has been well studied in plants, moss, bacteria, and many fungi (Hohe & Reski, 2005; Huang & Hull, 2017; Vesty et al., 2016). Unfortunately, information on the complex signaling involved in the regulation of germination, particularly in fungi remains lacking. This chapter will discuss germination of fungal spores covering our current understanding of the regulation, signaling, outcomes, and implications of germination of pathogenic fungal spores. Owing to the morphological similarities between the spore-hyphal and yeast-hyphal transition and their relevance for disease progression, relevant aspects of fungal dimorphism will be discussed alongside spore germination in this chapter.
真菌、藻类、植物、原生动物和细菌都被认为能形成孢子,特别是具有很强抗逆性和无处不在的繁殖结构,而且这些孢子通常也是疾病的病原体。孢子可以存活数千年,被冻结在永久冻土层中(Kochkina 等人,2012 年),从盐晶体中提取的最古老的有活力的孢子已有 2.5 亿年的历史(Vreeland、Rosenzweig 和 Powers,2000 年)。它们对高水平紫外线、干燥、压力、高温和低温的抗性使孢子能够在最恶劣的条件下存活(Setlow,2016 年)。例如,枯草芽孢杆菌孢子在经历类似于火星条件后仍能存活并保持活力(Horneck 等人,2012 年)。孢子通过环境因素传播。风和水或动物运输使孢子在整个环境中广泛传播。一旦暴露在有利条件下,孢子就会打破休眠并开始发芽。发芽是将孢子从休眠的生物有机体转化为能够进行有性或无性繁殖的营养生长的机制。发芽过程在植物、苔藓、细菌和许多真菌中都得到了很好的研究(Hohe 和 Reski,2005 年;Huang 和 Hull,2017 年;Vesty 等人,2016 年)。不幸的是,关于调节发芽所涉及的复杂信号的信息,特别是在真菌中仍然缺乏。本章将讨论真菌孢子的发芽,涵盖我们对致病性真菌孢子发芽的调节、信号、结果和影响的现有认识。由于孢子-菌丝和酵母-菌丝转化之间的形态相似性以及它们与疾病进展的相关性,本章将与孢子发芽一起讨论真菌二态性的相关方面。