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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 42 (1995), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . We have isolated a cDNA for an α-tubulin mRNA from L. donovani promastigotes and determined its complete nucleotide sequence. Both nucleotide and deduced amino acid sequence analysis of this cDNA showed significant similarity with a previously reported, partial sequence of an L. enriettiiα-tubulin and the complete sequence of human α-tubulin. Further, the in vitro translated L. donovaniaα-tubulin gene product was specifically immunoprecipitated with a monoclonal antibody against human α-tubulin. Northern blot analysis revealed that there was little change in the expression of the L. donovaniα-tubulin RNA during parasite differentiation from promastigote to the in vitro grown “amastigote” form. Southern blot analysis revealed a simple genomic organization for the L. donovaniα-tubulin gene with more than one copy of the α-tubulin gene in the parasite genome. To our knowledge, this is the first complete sequence of an α-tubulin for Leishmania to be reported in the literature.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 23 (1976), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. An extracellular surface coat was observed at the fine-structural level on the outer lamina of the pellicular and flagellar membranes of intact Trypanosoma musculi bloodstream forms. The surface coat had a mean width of 9.2 nm, and was composed of a somewhat electron dense, uneven, fibrillar-like matrix. Brief trypsin treatment of living blood forms completely removed the cell surface coat.Several cytochemical methods applicable to electron microscopy were used to detect the presence and distribution of carbohydrates in the trypanosome's surface coat and pellicular membrane. The polycationic dye compounds employed were: ruthenium red, ruthenium violet, Alcian blue chloride, and lanthanum nitrate. Electron-dense stain reaction products, indicative of polysaccharides, were evident in the surface coat of cells treated with these dyes, which also agglutinated both living and glutaraldehyde fixed cells. Like the surface coat, the pellicular membrane of trypsinized cells gave strong positive staining reactions with the several dyes, indicating the presence of membrane bounded carbohydrates, and living and glutaraldehyde-fixed trypsinized cells were agglutinated with the polycationic stains. Bloodstream forms were treated with the enzymes, α-amylase, dextranase, and neuraminidase. No obvious morphologic difference, however, was apparent between the surface coat of untreated cells and those subjected to treatment with any of the various glycoside hydrolase enzymes. Further, these enzymes had no apparent gross effect on the staining affinity of the surface coat for the several polycationic dyes. Cationized ferritin was used to visualize the negative cell surface charge of T. musculi bloodstream forms. Large quantities of cationized ferritin were bound in the surface coat matrix. Glycoside hydrolase enzyme treatments had no apparent effect on the amount of ferritin bound in the surface coat. Cationized ferritin was bound also to the outer lamina of the pellicular membrane in trypsinized cells, which had quantitatively less ferritin bound per surface unit area than bloodstream forms untreated by the enzyme. Living and glutaraldehyde-fixed cells were agglutinated with cationized ferritin. The results obtained in the various experiments indicated that polyanionic polysaccharides were constituent terminal ligands of the surface coat matrix and pellicular membrane in T. musculi bloodstream forms.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 27 (1980), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Cell surface pellicular membranes (PM) were isolated from promastigote forms of Leishmania donovani by differential and discontinuous sucrose gradient centrifugation procedures. the PM had a density equivalent of ∼ 1.19 g/cm3. As ascertained by electron microscopy, longitudinal parallel arrays of subpellicular microtubules (MT) remained attached to the isolated PM inner lamina, and this feature was used to assess membrane fraction purity. Gradient fractions having ∼ 95% of all membranes combined with MT were obtained routinely. the attached MT imparted a structural asymmetry to the PM permitting uniequivocal identification of the membrane external and cytoplasmic surfaces. the supramolecular structure of attached MT was evident in negatively stained PM. In ultrathin sections, PM had a mean width of ∼ 7.2 nm and attached MT a diameter of ∼ 29 nm. the MT were apparently cross-bridged both to each other and to the PM via a flocculent filamentoid nexus. As determined by sodium dodecylsulfate-polyacrylamide gel electrophoresis, isolated PM contained ∼ 40 peptide bands ranging in apparent molecular weight from ≤ 1.2 × 104 to ≥ 2.2 × 105daltons. of these, 19 were stained with periodic acid-Schiffs’ reagent suggesting that most PM carbohydrate constituents were present as glycopeptides. A presumpative glycolipid/polysaccharide PM constituent was also identified in such gels.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 28 (1981), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The interaction of Leishmania with lysosomes within macrophages in vivo has been investigated. Lysosomes labeled with colloidal gold in vivo fused with phagocytic vacuoles containing Leishmania amastigotes within the macrophages of infected footpad tissue of BALB/c mice. This localization of Leishmania within macrophage phagolysosomes in vivo is the first confirmation for any obligate intracellulaire protozoon that parasite-lysosome interactions in vitro occur in vivo.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 19 (1972), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Antigens were prepared from axenic Entamoeba histolytica, Entamoeba invadens, and Trichomonas gallinae; dixenic Dientamoeba fragilis; and agnotobiotic Histomonas meleagridis cultures. Antisera were developed in rabbits against each of these species by subcutaneous inoculations of homogenized organisms with complete Freund's adjuvant. The globulin fraction of each serum was conjugated with fluorescein isothiocyanate (FITC) and then processed on Sephadex G-25 and DEAE-cellulose columns. Fluorescein/protein ratios were determined for the several DEAE fractions obtained from each of the 5 conjugated globulins, and those with ratios of approximately 3.0 were selected for use in all experiments. Conjugated anti-Dientamoeba and anti-Histomonas fractions were absorbed with the bacterial flora present in the respective cultures before being used for staining. Intact, formalin-fixed organisms of each of the species were subjected to direct staining, inhibition staining, and staining with cross-absorbed conjugated fractions. The emitted fluorescence was measured in an ultramicrofluorimeter.Cross reactions among the 5 antigens and 5 conjugated antisera suggested that very few, if any, common antigens were shared by Trichomonas and Entamoeba. They indicated also a close antigenic relationship between Trichomonas and Histomonas on the one hand and between Histomonas and Dientamoeba on the other. Trichomonas and Dientamoeba appeared to be less closely related, and still less relationship was noted between Dientamoeba and Entamoeba. Only very weak reactions were recorded between Histomonas and Entamoeba. Entamoeba invadens emitted much fluorescence after being stained with anti-Entamoeba histolytica conjugate and similar results were obtained by reciprocal staining. The phylogenetic implications of the immunologic findings are discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 21 (1974), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Antigens prepared from Trichomonas gallinae, Histomonas meleagridis, Dientamoeba fragilis, Entamoeba invodens and Entamoeba histolytica were separated by electrophoresis in agar gels and reacted with antisera prepared in rabbits against each of the 5 species. The most numerous and strongest precipitin lines were obtained from reactions between the homologous antigens and antisera. Direct and cross-absorption reaction methods were employed with each antiserum and the various antigens to ascertain quantitatively the immunologic relationships among the several organisms. Trichomonas shared many common antigens with Histomonas, fewer with Dientamoeba and none with either species of Entamoeba. Histomonas was more closely related antigenically to Dientamoeba than to Trichomonas. The histomonad had only a few weakly cross-reacting antigens in common with the 2 Entamoeba species. Dientamoeba shared the most common antigens with Histomonas, fewer with Trichomonas and the fewest with Entamoeba. Somewhat stronger cross-reactivity was obtained with anti-Dientamoeba serum and E. invadens than between this immune serum and E. histolytica. The 2 species of Entamoeba shared the largest number of common antigens with each other, and to a much lesser extent both species cross reacted with Dientamoeba. Anti-Entamoeba sera had only a few weak cross-reacting precipitins with Histomonas. No antigenic relationship was found between either species of Entamoeba and Trichomonas.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 19 (1972), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Antisera were developed in rabbits against Trichomonas gallinae, Histomonas meleagridis, Dientamoeba fragilis, Entamoeba invadens, and Entamoeba histolytica. In reactions between these antisera and antigens prepared from each of the 5 species the most numerous and strongest precipitin lines appeared on gel diffusion agarose plates between the homologous antigens and antisera. Anti-Trichomonas serum cross-reacted most strongly with Histomonas, somewhat less with Dientamoeba, but gave no lines with the 2 species of Entamoeba. Anti-Histomonas serum cross-reacted strongly with both Trichomonas and Dientamoeba, and weakly with E. invadens and E. histolytica. Dientamoeba antiserum gave many precipitin lines with Histomonas, fewer with Trichomonas, and fewest with the 2 species of Entamoeba. Stronger reactions were noted between anti-Dientamoeba serum and E. invadens than between this serum and E. histolytica. Immune sera prepared against the 2 species of Entamoeba gave the most numerous precipitin lines in intrageneric cross-reactions, but the reaction between either of these antisera and Histomonas was weak. Somewhat stronger reactions were observed between the 2 anti-Entamoeba sera and Dientamoeba. Trichomonas failed to react with either of the anti-Entamoeba sera.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 18 (1971), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Antigens were prepared from each of 4 lines of Histomonas meleagridis: Hm-L1, a strain highly virulent for both turkeys and chickens; Hm-L1/C12, Hm-L1/C24, Hm-L1/C52, 3 avirulent substrains derived from Hm-L1 after 12, 24, 52 weeks of in vitro cultivation, respectively. Hm-L1 strain and the 3 substrains were maintained in liquid nitrogen. Antisera were developed in rabbits against Hm-L1 and Hm-L1/C24 parasites. Both antisera were reacted on gel diffusion plates with homologous and heterologous antigens. Two groups of precipitin lines and/or bands designated arbitrarily as A and B, were observed on the slides. Analysis of these bands revealed the common antigenic composition of the 4 histomonads with respect to some of the group A and group B antigens. The concentrations and numbers of precipitin lines in both groups increased, however, with the length of cultivation. These antigenic differences are discussed in the light of their possible relationship to pathogenicity.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 51 (2004), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . Promastigotes of all pathogenic Leishmania species secrete acid phosphatase (SAcP) activity during their growth in vitro. It has been suggested that this enzyme may play a role in the survival of the parasite within its sandfly-vector host. To carry out such functions, SAcP would have to be relatively resistant to endogenous sandfly gut-proteases. Therefore, the current study was undertaken to ascertain whether L. donovani SAcP activity was affected by treatment with various proteases. Native L. donovani SAcP was treated with a variety of serine-, thiol-, metallo- and mixed proteases and subsequently assayed for enzymatic activity. Of the eleven proteases tested, only bromelain and subtilisin treatments caused a pronounced reduction in SAcP activity. Treatment of SAcP with seven out of the remaining nine proteases, resulted in an overall enhancement in SAcP enzymatic activity ranging from ∼ 10% (e.g. with trypsin) to 〉 90% (e.g. with ficin). The resistance of the Leishmania SAcP to various proteases may prolong its functional life within the sandfly gut and help to facilitate parasite infection in this host.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 140 (1973), S. 177-186 
    ISSN: 1432-0878
    Keywords: Microtubules ; Microsporidia ; Nosema ; Tubulins ; Electron microscopy, Electrophoresis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Nosema michaelis spores possess a biologically unique external arrangement of microtubules. The microtubules were studied ultrastructurally with the use of thin sections, freeze-etched and negatively stained preparations. Tubules were sheared from the spores by repetitive freeze-thaw cycles and harvested by high speed centrifugation. Electron microscopic observations of negatively stained and freeze-etched samples revealed the globular subunit construction of the tubules. Suspensions of isolated microtubules and tubular fragments formed extended linear array at 4°C, apparently by autoaggregation. Tubule preparations were reduced and alkylated under various conditions and examined in several polyacrylamide disc gel systems. Two bands were obtained from completely reduced and alkylated microtubule proteins separated in polyacrylamide gels containing 8 M-urea, detergent-urea or detergent alone. The two subunit proteins (tubulins) had average molecular weights of ∼45000 and ∼53000. Incompletely reduced samples yielded two additional satellite bands of higher molecular weights, suggestive of homodimers.
    Type of Medium: Electronic Resource
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