Title of article :
The mutations frequency of enhancer II/HBx regions of hepatitis B virus in acutely infected Iranian patients: a cross-sectional study
Author/Authors :
Karami ، Chiman Department of Microbiology - School of Medicine - Ardabil University of Medical Sciences , Mollaei ، Hamidreza Department of Microbiology and Medical Virology - School of Medicine - Kerman University of Medical Sciences , Arabzadeh ، Alimohammad Department of Microbiology and Medical Virology - School of Medicine - Kerman University of Medical Sciences , Mazloum Jalali ، Kamyar Department of Microbiology and Medical Virology - School of Medicine - Kerman University of Medical Sciences , Amerkani ، Saman Department of Microbiology and Medical Virology - School of Medicine - Kerman University of Medical Sciences , Pashangzadeh ، Salar Iranian Research Center for HIV/AIDS, Iranian Institute for Reduction of High Risk Behaviors - Tehran University of Medical Sciences , Nikpour ، Najmeh Department of Microbiology and Medical Virology - School of Medicine - Kerman University of Medical Sciences
From page :
554
To page :
562
Abstract :
Background and Objectives: The viral transactivator HBx protein affect cellular, viral and pregenomic factors pathway. Mutations in this protein can produce new viruses with new antigenic determinants that are generally related to developing cancerous. Materials and Methods: In this cross-sectional study, 33 serum samples of patients diagnosed with acute HBV infection were investigated for HBeAg and HBV DNA viral load and HBx gene mutations. mutation in the HBx protein detected by sequencing analysis. Results: Out of the 33 samples, 19 samples were males (57.6%), and 14 samples were females. 15 (45.5%) were positive for HBx DNA and 18 patients were negative for HBx DNA (54.5%). After sequencing, three mutations were recognized in HBx at nucleotide positions 147, 148, and 391 that were stationed to G1524A, G1525A, and G1767C mutations. Conclusion: The analysis result of this study shows G1524A and G1525A mutations that an important role in altering the inhibition function of the HBx activity domain. The G1767C mutation inactivates HBx transactivation activity. These mutations have a critical role in the pathogenicity of the virus, and the intensity of hepatic tissue demolition and the development of cirrhosis or carcinoma in patients can be understood.
Keywords :
Hepatitis B virus , X protein , Infections , Enhancer II , Mutation , Liver diseases
Journal title :
IJM Iranian Journal of Microbiology
Journal title :
IJM Iranian Journal of Microbiology
Record number :
2725408
Link To Document :
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