<Emphasis Type="Italic">Sarcocystis</Emphasis> in the birds family Corvidae with description of <Emphasis Type="Italic">Sarcocystis cornixi</Emphasis> sp. nov. from the hooded crow (<Emphasis Type="Italic">Corvus cornix</Emphasis>)

Having studied 67 birds of six species of the family Corvidae, Sarcocystis cysts were found in 16 (23.9%) individuals belonging to three species. The highest prevalence of infection (35.9%) was determined in the hooded crow (Corvus cornix). Two types of sarcocysts, which were temporarily called cysts type I and type V, were determined in the corvids examined. By light microscope, type I cyst wall seemed to be thin (< 1.0 microm) and smooth. Banana shaped cystozoites measured 6.0-8.0 microm in length. By light microscope, type V cyst wall seemed striated and reached up to 2.5 microm. Banana shaped cystozoites measured 6.1-7.9 x 1.4-1.8 microm. Ultrastructurally, the cyst wall amounted to 2.1 microm and had stump-like protrusions that differed greatly in size and shape. The parasitophorous vacuolar membrane had indentations and clearly visible (up to 0.2 microm in length) microprojections, which also differed considerably in size and shape. The ultrastructure of type V cyst wall differed from all those Sarcocystis spp. described thus far. On the basis of this-Sarcocystis cornixi sp. nov.-is proposed for this type of sarcocysts. Partial sequences of 18S rRNA and 28S rRNA genes were determined for this species and a phylogenetic analysis of the Sarcocystidae family was performed. In the phylogenetic tree, S. cornixi is grouped together with Frenkelia microti, F. glareoli, S. muris, S. neurona and the unnamed Sarcocystis species whose intermediate hosts are birds. S. cornixi is the most closely related to Sarcocystis sp. (cyst type I) from the white-fronted geese.     

Identification of Sarcocystis rileyi from the mallard duck (Anas platyrhynchos) in Europe: cyst morphology and results of DNA analysis

Macroscopic cysts of Sarcocystis in ducks were recorded in Europe, but they were not investigated in more detail. Results of light and electron microscopy as well as 18S rDNA, 28S rDNA and ITS-1 region sequences of Sarcocystis macrocysts isolated from naturally infected mallard duck (Anas platyrhynchos) from Lithuania are presented in this paper. According to ultrastructure results, macrocysts examined corresponds to S. rileyi. Phylogenetic investigation showed S. rileyi to be the most closely related to two unnamed Sarcocystis species from anseriforms and to the S. mucosa. This is the first well-documented case of S. rileyi in Europe.     

<Emphasis Type="Italic">Sarcocystis</Emphasis> spp. in birds of the order Anseriformes

Having studied 342 birds of 20 species of the order Anseriformes, we found Sarcocystis cysts in 100 individuals (29.2±2.5%) belonging to 15 species. One macrocyst and four microcysts types have been determined. By means of light microscopy, the morphology of cyst walls and merozoites have been examined and morphometric data are presented. According to morphological features, macrocysts correspond to the S. rileyi species.     

The mallard duck (Anas platyrhynchos) as intermediate host for Sarcocystis wobeseri sp. nov. from the barnacle goose (Branta leucopsis)

Morphometric and DNA investigation results of Sarcocystis wobeseri sp. nov. from the barnacle goose (Branta leucopsis) and Sarcocystis sp. (cyst type IV) from the mallard duck (Anas platyrhynchos) are presented. No significant morphometric differences between the investigated Sarcocystis species were found. ITS-1, 18S rRNA, and 28S rRNA gene sequences of these species showed 100% identity. The conclusion is drawn that it is one and the same Sarcocystis species in different intermediate hosts.     

<Emphasis Type="Italic">Sarcocystis</Emphasis> sp. from the goldeneye (<Emphasis Type="Italic">Bucephala clangula</Emphasis>) and the mallard (<Emphasis Type="Italic">Anas platyrhynchos</Emphasis>): cyst morphology and ribosomal DNA analysis

By light microscopy, cysts of Sarcocystis sp. (cyst type I) from the goldeneye (Bucephala clangula) seemed filamentous with a smooth and thin (<1 μm) cyst wall. Ultrastructurally, the cyst wall surface was irregular with minute undulations of the primary cyst wall. These sarcocysts had type-1 cyst wall. Cystozoites were banana-shaped and measured 7.0–8.5 μm in length. By light microscopy, cysts of Sarcocystis sp. (cyst type II) from the mallard (Anas platyrhynchos) were ribbon-shaped, very long, and thin. On the surface of the wall (up to 1.5 μm), they had palisade-like villar protrusions closely crowded together. Electron micrographs showed villar protrusions (up to 1.3 μm in length) different in size and shape. The latter had short microprojections especially obvious in the oblique sections. Cystozoites were slightly bent with blunt ends, broader at one end, and measured 13.0–16.1 × 1.8–2.5 μm. Phylogenetic analysis based on the comparison of partial 28S rRNR gene sequences of Sarcocystis sp. (cyst type II) derived from the mallard, Sarcocystis sp. (cyst type I) and Sarcocystis sp. (cyst type III) both derived from the white-fronted goose (Anser albifrons) suggested that these sequences belonged to separate Sarcocystis species.     

Effect of lead and chromium on reproductive success of Japanese quail

An experimental model based on application of Japanese quail (Coturnix coturnix japonica) lines with high (H) and low (L) concentrations of plasma lactate was designed in order to investigate the effects of lead and chromium on embryonic development and reproductive success of experimental groups representing different genotypes. During the first stage of the trial, mature males from quail lines H and L (marked as generation T) were fed subchronically for 12 weeks with lead as Pb(NO(3))(2) and chromium as K(2)Cr(2)O(7) (dosage 0.8 and 0.142 g/kg, respectively, in the feed). In addition, a binary mixture of both lead and chromium was administered to the third group of males. The control group consisted of untreated birds. After mating with untreated females (8 female x 5 male in each group), progeny with four genotypes were obtained. The chicks were marked as generation F1 and used in the second stage of the trial. The data obtained show that heavy metals decreased the hatchability of sexually mature quail males: chromium (14%), lead (19%), and binary lead-chromium mixture (28%). Early embryonic mortality increased as much as 2-3 times. Single lead and binary lead-chromium additions decreased fertility after treating Japanese quail during the development of sexual maturity: lead increased the number of unfertile eggs up to 30% (twofold), binary lead and chromium, up to 50% (more than threefold) relative to untreated controls. There was no effect of chromium alone on fertility. In general, hatchability, fertility, embryonic mortality and reproductive success of Japanese quail were dependent on age, sex, genotypes, and on single or binary treatment with the inorganic salts of lead and chromium.     

Molecular and morphological investigations of Sarcocystis corvusi sp. nov. from the jackdaw (Corvus monedula)

One type of sarcocyst was found in two of eight investigated jackdaws (Corvus monedula) and proposed as Sarcocystis corvusi sp. nov. By light microscope, cysts resembled a thick thread and were very long (the largest fragment found amounted to 6 mm) and relatively thin (up to 60 μm). The cyst wall measured <1 μm and seemed smooth. Using a computerized image analysis system, knolls, which resembled protrusions, were visible on the wall surface. Ultrastructurally, the cyst wall was wavy and reached up to 1.1 μm. The waves were of different heights and resembled low protrusions. The parasitophorous vacuolar membrane had many invaginations. Lancet- or orange segment-shaped cystozoites were 5.9–7.3 μm long. These sarcocysts had type-1 tissue cyst wall. According to 18S rRNA, 28S rRNA genes and ITS-1 region sequences, it was shown that S. corvusi is a genetically separate species. On the basis of these genetic markers, S. corvusi was most closely related to S. columbae, S. calchasi and S. wobeseri which parasitize birds and are characterized by the same type of sarcocyst wall.     

Description of <Emphasis Type="Italic">Sarcocystis anasi</Emphasis> sp. nov. and <Emphasis Type="Italic">Sarcocystis albifronsi</Emphasis> sp. nov. in birds of the order Anseriformes

On the basis of the already published morphological, 18S rDNA, 28S rDNA data (Kutkienė et al., Parasitol Res 99:562–565, 2006; Parasitol Res 102:691–696, 2008; Parasitol Res 104:329–336, 2009), and ITS-1 region investigation results of sarcocysts presented in this paper, Sarcocystis albifronsi sp. nov. from the white-fronted goose (Anser albifrons) and Sarcocystis anasi sp. nov. from the mallard duck (Anas platyrhynchos) are described.