Action of Penicillin G on Endosymbiote Lambda Particles of Paramecium aurelia

The kinetics of loss from the cytoplasm and changes in ultrastructure of symbiont lambda particles after treatment of axenically cultivated lambda-bearing Paramecium aurelia with penicillin G was investigated. Low concentrations (1 to 2 unit/ml) of the antibiotic caused many particles within the cell to become filamentous; high concentrations (2,000 unit/ml) caused lysis of the particles without noticeably affecting the protozoan. The ED(50) value (2 to 3 unit/ml) was within the range of values found to cause lysis of many gram-negative bacteria. Rapidly dividing lambda were more vulnerable to the action of the antibiotic than slowly dividing particles. Nondividing particles were not affected by exposure to the antibiotic. Ultrastructural changes observed in lambda during lysis by penicillin G were consistent with the view that penicillin interferes with the synthesis of a vital component of the cell envelope of the particle, possibly a peptidoglycan similar to that found in the cell walls of bacteria. The deoxyribonucleic acid of lambda was dispersed throughout the particle as electron dense fibers enclosed within electron transparent areas. The cell envelope appeared to consist of at least two morphologically distinguishable layers, an inner layer homologous to the plasma membrane of bacteria and an outer layer homologous to the bacterial cell wall. Lambda may be regarded as a randomly distributed population of bacteria growing and dividing synchronously within the collective cytoplasm of its protozoan host.     

The effects of growth conditions on the esterases of Paramecium aurelia

The esterase isozymes of Paramecium aurelia grown in the presence and absence of bacteria were examined by starch gel electrophoresis. Where present, bacteria make a positive contribution to the esterase zymograms. Different bacteria contribute different esterases. Paramecia growing in axenic medium possess a different esterase which is not produced by the same parmecia growing in the presence of bacteria. This axenic esterase disappears when bacteria are added back to the medium.Supported by a research grant from the Science Research Council.     

Effects of static magnetic fields on growth of Paramecium caudatum

Little is known about the influence of magnetic fields on growth of primitive eukaryotes such as the ciliate Paramecium. The latter are known to exhibit interesting characteristics such as electrotaxis, gravitaxis, and membrane excitability not commonly encountered in higher organisms. This preliminary study reports the effects of static magnetic fields on growth of Paramecium caudatum. The microorganisms were either permanently or 24 h on-and-off exposed to North and South polarity magnetic fields of average field gradient 4.3 T/m, for a period of 96 h. The growth rate and lag phase of all exposed populations were not significantly different from control ones exposed to normal geomagnetic field (P > .05). However, a significant negative shift in t(max) (time taken for maximum growth) of 10.5%-12.2% and a significant decrease (P < .05) in population size of 10.2%-15.1% during the 96 h of experimental conditions were recorded for exposed populations compared to control. Our results suggest that magnetic fields, irrespective of polarity and exposure period reduce Paramecium growth by triggering early senescence of the population. The mechanisms underlying the small changes in population growth are unknown at this level, but various hypotheses have been suggested, including disorganization of swimming patterns resulting from (i) changes in cell membrane electric potential due to high speed movement through a gradient magnetic field and (ii) thermodynamic effect of anisotropic magnetic energies on cell membrane components affecting functioning of calcium channels. Altered swimming movements could in turn affect highly orchestrated processes such as conjugation, essential for survival of the organisms during development of adverse environmental conditions as thought to occur in the closed culture system used in this study.     

农药胁迫对草履虫个体生长和种群动态的影响

采用连续培养法探讨了草履虫(Paramecium caudatum)在甲胺磷、2,4-D丁酯和甲氰菊酯3种农药胁迫条件下的个体生长和种群动态,并利用Logistic种群增长模型对种群的增长曲线进行了分析.结果表明:甲胺磷和甲氰菊酯农药胁迫能改变草履虫细胞的大小和形态;不同农药不同浓度处理下,草履虫密度增长曲线均具有"S"型生长特点;农药胁迫下草履虫密度增长曲线符合Logistic模型(R2＞0.8),3种农药胁迫下K值明显降低;甲胺磷和甲氰菊酯农药胁迫下种群最大增长率低于2,4-D丁酯胁迫和对照.     

Studies on the macronucleus of Paramecium aurelia

Following specific incorporation of tritiated thymidine into the DNA of the macronucleus of Paramecium aurelia for varying periods of time the vast majority of silver grains in electron microscope autoradiographs are associated with the area containing the small bodies and matrix. At best only 5% of the silver grains overlying the macronucleus are attributable to the large bodies. This is consistent with the view that the large bodies are the nucleoli of the macronucleus.     

Photoreversal of nuclear and cytoplasmic effects of short ultraviolet radiation on Paramecium caudatum

1. Irradiation with three short ultraviolet (UV) wave lengths, 226, 233, and 239 mµ rapidly immobilizes Paramecium caudatum, the dosage required being smaller the shorter the wave length. 85 per cent of paramecia immobilized with wave length 226 mµ recover completely. Recovery from immobilizing doses is less the longer the wave length. 2. Irradiation continued after immobilization kills the paramecia in a manner which is markedly different for very short (226, 233, and 239 mµ) and longer (267 mµ) wave lengths. 3. An action spectrum for immobilization in P. caudatum was determined for the wave lengths 226, 233, 239, 248, and 267 mµ, and found to resemble the absorption of protein and lipide in the wave length region below 248 mµ. Addition of these data to those of Giese (1945 b) gives an action spectrum resembling the absorption by albumin-like protein. 4. Division of P. caudatum is delayed by doses of wave lengths 226, 233, and 239 mµ which cause immobilization, the longest wave length being most effective. 5. Immobilization at any of the wave lengths tested (226, 233, 239, 248, 267 mµ) is not photoreversible when UV-treated paramecia are concurrently illuminated. 6. Division delay resulting from immobilizing doses of 226, 233, and 239 mµ is photoreversible by exposure to visible light concurrently with the UV. 7. Division delay induced by exposure to wave length 267 mµ is reduced by exposure to visible light applied concurrently with UV or immediately afterwards. 8. The data suggest that the shortest UV wave length tested (226 mµ) affects the cytoplasm selectively, because it is absorbed superficially as indicated by unilateral fluorescence in UV. Consequently it immobilizes paramecia rapidly but has little effect on the division rate because little radiation reaches the nucleus. 9. The data support the view that nuclear effects of UV are readily photoreversed but cytoplasmic effects are not.     

Paramecium tredecaurelia of the Paramecium aurelia complex in Israel

The paper concerns the finding of a new habitat (Kiryat Motzkin, north of Haifa, Israel) of Paramecium tredecaurelia from the P. aurelia complex. This is only the forth known locality of the species in the world. Previously, its strains were obtained from widely separated localities: the River Seine, Paris, France; Benenitra, Madagascar, and the Cuernavaca Valley, Taxco, Mexico. The studied strain originating from Israel was identified as P. tredecaurelia on the basis of the strong (90%) conjugation between the complementary mating type of the examined clones with the appropriate standard strain 209 of P. tredecaurelia from Paris, France (restricted to odd mating type). However, the strain from Israel is restricted to the even mating type.     

Effect of local UV microirradiation on the nuclear apparatus and cytoplasm of the infusorian Paramecium caudatum]

The work is the first attempt to study nuclear dualism of ciliates with ultraviolet microbeam (UV-beam), which was not applied earlier for these purposes. The special advantage of the UV-beam is that it allow to inactivate selectively of the particular elements of nuclear apparatus of living ciliates is to observe consequences of operation on distant descendants of irradiated cell. On Paramecium caudatum the ways of UV-beam have been devised specifically. The original rotocompression chamber was employed for immobilization of cell in space of irradiation. The effective UV-doses were selected, the relative resistance of cytoplasm, macro-, micronucleus (Mi), and symbiotic bacteria of Mi -- omega particles -- was detected. The "pure" and infected cells were irradiated, in some different variants. The effect of UV-beam depends on dose and consists in a reduction the effectiveness of cell cloning, the loss of omega-particles from Mi, the appearance of the cells with 2--3 Mi, and, possibly, of amicronucleate cells. The injuries due to UV-beam are restored by photoreactivation of visible light.     

Studies on the surface coat of Paramecium aurelia

Summary The plasma membrane of Paramecium aurelia is covered with a ruthenium red stainable surface coat. Results obtained after digestion with pronase, trypsin and neuraminidase suggest the glycoprotein nature of this structure. Lipid extraction also affects the surface coat forming material. The results are consistent with the model proposed by Ginsburg and Kobata dealing with spatial configuration of the surface coat components.Authors are grateful to Mrs. D. Kucharczyk for very efficient technical assistence, to Mrs. Z. Kaminska for sectioning the material and Mr. A. Renski for help with the electron microscope service.     

Studies on the surface coat of Paramecium aurelia

Summary Correlations between the presence of surface coat and immobilization antigen of Paramecium tetraurelia were studied. Supravital, partial removal of the surface coat resulted in accelerated response of monobacterially and axenically grown cells to the homologous antiserum. Ciliates pretreated with trypsin or pronase (0.5mg/ml for 45 min at 0–4° C) were immobilized approximately twice as fast as untreated control cells. The probable localization of at least part, of the immobilization antigen within the surface coat of P. tetraurelia is discussed.The author thanks Prof. S. Dryl (Department of Cell Biology, M. Nencki Institute of Experimental Biology) and Prof. T.M. Sonneborn (Department of Zoology, Indiana University, Bloomington, USA) for donating antisera and for helpful discussion     

Paramecium sexaurelia of the Paramecium aurelia species complex in Thailand

The clones originating from Thailand, Phuket Island, were identified as Paramecium sexaurelia.     

Ultrastructural and functional differences in mitochondria isolated from Paramecium aurelia grown axenically and monoxenically.

Differences in the ultrastructure of mitochondria in $\text{P.}\text{aurelia}$ grown axenically and monoxenically have been observed. Functional mitochondria have been isolated from both cultures and various metabolic parameters have been tested; respiration rates, cytochrome content, oligomycin sensitive ATPase activity, and an attempt has been made to relate the observed structure and metabolic activity of the mitochondria to the growth conditions.