Description of Metchnikovella spiralis sp. n. (Microsporidia: Metchnikovellidae), with notes on the ultrastructure of metchnikovellids.

The present paper reports results of a transmission electron microscopy study of a new metchikovellid microsporidium. It was isolated from gregarines Polyrhabdina sp. inhabiting guts of polychaetes Pygospio elegans sampled at the White Sea silt littoral zone. Free sporogony (FS) occurred in the life cycle of the microsporidium alongside sac-bound sporogony (BS). Free spores resided in a parasitophorous vacuole and were of typical metchnikovellidean structure, uninucleate and oblong. They measured on sections 2·0-3·2×1·3-1·9 µm. The life cycle included pre-sporogonial stages represented by dikaryotic cells and 4-nucleate cells with coupled nuclei. A multinucleate sporogonial plasmodium of FS split in numerous (>10) sporoblasts. In BS segregation of sporoblasts occurred within thick-walled cysts by internal budding. Spore sacs of this microsporidium, measuring on average 11·6×4·7 µm, were limited by a thick electron-dense wall, externally ornamented with spirally wound cords of dense material. These oval spore sacs contained eight barrel-shaped spores, comparable in size and ultrastructure to FS spores. Ultrastructure of both types of spores and intracellular development of the new microsporidium and Metchnikovella spp. were similar, suggesting they belong to the same genus. In this paper we describe a new species Metchnikovella spiralis and discuss morphology of metchnikovellids in the context of putative evolutionary history of Microsporidia.

Fine structure of Metchnikovella incurvata Caullery and Mesnil 1914 (microsporidia), a hyperparasite of gregarines Polyrhabdina sp. from the polychaete Pygospio elegans.

Class Rudimicrosporea Sprague 1977, with its single family Metchnikovellidae, comprises hyperparasites of gregarines from the guts of marine invertebrates. Metchnikovellids remain poorly studied in spite of their significance to the evolutionary history of microsporidia; their ultrastructure and life cycles require further investigation. Here we present results of the light- and electron-microscopy study of Metchnikovella incurvata Caulleri and Mesnil 1914, isolated from lecudinid gregarines, parasitizing polychaetes Pygospio elegans in the White Sea littoral zone, and yet described only on the light-microscopic level. The life cycle of this microsporidium includes 2 sporogonies: free (FS) and sac-bound (SBS). In FS, sporonts develop into multinuclear cells (sporogonial plasmodia), which generate sporoblasts and free spores residing in direct contact with the host cytoplasm. Electron microscopy revealed their metchnikovellidean structure: a horseshoe-shaped nucleus, short manubrium perpendicular to the long axis of the spore, and a polar cap in a separate membrane container. Merogony was not observed. The earliest stages of SBS were chains of binucleate cells. They underwent a series of nuclear and cell divisions, produced extracellular envelopes, and split into boomerang-shaped spore sacs, containing up to 16 spores each. Ultrastructure and sizes of sac-bounded spores were similar to those of free-living ones. An amended diagnosis of M. incurvata is provided.

[Morphology of Urospora chiridotae (Sporozoa: Gregarinomorpha: Eugregarinida) from sea cucumber Chiridota laevis (Echinodermata: Holothuroidea: Apoda)]. / Morfologiia gamontov Urospora chiridotae (Sporozoa: Gregarinomorpha: Eugregarinida) iz goloturii Chiridota laevis (Echinodermata: Holothuroidea: Apoda).

Several morphological forms (morphotypes) of Urospora chiridotae gamontes are found in White Sea holothuroid Chiridota laevis. All these morphotypes are differed by localization in the body of host, form and cytological features. The gregarines are situated in several host biotopes, such as blood vessels, intestine and mesenteries. In the blood vessels elongate skittle-like cells supplied with long thin cytopillia are observed. On the external surface of the intestine spherical gregarines are found. These parasites commonly covered with one layer of coelomic epithelium's cells. In some holothuria intratissue spherical cells of parasites located in intestinal epithelium are presented. Both of these types of parasites lack cytopillia, and folds or ridges on its surface. On different mesenteries, connections between intestine and body wall, and also on intestine elongate ounce-shaped cells and gamontocysts are observed. These cells are situated on the apices of finger-like processes of the intestine and mesenteries surface. Ounce-shaped gregarines have cytopillia shorter than in skittle-like gregarines. The differences between morphotypes of Urospora chiridotae are probably caused by different environmental conditions. In the narrow rift of blood vessel elongate cells are developed. The cytopillia may serve for making more or less wide space around gregarines, which is necessary for food uptake. Spherical cells surrounded by host's cells and have the form typical for tissue parasites. In the wide coelomic cavity where convection of liquid proceeds better than in blood vessel, ounce-shaped gregarines with short cytopillia are developed. We found only typical for Urospora chiridotae ovoid oocysts with dissimilar ends, anterior collar and spine-like posterior end. Thus, the all above-mentioned morphotypes undoubtedly belong to the same species. The relationships between defense host cells and the different morphotypes of trophozoites are variable.