1.Immobilization-agglomeration reaction for the diagnosis of Trichomonas vaginalis infection.
The Korean Journal of Parasitology 1970;8(1):13-21
The Trichomonas immobilization-agglomeration reaction was studied using the sera from women with vaginal trichomoniasis and from rabbits inoculated with cultures of T. vaginalis. It was found that the greatest amount of immobilization occurred at 25 to 30 minutes, and that inactivation of the sera did not affect the results. An evidence of antigenic differences between T. vaginalis, T. hominis and C. albicans was confirmed. The immobilization reaction was positive in 80.3% of the 71 T. vaginalis positive cases, but in only 7.7% of the 77 persons of T. vaginalis negative cases. From the above results, it is suggested that immobilization reaction is a useful tool for the diagnosis of T. vaginalis infection.
parasitology-protozoology-Trichomonas vaginalis
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immobilization
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agglomeration
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human
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rabbit
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culture-media
2.Experimental study on bionomics of Giardia Part I. Localization and morphological variation of Giardia muris in various parts of the small intestine of laboratory mice.
The Korean Journal of Parasitology 1963;1(1):29-36
The localization of Giardia muris was determined in 8 Giardia-infected laboratory mice that were fed on a normal diet. The average total length of small intestine of the mice was 38.3 cm. Among 8 sections (to divide into 8 part from pylorus to cecal junction :Sect. I, Sect. II, ...... Sect. VIII), the optimum habitat ranged Sect. IV to Sect. V(from 14.5 cm to 24.4 cm posterior to the pylorus. Distribution rate of Giardia muris in posterior part of small intestine was higher than that in anterior part. The bile duct of 8 mice were examined, but no Giardia was found. The cyst of Giardia muris were found at the part posterior to the Sect. VII. The result of a comparison between varying average body length and body breadth of Giardia muris drawn at random from different part of small intestine of 5 laboratory mice was as follows : Maximum average dimension of the body length of the trophozoite was found at the part of Sect. IV and minimum average value was observed at the part of Sect. VIII. On average dimension of body length of the trophozoite, no significant difference was obtained among the parasites at Sect. II, Sect. IV, Sect. VI, but significant small dimension value was observed aat Sect. VIII. Coincidental figures on the part where the maximum distribution rate was shown and the part where the maximum average dimension of the body length of the trophozoite were considered as indicating the optimum site of the parasite.
parasitology-protozoology-Giardia muris
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mouse
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intestine
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habitat
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animal
3.The microfilarial density of the host and the infectivity of the mosquito vecter.
The Korean Journal of Parasitology 1963;1(1):7-10
In filariasis the infectivity of the appropriate mosquito vector is not consistent with the microfilarial density of the host. The reason may be attributed such factors as the time of microfilarial appearance in the peripheral blood of the host, the time of maximum biting activity of the arthropod vector, or the morphological adaptation of the feeding mechanism of the vector. However, it is quite puzzling to see why the number of microfilariae taken up by mosquitoes is subjected such a great variation, even though the same batch of mosquitoes are fed on the same filarial host under same laboratory conditions. The experiment was designed to observe more detail aspect of this relation. Adult Aedes togoi (Theobald, 1907) mosquitoes were reared from egg rafes colonized in an insectary. Animals used were Taiwan monkeys, Macaca cyclopsis which had been artificially infected with Wucheria malayi. The animals showed the microfilarial counts as low as nil to ten per slide of 20 cmm3 of blood, which seem to be rather fortunate for this kind of work. The microfilarial density of each animal was counted by taking each ten smears of 20 cmm(3) of peripheral blood the ear lobes before and after mosquito bite. Feeding were done in two occations, during 1600-1630 and 1900-1930 hours of the same day. The monkeys were immobilized and a rayon cage, housed 100 female mosquitoes for two days starvation, was exposed to the shaved abdomen of each animal. Fully engorged mosquitoes were transferred to a square rearing cage, which was later placed in the insectary, where kept temperature of 23-27degree C and relative humidity of 80-85 per cent. It was found that filarial larvae of the mosquito body usually develop to the third or infective stage in about 10 days after blood meal under these conditions. Daily dissections were made of these mosquitoes, either living or dead, after one week of rearing. Analysing of the result, the following conclusion was made. The rate and intensity of infection in mosquitoes are not directly related to the blood counts of microfilariae of the host animals. This is perhaps due to fluctuations of microbial outflow in the peripheral blood of individual animals. The reason of this would be no doubt due to a patch type of microfilarial distribution in the host blood.
parasitology-arthropodology-mosquito
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Aedes togoi
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Macaca cyclopsis
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monkey
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protozoology
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Brugia malayi
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microfilaria
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animal
4.Parasitological studies of Korean forces in South Vietnam I. Examination of blood films on malaria patients.
Byong Seol SEO ; Soon Hyung LEE ; Jong June YOON ; Yong Suk RYANG
The Korean Journal of Parasitology 1970;8(1):25-29
A parasitological study was performed with 452 malaria patients evacuated from South Vietnam by examinations of their peripheral blood. Results were as follows: The peripheral blood examinations revealed that 52.0% of the examined have parasitemia, of which 95.3% was P. falciparum, one case of P. vivax and the other 10 patients were mixed infected. Neither P. malaria nor P. ovale were found. A total of 1,500 thick and thin blood films was prepared and 707 slides of them (47.1%) showed positive. In P. falciparum, ring forms were found most frequently and the next was gametocytes. Eighty slides (50%) showed mixed together with both ring form and gametocytes. All of the erythrocytic stages were seen in three slides of P. vivax. Weekly periodical examinations showed 233.8 parasite density every 1,000 W.B.C count in average, while occasional at fever attacks 531.7.Size of gametocytes in P. falciparum was 9.31(+/-0.89) by 2.16(+/-0.53) in macrogametocyte and 6.61(+/-0.82) by 2.51(+/-0.35) in microgametocyte. Their sex ratio was 100 : 92. Repeated blood examinations showed increased detection rates. The positive rate of parasitemia was 52.0% in single examination, increasing in succession with repetitions.
parasitology-protozoology-malaria
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Plasmodium falciparum
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Plasmodium vivax
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Plasmodium ovale
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Plasmodium malariae
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ring form gametocyte
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epidemiologyk Vietnam
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parasitemia