Erlandsen S L, Bemrick W J, Wells C L, Feely D E, Knudson L, Campbell S R, van Keulen H, Jarroll E L
Department of Cell Biology and Neuroanatomy, University of Minnesota School of Medicine, Minneapolis 55455.
J Parasitol. 1990 Oct;76(5):717-24.
Trophozoites of Giardia ardeae were obtained from the great blue heron (Ardea herodias) and established in axenic culture using the TYI-S-33 medium. The generation time in culture for G. ardeae was 22-25 hr, which was 3-fold longer than for Giardia duodenalis (WB strain). A morphological comparison of trophozoites in the original intestinal isolate to those grown in culture revealed that they were identical for the following characteristics: a pyriform-shaped body, a ventral adhesive disc with a deep notch in the posterior border, teardrop-shaped nuclei, pleomorphism in median body structure ranging from a round-oval appearance (Giardia muris type) to that of a clawhammer (G. duodenalis type), and a single caudal flagellum on the right side (as viewed dorsally) with the left one being rudimentary. Analysis of the chromosomal migration patterns was performed by orthogonal-field-alternation gel electrophoresis and demonstrated that the pattern for G. ardeae was distinctly different from that for G. duodenalis (Portland 1-CCW strain). Bacterial symbionts were seen attached to trophozoites in the original isolate but could not be detected in cultured trophozoites using scanning electron microscopy, fluorescence light microscopy using the Hoechst 33258 dye for DNA localization, or by standard microbiological techniques using nonselective media for growing aerobic or anaerobic bacteria. This study demonstrated that avian-derived Giardia could be grown in axenic culture; based on morphological criteria and chromosomal migration patterns, that G. ardeae should be considered a distinct species; and that rationale for determining Giardia spp., based on median body structure alone, should no longer be considered adequate for classification at the species level.
从大蓝鹭(苍鹭)中获取了阿氏贾第虫滋养体,并使用TYI-S-33培养基在无菌培养中进行培养。阿氏贾第虫在培养中的世代时间为22 - 25小时,这比十二指肠贾第虫(WB株)长3倍。对原始肠道分离物中的滋养体与培养中生长的滋养体进行形态学比较,结果显示它们在以下特征上相同:梨形身体、腹侧附着盘后缘有深切口、泪滴形细胞核、中体结构多形性,范围从圆形 - 椭圆形外观(鼠贾第虫类型)到羊角锤形(十二指肠贾第虫类型),以及右侧(从背面看)有一条单一的尾鞭毛,左侧的则退化。通过正交场交变凝胶电泳对染色体迁移模式进行分析,结果表明阿氏贾第虫的模式与十二指肠贾第虫(波特兰1 - CCW株)明显不同。在原始分离物中可见细菌共生体附着在滋养体上,但使用扫描电子显微镜、使用Hoechst 33258染料进行DNA定位的荧光显微镜或使用用于培养需氧或厌氧细菌的非选择性培养基的标准微生物技术,在培养的滋养体中均未检测到。本研究表明,源自禽类的贾第虫可以在无菌培养中生长;基于形态学标准和染色体迁移模式,阿氏贾第虫应被视为一个独特的物种;并且仅基于中体结构来确定贾第虫物种的理论依据,在物种水平分类上不应再被认为是充分的。