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  • 1
    Electronic Resource
    Electronic Resource
    Extraintestinal Development of Caryospora simplex (Apicomplexa: Eimeriidae) in Experimentally Infected Mice, Mus musculus (1984)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 31 (1984), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Developmental stages of Caryospora simplex were found in connective tissue of the cheek, tongue, and nose of Swiss-Webster and C57 BL/6 mice (Mus musculus) from 8 through 70 days after oral inoculation with 50,000 or 250,000 oocysts, or 60,000 free sporocysts of the same species obtained from an Ottoman viper, Vipera xanthina xanthina. The earliest developmental stages were seen on day 8 post-inoculation (PI) and consisted of two types of meronts and gamonts (undifferentiated sexual stages). Gamonts, microgametocytes, macrogametes, and unsporulated oocysts were found on days 10 and 12 PI. Fully sporulated, thin-walled oocysts containing eight sporozoites surrounded by a thin sporocyst membrane were first seen 12 days PI. Monozoic cysts (caryocysts) were first seen 12 days PI and appeared fully viable throughout the duration of the study, 70 days PI. Four mice injected intra-peritoneally with 150,000 free sporozoites and killed 12 days PI contained unsporulated and sporulated oocysts in connective tissues of the cheek, tongue, and nose, suggesting that sporozoites may be carried to the site of infection via the lymphatic/circulatory system. Four cotton rats, Sigmodon hispidus, inoculated orally with 250,000 oocysts all had unsporulated and sporulated oocysts of C. simplex in connective tissue of the cheek, tongue, and nose when killed on day 12 PI, indicating extraintestinal development in the secondary host is not species specific. This is the first report of a heteroxenous coccidium with both asexual and sexual development in the primary (predator) and secondary (prey) hosts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1984.tb02985.x
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  • 2
    Electronic Resource
    Electronic Resource
    In Vitro Excystation of Caryospora simplex (Apicomplexa: Eimeriorina) (1984)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 31 (1984), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In vitro excystation of sporozoites of the heteroxenous coccidian Caryospora simplex Léger, 1904 (Apicomplexa: Eimeriorina) is described. Sporocysts freed mechanically from oocysts released a maximum of 51% of their sporozoites within 45 min at 25°C and a maximum of 74% within 20 min at 37°C when incubated in a 0.25% (w/v) trypsin–0.75% (w/v) sodium taurocholate (bile salt) excystation solution. At emergence from sporocysts, sporozoites were weakly motile then became highly active after about 2 min in excystation solution. Sporozoites within sporocysts exposed to bile salt only became highly motile within 25 min at 25°C and within 15 min at 37°C but did not excyst. When exposed only to trypsin at the above temperatures, the Stieda body dissolved; the substieda body remained intact, and the sporozoites exhibited only limited motility within sporocysts; only a few excysted. Intact, sporulated oocysts incubated at 25° or 37°C in 0.02 M cysteine-HC1 and a 50% CO2 atmosphere for 18 h had no morphologic changes in the oocyst wall. Further incubation of these intact oocysts in excystation solution for 30 min at 37°C caused neither motility of sporozoites within sporocysts nor excystation. Grinding oocysts for 30 sec in a motor-driven, teflon-coated tissue grinder caused motility of some sporozoites within sporocysts but did not result in excystation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1984.tb02964.x
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  • 3
    Electronic Resource
    Electronic Resource
    Hammondia pardalis sp. n. (Sarcocystidae) from the Ocelot, Felis pardalis, and Experimental Infection of Other Felines (1979)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 26 (1979), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Synopsis. Hammondia pardals sp. n. (Eimeriorina: Sarcocystidae) from Panama Canal Zone is described as an obligate heteroxenous coccidian, with felids as the final host and laboratory mice as the experimental intermediate host. Ovoid oocysts. measuring 40.8 (36–46) × 28.5 (25–35) m̈m. are shed unsporulated. Oocysts were infective only for the intermediate host. the laboratory mouse, Mus musculus, and the intracellular cysts were infective only for felids. Attempted passage of tissue cysts from mouse to mouse was unsuccessful.Mice fed 5 × 104 sporulated oocysts were found to harbor small intracellular cysts, 13–16 × 10–15 m̈m, in the mesenteric lymph nodes, lungs, and intestinal submucosa 15 days postinfection. The meronts in these early cysts were stubby and measured 3 × 6 m̈m. The prepatent period in the felids was 5 to 8 days and the patent period 5–13 days. Experimental infections of definitive hosts were successful with 6/6 domestic laboratory-reared kittens, Felis catus; 5/5 ocelots, F. pardalis; and 1/1 jaguarundi, F. yagouaroundi. None of the exposed raccoons, Procyon lotor, shed oocysts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1979.tb02728.x
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  • 4
    Electronic Resource
    Electronic Resource
    Development of the Swine Coccidium Eimeria debliecki Douwes, 1921 in Mammalian Cell Cultures (1985)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 32 (1985), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Sporozoites of Eimeria debliecki entered human fetal lung and porcine kidney cells grown in cultures and underwent one merogenous cycle, terminating in the production of second-generation trophozoites. Sporozoites were intracellular 1 h post-inoculation (PI) and developed into sporozoite-shaped meronts at 40 h PI. These meronts, one of which was motile, had from two to ten nuclei. Sporozoite-shaped meronts then developed into elongate or spheroidal meronts with 10 to 24 nuclei by two days PI. Ten to 26 first-generation merozoites were formed by budding from the meront surface. Mature first-generation merozoites were most numerous three days PI. Most meronts had ruptured and released nonmotile merozoites into the culture medium by four days PI. Merozoites that were not released became rounded and developed into second-generation trophozoites. Refractile bodies were present in all developmental stages. No further development was observed five through eight days PI.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1985.tb03099.x
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  • 5
    Electronic Resource
    Electronic Resource
    Life Cycle of Eimeria ferrisi Levine & Ivens, 1965 in the Mouse, Mus musculus (1975)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 22 (1975), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. The life cycle of Eimeria ferrisi is described from experimentally infected Mus musculus. The prepatent period was 3 days and the patent period was 3–4 days. The endogenous stages were found only in the cecum and colon. Three generations of schizonts were found. Mature 1st-generation schizonts first seen 24 hr postinoculation (PI) measured 10.9 (7–14) × 10.2 (6–13) μm and had 9.6 (7–14) merozoites. Some 2nd-generation schizonts had uninucleate merozoites and others had multinucleate merozoites. The former were first seen in small numbers 36 hr PI and were most abundant 48 hr PI. They measured 9.6 (5–13) × 7.9 (6–12) μm and had 18 (6–25) merozoites. Schizonts with multinucleate merozoites were seen 72 hr PI. Mature 3rd-generation schizonts were seen 72 hr PI. They measured 14.0 (12–18) × 11-0 (9–13) μm and had 12.5 (5–16) merozoites. Macrogamonts were first seen in 72 hr sections. Each young macrogamont had a large nucleus with a prominent nucleolus. Only one type of cytoplasmic granule appeared to be involved in the formation of the oocyst wall. Mature macrogamonts were 11.0 (5–14) × 10.0 (6–13) μm. Crescent-shaped bodies were observed in the parasitophorous vacuole of trophozoites and young macrogamonts. Early microgamonts were first recognized at 96 hr by the presence of darkly stained and irregularly shaped nuclei. Usually, mature microgametes were arranged in long, narrow whorls at the periphery of the microgamont or in whorls at the surface of 2–5 compartments.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1975.tb05177.x
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  • 6
    Electronic Resource
    Electronic Resource
    The Development of First Generation Schizonts of Eimeria bovis (1966)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 13 (1966), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. In young first generation schizonts of E. bovis, the nuclei appeared to have a random distribution. In calves killed 8 days after inoculation some of the schizonts had the nuclei arranged in a single layer at the periphery, with a few infoldings of this layer into the interior. In further development, such ingrowths of the nuclear layer resulted in the formation of compartments of varying size. In schizonts of calves killed 12 days after inoculation spherical or ellipsoidal bodies (blastophores), about 5–20 μ in diameter with a single peripheral layer of nuclei were formed. Merozoites developed as radial outgrowths from the blastophores, leaving residual bodies of variable size, which later disappeared. The response of the host cell to the presence of the schizont was characterized by marked growth of both the nucleus and cytoplasm. The nucleolus became greatly enlarged, and the chromatin was distributed in relatively fine granules. In the host cell cytoplasm, 2 concentric layers were observed; the inner was more dense than the outer. After growth of the schizont was completed its host cell was stretched into a thin covering layer about 1 μ thick. In some schizonts, the host cell disintegrated, and the schizont was then invaded by eosinophils, macrophages and other cells, which eventually destroyed the merozoites.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1966.tb01964.x
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  • 7
    Electronic Resource
    Electronic Resource
    Eimeria balphae n. sp. from the Ord Kangaroo Rat Dipodomys ordii (1967)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 14 (1967), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Eimeria balphae n. sp. is described from the Ord kangaroo rat Dipodomys ordii. The sporulated oocysts are broadly ellipsoidal to ovoid, averaging 16.7 by 14.3 μ. A single, large, homogenous body represents the oocyst residuum. A polar granule is present. There is no micropyle. The ovoid sporocysts average 8.7 by 5.9 μ. The sporocyst residuum is composed of 7–14 round, clear granules. This species of Eimeria was found in 1 of 82 D. ordii in northwestern Utah.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1967.tb02040.x
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  • 8
    Electronic Resource
    Electronic Resource
    Development of Eimeria alabamensis from Cattle in Mammalian Cell Cultures (1971)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 18 (1971), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Monolayer primary cultures of cells from bovine embryonic intestine (BEInt), kidney (BEK), spleen (BES), and thyroid (BETy) and cell line cultures of embryonic bovine trachea (EBTr) and synovium (BESy) as well as established cell line cultures of bovine kidney (Madin-Darby, MDBK), human intestine (Int 407) and Syrian hamster kidney (BHK) were inoculated with freshly excysted sporozoites of Eimeria alabamensis and observed for 4–5 days. Sporozoites penetrated all cell types; during the 1st 24 hr, intracellular sporozoites, trophozoites and binucleate schizonts were seen in all cell cultures. Mature schizonts were more numerous in BES and MDBK cells than in the others. Large schizonts, 14.2 (11–18.5) by 10.2 μ (8.5–11), with 6–14 short, stubby merozoites (each with 2 refractile bodies) occurred at 2 and 3 days in all cells except BESy, Int 407, and BHK. Small schizonts, 9.7 (5.5–13) by 6 μ (5–8.5), with 6–10 long, slender merozoites (each with 2 refractile bodies) were found 3 days after inoculation in all cell types. At 4 days, some intracytoplasmic merozoites and a few intranuclear 2nd generation trophozoites were found. After 4 days post-inoculation, intracellular parasites were rarely seen and these were apparently degenerate. Development within the host cell nucleus, the normal site of development in the host animal, was observed infrequently in cell cultures. Intranuclear sporozoites, found no earlier than 2 days after inoculation, developed similarly to those in the cytoplasm, and small intranuclear schizonts with 6–10 merozoites (each with 2 refractile bodies) occurred after 3 days in culture.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1971.tb03292.x
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  • 9
    Electronic Resource
    Electronic Resource
    Eimeria reedi sp. n. and E. chobotari sp. n. (Protozoa: Eimeriidae) from Heteromyid Rodents (1970)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 17 (1970), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS The oocysts of 2 new species of Eimeria are described from heteromyid rodents. The subspherical to ellipsoidal cocysts of Eimeria reedi from Perognathus formosus averaged 22.6 by 20.8 μ. An ellipsoidal polar granule was present. The oocyst residuum was a single globule about 8 μ in diameter. The ovoid sporocysts averaged 10.9 by 7.7 μ and had a residuum of 6-12 granules. A Stieda body and substiedal body were present in the sporocysts. Eimeria chobotari oocysts, from Dipodomys merriami and D. microps, were ellipsoidal to ovoid and averaged 47.7 by 35.2 μ. No polar granule was seen. The large oocyst residuum consisted of several granules of various sizes. The ovoid sporocysts averaged 15.8 by 11.3 μ and had a residuum of many small granules. A Stieda body and substiedal body were present in the sporocysts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1970.tb04713.x
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  • 10
    Electronic Resource
    Electronic Resource
    Eimeria procyonis sp. n., an Isospora sp., and a Redescription of E. nuttalli Yakimoff and Matikaschwili, 1932 (Protozoa: Eimeriidae) from the American Raccoon (Procyon lotor) (1972)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 19 (1972), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Thirty-two of 48 raccoons examined were infected with a previously undescribed species of Eimeria which is herein named E. procyonis. Of the 32 infected animals, 10 also harbored E. nuttalli and 1 had Isospora sp. oocysts.The ellipsoid to ovoid oocysts of E. procyonis measured 23.4 × 18.0 (16–29 × 13–24) μm; its sporocysts measured 12.1 × 9.3 (11.5–15 × 7–10) μm, each containing a slightly flattened substiedal body. The sporocyst residuum consisted of numerous scattered granules each ∼1 μm in diameter. The oocyst wall was double-layered. The outer layer appeared rough and pitted, measuring 1.5 μm, except at the micropyle where it was 1 μm thick. The oocysts of the Isospora sp. measured 16.8 × 13.7 (16–18.5 × 12.5–15.5) μm. The wall consisted of a single layer ∼0.5 μm thick. The sporocysts measured 11.2 × 9.1 (9.5–11.5 × 8–10) μm, and each contained 4 elongate sporozoites. The oocysts of E. nuttalli measured 17.5 × 13.6 (12-21 × 11-15) μm, with a smooth single-layered wall approximately 0.7 μm thick. The sporocysts measured 12.2 × 7.1 (9-13 × 5.5–11) μm. Each sporocyst had a thin, dark, Stieda body and the sporocyst residuum consisted of many fine granules.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1972.tb03445.x
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