Jang Hyunjung, Cho Mong, Heo Jeong, Kim Hyunghoi, Jun Hongki, Shin Woowon, Cho Byungman, Park Heekyung, Kim Cheolmin
Department of Microbiology, College of Medicine, Pusan National University, #10 1-Ga Ami-Dong Seo-Gu, Busan 602-739, Korea.
J Clin Microbiol. 2004 Sep;42(9):4181-8. doi: 10.1128/JCM.42.9.4181-4188.2004.
Hepatitis B virus (HBV) is one of the major causes of liver disease worldwide. It is important to conduct antiviral therapy against chronic hepatitis B to minimize the amount of liver damage. Lamivudine has been known to be an effective antiviral agent for the treatment of HBV infection. However, the emergence of viral mutants resistant to lamivudine is the main concern during the treatment of HBV-infected patients. Therefore, the detection of lamivudine-resistant mutants is of clinical importance. We have developed an oligonucleotide chip for the detection of lamivudine-resistant HBV which is rapid and accurate. The oligonucleotide chip consists of quality control probes, negative control probes, and specific oligonucleotide probes for the detection of lamivudine-resistant HBV. The specific probes consist of five probes for the detection of wild-type rtL180, rtM204, and rtV207 sequences and seven probes for the detection of HBV mutations. We tested 123 serum samples from patients with chronic HBV infection who had received lamivudine therapy. Eighty samples contained mutants with YMDD mutations. Among these, 17 contained rtM204V (YVDD), 24 contained rtM204I3 (YIDD3), 3 contained rtM204I2 (YIDD2), and 36 contained mixed types. We compared the results obtained with our oligonucleotide chip with those obtained by PCR-restriction fragment length polymorphism (RFLP) analysis and sequencing. The rate of concordance between the assay with the oligonucleotide chip and PCR-RFLP analysis for detection of the YMDD motif was 96.7%. The rate of concordance between the results obtained with the oligonucleotide chip for the detection of rtL180 and rtV207 and the results obtained by sequencing was 100%. Thus, the oligonucleotide chip is a reliable and useful tool for the detection of antiviral-resistant HBV.
乙型肝炎病毒(HBV)是全球肝病的主要病因之一。对慢性乙型肝炎进行抗病毒治疗以尽量减少肝脏损害的程度非常重要。已知拉米夫定是治疗HBV感染的一种有效抗病毒药物。然而,对拉米夫定耐药的病毒突变体的出现是治疗HBV感染患者过程中的主要关注点。因此,检测拉米夫定耐药突变体具有临床重要性。我们开发了一种用于检测拉米夫定耐药HBV的寡核苷酸芯片,它快速且准确。该寡核苷酸芯片由质量控制探针、阴性对照探针以及用于检测拉米夫定耐药HBV的特异性寡核苷酸探针组成。特异性探针包括用于检测野生型rtL180、rtM204和rtV207序列的5个探针以及用于检测HBV突变的7个探针。我们检测了123份接受拉米夫定治疗的慢性HBV感染患者的血清样本。80个样本含有YMDD突变的突变体。其中,17个含有rtM204V(YVDD),24个含有rtM204I3(YIDD3),3个含有rtM204I2(YIDD2),36个含有混合型。我们将用寡核苷酸芯片获得的结果与通过聚合酶链反应 - 限制性片段长度多态性(RFLP)分析和测序获得的结果进行了比较。寡核苷酸芯片检测YMDD基序与PCR - RFLP分析之间的一致性率为96.7%。寡核苷酸芯片检测rtL180和rtV207的结果与测序结果之间的一致性率为100%。因此,寡核苷酸芯片是检测抗病毒耐药HBV的可靠且有用的工具。