Department of Mycology, Translational Mycology Group, Institut Pasteur, Université Paris Cité, National Reference Center for Invasive Mycoses and Antifungals, Paris, France.
Laboratoire de parrasitologie-Mycologie, Hôpital Saint-Louis, Paris, France.
Methods Mol Biol. 2024;2775:349-358. doi: 10.1007/978-1-0716-3722-7_22.
Cryptococcus neoformans is the second major cause of death in patients with HIV. During a latent infection, this pathogenic fungus survives in the host for years without causing symptoms of active disease. Upon favorable conditions, such as immunosuppression due to HIV infection, or other conditions (steroid use or organ transplantation), the yeast may reactivate and cause active cryptococcosis. Hence, dormancy is an important phase in the pathogenesis of C. neoformans. Additionally, C. neoformans also persists during antifungal treatment and causes disease recurrence, which is a major medical problem, especially in low- and middle-income countries. To survive in the host, yeast cells must react to the stresses they are exposed to and generate a cellular response that is favorable for yeast survival. A prominent strategy used by C. neoformans to combat challenging surroundings is dormancy, which may translate into a viable, but nonculturable phenotype (VBNC). This chapter describes an in vitro protocol to generate and characterize dormant Cryptococci.
新型隐球菌是 HIV 患者的第二大致死原因。在潜伏感染期间,这种致病真菌在宿主体内存活数年而不引起显性疾病的症状。在有利条件下,如 HIV 感染引起的免疫抑制,或其他条件(使用类固醇或器官移植)下,酵母可能重新激活并导致显性隐球菌病。因此,休眠是新型隐球菌发病机制中的一个重要阶段。此外,新型隐球菌在抗真菌治疗期间也会持续存在并导致疾病复发,这是一个主要的医学问题,特别是在中低收入国家。为了在宿主体内存活,酵母细胞必须对其所暴露的应激作出反应,并产生有利于酵母生存的细胞反应。新型隐球菌用来应对挑战性环境的一个突出策略是休眠,这可能转化为一种可行但不可培养的表型(VBNC)。本章描述了一种体外方案,用于生成和表征休眠隐球菌。