Title of article :
Phylogenetic Analysis of HBV Based on PreS Region Iranian Hepatocellular Carcinoma Patients
Author/Authors :
GOODARZI, ZAHRA baqiyatallah university of medical sciences - Baqiyatallah Research Center for Gastroenterology and Liver Disease, تهران, ايران , MALEKZADEH, REZA tehran university of medical sciences tums, تهران, ايران , MONTAZERI, GHODRATOLLAH tehran university of medical sciences tums, تهران, ايران , ALAVIAN, SEYED MOAYED baqiyatallah university of medical sciences - Baqiyatallah Research Center for Gastroenterology and Liver Disease, تهران, ايران , QURBANALIZADEGAN, MEHDI baqiyatallah university of medical sciences, تهران, ايران , DARAM, MARYAM tehran university of medical sciences tums - FACULTY OF PUBLIC HEALTH - DEPARTMENT OF VIROLOGY, تهران, ايران , JAZAYERI, SEYED MOHAMMAD tehran university of medical sciences tums - FACULTY OF PUBLIC HEALTH - DEPARTMENT OF VIROLOGY, تهران, ايران
From page :
201
To page :
205
Abstract :
Background and Aims: There are eight genotypes (A-H) of hepatitis B virus (HBV), which show a characteristic worldwide distribution. Genotyping can be accomplished based on a partial sequence of HBV genome such as the PreS or S gene. The aim of this study was to determine the HBV genotypes in Iranian hepatocellular carcinoma (HCC) patients with chronic HBV infection. Methods: Serum sample of 10 HCC patients with chronic HBV infection were subjected to PreS Hemi-Nested PCR. The viral genotype of each sample was determined by bi-directional sequencing of the PreS amplicon and phylogenetic analysis by comparing the nucleotide sequence with 33 reference HBV strains obtained from the GenBank. Results: Phylogenetic analysis based on PreS region sequences disclosed that all isolated strains belonged to genotype D. Analysis of sequences revealed that all the sequences contained amino acid substitutions. In the PreS2 region of two samples, a point mutation in the start codon was found. There were some deletions with 3, 6 and 8 amino acids in PreS2 region of three samples. Conclusions: Despite the low number of samples, these data revealed that the HBV genotype D is dominant in Iranian HCCpatients. Most of the mutations are located at immunodominant epitopes involved in Borland T cell recognition.
Keywords :
HBV , Phylogenetic Analysis , PreS , Hepatocellular Carcinoma
Journal title :
Hepatitis Monthly
Journal title :
Hepatitis Monthly
Record number :
2581948
Link To Document :
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