The morphological characters of the microfilaria of Brugia malayi collected in Cheju-Do, Korea were described and compared with those or other local strains, already reported from the Malay Archipelago(Brug, 1927), Huchow, South China (Feng, 1933), Hachijo Kojima, Japan (Hayashi, 1951) etc. And it was found that there are no marked difference among these kinds of Microfilaria malayi. The percentage measurements of the fixed points in the Microfilaria malayi from Korea are summarized as follows; B.N.C.: 3.38%(2.90-3.72%), N.R.: 22.64% (17.36-25.81%), E.P.: 32.26% (27.49-36.60%), E.C.: 38.78% (34.90-41.72%), Inn. K. begin: 53.95% (49.50-58.84%) end: 67.87%(63.02-72.97%), G-1: 70.42% (60.22-75.23%), G-2:76.70% (75.10-78.32%), G-3:78.84% (77.81-79.59%), G-4:80.84%(79.82-81.35%), A.P.:82.94%(77.32-89.72%), Length: 193.39(+-12.3 micro-meter)(170.77-233.08 micro-meter), Width: 7.04+-0.37 micro-meter(5.99-7.99 micro-meter), Sheath: 268.48+-17.07 micro-meter(218.72-286.47 micro-meter), Ratio(Cephalic space): 1: 0.78
parasitology-helminth-nematoda ; Brugia malayi ; microfilaria

Malayain filariasis in Korea is reviewed in the point of history, parasitology, epdidemiology, pathology and clinical aspects, diagnosis and chemotherapy.
parasitology-helminth-nematoda ; Brugia malayi ; filariasis ; epidemiology ; pathology ; clinical finding ; diagnosis ; chemotherapy ; diethylcarbamazine ; Aedes togoi

The metacercariae of Metagonimus yokogawai were isolated from the sweetfish Plecoglossus altivelis, clollected at Hwagae, South Kyongsang Do, one of the newly known endemic foci of metagonimiasis in Korea. The body structure of metacercaria of M.yokogawai was described and the measurements of the excysted metacercaria were also made. In order to know the distribution of metacercariae within the host, the rate of infection and the intensity of infection, a total of 10 sweet fishes was examined and it was found all infected, from which a total of 38,511 metacercariae was isolated. The number of metacercariae in a fish varied from 219 to 14,427. The average number of metacercaria per fish was 3,851. The distribution of metacercariae in the four divided parts of fish was observed in the following order; number of metacercaria in the muscles; 2,417 (62.8%), in the subcutaneous tissues; 1,126.9 (29.3%), and on the scale; 291.9(7.7%). The development of the metacercaria of M. yokogawai in the mouse host was experimentally traced every day for 10 days after infection . In an earlier period of infection, the growth rate of the genital primordia was distinctly high, particularly in the testes. The seminal receptable and seminal vesicle became clearly recognized in measurable size at 4 days after infection. The vitelline follicles and their ducts were also first visible in the living specimens at 6 days after infection. The oral sucker was larger in size than the ventral sucker in an early stage of the worms, however after 7 days after infection it reversed. The posterior part of body began to extend since two days after infection. Fully matured worms were able to collect only after 7 days after infection. At this stage, the body of worm became 0.7 mm long and 0.3 mm wide. The first positive appearance of eggs in the uterine tubule and in feces was on the 6th day and 10th day of infection, respectively. In an earlier stage of infection, the worms were found mostly in the upper portion of small intestine and the recovery rates of the worms were high, however according to the course of infection in later stage they were seen rather in the lower part of the intestine and the recovery rate also decreased.
parasitology-helminth-trematoda ; Metagonimus yokogawai ; development ; metacercaria ; Plecoglossus altivelis

Cotylaspis coreensis sp. n., Cotylaspis sinensis Faust et Tang, 1936, Phyllodistomum parasiluri Yamaguti, 1934, Kaurma orientalis Yamaguti, 1937, Astiotrema reniferum (Looss, 1898), Astiotrema odhneri Bhalerao, 1936, Astiotrema sp. and Cephalogonimus japonicus Ogata, 1936 were collected from the intestine of freshwater mud-turtle, Amyda sinensis Wiegmann in Korea which were purchased at Namdaemoon Market of Seoul on October 1968 and May 1977. Cotylaspis coreensis differs from other members of the genus in relatively large size of pharynx, the number and distribution of vitelline follicles, size of testis, length of intestine and position of genital opening. Distribution of Cotylaspis sinensis was firstly recorded in Korea. Phyllodistomum parasiluri collected in this study was considered to be the first to recover from the reptilian host although the collected worms were still immatured. The genus Astiotrema collected in this study were divided into three species, A. reniferum which is hitherto unrecorded in Korea, A. odhneri which had been described as A. orientale, A. amydae and A. fukuii and another Astiotrema sp. which differs from the former two species in minor differences in size of suckers, size of ova and size of cirrus pouch. The distribution of Cephalogonimus japonicus was firstly recorded in Korea.
parasitology-helminth-trematoda ; Cotylaspis coreensis ; Phyllodistomum parasiluri ; Kaurma orientalis ; Astiotrema reniferum ; Astiotrema odhneri ; Astiotrema sp. ; Cephalogonimus japonicus ; turtle-Amyda sinensis ; epidemiology

The malic dehydrogenase activity was determined by the modified method of Ochoa (1955) using tissue homogenates of various parasitic helminths. Worm parasites were mostly collected from local abattoir, and removed from the organ or tissues of the naturally infected animal hosts, and some materials were also obtained from the human hosts. The helminths used in this experiment include 3 kinds of nematodes, 5 kinds of trematodes, and 8 kinds of cestodes. They were throughly washed and homogenized in glass tissue grinder in ice chilled water bath, and then centrifuged. The supernatants were designated as enzyme preparations. The hydrogen concentrations of buffer solution were pH 1.4, 2.7, 3.5, 4.2, 5.2, 7.4, 8.2, 9.3, 10.2, 11.6, and enzymatic reaction of this experiment was performed at incubation temperature of 20, 30, 40, and 50 C. The extinction of Nicotinamide Adenosine Dinucleotide (NAD) was measured by spectrophotometry at the wave length of 340 millimicron. The results of the experiment were as follows: The malic dehydrogenase activity occurred over all kinds of parasitic helminths used in this study. And the activity on sparganum turned out to be highest. All helminths displayed their maximum activity in the range of alkaline pH. A comparison of the effects of temperature and substrate concentration on the enzyme activity was made among these helminths. However, no definite relationship among them has been detected. The significance of the existence of this enzyme in the helminths was briefly discussed.
parasitology-helminth-trematoda-cestoda-nematoda ; Fasciola hepatica ; Eurytrema pancreaticum ; Paramphistomum sp. ; Taenia solium ; Taenia pisiformis ; Dipylidium caninum ; Diphyllobothrium mansoni ; Cysticercus cellulosae ; Cysticercus fasciolaris ; sparganum ; Ascaris lumbricoides ; Ascaridia galli ; Dirofilaria immitis ; Paragonimus westermani ; Clonorchis sinensis ; malic dehydrogenase-biochemistry-enzyme ; malic dehydrogenase ; Nicotinamide Adenosine Dinucleotide

In order to obtain some informations on the nature and relative activity of the phosphatases present in various helminths, biochemical studies have been made in thirteen kinds of worm parasites including the adults and larvae (Fasciola hepatica, Eurytrema pancreaticum, Paramphistomum sp., Taenia solium, Taenia pisiformis, Dipylidium caninum, Diphyllobothrium mansoni, Cysticercus cellulosae, Cysticercus fasciolaris and Sparganum). A comparison based on the analysis of pH-activity curves was made among these helminths. The worm materials were mostly obtained alive from an abattoir and removed from the organs or tissues of the animal hosts naturally infected. Sparganum and Cysticercus cellulosae, however, are collected from the subcutaneous tissue of the patients by surgical removal. The worms thoroughly washed were weighed and transferred with 0.1 M Tris buffer to a chilled glass grinder (Capacity; 15 ml) and homogenized in the cold. The homogenate was centrifuged at 5000 RPM for 30 minutes. The supernatant was pipetted off for determination of the phosphatase activity. Incubation mixtures consisted of 1 ml substrate, 1 ml buffer and 0.5ml extract. The buffers used were Tris (Hydroxymethyl) aminomethane and citric acid monohydrate and the substrate was paranitrophenyl phosphate (1 gm/25 ml). These mixtures were incubated at the temperature of 37 C for 30 minutes in water bath. The absorbance or transferance of mixture was determined colorimetrically by "Spectronic 20 "spectrophotometer at 410 nm against a distilled water blank. The amount of phenol liberated was then calculated from a standard curve using phenol solutions. Controls consisted of unincubated mixtures. The results were deducted from this experiment. The phosphatase activity occurred over all parasitic helminths used in this experiment. In trematodes, pH-activity curves have demonstrated two peaks of phosphatase activity in Fasciola hepatica and Paramphistomum species. However the acid phosphatase activity was predominantly found and the alkaline phosphatase activity was found distinctly to be low in all three species. In Eurytrema pancreaticum, the pH-activity curves displayed two peaks in acid phosphatase activity, one at pH 5.0 and the other pH 9.0. In cestodes, both alkaline and acid phosphatase activity displayed the pH optima 5.0 and 9.0 to 10.0 in the adult tapeworms. However, major activity in the adults is due to the alkaline phosphtases. In contrast to the adults, Cysticercus and sparganum showed the higher activity in acid phosphatases which predominates in the larvae. In all cases of nematodes, the pH optimum for acid phosphatase was 4.0 to 6.0. A preponderance of acid phosphatase activity was shown in the extract of intestine of Ascaris lumbricoides. The aspect that phosphatases are correlated with phosphorylated passage of substances through the cuticle of helminths and may also be involved in carbohydrate metabolism is discussed.
parasitology-helminth-trematoda-cestoda ; Fasciola hepatica ; Eurytrema pancreaticum ; Paramphistomum sp. ; Taenia solium ; Taenia pisiformis ; Dipylidium caninum ; Diphyllobothrium mansoni ; Cysticercus cellulosae ; Cysticercus fasciolaris ; sparganum ; alkaline phosphatase ; acid phosphatase ; biochemistry

The present study attempted to induce an acquired immunity against the dog hookworm, Ancylostoma caninum. The experiments were carried out to demonstrate and confirm whether an acquired resistance could be developed by the repeated lowgrade infections with the infective larvae of A. caninum in the abnormal host of mouse. In order to determined the distribution of hookworm larvae in the lungs and liver of mice after inoculation of infective larvae, 54 mice were inoculated with 1,000 larvae and sacrificed in batches daily up to 9 days after infection. It was found that in all cases the average total number of larvae recovered from the lungs and liver increased at 48 hours after infection, then began to decrease and reached 0 to 1 at the 9th day after inoculation. One hundred fifteen mice were immunized 2 or 4 times at 7 day intervals with 50 infective larvae, followed by challenging infection with 1,000 infective larvae and killed in batches at 48 hours after challenge. The interval between challenge and last immunization were from one to four weeks for each group. Sixty mice as the controls were given only challenging infection without previous immunization infection. Induced resistance was evaluated by the rate of recovery or the average total number of the larvae recovered from the lungs and liver in the challenged mice, compared with the controls. It was noted that the rates of recovery in the controls were twice or nearly higher than those in the previously infected mice in all instances and these remained low for the first 7 day intervals between the last immunizing infection and challenge, then gradually increased. From the above observations it is highly suggested that an acquired resistance can be produced by repeated previous infections with the larvae of A. caninum, even in low grade, in the abnormal host of mouse, and evaluated by the rate of recovery of the larvae after challenge.
parasitology-helminth-nematode-Ancylostoma caninum ; immunology ; recovery rate

The occurrence of Sarles' phenomenon (Cerkarien Hullen Reaktion) are proved in the excysted metacercariae of Clonorchis sinensis which were incubated in the sera from rabbits given a varying number of metacercariae of C. sinensis per orally. The precipitates were formed around the oral sucker and excretory bladder of the excysted larvae. Sarles' phenomenon began to be positive from the 2nd to 3rd week after infection. In the excysted larvae of C. sinensis precipitates were not produced in the sera of rabbits infected with Metagonimus yokogawai and Capillaria hepatica. The number of eggs in the feces (E.P.G.), intradermal reaction, the course of infection and Sarles' phenomenon was studied in 6 clonorchiasis patients. Sarles' phenomenon appeared in the sera of some clonorchiasis patients. However, it assumed that this phenomenon correlated with the degree and the course of infection of clonorchiasis.
parasitology-helminth-trematoda-Clonorchis sinensis ; Sarles' phenomena ; rabbit

Since Senoo and Lincicome (1951) first have brought up for attention to the existence of malayan filariasis in Korea, several reports on the epidemiological investigations of the disease had already been made by many workers. However it is little known what kind of mosquitoes are involved as the major vectors in main endemic areas. In Cheju-Do, known as one of main endemic areas in Korea, Aedes togoi is most likely suspected as an important vector because of their abundant collections and vigorous biting attack to human. As a part of studies on filariasis in Korea, an essential preliminary is to determiine whether this mosquito, Aedes togoi collected in the above areas is receptive to the microfilariae of B. malayi. Therefore, the present paper is concerned chiefly with the development of B. malayi in A. togoi. It is also hoped that the studies on the larval morphology in the mosquito host and the structure of microfilariae will provide the base line data required for later investigation of the different vector hosts. The studies were summarized as follows: The measurements of the fixed points in percentage of the body length of microfilariae from the Giemsa stained thick films were made, and they showed that cephalic space was 8 percent,cephalic space length to width, 1.3:1, nerve ring, 21.2 percent, excretory pore, 30.8 percent, excretory cell, 36.5 percent, R1 cell, 66. 5 percent, anus 80.4 percent and body length 202 micrometer(l81-228 micrometer) maximun width 7.6 micrometer. A study on the development of microfilaria malayi in the mosquito, Aedes togoi was carried out at room temperature (24-30 C). Mosquitoes used in this experiment were reared from larvae collected from the tide water rock pool in the coastal areas of Cheju-Do and they were fed with a blood meal of carrier donors whose microfilaria densities were in the range from 0.5 to 0.7 per cmm of blood. All of the microfilariae ingested by mosquito exsheathed in stomach, penetrated into the body cavity and then migrated into the thoracic muscles of the mosquitoes within 10 hours, after two moults in the mosquito host, the length of the developing 3rd stage larvae reached in size of 1.3-1.7 mm x 23-32 microns with anal ratio, 2.6 to 3.6. The first appearance of 3rd stage larvae in the mosquito host in this experiment was in 8th day after infection. The larvae were observed in the various cavities of mosquito, such as head, thoracic cavity, abdomen, halters, eye and legs. During the larval development in larval development in the host, the shortening of body length was first observed and then elnongation was followed until becoming 3rd stage larvae. Aedes togoi was proved to be the most suitable host for this species of microfilaria malayi in the above endemic areas.
parasitology-helminth-nematoda-Brugia malayi ; filariasis ; epidemiology ; mosquito ; life cycle ; vector

Radioactive C(14)-glycine was given to Clonorchis sinensis in Tyrode medium in order to trace the metabolic fate of the labeled carbon. The labeled carbon from glycine enters into every major fraction of Clonorchis sinensis and is highest in the fraction of protein and nucleic acid. Significant amount of C(14)-glycine is incorporated into respiratory carbon dioxide. Relatively high percentage of C(14)-glycine in medium is converted to amino acid fraction and lipid fraction of the worm. In general, glycine is continuously being utilized in the synthesis of proteins and for energy production despite the uptake rate of glycine decreased gradually as incubation proceeds.
parasitology-helminth-trematoda ; Clonorchis sinensis ; metabolism ; biochemistry ; glycine ; amino acid ; nucleic acid ; protein ; lipid ; Tyrode medium