Abstract |
The aim of the current study was to detect HBV by Real time - PCR in chronic hepatitis B patients. Fifty-eight sera of chronic hepatitis B patients were subjected during the period March 2009 to April 2010 in Ilam cities in West of Iran. Sera assayed by real-time PCR and ELISA methods. Twenty serum samples from healthy volunteers and non- hepatitis B patients and negative for hepatitis B seromarkers served as negative controls for the study. Among fifty-eight sera, ELISA showed fifty-five (94.8%) of the samples were positive for HBsAg and three (5.2%) negative results obtained while real-time PCR specified fifty-eight (100%) positive results in chronic hepatitis B patients. HBsAg status did not necessarily reflect HBV DNA level in the serum, as 5.2% of chronic Hepatitis B patients were positive for HBV DNA but negative for HBsAg. HBV DNA was not found to be positive amongst any of the negative controls. Real time - PCR is a sensitive and reproducible assay for HBV DNA quantization.
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Authors | Nourkhoda Sadeghifard, Reza Mohebi, Zamberi Sekawi, Sobhan Ghafourian, Hossien Kazemian, Mitra Rezaee |
Journal | Roumanian archives of microbiology and immunology
(Roum Arch Microbiol Immunol)
2012 Jan-Mar
Vol. 71
Issue 1
Pg. 53-5
ISSN: 1222-3891 [Print] Romania |
PMID | 22838221
(Publication Type: Journal Article)
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Chemical References |
- DNA, Viral
- Hepatitis B Surface Antigens
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Topics |
- DNA, Viral
(analysis)
- Hepatitis B Surface Antigens
(analysis, genetics)
- Hepatitis B virus
(genetics, isolation & purification)
- Hepatitis B, Chronic
(virology)
- Humans
- Prevalence
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