Nielsen Kirsten, Heitman Joseph
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Adv Genet. 2007;57:143-73. doi: 10.1016/S0065-2660(06)57004-X.
Over the past decade, opportunistic fungal infectious diseases have increased in prevalence as the population of immunocompromised individuals escalated due to HIV/AIDS and immunosuppression associated with organ transplantation and cancer therapies. In the three predominant human pathogenic fungi (Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus), a unifying feature is that all three retained the machinery needed for sex, and yet all limit their access to sexual reproduction. While less well characterized, many of the other human pathogenic fungi also appear to have the ability to undergo sexual reproduction. Recent studies with engineered pairs of diploid strains of the model yeast Saccharomyces cerevisiae, one that is sexual and the other an obligate asexual, provide direct experimental validation of the benefits of both sexual and asexual reproduction. The obligate asexual strain had an advantage in response to constant environmental conditions whereas the sexual strain had a competitive edge under stressful conditions (Goddard et al., 2005; Grimberg and Zeyl, 2005). The human pathogenic fungi have gone to great lengths to maintain all of the machinery required for sex, including the mating-type locus and the pheromone response and cell fusion pathways. Yet these pathogens limit their access to sexual or parasexual reproduction in unique and specialized ways. Our hypothesis is that this has enabled the pathogenic fungi to proliferate in their environmental niche, but to also undergo genetic exchange via sexual reproduction in response to stressful conditions such as new environments, different host organisms, or changes in the human host such as antimicrobial therapy. Further study of the sexual nature of the human pathogenic fungi will illuminate how these unique microbes have evolved into successful pathogens in humans.
在过去十年中,随着因艾滋病毒/艾滋病以及与器官移植和癌症治疗相关的免疫抑制导致免疫功能低下个体数量的增加,机会性真菌传染病的患病率有所上升。在三种主要的人类致病真菌(白色念珠菌、新型隐球菌和烟曲霉)中,一个共同特征是这三种真菌都保留了有性生殖所需的机制,但它们都限制了有性生殖的机会。虽然其他许多人类致病真菌的特征尚不明确,但似乎也都具有进行有性生殖的能力。最近对模式酵母酿酒酵母的工程化二倍体菌株对进行的研究,其中一种是有性的,另一种是专性无性的,为有性生殖和无性生殖的益处提供了直接的实验验证。专性无性菌株在应对恒定环境条件时具有优势,而有性菌株在压力条件下具有竞争优势(戈达德等人,2005年;格林伯格和泽尔,2005年)。人类致病真菌不遗余力地保留了有性生殖所需的所有机制,包括交配型基因座以及信息素反应和细胞融合途径。然而,这些病原体以独特而特殊的方式限制了它们进行有性或准性生殖的机会。我们的假设是,这使得致病真菌能够在其生态位中增殖,但也能在应对诸如新环境、不同宿主生物体或人类宿主变化(如抗菌治疗)等压力条件时通过有性生殖进行基因交换。对人类致病真菌有性本质的进一步研究将阐明这些独特的微生物是如何进化成为人类成功病原体的。