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H M Seitz

Publications and source records attributed to H M Seitz.

At least 19 recordsLinked to original sources

The effect of nosematosis on the development of Plasmodium falciparum in Anopheles stephensi.

To quantify the effect of Nosema algerae (Microsporidia, Nosematidae) on the development of Plasmodium falciparum in Anopheles stephensi (Diptera, Culicidae), we carried out infection experiments under standardized laboratory conditions. Apart from a mean reduction of 69% in oocyst development, smaller numbers of oocysts and fewer sporozoites were found in the Nosema-infected mosquitoes. In addition, nosematosis resulted in higher mortality. The potential role of Nosema algerae as a biological control agent is discussed.

Animals

The effects of Nosema algerae on the development of Plasmodium yoelii nigeriensis in Anopheles stephensi.

Experimental simultaneous infections of Anopheles stephensi (Diptera: Culicidae) with Nosema algerae (Microsporida: Nosematidae) and Plasmodium yoelii nigeriensis under standardized laboratory conditions showed partial suppression of the malaria parasite. At 9 days after an infective bloodmeal, the oocysts in the midgut were counted; 12.1%-66.6% of the double-infected mosquitoes exhibited no oocysts, whereas only 4.5%-12% of the control group showed no oocysts. The mean reduction in oocyst numbers under the influence of Nosema was 84.68%. At 14 days after infection with Plasmodium, the amount of sporozoites was examined; their mean reduction in eight experiments was 70%.

Animals

Plasmodium falciparum: effect of chloroquine, halofantrine and pyrimethamine on the infectivity of gametocytes for Anopheles stephensi mosquitoes.

The activity of chloroquine, halofantrine and pyrimethamine against the gametocytes and sporogonic stages of Plasmodium falciparum (strain NF54) was tested. Five-day-old gametocytes (stages I and II) from in vitro cultures were exposed to the drugs for 48 hours. The effect of the drugs on gametocyte development was assessed by counting gametocytes on days nine and 15 of culture and determining the infectivity of the drug-treated gametocytes to mosquitoes. Gametocytogenesis was partially inhibited by all three drugs; there were 71% of the number of gametocytes in drug-free control cultures in cultures with 3 x 10(-8) M chloroquine, 51% with 5 x 10(-8) M chloroquine, 78% with 5-7 x 10(-9) M halofantrine, and 48% with 10(-7) M pyrimethamine. Halofantrine- and pyrimethamine-treated gametocytes were found to be more infective to Anopheles stephensi than untreated controls. The three drugs were also administered to the mosquitoes, either in the first bloodmeal, which contained gametocytes from in vitro cultures, or in the second, parasite-free bloodmeal, given four days after infection. The sporontocidal activity of the drugs was evaluated by counting the number of oocysts on the midgut seven or eight days after infection, or the number of sporozoites in the salivary glands 15 days after infection. A sporontocidal effect was observed only when pyrimethamine was administered with the infective bloodmeal. Neither chloroquine nor halofantrine had any marked effect on sporogony at the concentrations tested.

Animals

A new model for testing gametocytocidal effects of some antimalarial drugs on Plasmodium falciparum in vitro.

A technique is described for obtaining pure gametocyte cultures of Plasmodium falciparum, using pyrimethamine at the minimum concentration for inhibition of asexual parasites. Routine cultures producing sexual stages were exposed to pyrimethamine on days 5 and 6. These cultures grew synchronously and contained gametocytes of stages II, III and V on day 7, 9 and 15 of the cultures respectively. The pyrimethamine-treated gametocytes were more infective to mosquitoes than were untreated controls. This model for the culture of pure gametocytes was used to observe the activity of chloroquine, halofantrine, pyrimethamine and quinine on the gametocyte stage III of Plasmodium falciparum strain NF54 in vitro. NF54 was shown to be sensitive to chloroquine, quinine and pyrimethamine, but the results showed that halofantrine was the most effective drug in reducing the number of gametocytes. A concentration of 3 x 10(-9) M halofantrine was lethal to both asexual parasites and gametocytes. The gametocytocidal EC90 of chloroquine (1 x 10(-6) M) and that of quinine (9 x 10(-7) M) were equal to the minimum inhibitory concentration of asexual stages of isolates of P. falciparum considered as highly resistant to these drugs. A high concentration of pyrimethamine (1 x 10(-4) M) had, in contrast, little effect on gametocytes.

Animals

Trials to infect Anopheles stephensi with Plasmodium yoelii nigeriensis by the membrane feeding technique.

The aim of this study was to find optimal conditions for the membrane feeding technique to obtain maximum infection rates of mosquitoes with Plasmodium yoelii nigeriensis. The results show that the malaria parasite Plasmodium yoelii nigeriensis is most infective to Anopheles stephensi mosquitoes on day 3 of the infection in the mice, 1 day before the peak of parasitaemia. The mortality rate of the mosquitoes fed on mice on day 3 after infection was the highest as compared to mosquitoes fed on other days after infection. Gametocytes from mice 3 days after infection were fed to mosquitoes by three different membrane feeding methods. The results indicate that feeding during the first 10 min after blood collection gave the highest infection rates. Keeping the blood meal at a pH of 7.2 yields higher infection rates than keeping it at pH of 8.5. Stirring of the blood and supplying it with CO2 is not necessary when feeding of the mosquitoes is completed within the first 10 min after collection of the blood.

Animals

[Malaria].

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Animals

Experiments on cryopreservation of Plasmodium falciparum.

A comparative study was carried out in order to assess the effectivity of the deep-freezing conditions for P. falciparum cultures: 1. by plunging them into liquid nitrogen, 2. by use of an established freezing program for lymphocytes. After thawing in a waterbath at 37 degrees C, samples were diluted with equal volumes of 3.5% sodium chloride solution or 15% phosphate-buffered saline supplemented glucose solution. Other samples were not diluted after thawing, but the medium was replaced twice during the first day in culture. Survival was evaluated by counting the parasites in Giemsa-stained smears taken on day 3 after thawing. We obtained the best survival rate using NaCl solution, whereas replacing the medium twice resulted in the lowest level of survival. In synchronized cultures we studied survival rates of the different developmental stages of the intraerythrocytic parasites: young trophozoites (ring stages) and schizonts. The results indicate that irrespective of the freezing technique used, the survival level of young trophozoites was high (40 and 60%). The more sensitive stages (late trophozoites and schizonts) were better protected by using the freezing program designed for lymphocytes.

Animals

Studies on the lethal effect of ultraviolet light on Trichomonas vaginalis.

Following cultivation in Asami medium, centrifugation and resuspension in saline or in water from a medicinal spring, Trichomonas vaginalis trophozoites were exposed to well-defined doses of ultraviolet (UV) light (254 nm). We used 24- and 48-h-old trichomonads at concentrations of 1 x 10(5) and 5 x 10(4) trophozoites/ml in a total volume of 20 ml for these studies. The apparatus for UV irradiation was especially constructed for batch experiments. After irradiation at doses ranging from 80 to 160 mJ/cm2, the mobility of the parasites was reduced and morphological alterations appeared: rounding of the cells, vacuolization of the cytoplasm and even cytolysis. A dose of 401.7 mJ/cm2 killed 99.8% of the 48-h-old trichomonads when irradiation occurred in saline at a cell density of 1 x 10(5) trichomonads/ml and 98.9% when irradiation was done at a cell density of 5 x 10(4) trichomonads/ml. A dose of 362.1 mJ/cm2 killed only the more sensitive 24-h-old trichomonads. In mineral water, 241 mJ/cm2 was sufficient to kill up to 99.5% of the 48-h-old trichomonads. When 48-h-old trichomonads that had been exposed to a radiation dose of 160-240 mJ/cm2 were subcultured, they lost their ability to propagate. At a dose of 80 mJ/cm2, both the trichomonads that had been harvested during the log phase and the 48-h-old organisms suspended in mineral water lost their ability to propagate on subculture. These results indicate that 24-h-old trichomonads were more sensitive than 48-h-old organisms. Furthermore, the experiments demonstrated that a higher dose of UV radiation must be applied to T. vaginalis trophozoites than to the more sensitive bacterial strain Escherichia coli ATCC 11229 so as to achieve comparable killing results.

Animals

Alveolar echinococcosis with involvement of the ureter and testis.

Alveolar echinococcosis is a rare disease of the liver, and occasionally of the lungs and brain, that is endemic across areas of Central Europe, the Soviet Union and Alaska. We describe a case of alveolar echinococcosis with involvement of the ureter and testis overshadowing the liver manifestation. The unusual presentation and nondemonstrable exposure to the organism caused misinterpretation of the histological findings and an initial misdiagnosis of tuberculosis.

Adult

The relation between the two forms of COPT and levels of total IgG and IgM in acute and chronic schistosomiasis mansoni.

COPT was performed on 55 acute and 48 chronic male patients with schistosomiasis mansoni as well as on 20 control normal subject. The percentage of the segmented and the bleb reactions were determined. The total levels of IgG, IgM and IgA were measured. There was no distinct evidence that COPT shows only bleb precipitations in acute cases and only segmented reactions in chronic cases. The total levels of IgG were higher in patients who showed segmented that in those who showed bleb reactions especially in the segmented but not the bleb reactions especially in chronic cases. IgM may be responsible for the bleb reactions in acute cases.

Animals

[Pneumocystis carinii pneumonia--a review].

Pneumocystis carinii pneumonia is a clinically, roentgenologically, and serologically uncharacteristic pneumonia of the immunodeficient patient and is caused by the opportunistic parasite Pneumocystis which is most likely a protozoon. The untreated disease is lethal. The epidemiologic, clinic, and histologic features of P. carinii pneumonia are different from those of the interstitial plasmacellular pneumonia that occurred in malnourished and premature infants between 1930 and 1960 in Europe and was caused by the same organism. P. carinii is restricted to the alveoli of the lung. Material for the direct microscopic diagnosis of the parasite can be produced by bronchoalveolar lavage. The trophozoites of P. carinii are preferably stained by Giemsa stain and the cystwalls by methenamine-silver. For a reliable diagnosis both methods should be used.

Acquired Immunodeficiency Syndrome

[Experiments in vitro with Litomosoides carinii (Nematoda: Filarioidea). I. Maintenance of adult females and microfilariae as well as release of microfilariae in different culture media (author's transl)].

Embryos of L. carinii continue intrauterine development to microfilariae and are totally released into the medium within 5--6 days when the latter (Tc 199) is changed daily and air is used as the gas phase. Oogenesis or further fertilization of eggs, however, does not occur in vitro in any of the media examined by us. One female releases 140 X 10(3) microfilaria/day on an average in vitro within 5--6 days. Mean initial numbers of 300 X 10(3) Mf/female/day are observed. Addition of equine serum inhibits microfilarial release in vitro; normal cotton rat serum prolongs survival of females while total numbers of released microfilariae or retained embryonic stages are not increased. The serum of post-patent animals does not influence the numbers of released microfilariae or their viability or survival of females. Microfilariae released in vitro in Tc 199 + 33% normal cotton rat serum survive for more than 8 days, when air is used as the gas phase and the medium is changed daily. Microfilariae isolated from the blood of patent animals survive for at most 6 days, at a 48-hourly change of medium survival does not even exceed 4 days.

Animals

[Light microscopic and scanning electron microscopic observations on phagocytosis of Plasmodium berghei infected erythrocytes by mouse macrophages [author's transl)].

Peritoneal macrophages from mice were cultured in Leighton tubes for 2 hours. Thereafter suspensions of washed red blood corpuscles originating from Plasmodium berghei-infected mice were offered to the cultured cells for phagocytosis. After 15 minutes of incubation 13,5% of the macrophages showed phagocytized parasites if the peritoneal cells came from malariaimmune mice. Cells from normal mice or from infected mice had lower rates (4,8/9,1%). After an incubation of 3 hours about 50% of the cells showed phagocytosis in all three groups. The system used allowed to estimate the halftimes for intracellular elimination of the parasites. The values are 27 minutes for cells from immune animals, 57 minutes for cells from normal animals, and 66 minutes for cells from infected animals. Details of the process of phatocytosis were recorded by scanning electron microscopic pictures.

Animals