Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Southeast Asian J Trop Med Public Health ; 2004 Jun; 35(2): 267-9
Article in English | IMSEAR | ID: sea-34325

ABSTRACT

Third-stage larvae were used as antigen in the diagnosis of gnathostomiasis in Western blot analysis. Normally, the larvae were obtained from digestion of eel's liver (Fluta alba) by the enzyme pepsin. We used pineapple juice (Ananus comosus) instead of enzyme pepsin in harvesting Gnathostoma spinigerum third-stage larvae. The difference in recovered larvae numbers, between pineapple juice and pepsin, were not statistically significantly different (p>0.05). The larvae from pepsin and pineapple juice digestion were cultivated on BME for 7 days; the survival rates were not significantly different (p>0.05). Thus, pineapple juice is another enzyme of choice for recovering Gnathostoma spinigerum third-stage larvae.


Subject(s)
Ananas/metabolism , Animals , Antigens, Helminth , Beverages , Blotting, Western , Digestion/physiology , Eels/parasitology , Fish Diseases/diagnosis , Food Parasitology , Gnathostoma/immunology , Larva/immunology , Larva Migrans, Visceral , Liver/parasitology , Pepsin A/diagnosis , Solutions/diagnosis , Spirurida Infections/diagnosis
2.
Southeast Asian J Trop Med Public Health ; 2004 Jun; 35(2): 270-4
Article in English | IMSEAR | ID: sea-32525

ABSTRACT

A detection method of Toxoplasma gondii oocysts from soil was evaluated using the sucrose flotation technique with modification involving addition of 0.1% gelatin into washing and floating solutions. PCR was performed on untreated samples and after treatment with polyvinylpyrrolidone (PVP), heating and cooling, and NaCl. The addition of gelatin in the sucrose solution yielded a higher number of oocysts. A very thin band was observed when DNA extract was diluted to 1:1024, indicating the presence of PCR inhibitor in the soil. PCR performed on untreated DNA, on PVP-treated, and on PVP-treated with heating and cooling without added bovine serum albumin (BSA) showed a band only at higher dilutions (1:1024 and 1:512) but at a much lower dilution (1:8) with BSA. In contrast, DNA treated with all three agents showed a band at a much lower dilution (1:64), even without added BSA, and no dilution was required when BSA was added. The PCR inhibitors present in the soil were removed by employing various treatment procedures during DNA extraction, and BSA in PCR. Furthermore, the detection limit with the method was 1 oocyst/g of soil, indicating that this method is useful in epidemiological studies.


Subject(s)
Animals , Cats , Cell Fractionation/methods , Centrifugation , DNA, Protozoan/analysis , Feces/parasitology , Japan , Oocysts/genetics , Polymerase Chain Reaction/methods , Silicon Dioxide/analysis , Soil/parasitology , Solutions/diagnosis , Sucrose/diagnosis , Toxoplasma/genetics
SELECTION OF CITATIONS
SEARCH DETAIL