This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marshall, D. J.
Right arrow Articles by de Arruda, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marshall, D. J.
Right arrow Articles by de Arruda, M.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, Dec 1997, 3156-3162, Vol 35, No. 12
Copyright © 1997 by the American Society for Microbiology. All rights reserved.

Determination of hepatitis C virus genotypes in the United States by cleavase fragment length polymorphism analysis [In Process Citation]

DJ Marshall, LM Heisler, V Lyamichev, C Murvine, DM Olive, GD Ehrlich, BP Neri and M de Arruda
Third Wave Technologies, Inc., Madison, Wisconsin 53711, USA.

We describe the application of a new DNA-scanning method, which has been termed Cleavase Fragment Length Polymorphism (CFLP; Third Wave Technologies, Inc., Madison, Wis.), for the determination of the genotype of hepatitis C virus (HCV). CFLP analysis results in the generation of structural fingerprints that allow discrimination of different DNA sequences. We analyzed 251-bp cDNA products generated by reverse transcription-PCR of the well-conserved 5'-noncoding region of HCV. We determined the genotypes of 87 samples by DNA sequencing and found isolates representing 98% of the types typically encountered in the United States, i.e., types 1a, 1b, 2a/c, 2b, 3a, and 4. Blinded CFLP analysis of these samples was 100% concordant with DNA sequencing results, such that closely related genotypes yielded patterns with strong familial resemblance whereas more divergent sequences yielded patterns with pronounced dissimilarities. In each case, the aggregate pattern was indicative of genotypic grouping, while finer changes suggested subgenotypic differences. We also assessed the reproducibility of CFLP analysis in HCV genotyping by analyzing three distinct isolates belonging to a single subtype. These three isolates yielded indistinguishable CFLP patterns, as did replicate analysis of a single isolate. This study demonstrates the suitability of this technology for HCV genotyping and suggests that it may provide a low- cost, high-throughput alternative to DNA sequencing or other, more costly or cumbersome genotyping approaches.


This article has been cited by other articles:

  • Ilina, E. N., Malakhova, M. V., Generozov, E. V., Nikolaev, E. N., Govorun, V. M. (2005). Matrix-Assisted Laser Desorption Ionization-Time of Flight (Mass Spectrometry) for Hepatitis C Virus Genotyping. J. Clin. Microbiol. 43: 2810-2815 [Abstract] [Full Text]  
  • Pincas, H., Pingle, M. R., Huang, J., Lao, K., Paty, P. B., Friedman, A. M., Barany, F. (2004). High sensitivity EndoV mutation scanning through real-time ligase proofreading. Nucleic Acids Res 32: e148-e148 [Abstract] [Full Text]  
  • Cahill, P., Bakis, M., Hurley, J., Kamath, V., Nielsen, W., Weymouth, D., Dupuis, J., Doucette-Stamm, L., Smith, D. R. (2003). Exo-Proofreading, A Versatile SNP Scoring Technology. Genome Res 13: 925-931 [Abstract] [Full Text]  
  • Pourmand, N., Elahi, E., Davis, R. W., Ronaghi, M. (2002). Multiplex Pyrosequencing. Nucleic Acids Res 30: e31-e31 [Abstract] [Full Text]  
  • Dong, F., Allawi, H. T., Anderson, T., Neri, B. P., Lyamichev, V. I. (2001). Secondary structure prediction and structure-specific sequence analysis of single-stranded DNA. Nucleic Acids Res 29: 3248-3257 [Abstract] [Full Text]  
  • Dufour, D. R., Lott, J. A., Nolte, F. S., Gretch, D. R., Koff, R. S., Seeff, L. B. (2000). Diagnosis and Monitoring of Hepatic Injury. I. Performance Characteristics of Laboratory Tests. Clin. Chem. 46: 2027-2049 [Abstract] [Full Text]  
  • Olive, D. M., Bean, P. (1999). Principles and Applications of Methods for DNA-Based Typing of Microbial Organisms. J. Clin. Microbiol. 37: 1661-1669 [Full Text]  
  • Charrel, R. N., Lévy, N., Tesh, R. B., Chandler, L. J. (1999). Use of Base Excision Sequence Scanning for Detection of Genetic Variations in St. Louis Encephalitis Virus Isolates. J. Clin. Microbiol. 37: 1935-1940 [Abstract] [Full Text]  
  • Cockerill, F. R. III (1999). Genetic Methods for Assessing Antimicrobial Resistance. Antimicrob. Agents Chemother. 43: 199-212 [Full Text]  
  • Sreevatsan, S., Bookout, J. B., Ringpis, F. M., Pottathil, M. R., Marshall, D. J., De Arruda, M., Murvine, C., Fors, L., Pottathil, R. M., Barathur, R. R. (1998). Algorithmic Approach to High-Throughput Molecular Screening for Alpha Interferon-Resistant Genotypes in Hepatitis C Patients. J. Clin. Microbiol. 36: 1895-1901 [Abstract] [Full Text]