Four of 28 wild boodies or burrowing bettongs, Bettongia lesueur (Quoy et Gaimard) passed oocysts of species of Eimeria Schneider, 1875. The boodies are surviving on off-shore islands and in large predator-proof sanctuaries on the mainland where they were reintroduced. The boodie is a potoroid marsupial extinct from the mainland of Australia due to predation from red foxes and feral cats. Comparison with other species of the genus Eimeria indicates that the coccidium found represents a new species. Sporulated oocyst of Eimeria burdi sp. n. are pyriform, 21.0-24.0 µm (mean 22.6 µm) by 14.0-16.0 µm (14.9 µm), with a length/width ratio 1.31-1.71 (1.52) and 1-µm-thick yellowish bilayered wall. Micropyle is present at the thinner apex end filled with hyaline body. Polar granules are absent. Sporocysts are ellipsoidal, 10.0-13.5 µm (11.8 µm) by 7.0-8.5 µm (7.4 µm), shape index is 1.42-1.89 (1.63) and a very thin, poorly defined unilayered sporocyst wall is 0.2 µm thick with a domelike almost indistinct Stieda body. Substieda body is indistinct., Frances Hulst, Leah F. Kemp, Jan Šlapeta., and Obsahuje bibliografii
Parasitological examination of two ornate Nile monitors Varanus ornatus (Daudin, 1803) imported from Benin revealed the presence of a new species of Caryospora. Oocysts of Caryospora varaniornati sp. n. are spherical to slightly subspherical, 12.0 (11-12.5) × 11.5 (11-12) µm, without a micropyle and oocyst residuum, and occasionally possessing one small polar granule. Sporocysts are broadly ellipsoidal, 8.8 (8.5-9.5) × 6.7 (6.5-7) µm; a lentil-like Stieda body is present, ca. 0.5 × 1 µm; substieda body not visible. Experimental infection of a closely related host, Varanus niloticus (L.), did not lead to the oocyst excretion despite the fact that one of the experimentally inoculated monitors was immunosuppressed by dexamethasone. Histological examination did not reveal stages of coccidian development. Therefore, it is possible that C. varaniornati is strictly host specific.
Faecal samples from the rock hyrax (Procavia capensis jayakari Thomas) were collected from the Ibex Reserve in central Saudi Arabia. Eimerian oocysts, which are believed to represent a new species described here as Eimeria tamimi sp. n., were detected in 40 out of 93 samples. Oocysts were fully sporulated in 24-48 hours at 25 ± 2 °C. Sporulated oocysts of E. tamimi sp. n. were ovoid, measuring 35-42 × 19-25 μm (39 × 23 μm), a length/width ratio 1.5-2 (1.7). Oocyst wall was bilayered and measured 1.5 μm in thickness. Micropyle, oocyst residuum and polar granules were not present. Sporocysts are elongate, measuring 12-18 × 9-12 μm (15 × 10 μm), with a length/width ratio 1.1-1.8 (1.5) prominent Stieda bodies and sporocyst residuum. Experimental infection of two clinically healthy rock hyraxes with sporulated oocysts of E. tamimi sp. n. resulted in shedding unsporulated oocysts 5-10 days post infection. Partial sequences of 18S ribosomal RNA (18S rDNA) and cytochrome C oxidase subunit 1 (COI) regions were amplified using the polymerase chain reaction (PCR) and sequenced. Phylogenetic analysis based on 18S rDNA using maximum likelihood (ML) and Bayesian inference (BI) methods revealed that E. tamimi sp. n. grouped with Eimeria quokka Barker, O'Callaghan et Beveridge, 1988, E. mundayi Barker, O´Callaghan et Beveridge, 1988, E. potoroi Barker, O'Callaghan et Beveridge, 1988 and E. gaimardi Barker, O'Callaghan et Beveridge, 1988 marsupials. Eimerian species have been regarded as a paraphyletic group and the present investigation confirmed the conflict between phenotypic traits, used widely in the classification of this group of parasites., Osama B. Mohammed, Manei M. Aljedaie, M. S. Alyousif and Nabil Amor., and Obsahuje bibliografii
Coccidiosis is a parasitic disease caused by protists (apicomplexans) of the genus Eimeria Schneider, 1875 and is considered to be the most important disease faced by rabbit breeders due to its high morbidity. In the present study, the antioxidant status and changes in apoptosis and in the expression of some genes were quantified in rabbits' ilea following infection with Eimeria intestinalis Cheissin, 1948. Rabbits, orally infected with 1 × 105 sporulated oocysts of E. intestinalis, started to shed oocysts in their faeces on 8 days post infection (dpi) and reached maximum excretion on 10 dpi, with approximately 5 million oocysts. This was accompanied by a significant decrease in the live body weight of infected rabbits. Also, malondialdehyde and nitric oxide were significantly increased while catalase and glutathione were significantly decreased in the ileum tissues of the infected rabbits. In addition, a significant increase was observed in the percentages of apoptotic cells in the ilea of the infected rabbits. Furthermore, interleukin-1β and interleukin-2 mRNA levels were significantly down-regulated and mRNA levels of interleukin-6, interferon gamma and inducible nitric oxide synthase were significantly up-regulated, while those of C-reactive protein remained unchanged. We conclude that infection with E. intestinalis induces oxidative stress, a significant increase in the percentage of apoptotic cells and a diverse and robust Th1 and Th1-related cytokine response in the ileum tissues., Heba M. Abdel-Haleem, Shawky M. Aboelhadid, Thabet Sakran, Gamal El-Shahawy, Huda El-Fayoumi, Saleh Al-Quraishy, Abdel-Azeem S. Abdel-Baki., and Obsahuje bibliografii
To date, three species of Isospora Schneider, 1881 have been described from lizards of the genus Acanthodactylus Wiegmann. Two of these, although representing separate species parasitizing two different hosts, Acanthodactylus boskianus Daudin in Egypt and A. schmidti Haas in Saudi Arabia, were described under the name Isospora acanthodactyli. The third species is Isospora abdallahi Modrý, Koudela et Šlapeta, 1998 from A. boskianus in Egypt. In the present study, Isospora alyousifi nom. n. is proposed to accommodate Isospora acanthodactyli Alyousif et Al-Shawa, 1997 (homonym of I. acanthodactyli Sakran, Fayed, El-Toukhy et Abdel-Gawad, 1994) and its redescription based on newly collected material is provided.
The present study was designed to determine the influence of temperature and the addition of potassium dichromate solution (K2Cr2O7) on the efficiency of sporulation of Eimeria bovis (Zublin, 1908), a coccidian species most commonly diagnosed in European bison Bison bonasus (Linnaeus). Sporulation under conventional conditions (2.5% dichromate solution, 23 °C) was completed on the fourth day of incubation (control), whereas the oocyst development took two days more at the temperature of 18 °C, and two days less at 28 °C. Additionally, experimental sporulation of E. bovis at the temperature of 23 °C in the environment of sterilised tap water (without any preservation) took 9 days more compared to control. Finally, oocyst development took 16 weeks when the faces were stored in the refrigerator (3-5 °C) without any special additives. Overall, our results indicate that K2Cr2O7, besides the temperature, plays a crucial role in the process of sporulation of oocysts under laboratory conditions, as the longest delay in sporogony was observed when the faeces were stored without any other additives in the temperature of the refrigerator., Anna M. Pyziel, Aleksander W. Demiaszkiewicz., and Obsahuje bibliografii
Eimeria dorcadis Mantovani, 1966 is redescribed from dorcas gazelle (Gazella dorcas (L.)) from Saudi Arabia. Oocysts were detected in 7 out of 22 faecal samples (32%) using floatation method. The sporulated oocysts are cylindrical, slightly flattened at the micropylar pole, measure in average 32 × 19 μm (27-36 × 16-24 μm), length/width ratio being 1.7 (1.5-2.1). Oocyst wall is 1.2 μm thick, smooth, double-layered; outer layer is slightly thicker, light blue in colour; inner layer brownish, with micropyle in the inner layer and apparently continual outer one, measures 2.2 μm, but lacks a micropylar cap. The sporocyst elongate-ellipsoidal, measures 14 × 8 μm (12-17 × 6-9 μm), length/width ratio being 1.8, with sporocyst residuum as circular compact, coarse, refractile granules. Stieda body is present, while substieda body is absent. Sporozoites banana-shaped, measure 11 × 2.5 μm, each with a large spheroidal refractile body at the wider pole. Sporulation time is 2-3 days at 25 ± 2 °C.