Literature DB >> 27535686

Detection of Anti-Hepatitis B Virus Drug Resistance Mutations Based on Multicolor Melting Curve Analysis.

Yi Mou1,2, Muhammad Ammar Athar1,2, Yuzhen Wu1,2, Ye Xu1,2, Jianhua Wu3, Zhenxing Xu3, Zulfiqar Hayder4, Saeed Khan5, Muhammad Idrees6, Muhammad Israr Nasir7, Yiqun Liao8,9, Qingge Li8,2.   

Abstract

Detection of anti-hepatitis B virus (HBV) drug resistance mutations is critical for therapeutic decisions for chronic hepatitis B virus infection. We describe a real-time PCR-based assay using multicolor melting curve analysis (MMCA) that could accurately detect 24 HBV nucleotide mutations at 10 amino acid positions in the reverse transcriptase region of the HBV polymerase gene. The two-reaction assay had a limit of detection of 5 copies per reaction and could detect a minor mutant population (5% of the total population) with the reverse transcriptase M204V amino acid mutation in the presence of the major wild-type population when the overall concentration was 104 copies/μl. The assay could be finished within 3 h, and the cost of materials for each sample was less than $10. Clinical validation studies using three groups of samples from both nucleos(t)ide analog-treated and -untreated patients showed that the results for 99.3% (840/846) of the samples and 99.9% (8,454/8,460) of the amino acids were concordant with those of Sanger sequencing of the PCR amplicon from the HBV reverse transcriptase region (PCR Sanger sequencing). HBV DNA in six samples with mixed infections consisting of minor mutant subpopulations was undetected by the PCR Sanger sequencing method but was detected by MMCA, and the results were confirmed by coamplification at a lower denaturation temperature-PCR Sanger sequencing. Among the treated patients, 48.6% (103/212) harbored viruses that displayed lamivudine monoresistance, adefovir monoresistance, entecavir resistance, or lamivudine and adefovir resistance. Among the untreated patients, the Chinese group had more mutation-containing samples than did the Pakistani group (3.3% versus 0.56%). Because of its accuracy, rapidness, wide-range coverage, and cost-effectiveness, the real-time PCR assay could be a robust tool for the detection if anti-HBV drug resistance mutations in resource-limited countries.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2016        PMID: 27535686      PMCID: PMC5078540          DOI: 10.1128/JCM.00439-16

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  28 in total

Review 1.  Antiviral drug-resistant HBV: standardization of nomenclature and assays and recommendations for management.

Authors:  Anna S Lok; Fabien Zoulim; Stephen Locarnini; Angeline Bartholomeusz; Marc G Ghany; Jean-Michel Pawlotsky; Yun-Fan Liaw; Masashi Mizokami; Carla Kuiken
Journal:  Hepatology       Date:  2007-07       Impact factor: 17.425

2.  Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing.

Authors:  Jin Li; Lilin Wang; Harvey Mamon; Matthew H Kulke; Ross Berbeco; G Mike Makrigiorgos
Journal:  Nat Med       Date:  2008-04-13       Impact factor: 53.440

3.  Application of coamplification at lower denaturation temperature-PCR sequencing for early detection of antiviral drug resistance mutations of hepatitis B virus.

Authors:  Danny Ka-Ho Wong; Ottilia Tsoi; Fung-Yu Huang; Wai-Kay Seto; James Fung; Ching-Lung Lai; Man-Fung Yuen
Journal:  J Clin Microbiol       Date:  2014-06-20       Impact factor: 5.948

4.  Rapid detection of isoniazid resistance in Mycobacterium tuberculosis isolates by use of real-time-PCR-based melting curve analysis.

Authors:  Siyu Hu; Guoli Li; Hui Li; Xiaoli Liu; Jianjun Niu; Shengmao Quan; Feng Wang; Huixin Wen; Ye Xu; Qingge Li
Journal:  J Clin Microbiol       Date:  2014-03-05       Impact factor: 5.948

5.  Quantitation of hepatitis B virus genomic DNA by real-time detection PCR.

Authors:  A Abe; K Inoue; T Tanaka; J Kato; N Kajiyama; R Kawaguchi; S Tanaka; M Yoshiba; M Kohara
Journal:  J Clin Microbiol       Date:  1999-09       Impact factor: 5.948

Review 6.  Recent developments in antivirals against hepatitis B virus.

Authors:  Ya-Juan Wang; Li Yang; Jian-Ping Zuo
Journal:  Virus Res       Date:  2015-12-28       Impact factor: 3.303

7.  Comprehensive evaluation of hepatitis B virus reverse transcriptase substitutions associated with entecavir resistance.

Authors:  Carl J Baldick; Daniel J Tenney; Charles E Mazzucco; Betsy J Eggers; Ronald E Rose; Kevin A Pokornowski; Cheng F Yu; Richard J Colonno
Journal:  Hepatology       Date:  2008-05       Impact factor: 17.425

Review 8.  Hepatitis B virus resistance to nucleos(t)ide analogues.

Authors:  Fabien Zoulim; Stephen Locarnini
Journal:  Gastroenterology       Date:  2009-09-06       Impact factor: 22.682

9.  A one-year trial of lamivudine for chronic hepatitis B. Asia Hepatitis Lamivudine Study Group.

Authors:  C L Lai; R N Chien; N W Leung; T T Chang; R Guan; D I Tai; K Y Ng; P C Wu; J C Dent; J Barber; S L Stephenson; D F Gray
Journal:  N Engl J Med       Date:  1998-07-09       Impact factor: 91.245

10.  Adefovir dipivoxil alone or in combination with lamivudine in patients with lamivudine-resistant chronic hepatitis B.

Authors:  Marion G Peters; H w Hann Hw; Paul Martin; E Jenny Heathcote; P Buggisch; R Rubin; M Bourliere; K Kowdley; C Trepo; D f Gray Df; M Sullivan; K Kleber; R Ebrahimi; S Xiong; Carol L Brosgart
Journal:  Gastroenterology       Date:  2004-01       Impact factor: 22.682

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  3 in total

1.  A novel multiplex PCR for virus detection by melting curve analysis.

Authors:  Pengcheng Liu; Lijuan Lu; Menghua Xu; Huaqing Zhong; Ran Jia; Liyun Su; Lingfeng Cao; Zuoquan Dong; Niuniu Dong; Linfu Zhou; Jin Xu
Journal:  J Virol Methods       Date:  2018-09-26       Impact factor: 2.014

Review 2.  Hepatitis B Virus: From Diagnosis to Treatment.

Authors:  Meryem Guvenir; Ayse Arikan
Journal:  Pol J Microbiol       Date:  2020-12-27

3.  Fast and Sensitive Real-Time PCR Detection of Major Antiviral-Drug Resistance Mutations in Chronic Hepatitis B Patients by Use of a Predesigned Panel of Locked-Nucleic-Acid TaqMan Probes.

Authors:  Son V Chu; Son T Vu; Hang M Nguyen; Ngan T Le; Phuong T Truong; Van T T Vu; Thuy T B Phung; Anh T V Nguyen
Journal:  J Clin Microbiol       Date:  2021-07-28       Impact factor: 5.948

  3 in total

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