Coccidia of wombats: correction of host-parasite relationships. Eimeria wombati (Gilruth and Bull, 1912) Comb. Nov. and Eimeria ursini Supperer, 1957 from the hairy-nosed wombat and Eimeria arundeli sp. n. from the common wombat.

Coccidial oocysts morphologically consistent with Eimeria ursini Supperer 1957, and E. tasmaniae Supperer 1957 were recovered from the feces of wild and captive hairy-nosed wombats (Lasiorhinus latifrons) in Australia. Eimeria arundeli so. n. was recovered from the feces of wild and captive common wombats (Vombatus ursinus). Eimeria arundeli oocysts are ellipsoidal to slightly ovoid 60.2--67.2 (63.7) X 40.6--47.6 (43.4); micropyle 3 in diameter usually visible; with oocyst wall granular, dark brown and occasionally opaque, 4--7 thick; inner oocyst wall clear, about 1.5 thick; small oocyst residuum present, four sporocysts ovoid 22.4--29.4 (25.8) X 12.6--15.4 (14.1) with protuberant Stieda body; opposite end of sporocyst also often slighly pointed; large granular sporocyst residuum obscuring sporozoites. Gametocytes of E. arundeli sp. n. and of an organism which is consistent with E. tasmaniae, are described developing in the lamina propria of villi in the small intestine. The stages in the hairy-nosed wombat are those described as Ileocystis wombati Gilruth and Bull 1912. It is suggested that the identification of the host of Supperer's E. ursini and E. tasmaniae as V. ursinus was in error and that the allopatric L. latifrons is the natural host. Eimeria tasmaniae Supperer 1957 is suppressed and E. wombati (Gilruth and Bull, 1912) comb. nov. is proposed and redescribed. No schizonts were identified among the endogenous stages, consistent with observations in the literature on other coccidia with similar gametocyte and oocyst structure.     

Eimeria (Protozoa: Eimeriidae) of the Cottontail Rabbit Sylvilagus audubonii in Northeastern Colorado, with Descriptions of Three New Species

SYNOPSIS. All of 100 cottontail rabbits Sylvilagus audubonii were found to be infected with 1-6 species of Eimeria. Three new species, E. audubonii, E. neoirresidua and E. poudrei are described from this host. Sub-spherical oocysts of E. audubonii average 21.2 by 17.1 μ; polar body, micropyle, oocyst residuum and sporocyst residuum are all absent; ellipsoidal sporocysts average 12.9 by 5.8 μ. Ovoid to ellipsoidal oocysts of E. neoirresidua average 25.7 by 17.9 μ; polar body and oocyst residuum are absent; micropyle and sporocyst residuum are present; ellipsoidal sporocysts average 14.5 by 6.4 μ. Ovoid to ellipsoidal oocysts of E. poudrei average 26.0 by 18.1 μ; polar body is lacking; micropyle, oocyst residuum and sporocyst residuum are present; ellipsoidal sporocysts average 14.4 by 6.4 μ. Three species of Eimeria previously described in the literature, E. maior Honess, 1939, E. media form honessi Carvalho, 1943 and E. environ Honess, 1939 are redescribed. A detailed structural and statistical analysis of each species is presented with at least 200 sporulated oocysts measured in each instance. A host list and a key to the Eimeria of cottontails is given. The use of detailed studies of oocyst size and structure as a tool for specific diagnosis of the Eimeria of cottontails is discussed.     

Demonstration of acid phosphatase in Eimeria spp.: partial characterization of the enzyme in E. vermiformis

Sporozoite extracts of E. vermiformis, E. stiedai, and E. tenella are rich in acid phosphatase activity. They contain specific enzyme activities equal to or greater than those reported for other highly virulent protozoan parasites. The absolute amount of enzyme activity per oocyst dramatically increases during sporulation of E. stiedai and E. vermiformis. Partial characterization of the acid phosphatase activity of E. vermiformis indicates that sporozoites account for greater than 92% of the total activity in sporulated oocysts, that the enzyme is resistant to inhibition by tartrate, and that it can be separated into two forms by anion exchange chromatography.     

Eimeria caprina sp. n. from the domestic goat, Capra hircus, from the USA

The ellipsoidal to slightly ovoid oocysts of Eimeria caprina sp. n. from the domestic goat, Capra hircus, are 27--40 x 19.5--26 micrometers (mean 31.8 x 23.1 micrometers); their sporocysts are 13--17 x 7--10 micrometers (mean 15.3 x 8.5 micrometers). The oocyst wall is 1.7 micrometers thick, smooth, dark brown to brownish-yellow, and 2-layered. Micropyle, polar granule, and sporocyst residuum are present; micropylar cap and oocyst residuum are absent. These features distinguish the new species from other species in the genus which have a micropylar cap, or are smaller, or have a small micropyle with a small internal plug.     

Eimeria lipura and E. landersi n. spp. (Protozoa,Eimeriidae) from the Long-tailed Porcupine Trichys lipura Günther, 1876 in Malaysia1

SYNOPSIS. Oocysts of 2 new species of Eimeria are described from the long-tailed porcupine Trichys lipura. The ovoid, 2-layered oocysts of E. lipura average 33.1 by 24.4 μ. A micropyle and polar granules are present; an oocyst residuum is absent. Ovoid sporocysts average 10.9 by 9.3 μ. A sporcyst residuum is present; Stieda body is absent. The subspherical, 3-layered oocyst of E. landersi averages 25.2 by 24.2 μ. An oocyst residuum is absent; a polar granule is present. Ovoid sporocysts average 11.7 by 7.9 μ. A sporcysts residuum is present; a Stieda body is absent.     

Phylogenetic relationships among rodent Eimeria species determined by plastid ORF470 and nuclear 18S rDNA sequences

Phylogenetic analyses for 10 rodent Eimeria species from different host genera based on plastid ORF470 and nuclear 18S rDNA sequences were done to infer the evolutionary relationships of these rodent Eimeria species and their correlation to morphology and host specificity. The phylogenies based on both data sets clearly grouped the 10 rodent Eimeria species into two major lineages, which reflect more their morphological differences than host specificity. Species in lineage A have spheroidal to subspheroidal sporulated oocysts, are similar in size (18-29 x 17-23; xbar = 22 x 20 microm), have an oocyst residuum and one-two polar granules; these include Eimeria albigulae (Neotoma), Eimeria arizonensis (Peromyscus, Reithrodontomys), Eimeria onychomysis (Onychomys) and Eimeria reedi (Perognathus). Species in lineage B, including Eimeria falciformis (Mus), Eimeria langebarteli (Reithrodontomys), Eimeria nieschulzi (Rattus), Eimeria papillata (Mus), Eimeria separata (Rattus) and Eimeria sevilletensis (Onychomys) have different shapes (ovoid, ellipsoid, elongated ellipsoid, etc.), differ greatly in size (10-27 x 9-24; xbar = 19 x 16 microm) and all lack an oocyst residuum. Thus, The oocyst residuum was the most determinant feature that differentiated the two lineages. The accession numbers of ORF470 of E. albigulae, E. arizonensis, E. falciformis, E. nieschulzi, E. onychomysis, E. papillata, E. reedi, E. separata, E. sevilletensis, E. langebarteli are AF311630-AF311639 and 18S rDNA of E. langebarteli, E. papillata, E. reedi, E. separata, E. sevilletensis are AF311640-AF311644.     

Formation of sulfhydryl groups in the walls of Eimeria stiedai and E. tenella oocysts subjected to in vitro excystation.

Eimeria stiedai or Eimeria tenella oocysts were incubated in aqueous cysteine hydrochloride (cysHCl) under carbon dioxide (CO2), aqueous cysHCl under air, water under CO2 or water under air, and analyzed for sulfhydryl (-SH) groups. The cysHCl-CO2 treatment produced more -SH groups than the other treatments and was effective in allowing activation of intact and sodium hypochlorite (NaOCl)-treated E. stiedai oocysts as well as NaOCl-treated E. tenella oocysts. The CO2-cysHCl complex may act directly on the oocyst wall, especially in the micropylar region, to unmask lipid-shielded disulfide bridges, which are reduced to -SH groups. The reduction apparently disturbs the protein superstructure of the oocyst wall, promotes opening of the micropyle, and changes the impermeable state of the sporulated oocyst.     

Eimeria azul sp. n. (protozoa: Eimeriidae) from the eastern cottontail, Sylvilagus floridanus, in Pennsylvania.

Eimeria azul sp. n. is described from the cottontail rabbit, Sylvilagus floridanus, in central Pennsylvania. The oval oocysts are 19.5--27.0 micrometer by 15.0--19.0 (mean - 22.9 X 16.7 micrometer). The fusiform sporocysts are 7.8--14.0 micrometer by 3.3--6.5 micrometer (mean = 11.8 X 5.8 micrometer). A Stieda Body is present. There is no micropyle, oocyst residuum or polar granule. The sporocyst has a residuum which is variable in appearance. The oocysts are characterized by a blue tint when viewed with an apochromatic objective lens.     

Eimeria cicaki sp. n. and Isospora thavari sp. n. from the house lizard Gehyra mutilata Boulenger in Malaysia.

Oocysts and endogenous stages of new species of Eimeria and Isospora from the house lizard, Gehyra mutilata, are described. The ellipsoid to subspherical 2-layered oocysts of E. cicaki averaged 24.0 X 21.0 mum. Polar granules are present. Micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.2 X 9.0 mum. A sporocyst residuum is present, but the Stieda body is absent. Endogenous stages are in epithelial cells of the small intestine. The subspherical single-layered oocysts of I. thavari average 23.8 X 22.8 mum. The polar granule is present; micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.8 X 9.4 mum. Stieda body and sporocyst residuum are present. There are endogenous stages in epithelial cells of the small intestine.     

Eimeria cicaki sp. n. and Isospora thavari sp. n. from the House Lizard Gehyra mutilata Boulenger in Malaysia*

SYNOPSIS. Oocysts and endogenous stages of new species of Eimeria and Isospora from the house lizard, Gehyra mutilata, are described. The ellipsoid to subspherical 2-layered oocysts of E. cicaki averaged 24.0 × 21.0 μm. Polar granules are present. Micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.2 × 9.0 μm. A sporocyst residuum is present, but the Stieda body is absent. Endogenous stages are in epithelial cells of the small intestine. The subspherical single-layered oocysts of I. thavari average 23.8 × 22.8 μm. The polar granule is present; micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.8 × 9.4 μm. Stieda body and sporocyst residuum are present. There are endogenous stages in epithelial cells of the small intestine.     

Eimeria ovata n. sp. and Other Coccidia of the Eastern Chipmunk Tamias striatus in Massachusetts

SYNOPSIS. Eimeria vilasi, E. wisconsinensis , and E. ovata n. sp. were found in the intestinal contents of eastern chipmunks Tamias striatus in Massachusetts. The oocysts of E. ovata are ovoid with mean dimensions of 26.1 × 16.7 μ. The outer oocyst wall is rough, with small pits. Micropyle and oocyst residuum are absent. Sporulation time at room temperature is 7–8 days.     

Eimeria clethrionomysis sp. n., Eimeria gallatii sp. n., Eimeria pileata sp. n. and Eimeria marconii sp. n. from the red-backed vole Clethrionomys gapperi Vigors, from Pennsylvania.

Four new eimerian species are described from red-backed voles, Clethrionomys gapperi in Pennsylvania. Sporulated oocysts of Eimeria clethrionomyis sp. n. are ellipsoidal, 18.8 (16.5-21.5) x 14.9 (14.0-16.5) with elongate, ovoid sporocysts, 10.6 (9.5-12.0) x6.1 (5.5-7.0). The oocyst wall is smooth, with 2 layers, and thins, with terminal cap at one or both ends. Polar granules, dark Stieda body and sporocyst residuum are present. The oocyst residuum is absent. Sporulated oocysts of Eimeria gallatii sp. n. are ellipsoidal, 27.7 (21-32) x 19.3 (17-24) with ovoid sporocysts, 13.5 (12-15) x 8.8 (8-10). The oocyst wall is smooth, 2-layered, with a micropyle and thin wall at the end opposite the micropyle. Polar granules, Stieda body and sporocyst residuum are present. The oocyst residuum is atypical, of cobwebby material. Sporulated oocysts of Eimeria pileata sp. n. are subspherical to spherical, 25.2 (20.5-29.5) x 22.5 (19.5-25.5) with ellipsoidal sporocysts, 13.4(10.5-15.0) x 8.4 (7.5-9.5). The oocyst wall is rough, pitted, striated, 2-layered, with no micropyle. Polar granules, oocyst and sporocyst residuum, Stieda body and stiedal cap are present. Sporulated oocysts of Eimeria marconii sp. n. are ellipsoidal, 13.0 (10.5-15-0) x 10.6 (9.5-12.0) with elongate, ovoid sporocysts, 7.7 (7.0-8.5) x 4.2 (3.0-4.5). The oocyst wall is smooth, single-layered, with no micropyle. Polar granules, dark Stiedal body and sporocyst residuum are present. There is no oocyst residuum.     

Two new species of coccidia, Eimeria leucuri and E. oreoecetes (Protozoa: Eimeriidae), in grouse from Colorado.

Eimeria leucuri is described from white-tailed ptarmigan (Lagopus leucurus), and E. oreoecetes from white-tailed ptarmigan and blue grouse (Dendragapus obscurus) from Colorado. Oocysts of E. leucuri are ellipsoidal, 26.6 by 17.7 micron, each bearing a micropyle, micropyle cap, up to 4 polar granules, but no oocyst residuum. The lemon-shaped sporocysts are 15.4 by 6.7 micron, and have Stieda bodies and large amounts of sporocyst residuum. The sporocyst contents are enclosed in a membrane. Oocysts of E. oreoecetes are subspherical, 26.0 by 22.6 micron, and have up to 4 polar granules. The lemon-shaped sporocysts are 14.6 by 8.8 micron, and have both Stieda bodies and substiedal bodies and a large amount of sporocyst residuum. The sporocyst contents are enclosed in a membrane. These are the first coccidia to be described from these tetraonids.     

Six new Eimeria species from vespertilionid bats of North America.

Twenty species of bats (Molossidae, Vespertilionidae) were collected from California, New Mexico, Oregon, South Carolina, Utah, and Baja California Norte (Mexico), and 29 of 404 (7%) animals, including Antrozous pallidus, Eptesicus fuscus, Myotis auriculus, Myotis californicus, Myotis ciliolabrum, Myotis evotis, Myotis lucifugus, Myotis thysanodes, Myotis vivesi, Myotis volans, Myotis yumanensis, and Nycticeius humeralis were infected with Eimeria spp., which represent 6 new species. Sporulated oocysts of a new species from A. pallidus are subspheroidal, 24.8 x 21.6 (22-27 x 19-24) microm with a polar granule and a large globular residuum. The oocyst wall is sculptured, with 2 layers, approximately 1.5 thick. Ovoidal sporocysts are 11.5 x 7.8 (9-13 x 7-10) microm, with Stieda body and residuum of many large granules. Sporulated oocysts of a new species from M. californicus are subspheroidal, 20.7 x 18.2 (19-23 x 16-20) microm, with 1-7 tiny polar granules, but without oocyst residuum. The oocyst wall is rough, with 2 layers, approximately 1.4 thick. Ovoidal sporocysts are 11.2 x 7.3 (10-12 x 7-8) microm, with Stieda body and a globular residuum. Sporulated oocysts of a second new species from M. californicus are subspheroidal, 23.1 x 20.7 (20-26 x 19-23) microm, with residuum and 1 polar granule, but a micropyle is absent. The oocyst wall is rough with 2 layers, approximately 1.5 thick. Ovoidal sporocysts are 12.5 x 7.2 (11-14 x 7-8) microm, with a Stieda body and residuum. Sporulated oocysts of a new species from M. ciliolabrum are subspheroidal, 24.9 x 20.1 (18-27 x 17-23) microm, with 1-2 polar granules, but without micropyle and residuum. The oocyst wall is rough with 2 layers, approximately 1.5 thick. Ellipsoidal sporocysts are 12.5 x 9.0 (8-14 x 7-10) microm, with Stieda and substieda bodies and residuum. Sporulated oocysts of a new species from M. evotis are subspheroidal, 21.3 x 18.6 (20-24 x 15-20) microm, with a prominent polar granule, but without micropyle and residuum. The oocyst wall is smooth with 2 layers, approximately 1.0 thick. Ovoidal sporocysts are 12.2 x 8.0 (11-13 x 7.5-9) microm, with Stieda and substieda bodies and residuum. Sporulated oocysts of the new species from N. humeralis are subspheroidal, 22.4 x 18 (21-24 x 17-20) microm, with 1-3 polar granules, but residuum and micropyle are absent. The oocyst wall is lightly sculptured with 2 layers, approximately 1.4 thick. Ovoidal sporocysts are 10.9 x 7.7 (9-12 x 6-8) microm, with Stieda body and residuum. Sporulated oocysts of E. pilarensis Scott and Duszynski, 1997 and those of at least 12 other morphological forms were seen in the other infected bats; these latter forms were seen in too few numbers to be adequately described as new species.     

Eimeria galateai sp. n. from the Paradise Kingfisher, and Eimeria duncani sp. n. from the Sacred Kingfisher in Papua New Guinea

SYNOPSIS. Eimeria galateai sp. n. from the paradise kingfisher ( Tanysiptera galatea Gray) and Eimeria duncani sp. n. from the sacred kingfisher ( Halcyon sancta Vigors & Horsfield) have been described from Papua New Guinea. Four of 11 paradise kingfishers were infected with E. galateai oocysts, measuring 13 (11–16) × 9 (8–11) μm. The oocysts were ovoid with nipple-like protrusion at one pole. Micropyle and polar granule were absent, while oocyst residuum (5 × 4 μm) was present. Sporocysts, measuring 5 (4–6) × 2 μm, were elongate-ovoid, and had a distinct convex Stieda body; the sporocyst residuum was absent. Two of 9 sacred kingfishers were infected with ovoid-truncated, 22 (19–25) × 16 (12–18) μm oocysts of E. duncani . Polar granule (5 × 2) was present in the oocysts, but there was no micropyle or oocyst residuum. Sporocysts were ovoid, measuring 9 (8–10) × 5 (4–6) μm, with a prominent Stieda body, and granular sporocyst residuum. Eimeria galateai and E. duncani are the first species of this genus to be described from birds of the order Coraciiformes.     

Descriptions of two new species of coccidia (Protozoa: Eimeriidae) and redescriptions of Eimeria ivensae and Eimeria odocoilei from captive white-tailed deer, Odocoileus virginianus

Two new species of Eimeria were observed in the feces of captive white-tailed deer fawns, Odocoileus virginianus, from Alabama. The first new species was easily recognized because of its small size. Sporulated oocysts are spherical, average 10.2 by 10.0 microm, and lack a micropyle and oocyst residuum. Oocysts contain a polar granule and elongate-ellipsoidal sporocysts that measure 6.7 by 3.1 microm. A Stieda body is present on the sporocysts. Oocysts were observed in the feces, and gamonts and oocysts were observed in the jejunum of a month-old fawn from Minnesota that died from enteritis due to this species. Oocysts of this small species were present in 5 of the 6 white-tailed deer fawns examined. Oocysts of a second new species are ellipsoidal and average 29.5 by 24.6 microm. The oocyst encloses an oocyst residuum, polar granule, and elongate-ellipsoidal sporocysts that average 16.0 by 9.0 microm. A Stieda body and substieda body are present on the sporocysts. Oocysts of the second new species were present in 4 of the 6 white-tailed deer fawns examined. Oocysts of E. ivensae are ovoid or flask-like and average 32.0 by 20.8 microm. The oocyst wall is rough, contains a micropyle, and encloses elongate-ellipsoidal sporocysts that average 16.5 by 7.8 microm. A Stieda body is present on the sporocysts. Oocysts of E. ivensae were present in 4 of the 6 white-tailed deer fawns. Oocysts of E. odocoilei are spherical or slightly subspherical and measure 24.7 by 21.5 microm. They enclose ovoid sporocysts that average 12.7 by 8.8 microm. A Stieda and substieda body are present on the sporocyst. Oocysts of E. odocoilei were present in 4 of the 6 white-tailed deer fawns.     

A new Eimeria (Apicomplexa: Eimeriidae), possessing mitra-shaped oocysts, from the Neotropical chelid turtle Batrachemys heliostemma (Testudines: Chelidae), and its comparison with Eimeria mitraria (Laveran & Mesnil 1902)

Eimeria jirkamoraveci sp. n. is described from faeces of two specimens of the toad-headed, side-necked turtle Batrachemys heliostemma collected at Iquitos in Peru. Oocysts are ovoid to almost spherical, 10.6 (8-12) x 8.9 (7-10) microm, without micropyle, polar granule and oocyst residuum. One conically stretched end and three blunt conical tubercles at the opposite end of oocyst give it mitra-like appearance. Sporocysts are elongated, ellipsoidal, 7.2 (6-8) x 4.1 (4-4.5) microm, with a small, knob-like Stieda body and sporocyst residuum composed of fine granules. To avoid possible conspecificity, the described new species is thoroughly compared with the most similar coccidium, E. mitraria, collected from its type host, Chinemys reevesii.     

Coccidia of Malaysian Mammals: New Host Records and Descriptions of Three New Species of Eimeria*

SYNOPSIS. In a survey of parasites of wild mammals of Malaysia 3 new species of Eimeria were found. Eimeria tupaiae sp. n. is described from the common tree shrew, Tupaia glis. Its ellipsoidal to spherical, 3-layered oocysts average 20 × 19 μm. A micropyle is absent; an oocyst residuum and polar granule are present. Ellipsoidal sporocysts average 11 × 7 μm. A sporocyst residuum and Stieda body are present. Eimeria ptilocerci sp. n. is described from the pen-tail tree shrew, Ptilocercus lowii. The ellipsoidal to spherical, 2-layered oocysts average 23 × 20 μm. A micropyle and oocyst residuum are absent; polar granules are present. The ellipsoidal sporocysts average 13 × 7 μm. A sporocyst residuum and Stieda body are present. Eimeria muuli sp. n. is described from the pencil-tailed tree mouse, Chiropodomys gliroides. The ellipsoidal single-layered oocysts average 25 × 19 μm. A micropyle and oocyst residuum are absent; a polar granule is present. The ellipsoidal sporocysts average 13 × 8 μm. A sporocyst residuum and Stieda body are present. In addition, new host records are reported as follows: E. miyairii Ohira from Whitehead's rat Rattus whiteheadi and the Malaysian wood rat, R. tiomanicus; E. separata Becker & Hall from Mueller's rat, R. muelleri, the chestnut rat, R. fulvescens, and the Malaysian wood rat, R. tiomanicus; E. nieschulzi Dieben from the red spiny rat, R. surifer and the chestnut rat, R. fulvescens; and E. callosciuri Colley from the grey-bellied squirrel, Callosciurus caniceps and the black-banded squirrel, C. nigrovittatus.     

Eimeria urosauris n. sp., a Coccidium from the Lizard Urosaurus graciosus Hollowell, in California

SYNOPSIS. A new species of coccidium is described: Eimeria urosauris n. sp., in the gall bladder of the lizard Urosaurus graciosus Hollowell, from the Mojave Desert in California. The oocyst of E. urosauris is smooth, bilaminar, nearly cylindrical, with long borders only slightly convex, ends rounded and very nearly hemispherical. It is usually 32 × 20 μ, and its length/width ratio is 1.6. It contains 4 ellipsoid sporocysts, each 10.5 × 9 μ, for which 1/w is 1.17. Each sporocyst contains 2 tapered bent sporozoites with rounded ends, 11 μ long, 4 μ in diameter at the larger end, and 1.5 μ in diameter at the smaller end. Each sporocyst also contains a central granular sporocyst residuum 3.5 μ in diameter. The oocyst lacks a micropyle and oocyst residuum, and there is no Stieda body on the sporocyst. Sporulation time is 6–10 hr. Endogenous development, with reinfection by liberated sporozoites, occurs in the epithelial lining of the gall bladder. E. urosauris is compared to other morphologically similar lacertilian eimerias with which it might be confused.