Romeiro A, Solé-Cava A, Sousa M A, de Souza W, Attias M
Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Brazil.
J Eukaryot Microbiol. 2000 May-Jun;47(3):208-20. doi: 10.1111/j.1550-7408.2000.tb00040.x.
Promastigote forms of a trypanosomatid were isolated from the third and fourth ventricles of the midgut and from the hindgut of the phytophagous hemipteran Oncopeltus fasciatus. Some individuals had adhered to its anterior region, close to the flagellar pocket, or to the flagellum up to four rounded aflagellated forms known as straphangers cysts. Scanning electron microscopy revealed that the flagellated forms presented a twisted cell body and a long flagellum, and the cysts, smaller than the parental promastigote, had a nascent flagellum. Transmission electron microscopy showed that promastigotes were typical, while cystic forms were ovoid dense cells devoid of a cyst wall, but presenting a cell coat, a special subpellicular region limited by a membrane unit, and a condensed cytoplasm. The kinetoplast-DNA fibrils appeared as dense spots and the condensed chromatin was arranged in a labyrinthic structure. Desmosome-like structures, observed in the region of adhesion of the precystic forms to the parental promastigote, could explain how cysts remain attached to the mother cell during the encystation process. Release of membranes from the surface of promastigotes and cysts seems to be correlated with the condensation of the cytoplasm during encystment. Morphological and isozyme analyses indicated that this trypanosomatid belongs to the genus Leptomonas. The molecular karyotype of this isolate was compared with that of a strain of Leptomonas oncopelti obtained from Oncopeltus varicolor by contour-clamped homogeneous electric field (CHEF) electrophoresis and revealed similar DNA banding patterns between 2,200-825 Kb, but not in lower bands (825-225 Kb). This suggested that the isolate from O. fasciatus and that from O. varicolor were not identical. Based on our findings we are describing Leptomonas wallacei n. sp. for our isolate from O. fasciatus.
从植食性半翅目昆虫红蝽(Oncopeltus fasciatus)的中肠第三和第四脑室以及后肠中分离出锥虫的前鞭毛体形式。一些个体附着在其前部区域,靠近鞭毛袋,或附着在鞭毛上,形成多达四个圆形无鞭毛形式,即所谓的“搭便车者”囊肿。扫描电子显微镜显示,有鞭毛的形式呈现出扭曲的细胞体和长鞭毛,而囊肿比亲代前鞭毛体小,有一个新生的鞭毛。透射电子显微镜显示,前鞭毛体是典型的,而囊性形式是卵形致密细胞,没有囊壁,但有细胞被膜、一个由膜单元界定的特殊表膜下区域和浓缩的细胞质。动质体DNA纤维呈现为致密斑点,浓缩的染色质排列成迷宫状结构。在囊前期形式与亲代前鞭毛体的附着区域观察到的桥粒样结构,可以解释囊肿在包囊形成过程中如何保持附着在母细胞上。前鞭毛体和囊肿表面膜的释放似乎与包囊形成过程中细胞质的浓缩有关。形态学和同工酶分析表明,这种锥虫属于细滴虫属(Leptomonas)。通过轮廓钳位均匀电场(CHEF)电泳,将该分离株的分子核型与从变色红蝽(Oncopeltus varicolor)获得的一株细滴虫(Leptomonas oncopelti)的分子核型进行比较,结果显示在2200 - 825 Kb之间有相似的DNA条带模式,但在较低条带(825 - 225 Kb)中没有。这表明来自fasciatus的分离株与来自varicolor的分离株不相同。基于我们的发现,我们将从fasciatus分离出的菌株描述为新种华莱士细滴虫(Leptomonas wallacei n. sp.)。