Hoffman Rebecca M, Marshall Marilyn M, Polchert David M, Jost B Helen
Wisconsin State Laboratory of Hygiene, University of Wisconsin-Madison, Madison, Wisconsin 53718, USA.
Appl Environ Microbiol. 2003 Aug;69(8):4966-70. doi: 10.1128/AEM.69.8.4966-4970.2003.
Microsporidia are obligate intracellular protozoa that have been shown to be pathogenic to most living creatures. The development of in vitro cell culture propagation methods has provided researchers with large numbers of spores and facilitated the study of these organisms. Here, we describe heterogeneity within cell culture-propagated Encephalitozoon intestinalis suspensions. Flow cytometer histograms depicting the log side scatter and forward-angle light scatter of spores from nine suspensions produced over 12 months consistently showed two populations differing in size. The suspensions were composed primarily of the smaller-spore subpopulation (76.4% +/- 5.1%). The presence of two subpopulations was confirmed by microscopic examination and image analysis (P < 0.001). Small subpopulation spores were noninfectious in rabbit kidney (RK13) cell culture infectivity assays, while the large spores were infectious when inocula included > or = 25 spores. The small spores stained brilliantly with fluorescein isothiocyanate-conjugated monoclonal antibody against Encephalitozoon genus spore wall antigen, while the large spores stained poorly. There was no difference in staining intensities using commercial (MicroSporFA) and experimental polyclonal antibodies. Vital-dye (DAPI [4',6'-diamidino-2-phenylindole], propidium iodide, or SYTOX Green) staining showed the spores of the small subpopulation to be permeable to all vital dyes tested, while spores of the large subpopulation were not permeable in the absence of ethanol pretreatment. PCR using primers directed to the 16S rRNA or beta-tubulin genes and subsequent sequence analysis confirmed both subpopulations as E. intestinalis. Our data suggest that existing cell culture propagation methods produce two types of spores differing in infectivity, and the presence of these noninfective spores in purified spore suspensions should be considered when designing disinfection and drug treatment studies.
微孢子虫是专性细胞内原生动物,已被证明对大多数生物具有致病性。体外细胞培养繁殖方法的发展为研究人员提供了大量孢子,并促进了对这些生物体的研究。在此,我们描述了细胞培养繁殖的肠脑炎微孢子虫悬浮液中的异质性。描绘12个月内产生的9种悬浮液中孢子的对数侧向散射和前向角光散射的流式细胞仪直方图始终显示出两个大小不同的群体。悬浮液主要由较小孢子亚群组成(76.4%±5.1%)。通过显微镜检查和图像分析证实了两个亚群的存在(P<0.001)。在兔肾(RK13)细胞培养感染性试验中,小亚群孢子无感染性,而当接种物包含≥25个孢子时,大亚群孢子具有感染性。小孢子用异硫氰酸荧光素偶联的抗肠脑炎微孢子虫属孢子壁抗原单克隆抗体染色明亮,而大亚群孢子染色较差。使用商业(MicroSporFA)和实验性多克隆抗体时,染色强度没有差异。活体染料(4',6'-二脒基-2-苯基吲哚、碘化丙啶或SYTOX Green)染色显示,小亚群孢子对所有测试的活体染料均具有渗透性,而在没有乙醇预处理的情况下,大亚群孢子不具有渗透性。使用针对16S rRNA或β-微管蛋白基因的引物进行PCR并随后进行序列分析,证实两个亚群均为肠脑炎微孢子虫。我们的数据表明,现有的细胞培养繁殖方法产生了两种感染性不同的孢子,在设计消毒和药物治疗研究时,应考虑纯化孢子悬浮液中这些无感染性孢子的存在。