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Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection

Lamivudine, a nucleoside analogue, has been used widely as an effective antiviral agent for the treatment of patients with chronic hepatitis B virus (HBV) infection. However, the YMDD motif mutation of HBV polymerase resistant to lamivudine occurs very frequently after long term therapy. We develope...

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Autores principales: Heo, Jeong, Cho, Mong, Kim, Hyung Hoi, Shin, Young Min, Jang, Hyun Jung, Park, Hee Kyung, Kim, Cheol Min, Kim, Gwang Ha, Kang, Dae Hwan, Song, Geun Am, Yang, Ung Suk
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816888/
https://www.ncbi.nlm.nih.gov/pubmed/15308845
http://dx.doi.org/10.3346/jkms.2004.19.4.541
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author Heo, Jeong
Cho, Mong
Kim, Hyung Hoi
Shin, Young Min
Jang, Hyun Jung
Park, Hee Kyung
Kim, Cheol Min
Kim, Gwang Ha
Kang, Dae Hwan
Song, Geun Am
Yang, Ung Suk
author_facet Heo, Jeong
Cho, Mong
Kim, Hyung Hoi
Shin, Young Min
Jang, Hyun Jung
Park, Hee Kyung
Kim, Cheol Min
Kim, Gwang Ha
Kang, Dae Hwan
Song, Geun Am
Yang, Ung Suk
author_sort Heo, Jeong
collection PubMed
description Lamivudine, a nucleoside analogue, has been used widely as an effective antiviral agent for the treatment of patients with chronic hepatitis B virus (HBV) infection. However, the YMDD motif mutation of HBV polymerase resistant to lamivudine occurs very frequently after long term therapy. We developed an oligonucleotide chip for the detection of YMDD motif mutants resistant to lamivudine and investigated the prevalence of the mutants in patients with chronic HBV infection who had not been treated by lamivudine before. Forty patients who had not been treated with lamivudine were included in this study. Serum samples were tested by the oligonucleotide chips designed for detection of wild-type YMDD motif, M552V and M552I. Samples were confirmed by restriction fragment length polymorphism (RFLP) and direct sequencing. M552I mutants were detected by the oligonucleotide chips in 7.5% (3/40) of chronic HBV infected patients (2 chronic hepatitis and 1 cirrhosis). The results were in accordance with those of RFLP. YMDD motif mutants occur as natural genome variabilities in patients with chronic HBV infection who had not been treated with lamivudine before. Oligonucleotide chip technology is a reliable and useful diagnostic tool for the detection of mutants resistant to antiviral therapy in chronic HBV infection.
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spelling pubmed-28168882010-02-12 Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection Heo, Jeong Cho, Mong Kim, Hyung Hoi Shin, Young Min Jang, Hyun Jung Park, Hee Kyung Kim, Cheol Min Kim, Gwang Ha Kang, Dae Hwan Song, Geun Am Yang, Ung Suk J Korean Med Sci Original Article Lamivudine, a nucleoside analogue, has been used widely as an effective antiviral agent for the treatment of patients with chronic hepatitis B virus (HBV) infection. However, the YMDD motif mutation of HBV polymerase resistant to lamivudine occurs very frequently after long term therapy. We developed an oligonucleotide chip for the detection of YMDD motif mutants resistant to lamivudine and investigated the prevalence of the mutants in patients with chronic HBV infection who had not been treated by lamivudine before. Forty patients who had not been treated with lamivudine were included in this study. Serum samples were tested by the oligonucleotide chips designed for detection of wild-type YMDD motif, M552V and M552I. Samples were confirmed by restriction fragment length polymorphism (RFLP) and direct sequencing. M552I mutants were detected by the oligonucleotide chips in 7.5% (3/40) of chronic HBV infected patients (2 chronic hepatitis and 1 cirrhosis). The results were in accordance with those of RFLP. YMDD motif mutants occur as natural genome variabilities in patients with chronic HBV infection who had not been treated with lamivudine before. Oligonucleotide chip technology is a reliable and useful diagnostic tool for the detection of mutants resistant to antiviral therapy in chronic HBV infection. The Korean Academy of Medical Sciences 2004-08 2009-05-20 /pmc/articles/PMC2816888/ /pubmed/15308845 http://dx.doi.org/10.3346/jkms.2004.19.4.541 Text en Copyright © 2004 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Heo, Jeong
Cho, Mong
Kim, Hyung Hoi
Shin, Young Min
Jang, Hyun Jung
Park, Hee Kyung
Kim, Cheol Min
Kim, Gwang Ha
Kang, Dae Hwan
Song, Geun Am
Yang, Ung Suk
Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title_full Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title_fullStr Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title_full_unstemmed Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title_short Detection of YMDD Motif Mutants by Oligonucleotide Chips in Lamivudine-Untreated Patients with Chronic Hepatitis B Virus Infection
title_sort detection of ymdd motif mutants by oligonucleotide chips in lamivudine-untreated patients with chronic hepatitis b virus infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816888/
https://www.ncbi.nlm.nih.gov/pubmed/15308845
http://dx.doi.org/10.3346/jkms.2004.19.4.541
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