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  • 1980-1984  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 31 (1984), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Morphologic and biometric data on bloodstream stages of Trypanosoma melophagium are presented. An increasing parasitemia with 111 trypomastigote stages of T. melophagium were found in Giemsa-stained thin blood smears taken from a splenectomized, cortisone-treated sheep recently infested with Melophagus ovinus infected with T. melophagium. The arithmetic mean and standard deviation in μm of the distances between posterior end and kinetoplast were 14.7 and 2.9, from the kinetoplast to the center of the nucleus 5.1 and 1.1, and from there to the anterior end 19.5 and 1.9. The free flagellum measured 6.0 μm ± 1.6 μm. The median and the range of the central 70% of values (median ± 35%) of the nuclear index were 1.1 and 0.9–1.2 and of the kinetoplastic index 3.8 and 3.3–4.9. The same data in μm for the maximal width were 3.1 and 2.1–4.6, and for the width at the level of the nucleus 2.9 and 2.2–4.6. The larger and smaller diameters of the nucleus measured 2.6 (2.2–3.7) μm and 1.7 (1.3–1.7) μm, respectively. The corresponding kinetoplast diameters were 1.1 (0.9–1.3) μm and 0.9 (0.6–0.9) μm, respectively.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Parasitology research 70 (1984), S. 687-689 
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Conclusions The host cells ofT. annulata can be infected withT. parva. With the superinfection of untreatedT. annulata cultures it is not clear if only the few cells not carrying a schizont were susceptible to infection withT. parva or if cells with aT. annulata schizont also became infected withT. parva. In the latter case,T. parva parasites, while going through non-dividing stages (sporozoite, trophozoite, early schizont), may have been diluted out by the rapidly growing and dividing cells transformed byT. annulata. When the propagation of the cells infected byT. annulata was stopped by the schizonticidal treatment, a high infection rate withT. parva was achieved. However, eventuallyT. annulata-infected cells reappeared in the cultures and by 6 weeks appeared to be overgrowing theT. parva-infected cells. Nevertheless, for a period of 2–3 weeks the cultures consisted of cells, more than 99% of which were infected withT. parva. When inoculated into cattle at a dose of 6×105, these cells failed to initiate infection or induce immunity. In view of the fact that as few as 104 of these cells infected withT. annulata can induce infection and a serological response in cattle, these results indicate that the difference in the capacity of the twoTheileria species to transfer infection is a property of the parasite rather than the host cell type which becomes infected.
    Type of Medium: Electronic Resource
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