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1.
Clinical and Molecular Hepatology ; : 249-250, 2014.
Article in English | WPRIM | ID: wpr-106802
2.
Clinical and Molecular Hepatology ; : 251-260, 2014.
Article in English | WPRIM | ID: wpr-106801

ABSTRACT

BACKGROUND/AIMS: Occult HBV infection can persist following HBsAg loss and be transmitted, but the virological features are not well defined. METHODS: Here we investigated 25 Korean patients who lost HBsAg during follow up, either spontaneously or subsequent to therapy. RESULTS: Whereas subtype adr (genotype C) was found in 96% of HBsAg positive patients, 75 % of patients who lost HBsAg spontaneously were seemed to be infected with the ayw subtype with sequence similar to genotype D. Mutations in the major hydrophilic region (MHR) of HBsAg were found in 7 patients who lost HBsAg spontaneously. The mutations include T123S, M125I/N, C139R, D144E, V177A, L192F, and W196L, some of which have not been reported before. Functional analysis via transfection experiments indicate that the C139R and D144E mutations drastically reduced HBsAg antigenicity, while the Y225del mutation found in one interferon-treated patient impaired HBsAg secretion. CONCLUSIONS: Lack of detectable HBsAg in patient serum could be explained by low level of ccc DNA in liver tissue, low antigenicity of the surface protein, or its secretion defect.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Amino Acid Sequence , Antiviral Agents/therapeutic use , DNA, Circular/analysis , Genotype , Hep G2 Cells , Hepatitis B/drug therapy , Hepatitis B Surface Antigens/blood , Hepatitis B virus/genetics , Liver/virology , Molecular Sequence Data , Mutation , Remission, Spontaneous , Republic of Korea , Serotyping
3.
Mem. Inst. Oswaldo Cruz ; 86(4): 379-85, Oct.-Dec. 1991. tab, ilus
Article in English | LILACS | ID: lil-109137

ABSTRACT

Four Trypanosoma cruzi strains from zymodermes A, B, C and D were successively clonedon BHI-LIT-agar-blood BLAB). Twenty clones from the first generation (F1), 10 from The second (F2) and 4 from the third (F3) from the strains A138, B147 and C23 were isolated. The D150 strain provied 29 F1 and F2 clones. The strains and clones had their isoenzyme and K-DNA patterns determined. The clones from A138, Bl47 and C231 strains presented isoemzyme and K-DNA patterns identical between thewmselves and their respective parental strains. Therefore showing the homogenety and stability of isoenzyme and K-DNA patterns after successive cloning. The Dl50 strain from zymodeme D (ZD) showed heterogeneity. Twenty-eight out of 29 clones of the first generation were of zymodeme A and only one was of zymodeme C, confirming previous reports that ZD strains consisted of ZA and ZC parasite populations. The only D150 strain clone of zymodeme C showed a K-DNA pattern identical to its parental strain. The remining clones although similar among themselves were different from the parental strain. Thus the T. cruzi strains had either homonogeneus or heterogeneous populations. The clones produced by successive cloning provided genetically homonogeous populations. Their experimental use will make future results more reliable and reproducible


Subject(s)
Animals , DNA, Circular/analysis , Isoenzymes/analysis , Trypanosoma cruzi/physiology , Cloning, Molecular , Electrophoresis , Trypanosoma cruzi/genetics
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