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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16171
Title: A PCR-RFLP based protocol for the detection of hepatitis B virus variants in some lamivudine-untreated chronic hepatitis B virus carriers in Pakistan
Authors: Isfahan Tauseef
Furhan Iqbal
Wajid Rehman
Muhammad Ali
Qureshi, Javed Anver
Muhammad Assad Aslam
Keywords: YMDD mutations
chronic hepatitis B
PCR-RFLP
polymerase gene
lamivudine
Issue Date: 9-Apr-2012
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi
Citation: Tauseef, I., Iqbal, F., Rehman, W., Ali, M., Qureshi, J. A., & Aslam, M. A. (2012). A PCR-RFLP based protocol for the detection of hepatitis B virus variants in some lamivudine-untreated chronic hepatitis B virus carriers in Pakistan. Pakistan Journal of Pharmaceutical Sciences, 25(2).
Abstract: Hepatitis B virus (HBV) affects more than 350 million people worldwide and is a leading cause of morbidity and mortality in developing countries like Pakistan. Lamivudine has potential to inhibit hepatitis B virus (HBV) replication but long term lamivudine treatment results in mutations in YMDD region of HBV, making this therapy ineffective. In this study, we have optimized a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) based protocol to detect two mutations in HBV DNA polymerase gene (at codon 528 and 552) in chronic hepatitis patients, without any prior lamivudine treatment. HBV genome was extracted and tested by PCR-RFLP for detection of mutations in polymerase gene. Variations in HBV genome were not detected in enrolled patients confirming that lamivudine can be used to treat chronic Hepatitis B in these patients. Several studies have reported the natural occurrence of mutation in YMDD motif of polymerase gene in chronic hepatitis B patients, not treated with lamivudine, but these mutants were not detected in Pakistani lamivudine-untreated chronic hepatitis B patients.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/16171
ISSN: 1011-601X
Appears in Collections:Issue 02

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