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DENNIS M. SCHMATZ MARK S. J. CRANE P. KEITH MURRAY 《The Journal of eukaryotic microbiology》1986,33(1):109-114
ABSTRACT. An assay has been developed using parasite-specific incorporation of 3H-uracil to assess the intracellular growth of Eimeria tenella in vitro. As shown by both scintillation counts and autoradiography, 3H-uracil was incorporated specifically into intracellular parasites from the onset of infection and continued throughout development of the first generation schizonts. Mature schizonts and first generation merozoites did not continue to incorporate additional 3H-uracil, indicating that RNA synthesis had halted in these stages. Based on these findings, a semi-automated microscale uracil incorporation assay was developed to determine parasite viability. This method should be useful for biochemical studies with intracellular parasites and for screening compounds for anticoccidial activity. The ease, rapidity, and quantitative nature of this assay contrasts favorably with standard morphometric approaches of determining parasite development. In addition, parallel studies using host cell incorporation of 3H-uridine have been introduced as a method of determining whether antiparasitic activity is direct or indirect in relation to effects on the host cell. 相似文献
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Biochemical characterisation of Pythium spp. involved in cavity spot of carrots in France 总被引:1,自引:0,他引:1
The pathogenicity and growth rate in vivo were assessed on 27 isolates of Pythium spp. recovered from cavity spot lesions on carrots grown in various parts of northwest France. Polyacrylamide gel electrophoresis of isoesterases was used to identify the Pythium spp. involved. Slow-growing isolates were more aggressive than fast-growing ones when inoculated on carrot tap roots. Isoesterase patterns identified the slow-growing isolates as P. violae and P. sulcatum; P. ultimum and P. intermedium were identified among the less aggressive fast-growing isolate group, in which some isolates were also classed as P. sylvaticum or P. irregulare, which have similar electrophoretic profiles. The incidence of Pythium spp. associated with the disease in France is discussed in regard to cavity spot in other countries. 相似文献
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Bryophytes and nutrient cycling 总被引:11,自引:0,他引:11
DENNIS H. BROWN JEFFREY W. BATES 《Botanical journal of the Linnean Society. Linnean Society of London》1990,104(1-3):129-147
Direct information on nutrient cycling through bryophytes is limited and often incomplete. Evidence bearing on the sources and pathways by which nutrient elements are acquired (e.g. aerial deposition, throughfall and substratum) and lost (e.g. leaching and decomposition) is critically discussed. The need to distinguish between the extracellular and intracellular location of elements is emphasized. The involvement of microorganisms and the problems of accurately measuring decomposition are considered. A summary is given of recent laboratory work on the internal redistribution of elements in Rhytidiadelphus squarrosus and of field experiments involving fertilizer addition to Pseudoscleropodium purum; their significance is assessed. 相似文献
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The cell cycle in Silene coeli-rosa shoot apices was measuredto test whether or not early components of the floral stimulus,produced during the 2nd and 3rd long days (LD) of an inductiveLD treatment, resulted in an increase in the duration of G2phase in constant 2024 h cell cycles. Plants were grownat 20°C in short days (SD) of 8 h light and 16 h darknessfor 28 d (day 0). Starting on day 0, plants were given SD or3 LD each comprising an identical 8 h day and 16 h photo-extension,or 3 dark-interrupted (d.i.) non-inductive LD, interrupted at1700 h of each day with 1 h of darkness. The cell cycle (percentagelabelled mitoses method) and changes in cell number were determinedin the shoot apical meristem. During days 12 of the SDtreatment, the cell cycle and mean cell generation time (MCGT)was 18 and 32 h, respectively, giving a growth fraction of 56%.During days 23, the cell cycle and MCGT shortened to15 and 23 h, respectively (growth fraction = 65%). During days12 of the LD and d.i. LD treatments, cell cycles andMCGTs were 910 and 2729 h, respectively, resultingin smaller growth fractions (about 33%). Thus, shortened cellcycles and altered growth fractions occurred regardless of whetheror not the treatment was inductive. The LD treatment resultedin a marked shortening of G1 and, to a lesser extent, S-phase,whilst G2 remained constant. These changes were consistent withincreases in the proportion of cells in G2 during the photoextensionof each LD which were suppressed during the comparable periodsof the d.i. LD treatment. The latter treatment resulted in eachphase occupying virtually identical proportions of the cellcycle as in the SD treatment. Thus, the unique cell cycle responsesto the initial part of the inductive LD treatment were increasesin the proportion of cells in G2 coupled with G1 and G2 beingof similar duration. Cell cycle, mean cell generation time, shoot apex, Silene coeli-rosa 相似文献
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