Clinical Chemistry
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Clinical Chemistry 51: 1123-1131, 2005. First published May 12, 2005; 10.1373/clinchem.2004.047506
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(Clinical Chemistry. 2005;51:1123-1131.)
© 2005 American Association for Clinical Chemistry, Inc.


Molecular Diagnostics and Genetics

Population Genotyping of Hepatitis C Virus by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry Analysis of Short DNA Fragments

Yoon Jun Kim1,2, Soo-Ok Kim2,2, Hyun Jae Chung2, Mi Sun Jee2, Byeong Gwan Kim1, Kang Mo Kim1, Jung-Hwan Yoon1, Hyo-Suk Lee1, Chung Yong Kim1, Sukjoon Kim2, Wangdon Yoo2 and Sun Pyo Hong2,a

1 Department of Internal Medicine, Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
2 GeneMatrix, Seoul, Korea.

aAddress correspondence to this author at: GeneMatrix, 8F, Cancer Research Institute, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul 110-799, Korea. Fax 82-2-764-8076; e-mail sunphong{at}genematrix.net.

Background: Identifying hepatitis C virus (HCV) genotypes has become increasingly important for determining clinical course and the outcome of antiviral therapy. Here we describe the development of restriction fragment mass polymorphism (RFMP) analysis, a novel matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) assay suitable for high-throughput, sensitive, specific genotyping of multiple HCV species.

Methods: The assay is based on PCR amplification and mass measurement of oligonucleotides containing genotype-specific motifs in the 5' untranslated region, into which a type IIS restriction endonuclease recognition was introduced by PCR amplification. Enzymatic cleavage of the products led to excision of multiple oligonucleotide fragments representing variable regions whose masses were determined by MALDI-TOF MS.

Results: The RFMP assay identified viral genotypes present at concentrations as low as 0.5% and reliably determined their relative abundance. When sera from 318 patients were analyzed, the RFMP assay exhibited 100% concordance with results obtained by clonal sequencing and identified mixed-genotype infections in 22% of the samples, in addition to several subtype variants.

Conclusions: The RFMP assay has practical advantages over existing methods, including better quantitative detection of mixed populations and detection of genotype variants without need for population-based cloning, enabling reliable viral genotyping in laboratories and efficient study of the relationship between viral genotypes and clinical outcome.




The following articles in journals at HighWire Press have cited this article:


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J. Clin. Microbiol.Home page
M. I. L. Sjoholm, J. Dillner, and J. Carlson
Multiplex Detection of Human Herpesviruses from Archival Specimens by Using Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry
J. Clin. Microbiol., February 1, 2008; 46(2): 540 - 545.
[Abstract] [Full Text] [PDF]


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Clin. Chem.Home page
L. Cook and K. R. Jerome
Mass Spectrometry for Genotyping Hepatitis C Virus: A Promising New Approach
Clin. Chem., July 1, 2005; 51(7): 1091 - 1092.
[Full Text] [PDF]




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