Showing papers in "Journal of Eukaryotic Microbiology in 1984"
TL;DR: Determinations of physiological and behavioral characteristics that are now becoming available should be included in species definitions wherever possible and may vary according to the parasite and host studied.
Abstract: The paper is concerned with the principles upon which coccidia of the genus Eimeria may be characterized. Reference strains for comparative purposes usually are not available and the limitations of morphological data for speciation are discussed. The value of other parameters are considered such as host and site specificity, pathogenicity, immunological specificity, pre-patent period, sporulation time, enzyme variation, and DNA buoyant density. The weight afforded to each of these parameters for specific identification may vary according to the parasite and host studied. Determinations of physiological and behavioral characteristics that are now becoming available should be included in species definitions wherever possible.
165 citations
TL;DR: Reports of Cryptosporidium in various hosts and cross-transmission experiments are reviewed and it is concluded that only four "species" should be considered valid at present.
Abstract: Reports of Cryptosporidium in various hosts and cross-transmission experiments are reviewed. Cryptosporidium has been found in mammals (Primates, Artiodactyla, Perissodactyla , Carnivora, Lagomorpha, and Rodentia), birds, reptiles, and fish. The only cross-transmission attempts that have been made have been from mammals to other mammals and to a few birds. Names have been given to 19 "species," but it is concluded that only four of these should be considered valid at present. These are: C. muris Tyzzer, 1907 in mammals, C. meleagridis Slavin , 1955 in birds, C. crotali Triffit , 1925 in reptiles, and C. nasorum Hoover , Hoerr , Carlton , Hinsman & Ferguson, 1981 in fish.
155 citations
TL;DR: It is deduced that intracystic bodies resulting from meiotic nuclear division are haploid and, after excystation, they are haploids trophozoites, and this process can be called sporogony.
Abstract: Evidence for meiosis was demonstrated electron microscopically for the first time in Pneumocystis carinii in rat alveoli by the observation of synaptonemal complexes followed by nuclear divisions Synaptonemal complexes indicating meiotic nuclear divisions were observed in uninuclear precysts Additionally, owing to the use of tannic acid as a fixative, spindle microtubules were also observed for the first time in the precyst Based on these facts, a new life cycle of the organism is proposed The precyst has generally been considered an intermediate form between the trophozoite and the cyst The present paper proposes that the precyst is additionally defined as the cell in which eight intracystic bodies are produced through meiotic reduction The most characteristic feature of the precyst is a clump of mitochondria in the cytoplasm We divide the precyst phase into three forms, which are named early, intermediate, and late Synaptonemal complexes were only observed in the early precyst, which is a uninuclear cell with a thin pellicle In the intermediate precyst, nuclear divisions are observed as follows: meiosis I produces two haploid nuclei and each of these divides at meiosis II producing four nuclei After that, another postmeiotic mitosis takes place, resulting in eight haploid nuclei In the late precyst, a delimiting membrane originates from the mother plasmalemma and surrounds the daughter nuclei and a small portion of the adjacent cytoplasm Finally, when the eight intracystic bodies are complete, the precyst changes to a cyst Thus, we deduce that intracystic bodies resulting from meiotic nuclear division are haploid and, after excystation, they are haploid trophozoites We consider that this process can be called sporogony(ABSTRACT TRUNCATED AT 250 WORDS)
135 citations
TL;DR: It is concluded that endocytic vesicles fuse with the food vacuole and that treatment of infected cells with therapeutic concentrations of chloroquine inhibited the last step of the feeding process, i.e. vacuolar degradation.
Abstract: Ultrastructural investigations of P. falciparum cultivated in vitro in human erythrocytes revealed new features of the feeding mechanism of the parasite. Mature trophozoites and schizonts take up a portion of the host cytosol by endocytosis which is restricted to cytostomes and which involves the invagination of both parasitophorous and parasite membranes. The resulting endocytic vesicles, surrounded by two concentric membranes, migrate towards the central food vacuole membrane. The external membrane of the endocytic vesicles apposes that of the food vacuole, leading to the internalization of vesicles bounded by a single membrane into the vacuolar space where they are rapidly degraded. We conclude from this sequence of events that endocytic vesicles fuse with the food vacuole. Treatment of infected cells with therapeutic concentrations of chloroquine inhibited the last step of the feeding process, i.e. vacuolar degradation. This was manifested by the accumulation within the vacuolar space of intact vesicles bounded by single membranes. The implications of these findings for the antimalarial activity of chloroquine are discussed.
133 citations
TL;DR: Infectivity studies in vitro with sporozoites showed that they were viable after purification and were at least as infectious as the unpurified sporozoite material.
Abstract: An anion exchange column of DE-52 has been used to purify Eimeria sporozoites from a post- excystation mixture of oocysts, oocyst shells, sporocysts, sporocyst shells, and sporozoites. The mean recovery from several experiments was 94% and virtually all non-sporozoite material was removed. Infectivity studies in vitro with sporozoites showed that they were viable after purification and were at least as infectious as the unpurified sporozoites; furthermore, oocysts in the crude preparation could be recovered from the DE-52 cellulose by resuspending them in a 20% (w/v) sodium chloride solution.
130 citations
TL;DR: Sarcocystis falcatula Stiles, 1893 is re-described in this paper, intermediate hosts of the parasite are species of passeriform, psittaciform, and columbiform birds, muscle zoites are 6.88 X 2.19 (4.8-8.4) micron and are enclosed in a cyst wall with regular protrusions.
Abstract: Sarcocystis falcatula Stiles, 1893 is re-described. Intermediate hosts of the parasite which was earlier described as Sarcocystis debonei Vogelsang, 1929 are species of passeriform, psittaciform, and columbiform birds. In these birds, muscle zoites are 6.88 X 2.19 (4.8-8.4 X 1.2-3.6) micron and are enclosed in a cyst wall with regular protrusions, 1-5 micron long. The convoluted primary wall has multiple thin areas in the osmiophilic layer. Microtubules originate in the ground substance and extend to the tips of the protrusions. The only known definitive host is the opossum, Didelphis virginiana; rats, cats, a dog, and a ferret could not be infected from muscle cysts. Sporocysts from opossums infected from five different infected avian sources measure 11.2 X 7.4 (9.6-12.0 X 6.0-8.4) micron.
98 citations
TL;DR: Findings provide circumstantial evidence that oocysts of Cryptosporidium can excyst in extraintestinal sites and liberate sporozoites that can initiate autoinfection.
Abstract: . Whereas excystation of sporozoites from oocysts of most coccidian species requires exposure to reducing conditions followed by pancreatic enzymes and bile salts, sporozoites of a bovine isolate of Cryptosporidium excysted without exposure to either reducing conditions or to pancreatic enzymes and bile salts. Without prior exposure to reducing conditions, a high percent excysted after incubation in a mixture of trypsin and bile salts in Ringer's solution; fewer excysted after incubation in tap water, even fewer after incubation in salt solutions, and none after incubation in saliva. Excystation, generally greater at pH 7.6 than at pH 6.0 and at 37°C than at 20°C, was observed as early as 1 h after incubation in water or the trypsin-bile mixture. These findings provide circumstantial evidence that oocysts of Cryptosporidium can excyst in extraintestinal sites and liberate sporozoites that can initiate autoinfection.
98 citations
TL;DR: The ultrastructure of the sexual stages of Plasmodium gallinaceum during gametogenesis, fertilization, and early zygote transformation is described and new observations are made regarding the parasitophorous vacuole of gametocytes and the process of emergence in male and female gametocyte.
Abstract: The ultrastructure of the sexual stages of Plasmodium gallinaceum during gametogenesis, fertilization, and early zygote transformation is described New observations are made regarding the parasitophorous vacuole (PV) of gametocytes and the process of emergence in male and female gametocytes Whereas female gametocytes readily disrupted both the PV membrane and host cell plasmalemma during emergence, male gametocytes frequently failed to break down the plasmalemma of the host cell New observations and hypotheses are presented on the behavior of the male gamete nucleus Following fertilization, the male nucleus appears to travel through a channel of endoplasmic reticulum in the female gamete before fusing with the female nucleus at a region in which the nuclear envelope is thrown into extensive convoluted folds Polarization of the zygote nucleus, in association with the appearance of a perinuclear spindle of cytoplasmic microtubules, preceded all other changes in the developing zygote After nuclear polarization becomes apparent, electron-dense material is deposited beneath the zygote pellicle, and a canopy is formed which eventually extends over the entire apical end of the developing ookinete As the apical end begins to extend outward, polar rings, micronemes, and subpellicular microtubules become visible in this portion and a “virus-like” inclusion known as a crystalloid is formed in the posterior portion of the zygote When female gametes are prevented from being fertilized, the cytoplasm at 24 h after gametogenesis is devoid of most of those organelles found in the developing zygote or the mature ookinete The cell is surrounded only by a single membrane Although at various points beneath the membrane there are deposits of electron-dense material reminiscent of those deposited in the zygote, no further development of ookinete structures takes place in the unfertilized female gamete
75 citations
TL;DR: The results demonstrate that more than one strain of T. cruzi can coexist in the same host; the timing and method of parasite isolation from the vertebrate host act as selective factors, and further passages may completely eliminate one (or more) strain from originally mixed trypanosome population.
Abstract: Groups of mice received double infections with the Y and F strains of Trypanosoma cruzi, the first inoculum of either strain being followed by a second inoculum of the other strain on day 5, 15, 30-40, or 60-65. Parasites were re-isolated from blood into culture, either directly or with an intermediate passage in gamma-irradiated mice, at intervals between 7 and 35 days after the second inoculation. Strain identification in the re-isolated material was by electrophoresis of kDNA fragments generated by the EcoRI restriction endonuclease and by electrophoresis for glucosephosphate isomerase isozymes. Both strains were identified in 22% of re-isolates originating from the experimental mice and only one of them was present in the remaining re-isolates, strain F being the most frequent. In some instances either Y or F was re-isolated from the same blood source, depending on whether culturing had been preceded or not by passage through a mouse. These results are certainly related to strain differences in the various aspects of host-parasite relationship and, possibly, growth rates in culture. The results demonstrate that: (1) more than one strain of T. cruzi can coexist in the same host; (2) the timing and method of parasite isolation from the vertebrate host act as selective factors, and further passages (in mice or cultures) may completely eliminate one (or more) strain from originally mixed trypanosome population, and (3) kDNA restriction "fingerprints" and isozyme profiles are simple, sensitive, and reliable techniques for strain identification both in single and mixed preparations.
74 citations
TL;DR: It is shown that polyamine biosynthesis from ornithine is required for growth of G. lamblia and that E. histolytica and T. vaginalis, two unrelated mucosal-dwelling parasites of humans, was not inhibited by 20 mM DFMO.
Abstract: Difluoromethylornithine (DFMO) is a specific and irreversible inhibitor of ornithine decarboxylase, an enzyme which catalyzes the first step in the biosynthetic pathway of the polyamines. We tested the effect of DFMO on the growth of Giardia lamblia, Entamoeba histolytica, and Trichomonas vaginalis. Growth of G. lamblia was inhibited by DFMO at concentrations of greater than or equal to 1.25 mM. Culture doubling time increased with increasing DFMO concentration. Growth inhibition was reversed if spermidine was added within 53 h of addition of DFMO; no growth was observed if spermidine was added later, indicating eventual parasite death. The growth of E. histolytica and T. vaginalis, two unrelated mucosal-dwelling parasites of humans, was not inhibited by 20 mM DFMO. These studies indicate that polyamine biosynthesis from ornithine is required for growth of G. lamblia.
73 citations
TL;DR: During the spring of 1981, trichodinid protozoa were collected from the gills or urinary bladder of the following species of fishes of Rybinsk Reservoir, USSR, located on the upper reaches of the Volga River system: Esox lucius, Rutilus rutilus, Leuciscus idus, Blicca bjoerkna, Abramis ballerus, Pelecus cultratus, Lota lota, and Perca
Abstract: During the spring of 1981, trichodinid protozoa were collected from the gills or urinary bladder of the following species of fishes of Rybinsk Reservoir, USSR, located on the upper reaches of the Volga River system: Esox lucius, Rutilus rutilus, Leuciscus idus, Blicca bjoerkna, Abramis ballerus, Pelecus cultratus, Lota lota, and Perca fluviatilis. A total of 13 species of Trichodinidae was recovered from Rybinsk fishes, among which are three new species of the genus Trichodina: T. izyumovae n. sp. from the gills of L. idus, T. borokensis n. sp. from the gills of P. cultratus, and T. kupermani n. sp. from the gills of A. ballerus. Other species of trichodinids reported are T. modesta Lom, 1980; T. nigra Lom, 1969; T. pediculus (O. F. Muller, 1786); T. prowazeki Grupcheva & Lom, 1980; T. rostrata Kulemina, 1968; T. urinaria Dogiel, 1940; T. ophiocephalus Kostenko & Karaev, 1976; Paratrichodina incisa (Lom, 1959); Trichodinella epizootica (Raabe, 1950); and Tripartiella copiosa Lom, 1959. Photomicrographs and morphometric data are presented for each species and aspects of their host and geographic distribution discussed. Trichodina algonquinensis Li & Desser, 1983 is considered a synonym of T. urinaria Dogiel, 1940.
TL;DR: Results indicate that the polaroplast organelle may provide the new plasma membrane for discharged microsporidian sporoplasms.
Abstract: Electron microscopic examinations of Glugea hertwigi and Spraguea lophii spores indicated the presence of a single plasma membrane; however, this membrane remained in the spore during the discharge of the sporoplasm from the spore. Although discharged spores retained the old plasma membrane, the extruded sporoplasms acquired a new plasma membrane. In order to determine where the new plasma membrane came from, we used two fluorescent probes with membrane affinities. The markers were tested on unfired and discharged spores. The probe, N-phenyl-1-naphthylamine (NPN), labeled the polaroplast membrane in addition to the apolar groups in the posterior vacuoles of unfired spores. After spore discharge, NPN label disappeared from the spore ghosts except for a slight fluorescence on residual plasma membranes. Much of the NPN-labeled membrane reappeared after spore discharge on the outer envelope of discharged sporoplasms. The probe chlorotetracycline (CTC) labeled calcium-associated membranes of spore polaroplasts. During spore discharge, the CTC fluorescence shifted from the polaroplast organelle of unfired spores to the outer envelope of discharged sporoplasms. These results indicate that the polaroplast organelle may provide the new plasma membrane for discharged microsporidian sporoplasms.
TL;DR: Two new species of Myxozoa from the brain of the green knife fish Eigemannia virescens are described: Myxobolus inaequus sp.
Abstract: Two new species of Myxozoa from the brain of the green knife fish Eigemannia virescens are described: Myxobolus inaequus sp. n. has an unusually large spore body and extremely unequal polar capsules, and Henneguya theca sp. n. has an attenuated spore encased in a sheath not previously described in other Myxozoa . Only spores of the two species were observed, and infections caused no obvious pathological changes in the brain.
TL;DR: It was concluded that T. cruzi strains with heterozygous isoenzyme profiles predominate in domestic transmission cycles in this highly endemic area of the Paraguayan Chaco.
Abstract: At Makthlawaiya, in the Paraguayan Chaco, the prevalence of Trypanosoma (Schizotrypanum) cruzi infection among both domestic Triatoma infestans and domestic dogs was 38%, and IgG anti-T. cruzi antibody was detected by the quantitative enzyme-linked immunosorbent assay (ELISA) in 80% (105/133) of human sera. Ninety percent (25/28) of T. cruzi strains isolated from both T. infestans and dogs showed heterozygous isoenzyme profiles for glucose phosphate isomerase, phosphoglucomutase and 6-phosphogluconate dehydrogenase. These strains appeared to be closely related to Bolivian zymodeme 2. Three Paraguayan T. cruzi strains showed homozygous isoenzyme profiles, similar to those of major Brazilian zymodemes. It was concluded that T. cruzi strains with heterozygous isoenzyme profiles predominate in domestic transmission cycles in this highly endemic area of the Paraguayan Chaco.
TL;DR: Calyptospora n.
Abstract: Calyptospora n. g. was erected for Eimeria funduli because the sporocyst of that species lacks Stieda and sub-Stieda bodies, has a veil supported by sporopodia, and has an anterior apical opening. A suture may be present, but it does not completely divide the sporocyst into two valves. Because C. funduli has an obligatory invertebrate intermediate host, we established Calyptosporidae n. fam. to accommodate Calyptospora and tentatively to accept Goussia. A new subgenus, Plagula, is erected for species of Goussia with a sporocystic veil not supported by sporopodia. We consider the family more primitive than Eimeriidae, Sarcocystidae, and possibly Lankesterellidae.
TL;DR: The results demonstrate that the pathogenic strains of amebas have a collagenolytic activity that closely correlates with their in vivo capacity to produce liver lesions, and suggest that species susceptibility to invasive infection may depend on the characteristics of the extracellular components of host tissues.
Abstract: Several axenic strains of pathogenic and nonpathogenic Entamoeba histolytica were tested for their capacity to digest native radioactive type I collagen gels and to produce liver abscesses when injected into the liver of newborn hamsters. The results demonstrate that the pathogenic strains of amebas (HM1:IMSS, HM3:IMSS, HM38:IMSS, and HK9) have a collagenolytic activity that closely correlates with their in vivo capacity to produce liver lesions. The nonpathogenic isolate (Laredo) did not show collagenolytic activity and failed to produce lesions in the liver of newborn hamsters. The results also demonstrate that type I collagen obtained from rodents and cats is degraded less by amebic collagenase than is bovine collagen, which is similar to human collagen. These findings suggest that species susceptibility to invasive infection may depend, among other factors, on the characteristics of the extracellular components of host tissues.
TL;DR: Naegleria australiensis does not appear to be as homogenous a species as N. fowleri and seems to be more widespread than previously thought.
Abstract: Fourteen strains of Naegleria australiensis, including the type strain, were compared for virulence for mice, maximum growth temperature, lectin agglutination, isoenzyme pattern, and total protein banding pattern. Their relation to other species of Naegleria also was compared by immunoelectrophoretic analysis. Strains with high virulence, comparable to that of N. fowleri, were found to be different in concanavalin A agglutination as well as with regard to zymograms and total protein patterns. Although serologically different from N. fowleri and reacting with N. australiensis antiserum in the fluorescent antibody test, these high-virulence strains differed in number of immunoelectrophoretic precipitin bands. Because of these results, the high-virulence strains are considered to be a subspecies of N. australiensis. The low-virulence strains showed minor differences from the type strain. Thus, N. australiensis does not appear to be as homogenous a species as N. fowleri. Pathogenic N. australiensis also seems to be more widespread than previously thought.
TL;DR: Methods by which variant surface glycoproteins of Trypanosoma brucei may be isolated, uncontaminated by water-soluble VSG ( mfVSG ) are presented and the sensitivity to different metal ions of the enzyme that mediated the conversion event is discussed.
Abstract: Variant surface glycoproteins (VSG) of Trypanosoma brucei are released in a water soluble form on impairment of membrane integrity. We have previously shown that this release is the result of an enzyme-mediated event which converts the hydrophobic membrane form VSG into the hydrophilic water-soluble form. We now present further details of the methods by which membrane form VSG ( mfVSG ) may be isolated, uncontaminated by water-soluble VSG ( sVSG ). The sensitivity to different metal ions of the enzyme that mediated the conversion event is discussed, and some biochemical characteristics of different mfVSG preparations are presented.
TL;DR: The blastogenic effects of specific parasite antigen and of mitogens on the lymphocytes of chickens infected with Eimeria tenella were examined, suggesting that soluble suppressor factors are generated during infection.
Abstract: The blastogenic effects of specific parasite antigen and of mitogens on the lymphocytes of chickens infected with Eimeria tenella were examined. Lymphocytes from infected chickens were stimulated to divide when cultured with parasite antigen, but their responses to the T-cell mitogen, phytohemagglutinin (PHA), were depressed throughout the period of infection. Responses to the B-cell mitogen, lipopolysaccharide (LPS), were depressed during the first week of infection but enhanced in the second week. The inclusion of plasma samples from infected chickens in the culture medium depressed the responses of normal spleen lymphocytes to PHA, suggesting that soluble suppressor factors are generated during infection.
TL;DR: Mice were totally immune to reinfection with E. vermiformis 30 and 105 days after inoculation and cross immunity was not observed between E. VermiformIS and E. ferrisi.
Abstract: . Pathological changes and immunity induced by Eimeria vermiformis (Ernst, Chobotar & Hammond, 1971) were studied in outbred Swiss mice inoculated with 5000, 10,000, 20,000, or 40,000 oocysts. Cross immunity to E. ferrisi was also studied. In the case of E. vermiformis, mortality was dose dependent; most deaths were observed in the intermediate-dose groups. Most deaths also correlated with peak oocyst output. Histopathologic changes consisted of an early neutrophil and mononuclear cell infiltration in the small intestine. Later, villus atrophy and crypt hyperplasia caused a decrease in the villus-crypt ratio. During the acute phase (8-10 days after inoculation), villus tips were eroded and parasites with necrotic debris filled the cryptal and intestinal lumina. Vacuolar changes were observed in epithelial cells of the small intestine. Neither parasites nor significant pathological changes were observed in extra-intestinal organs. Mice were totally immune to reinfection with E. vermiformis 30 and 105 days after inoculation. Cross immunity was not observed between E. vermiformis and E. ferrisi.
TL;DR: The freeze-fracture electron micrographs provided a more complete understanding of the fine structure of undulating membranes of Trichomonadinae, as represented by Trichomoas vaginalis, and of Tritrichomonas augusta, as exemplified by TritRichomonas foetus than was gained from previous transmission and scanning electron microscope studies.
Abstract: Two strains of Trichomonas vaginalis, JH162A , with low pathogenicity, and Balt 44, with high pathogenicity, as well as one highly pathogenic strain, KV-1, of Tritrichomonas foetus were studied by freeze-fracture electron microscopy. The protoplasmic faces ( PFs ) of the cell membranes of all three strains of both species had similar numbers of intramembranous particles (IMPs); however, the particles in the external faces (EFs) of these membranes were least abundant in Trichomonas vaginalis strain Balt 44 and most numerous in those of strain JH162A of this species. In Tritrichomonas foetus strain KV-1 the number of IMPs in the EF was close to but somewhat lower than that in the mild strain of the human urogenital trichomonad . In both species, the anterior, but not the recurrent, flagella had rosette-like formations, consisting of approximately 9 to 12 IMPs on both the PFs and EFs. The numbers and distribution of the rosettes appeared to vary among different flagella and in different areas of individual flagella of a single organism belonging to either species. The freeze-fracture electron micrographs provided a more complete understanding of the fine structure of undulating membranes of Trichomonadinae , as represented by Trichomonas vaginalis, and of Tritrichomonadinae (the Tritrichomonas augusta -type), as exemplified by Tritrichomonas foetus, than was gained from previous transmission and scanning electron microscope studies. Typically three longitudinal rows of IMPs on the PF of the recurrent flagellum of Trichomonas vaginalis were noted in the area of attachment of this flagellum to the undulating membrane. The functional aspects of the various structures and differences between certain organelles revealed in the two trichomonad species by the freeze-fracture method are discussed.
TL;DR: Scanning electron microscopy confirmed the previous finding that toxoplasmas actively invade mouse peritoneal cells that are inhibited from phagocytosis and provided clues to possible mechanisms of toxoplasma locomotion and host-cell invasion.
Abstract: Scanning electron microscopy confirmed our previous finding that toxoplasmas actively invade mouse peritoneal cells that are inhibited from phagocytosis. The parasites entered cells with the conoid end first and sometimes showed a counter-clockwise torsion of the body during invasion. Counter-clockwise torsion was also noted in free toxoplasmas. Host-cell responses to active invasion varied with experimental conditions and with the type of host cell. Under adverse culture conditions for phagocytosis, normal macrophages formed rudimentary filopodia or lamellipodia around the tips of in vading toxoplasmas; macrophages subjected to hyperthermia before similar incubation with toxoplasmas showed little or no response to invasion. Normal and heat-treated lymphocytes showed little surface reaction to invasion, but occa ionally a flocculent collar was seen around the tip of an invading toxoplasma. Scanning electron microscopy provides clues to possil'e mechanisms of toxoplasma locomotion and host-cell invasion.
TL;DR: Ten years of research on digestive vacuoles of Paramecium caudatum have revealed sequential changes both within the vacuole lumen as well as within the surrounding membrane.
Abstract: Ten years of research on digestive vacuoles (phagosomes) of Paramecium caudatum have revealed sequential changes both within the vacuole lumen as well as within the surrounding membrane. Four vacuole stages can be recognized by a combination of thin section and freeze-fracture ultrastructural features. Three sets of vesicles (discoidal vesicles, acidosomes, and lysosomes) fuse with the vacuole, each at a predetermined stage, to bring about these membrane and physiological changes. At various times membrane is removed as vesicles from the vacuole surface, which has the effect of regulating vacuole size. Membrane recycling, membrane replacement, and specific membrane to membrane recognition all appear to be operating during the digestive cycle. Details of these events are summarized in this address and a number of unanswered questions suggest areas for future research.
TL;DR: The ultrastructure of the freshwater, heterotrophic dinoflagellate Peridiniopsis berolinense (Lemm.) Bourrelly resembles other dinof lagellates in the structure of its nucleus, theca, flagella, and mitochondria, and of particular interest is the transitional helix present in the longitudinal flagellum.
Abstract: The ultrastructure of the freshwater, heterotrophic dinoflagellate Peridiniopsis berolinense (Lemm.) Bourrelly resembles other dinoflagellates in the structure of its nucleus, theca, flagella, and mitochondria. Other features less frequently reported in related organisms include fine sub-sulcal fibers, collared pits in the flagellar base region, and unusual structures herein termed fibrillar lamellae. Numerous vesicles are present, some of whose contents are distinctly crystalline, while others contain what appears to be membranous material arranged in either whorls or parallel stacks; still other vesicles contain electron-dense, granular spheres. Of particular interest is the transitional helix present in the longitudinal flagellum, this being the first report of such a structure among the dinoflagellates. Plastids of any kind are lacking, and a peduncle is present and is used during phagotrophy.
TL;DR: Protein comparisons included in the present study indicate that strain Tur, previously identified as a strain of T. vorax, is distinct from all other macrostome-forming species.
Abstract: The potential utility of protein arrays visualized by SDS-PAGE in taxonomic studies of protozoa has been investigated within the genus Tetrahymena. Matching coefficients have been obtained from one-dimensional separations of cytoskeletal proteins in a study involving 40 strains of Tetrahymena. In separate studies, the method was estimated to be accurate to within 10%, and the limit of intraspecific variation within the genus was estimated at ≅ 30%. Accordingly, it is suggested that strains showing matching coefficients 0.6 in these preparations probably represent different species. Further tests using strains identified to species by breeding criteria have shown that the 0.6 rule is asymmetric, i.e. although matching coefficients lower than this indicate separate species, values higher than this do not prove identity. Protein comparisons included in the present study indicate that strain Tur, previously identified as a strain of T. vorax, is distinct from all other macrostome-forming species. It is here designated Tetrahymena leucophrys n. sp.
TL;DR: It is concluded that the phenomenon of antigenic variation is a complex problem in ecology and population dynamics as well as molecular regulation.
Abstract: A detailed molecular analysis using recombinant DNA technologies is extremely important to our understanding of the phenomena of antigenic variation in the African trypanosomes; however, by itself, it may not completely explain antigenic variation as it occurs in vivo. Several laboratories have demonstrated the ability of one variant population to replace another in vivo as well as the presence of heterogeneous populations of trypanosomes within an individual animal. These two phenomena do not permit us to explain antigen variation solely on the basis of the molecular regulation of variant antigen expression. In addition to studies in molecular biology, it will be necessary to define clearly the differences in growth rates of variant populations and the role of competition between these variants in a single anatomical site. It will also be necessary to determine the influence of various physiological environments on growth rates and the competition between the different variants of a single repertoire. It is concluded that the phenomenon of antigenic variation is a complex problem in ecology and population dynamics as well as molecular regulation. This paper is designated to examine a variety of the ecological parameters presumably involved in antigenic variation.
TL;DR: A method for the isolation of Leishmania donovani amastigotes from infected hamster spleen and liver tissues is described and an active glutamate dehydrogenase is demonstrated, thus linking amino acid metabolism with carbohydrate metabolism.
Abstract: A method for the isolation of Leishmania donovani amastigotes from infected hamster spleen and liver tissues is described. Over 85% of the isolated amastigotes were viable as judged by acridine orange-ethidium bromide staining and in vitro transformation to the promastigote form. A comprehensive survey of the enzymes of carbohydrate metabolism in L. donovani amastigotes and promastigotes was conducted. Amastigotes and promastigotes possess all of the enzymes of the Embden-Meyerhof pathway, hexose monophosphate shunt, and tricarboxylic acid cycle. Cell-free extracts of both forms demonstrate an active glutamate dehydrogenase, thus linking activity which permits entry of pyruvate into the tricarboxylic acid cycle. Both forms demonstrate an active glutamate dehydrogenase, thus linking amino acid metabolism with carbohydrate metabolism. Pyruvate carboxylase, the enzyme responsible for replenishment of C4 acids by heterotrophic CO2 fixation into pyruvate, was also demonstrable in the tissue and insect forms. In general, activities of promastigote enzymes are higher than the amastigote enzymes. Differences between the vertebrate (amastigote) and invertebrate (promastigote) forms in their potential to utilize carbohydrates as substrates would appear to be quantitative rather than qualitative.
TL;DR: Sur the base of the resultats obtenus une nouvelle classification peut etre avancee de similarite en considerant 122 caracteres ultrastructuraux, morphologiques, stonatogenetiques, nucleaires ou de reproduction asexuee.
Abstract: Les relations de similarite ont ete calculees par analyse phenetique entre 59 genres et especes en considerant 122 caracteres ultrastructuraux, morphologiques, stonatogenetiques, nucleaires ou de reproduction asexuee. Sur la base des resultats obtenus une nouvelle classification peut etre avancee. Trois subphylums sont discernables: Karyorelictophora; Kinetophragminophora et Hymenophora avec respectivement 1 classe (Karyorelictea) 4 classes (Colpodea, Hypostomea, Spirotrichea et Hymerostomea) et 2 classes (Phyllopharyngea, Gymnostomea)
TL;DR: The antigens that are present in the coccidian parasites Toxoplasma gondii and Hammondia hammondi were demonstrated and defined by using SDS-PAGE and immunoenzymatic techniques with 125I-labeled and unlabeledAntigens of T. Gondii that were recognized by antibodies in the sera of mice infected orally or intraperitoneally with H. hammond i.
Abstract: The antigens that are present in the coccidian parasites Toxoplasma gondii and Hammondia hammondi were demonstrated and defined by using SDS-PAGE and immunoenzymatic techniques with 125I-labeled and unlabeled antigens of T. gondii and sera of mice infected orally or intraperitoneally with H. hammondi . All cell surface antigens of T. gondii that were labeled with 125I were recognized by antibodies in the sera of the mice infected with H. hammondi except the antigen of approximate molecular weight of 21.5 Kd. This suggests that this antigen is specific for T. gondii. Various antigens in the T. gondii-lysed antigen preparations were recognized by antibodies to H. hammondi . The number of recognized antigens increased as the infection of the mice with H. hammondi progressed. Oral infection with H. hammondi appeared to induce the formation of antibodies that recognized more T. gondii antigens than infection by intraperitoneal inoculation.