Sarcocystis Infection in Wild Reindeer (Rangifer Tarandus) From Hardangervidda in Southern Norway: with a Description of The Cysts of Sarcocystis Hardangeri N. Sp.

Fresh preparations of micro-isolated sarcosysts from skeletal muscle of 5 wild reindeer were examined by light microscopy. Slender, spindelshaped cysts measuring 821 × 60 µm, and having short knob-like cyst wall protrusions were found in all animals. In 1 animal cysts different in structure from the cysts of the 4 previously known Sarcocystis spp. of reindeer were found, These cysts are considered to be cysts of a new Sarcocystis sp. of reindeer, for which the name Sarcocystis hardangeri has been proposed. S. hardangeri n. sp. had macroscopic, ovoid to cylindrical cysts measuring 1667 (900–2570) × 819 (450–1575) µm. The cysts were surrounded by a 8–10 µm thick layer of fibrillar material. After removal of this layer, relatively few and irregularly spaced, slanting protrusions became visible. The 20–30 µm long protrusions were tongue-like, and were lying close to the surface of the cyst. Cysts of S. grueneri, S. rangiferi and S. tarandi were not demonstrated in the 5 wild reindeer examined.     

Ultrastructure of the cysts of Sarcocystis grueneri from cardiac muscle of reindeer (Rangifer tarandus tarandus)

Cysts of Sarcocystis grueneri from cardiac muscle of reindeer (Rangifer tarandus) in Norway were examined by transmission electron microscopy. The limiting unit membrane of the cyst proper formed regularly spaced invaginations into the cyst at numerous sites coinciding with interruptions in the underlying osmiophilic layer. The primary cyst wall formed numerous strip-like, sinuous protrusions, which were 30-40 nm thick, 150-300 nm wide and up to 4.5 microns long, and were running in parallel with the surface of the cyst. Generally the protrusions were arranged in several closely spaced layers compressed against the cyst. The nature and arrangement of the protrusions render them undetectable by light microscopy. Cyst ground substance divided the interior of the cyst into compartments containing typical sarcosporidian metrocytes and cystozoites. The cysts of S. grueneri from reindeer were ultrastructurally similar to cysts reported from red deer, roe deer and moose by other workers. The possibility that these cervids are hosts for a common Sarcocystis species is discussed.     

Sarcocystis dubeyella n. sp. and Sarcocystis phacochoeri n. sp. (Protozoa: Sarcocystidae) from the Warthog (Phacochoerus aethiopicus) in South Africa

ABSTRACT Sarcocystis dubeyella n. sp. and S. phacochoeri n. sp. from muscle fibers of the skeletal musculature of two warthogs in South Africa are described by light and and electron microscopy. Sarcocystis dubeyella sarcocysts are macroscopic (up to 12 mm long and 1 mm wide), with a parasite-induced encapsulation of the host muscle fiber in which the plasma membrane of the latter remained unaltered. The sarcocyst wall is characterized by evenly arranged, irregularly semicircular or rectangular villar protrusions (5.0 T. 2.8-11.0 μm) with indented margins and no specific content. Sarcocystis phacochoeri formed filiform microcysts (up to 4 mm long and 0.13 mm wide). Its cyst wall is provided with tightly packed, molarlike villar protrusions (1.6-3.3 T. 1.7-3.3 μm), with smooth margins, hollow on one side, and with longitudinal condensations of the fine granular matrix at various locations in the interior.     

Infections with Sarcocystis wenzeli are prevalent in the chickens of Yunnan Province, China, but not in the flocks of domesticated pigeons or ducks

The distribution and prevalence of infections with species of Sarcocystis in domestic fowl in Asia are poorly known. Here, ducks, pigeons, and chickens from Yunnan Province, China were examined for evidence of parasitic infection with Sarcocystis spp. One hundred and ninety one chickens, 514 ducks, and nine pigeons were investigated. Whereas the ducks and pigeons lacked tissue cysts in their muscle, brain or peripheral nervous system, cysts of Sarcocystis wenzeli were identified in 17 of 191 chickens (8.9%). Morphologically, the cysts were thread-like, ranging in size from 334-3169 × 41-117 μm (mean 1093 × 65 μm). Cysts were septate with dense, short finger-like protrusions which appeared radially striated. The cyst wall was 1.4-3.5 μm (mean 2.4 μm) thick. The bradyzoites were lancet shaped and measured 12.2-17.7 × 1.8-2.9 μm (mean 14.6 × 2.5 μm). Ultrastucturally, the primary sarcocyst wall had stubby villar protrusions, corresponding to the 'type 9' class previously designated. The protrusions measured 0.87-1.89 × 0.47-0.91 μm (mean 1.27 × 0.59 μm; n = 57). These findings confirm previous work from the vicinity of Kunming concerning the occurrence of S. wenzeli in chickens, and its use of both cats and dogs as definitive hosts, but indicate that corresponding infections may not occur in the regional domestic flocks of other types of fowl.     

Description of Sarcocystis falcatula Stiles, 1893, a Parasite of Birds and Opossums1

ABSTRACT. Sarcocystis falcatula Stiles, 1893 is re-described. Intermediate hosts of the parasite which was earlier described as Sarcocystis debonei Vogelsang, 1929 are species of passeriform, psittaciform, and columbiform birds. In these birds, muscle zoites are 6.88 × 2.19 (4.8-8.4 × 1.2-3.6) μm and are enclosed in a cyst wall with regular protrusions, 1-5 μm long. The convoluted primary wall has multiple thin areas in the osmiophilic layer. Microtubules originate in the ground substance and extend to the tips of the protrusions. The only known definitive host is the opossum, Didelphis virginiana; rats, cats, a dog, and a ferret could not be infected from muscle cysts. Sporocysts from opossums infected from five different infected avian sources measure 11.2 × 7.4 (9.6?12.0 × 6.0-8.4)μm.     

Fine structure and development of Sarcocystis aucheniae in llamas

Isolated cysts of Sarcocystis aucheniae of the llama (Lama glama) were fed to one dog and one cat. Only the dog excreted sporocysts, measuring 13.1-15.7 (15.0 +/- 0.54) X 9.0-11.3 (10.4 +/- 0.36) micron after 11 days for 21 days. A second cat, which had ingested meat of a llama containing macrocysts of S. aucheniae as well as sarcosporidial cysts visible only under a microscope also did not excrete sporocysts. The cysts of S. aucheniae are surrounded by a folded primary cyst wall forming cauliflower-like protrusions into the muscle fibre. The protrusions contain numerous microfilaments. In addition, the primary cyst wall forms numerous tiny vesicles. The parasitized muscle fibre is located in a large cavity within the normal muscle tissue. The cyst wall of S. aucheniae is similarly structured to that of S. gigantea of the sheep.     

Muscular sarcocystosis in coyotes from Oklahoma

In a recent survey in Oklahoma (USA), 52 free-ranging coyotes were examined for the presence of sarcocysts. Two of these coyotes were found infected with sarcocysts in skeletal muscle. By light microscopy, the cyst wall was thin and smooth. Ultrastructurally, the cyst wall had minute villar protrusions. The sarcocysts were 14.4 to 50.4 microm wide and 46.8 to 99 microm long. This is the first report of Sarcocystis sp. sarcocysts in the skeletal muscle of coyotes.     

Ultrastructure of Sarcocystis sp. from the muscle of a white-tailed deer (Odocoileus virginianus)

Sarcocystis sp. from the muscle of naturally infected white-tailed deer (Odocoileus virginianus) was examined by transmission electron microscopy. The primary cyst wall forms regularly spaced protrusions filled with electron-lucent ground substance; no fibrils are present in the protrusions. The cysts are divided by septa into compartments containing typical coccidian metrocytes and merozoites. Taxonomy of the protozoon from the white-tailed deer-dog is discussed.     

Light and electron microscope study of Sarcocystis sp. from the fallow deer (Cervus dama)

By means of light and electron microscopy a study was made of Sarcocystis sp. from 11 fallow deer (Cervus dama). Cysts of Sarcocystis sp. were found in the tongue and abdominal muscle of 3 of 11 deer from forests near Bonn (FRG). These measured 212-560 micron in length and 54-120 micron in width and contained metrocytes and merozoites. The cyst wall, which had narrow band-like protrusions, is compared with other Sarcocystis sp. from Cervidae.     

Effects of frozen storage on the structure of sarcocysts in pig muscle and implications in taxonomic studies

The morphology of the cyst wall of Sarcocystis has unique characteristics that can be used in species identification. To find a suitable way to preserve Sarcocystis cyst samples for species identification, by light microscopy and electron microscopy, we recorded the morphological changes in the cysts of Sarcocystis suihominis and Sarcocystis miescheriana from pig muscle, induced by storage at -20 degrees C. Comparisons were made between fresh cysts and those subjected to frozen storage for periods of 3 days, 20 days and 30 days. Results: cyst wall of the two Sarcocystis species appeared unaffected by storage. There was no obvious change in the length, nor in the width of the protrusions after storage (P>0.05), but the structure of the bradyzoite in the sarcocyst was in many cases disintegrated at -20 degrees C in 20 days for S. miescheriana and 30 days for S. suihominis. To our knowledge this is the first report that Sarcocystis cyst in muscle can be stored at -20 degrees C before and remain suitable for ultrastructural morphological study. Consequently, this paper proposes freezing as a convenient storage method for samples used in taxonomic studies of Sarcocystis.     

Prevalence of Sarcocystis sp. in stranded Atlantic white-sided dolphins (Lagenorhynchus acutus)

In January 1998 and 1999, two mass strandings of dolphins occurred in Wellfleet, Massachusetts. The strandings were composed of 97 and 53 animals, respectively. Tissues from 35 Atlantic white-sided dolphins (Lagenorhynchus acutus) from the 1998 stranding and 52 from the 1999 stranding were examined histologically. In the 1998 stranding, unidentified protozoal tissue cysts were seen in skeletal muscle from 11 of 28 (39%) dolphins. In addition, two dolphins had a protozoal tissue cyst in cardiac muscle. In the 1999 stranding, nine of 23 (39%) dolphins had the same protozoal tissue cysts in skeletal muscle. The identification of these protozoal tissue cysts as Sarcocystis sp. was confirmed by light and transmission electron microscopy. The high prevalence of sarcocysts in these dolphins suggests that they are likely intermediate hosts for previously undescribed Sarcocystis spp. The ultrastructure of the sarcocyst walls suggests that more than one species of Sarcocystis are present in dolphins.     

Ultrastructure of the cyst and life cycle of Sarcocystis sp. from wild sheep (Ovis musimon)

Sarcocystis sp. (Eimeriina: Sarcocystidae) is described as a heteroxenous coccidian with domestic dogs as an experimental definitive host and wild sheep (Ovis musimon) as natural intermediate hosts. Mature sarcocysts of this Sarcocystis sp. were examined by transmission electron microscopy. Sarcocysts in various muscle tissues were microscopic, had a thin primary cyst wall and septa and measured 81.0 x 30.5 microns. The cysts were located within muscle cells and were limited by a primary cyst wall (PCW). The cyst surface was highly folded forming densely packed projections. Between the PCW projections the surface of the cyst was marked with pit-like invaginations. The ground substance of the cyst formed a layer at the periphery of the cyst, filled the projections and formed septa which divided the cyst into compartments. Sarcocysts contained numerous bradyzoites that were 15.2 x 3 microns and few metrocytes 11.5 x 3.5 microns. Twelve days after ingesting Sarcocystis sp.-infected wild sheep meat, four dogs began passing sporocysts in their feces: two domestic cats did not pass oocysts or sporocysts after ingesting meat from the same animals. Sporocysts measured 14.8 x 9.9 microns.     

Sarcocystis speeri N. sp. (Protozoa: Sarcocystidae) from the opossum (Didelphis virginiana)

The North American opossum (Didelphis virginiana) is host to at least 3 species of Sarcocystis: Sarcocystisfalcatula, Sarcocystis neurona, and a recently recognized Sarcocystis sp. A new name, Sarcocystis speeri, is proposed for the third unnamed Sarcocystis. Immunodeficient mice are an experimental intermediate host for S. speeri. Sarcocystis speeri sporocysts are 12-15 x 8-10 microm in size, and its schizonts are found in many organs of mice. Sarcocysts of S. speeri are found in skeletal muscles and they are up to 5 mm long and filiform. By light microscopy, the sarcocyst wall is thin (<1 microm thick); ultrastructurally, the cyst wall is up to 1.8 microm thick and has characteristic steeple-shaped villar protrusions surmounted by a spire. Sarcocystis speeri schizonts are morphologically and antigenically distinct from schizonts of S. neurona, and S. speeri sporocysts were not infective to budgerigars (Melopsittacus undulatus).     

Three new coccidians (<Emphasis Type="Italic">Cyclospora</Emphasis>, <Emphasis Type="Italic">Eimeria</Emphasis>) from eastern moles, <Emphasis Type="Italic">Scalopus aquaticus</Emphasis> (Linnaeus) (Mammalia: Soricomorpha: Talpidae) from Arkansas,USA

Three new species of coccidians (Apicomplexa: Eimeriidae) are described from eastern moles, Scalopus aquaticus (Linnaeus) from Arkansas. Oöcysts of Cyclospora duszynskii n. sp. are subspheroidal with a smooth bi-layered wall, measure 11.4 × 10.0 µm, and have a length/width (L/W) ratio of 1.1; both micropyle and oöcyst residuum are absent, but a single polar granule is present. Sporocysts are ellipsoidal and measure 7.2 × 5.4 µm, L/W 1.3; an indistinct Stieda body is present, but the sub-Stieda and para-Stieda bodies are absent and the sporocyst residuum is composed of medium to large granules of different sizes along the edge of the sporocyst. Oöcysts of Cyclospora yatesi n. sp. are subspheroidal to ovoidal with an ornate outer wall, measure 17.0 × 15.2 µm, L/W 1.1; both micropyle and oöcyst residuum are absent, but a single polar granule is present. Sporocysts are ellipsoidal and measure 9.7 × 7.3 µm, L/W 1.3; an indistinct Stieda body is present, but sub-Stieda and para-Stieda bodies are absent and the sporocyst residuum is composed of medium to large granules of different sizes along the edge of the sporocyst. Oöcysts of Eimeria paulettefordae n. sp. are ovoidal to ellipsoidal with an ornate outer wall, measure 30.0 × 25.4 µm, L/W 1.2; both micropyle and oöcyst residuum are absent, but a single polar granule is present. Sporocysts are ellipsoidal and measure 12.6 × 9.2 µm, L/W 1.4; a button-like Stieda body is present, but sub-Stieda and para-Stieda bodies are absent and the sporocyst residuum is composed of medium to large granules of different sizes along the edge of the sporocyst. These are the first coccidians described from Arkansas populations of S. aquaticus. In addition, a summary is provided on the cyclosporans and eimerians from North American talpids.     

A comparative scanning electron microscopic study of the cyst wall in 11 Sarcocystis species of mammals

Sarcocysts found in the musculature of necropsied mammals were dried with hexamethyldisilazane and examined by scaning electron microscopy. The object of research in this morphological study was the outer surface configuration of the cyst wall. A smooth cyst wall without villar protrusions ( Sarcocystic cf. sebeki European badger, Meles meles ) was compared with 10 others each with its distinctly characterized villar protrusinos. In scanning electron microscopy these resembled stumpy nails with angular heads ( Sarcocystis sp./serow, Capricornis crispus ), tongues ( S. sp./sambar, Cervus unicolor ), ears ( S. sp./ wapiti, Crevus elaphus canadensis ), elongated cones or clubs ( S. sp./domestic horse, Equus caballus ), hairs ( S. sp./Mongolian gazelle, Procapra gutturosa ), and molar teeth (another S. sp./Mongolian gazelle). This study revealed that what appeared in light microscopy to be finger-like protrusions of Sarcocystis hofamanni in roe deer ( Capreolus capreolus ), of Sarcocystis hominis in bison ( Bison bison ), of Sarcocystis hirsuta in cattle ( Bos taurus ), and of Sarcocystis tenella in sheep ( Ovis aries ) were more similar to columns ( S. hofmanni ), straps ( S. hominis ), stalked polyhedrons ( S. hirsuta ), or cylinders ( S. tenella ).     

Sarcocystis gracilis n. sp. from the Brazilian Tortoise Kinosternon scorpioides*

SYNOPSIS. Sarcocystis gracilis n. sp. is described in the tortoise Kinosternon scorpioides (Reptilia, Chelonia) from the Island of Marajó, north Brazil. This appears to be the first record of a sarcosporidian from this group of reptiles. The cysts are restricted to the skeletal musculature and may reach up to 8.0 mm in length. The cyst wall is extremely delicate, with no visible striations or spines: the trabeculae are well developed and growth of the cyst appears to be largely from caps of proliferative cells at the poles. The zoites are long and slender, averaging 18.4 × 1.4 μ in fresh preparations. They undergo sudden and rapid gliding movements. The parasite produces striking pathologic changes in the muscle.     

Prevalence and development of two Sarcocystis spp. in the horse (author's transl)

The prevalence of Sarcocystis spp. in horses was investigated in a survey at the Munich abattoir during 1978/79. Muscle specimens (oesophagus, diaphragm, sublingual muscle, myocardium) were examined using tryptic digestion. Out of 200 horses 31 (15.5%) were found to be carriers of sarcocysts. No parasites were found in the myocardium. In three animals sarcocysts could be isolated and differentiated in fresh preparations. Cysts with 5 to 11 microns by less than 0.5 microns hairlike, unstable protrusions were classified as Sarcocystis equicanis, whereas those with 2.5 to 4.5 microns by 0.8 to 1.0 microns fingerlike, stabile protrusions were assigned to be S. fayeri. Histologically S. equicanis cysts were thin-walled and S. fayeri cysts were thick-walled and often striated. For both species the dog acts as final host. A mixture of sporocysts of both species measured: 12.0--14.4 (13.4 +/- 0.7) X 9.3--10.5 (9.8 +/- 0.4) microns. The prepatent period is 11 to 17 days. Two ponies experimentally infected with 100,000 sporocysts each did not show clinical signs. In fresh preparations and in histopathological examinations of biopsied (111th, 130th, 152th, and 165th day post-infection (p.i.) and postmortem material (167th and 189th day p.i.) different developmental stages of sarcocysts of both species were seen and the following pathological alterations observed: circumscribed non-purulent inflammation, moderate Zenker's degeneration of muscle fibres, and degenerated cysts, of which sometimes only parts of the cyst wall were left. In fresh preparations S. equicanis and S. Fayeri could be differentiated 111 days p.i. The observed disappearance of the sarcocysts is suggested to be a self-cleaning process.     

Life cycle of Sarcocystis tenella in sheep and dog

For Sarcocystis tenella, the second microscopic sarcocyst in sheep, the dog was shown to act as final host shedding sporocysts measuring 13.75-15.8 (14.8 +/- 0.8) X 9.7-10.8 (10.1 +/- 0.4) micron after a prepatent period of 8-13 days. The clinical signs and the course of experimental infections in sheep were most similar to S. ovicanis. After high doses of sporocysts sheep had temperatures up to 42 degrees C, anaemia, and paresis; they finally died from haemorrhagic diathesis. The development of S. tenella in sheep was studied and it resulted in microscopic cysts in the musculature that measured 300-650 X 20-50 micron. They showed hair-like delicate protrusions of the cyst wall measuring 6-8 X less than 0.5 micron, by which S. tenella could be clearly differentiated from S. ovicanis from day 60 p.i. onwards. The decreasing number of S. tenella through degeneration of cysts is suggested to be a self-cleaning process.