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  • 1965-1969  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 13 (1966), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Macrophages were infected in vivo with the intracellular form of Leishmania donovani (LDs), harvested from the previously saline-stimulated peritoneal cavities of hamsters and explanted into Leighton tubes containing removable coverslips. Serum from either rabbit, chicken, human, calf, hamster or cotton rat blood was used as the 40% component of a Hanks' BSS60 serum40 medium used to maintain these Leighton tube cultures at 37 C. After varying lengths of time coverslips were removed from tubes, stained with Giemsa, and the parasites per infected macrophage, total number of hamster cells and total number of parasites on each coverslip were counted.Maerophages constituted more than 90% of the explanted cells on the coverslips. When cotton rat serum was used as a component of the medium, fibroblastic overgrowth of the coverslips followed. Some similarities and differences in the numbers of macrophages, fibroblasts and parasites were noted with regard to the serum used as part of the medium. Except for cotton rat serum, the serum component of the medium used apparently did not influence, to any great degree, the morphology of either the macrophages or parasites therein. Thus, vacuolarization and granularization of macrophages did not appear to be very distinctly correlated with the time of sampling or the type of serum in the medium used for maintenance nor could any morphologic variations of the LDs be ascribed to these factors.When cotton rat serum, but not any of the other sera, was the serum component of the medium, leptomonads were noted in the overlay fluid of the cultures after 6 days.Under these conditions of cell culture, fibroblasts could not be infected with LDs although macrophages on the same coverslip were heavily parasitized.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 15 (1968), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Monkey kidney cells (LLC-MK2) grown in flasks and on coverslips in Leighton tubes were used as host cells for the growth of the intracellular stage, Leishman-Donovan bodies (LDs), of Leishmania donovani obtained from hamster spleen. These parasitized cultures were then used to determine the ability of acriflavin to induce dyskinetoplastic LDs.LD-infected cells were somewhat fewer in number than uninfected cells at all times except for the 1st day after infection. The parasites attained their maximum numbers on the 5th day after infection of the cultures having a 1.9-fold increase at that time.When acriflavin was added to the cell culture medium (250 mμ/ml) the numbers of monkey kidney cells did not differ greatly from non-treated cultures until 6–7 days after treatment with acriflavin. Similarly, the numbers of LDs in acriflavin-treated cell cultures, altho somewhat below those of untreated cultures, did not differ greatly from them.The combined effect of acriflavin and LDs reduced the numbers of monkey kidney cells in treated, LD-infected cell cultures more than either alone.Dyskinetoplastic LDs appeared in considerable numbers in acriflavin-treated, LD-infected cell cultures. Dyskinetoplastic and normal LDs harvested from cell cultures were inoculated into NIH medium and incubated at 27 C for transformation into leptomonads. There was no indication that dyskinetoplastic LDs were capable of transforming into leptomonads.
    Type of Medium: Electronic Resource
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