Université Lille Nord de France, Lille, France.
PLoS One. 2011;6(6):e20935. doi: 10.1371/journal.pone.0020935. Epub 2011 Jun 14.
Once regarded as an AIDS-defining illness, Pneumocystis pneumonia (PcP) is nowadays prevailing in immunocompromised HIV-negative individuals such as patients receiving immunosuppressive therapies or affected by primary immunodeficiency. Moreover, Pneumocystis clinical spectrum is broadening to non-severely-immunocompromised subjects who could be colonized by the fungus while remaining asymptomatic for PcP, thus being able to transmit the infection by airborne route to susceptible hosts. Although the taxonomical position of the Pneumocystis genus has been clarified, several aspects of its life cycle remain elusive such as its mode of proliferation within the alveolus or its ploidy level. As no long-term culture model exists to grow Pneumocystis organisms in vitro, an option was to use a model of immunosuppressed rat infected with Pneumocystis carinii and sort life cycle stage fractions using a high-through-put cytometer. Subsequently, ploidy levels of the P. carinii trophic and cystic form fractions were measured by flow cytometry. In the cystic form, eight contents of DNA were measured thus strengthening the fact that each mature cyst contains eight haploid spores. Following release, each spore evolves into a trophic form. The majority of the trophic form fraction was haploid in our study. Some less abundant trophic forms displayed two contents of DNA indicating that they could undergo (i) mating/fusion leading to a diploid status or (ii) asexual mitotic division or (iii) both. Even less abundant trophic forms with four contents of DNA were suggestive of mitotic divisions occurring following mating in diploid trophic forms. Of interest, was the presence of trophic forms with three contents of DNA, an unusual finding that could be related to asymmetrical mitotic divisions occurring in other fungal species to create genetic diversity at lower energetic expenses than mating. Overall, ploidy data of P. carinii life cycle stages shed new light on the complexity of its modes of proliferation.
曾经被认为是艾滋病定义性疾病的卡氏肺孢子菌肺炎(PcP)如今在免疫功能低下的 HIV 阴性个体中更为普遍,如接受免疫抑制治疗的患者或患有原发性免疫缺陷的患者。此外,卡氏肺孢子菌的临床谱正在扩大到非严重免疫功能低下的患者,这些患者可能被真菌定植,但无症状的 PcP,因此能够通过空气传播途径将感染传播给易感宿主。尽管卡氏肺孢子菌属的分类地位已经得到澄清,但它的生命周期的几个方面仍然难以捉摸,例如它在肺泡内的增殖方式或它的倍性水平。由于没有长期的体外培养模型来生长卡氏肺孢子菌,因此可以选择使用免疫抑制大鼠感染卡氏肺孢子菌的模型,并使用高通量细胞仪对生命周期阶段进行分类。随后,通过流式细胞术测量卡氏肺孢子菌营养体和囊体形式的倍性水平。在囊体形式中,测量到 8 个 DNA 含量,从而证实每个成熟的囊体包含 8 个单倍体孢子。释放后,每个孢子都会演变成营养体形式。在我们的研究中,营养体形式的大部分是单倍体。一些较少的营养体形式显示出两个 DNA 含量,这表明它们可能经历(i)交配/融合导致二倍体状态,或(ii)无性有丝分裂,或(iii)两者兼而有之。更稀少的营养体形式,具有四个 DNA 含量,提示有丝分裂分裂发生在二倍体营养体的交配之后。有趣的是,存在具有三个 DNA 含量的营养体形式,这是一个不寻常的发现,可能与其他真菌物种中发生的不对称有丝分裂分裂有关,以较低的能量成本创造遗传多样性,而不是交配。总的来说,卡氏肺孢子菌生命周期阶段的倍性数据为其增殖方式的复杂性提供了新的认识。