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A web resource to manage the classification and genotype and subtype assignments of hepatitis C virus
Donald B. Smith, Jens Bukh, Carla Kuiken, A. Scott Muerhoff, Charles M. Rice, Jack T. Stapleton and Peter Simmonds
This web page maintains a regularly updated list of confirmed HCV genotype and subtype assignments (Table 1). This maintained resource is designed to assist researchers investigating the diversity of HCV in designating appropriate assignments for new sequences and maintaining consistency in both the names designated and ensuring that guidelines for their assignment (originally proposed in the published consensus paper (3) and updated recently (4)) are appropriately followed. Although the 2005 proposal was supported by by the establishment of curated databases that organised HCV sequences as they became available (Los Alamos HCV Sequence Database, (2) and euHCVdb (1)), neither of these are now actively maintained. This web resource is designed to maintain this function for HCV researchers.
Based upon analysis of > 1300 nearly complete coding region sequences obtained from the Genbank and Los Alamos databases in May 2013 (4), the number of confirmed genotypes has increased from the 18 listed in 2005 (3) to 67 (Table 1). A neighbour joining phylogenetic tree of maximum composite likelihood nucleotide distances between the coding regions of these isolates, together with other isolates that have yet to be assigned a subtype (indicated by *) is shown below. Filled circles indicate selected clades with 100% bootstrap support.
Rules for genotype assignments:
As proposed in the 2005 consensus proposal (3), for an HCV isolate to be considered as a new confirmed genotype or subtype, a complete coding region sequence should be obtained that:
a) Forms a distinct phylogenetic group from previously described sequences
b) Is represented by at least three epidemiologically unlinked isolates
c) Does not represent a recombinant between other genotypes or subtypes.
Novel complete coding region sequences that are represented by an insufficient number of isolates are listed in Table 2. Novel genotypes or subtypes based on partial genome sequences and/or an insufficient number of isolates will no longer be assigned provisional names; previous provisional assignments awaiting confirmation are listed in Table 3. A list of recombinant forms of HCV is listed in Table 4. Reference alignments are being prepared that will be available as downloads.
We urge all researchers describing new variants to contact Donald Smith (D.B.Smith@ed.ac.uk) or Peter Simmonds (Peter.Simmonds@ed.ac.uk) before publishing assignments so that naming conflicts can be avoided and appropriate classifications can be made. All sequence data provided will be treated as strictly confidential.
1. Combet, C., F. Penin, C. Geourjon, and G. Deleage. 2004. HCVDB : Hepatitis C Virus Sequences Database. Appl. Bioinformatics. 3:237-240
2. Kuiken, C., K. Yusim, L. Boykin, and R. Richardson. 2005. The Los Alamos hepatitis C sequence database. Bioinformatics. 21:379-384
3. Simmonds, P., J. Bukh, C. Combet, G. Deleage, N. Enomoto, S. Feinstone, P. Halfon, G. Inchauspe, C. Kuiken, G. Maertens, M. Mizokami, D. G. Murphy, H. Okamoto, J. M. Pawlotsky, F. Penin, E. Sablon, I. Shin, L. J. Stuyver, H. J. Thiel, S. Viazov, A. J. Weiner, and A. Widell. 2005. Consensus proposals for a unified system of nomenclature of hepatitis C virus genotypes. Hepatology 42:962-973
4. Smith, D. B., Bukh, J., Kuiken, C., Muerhoff, A.S., Rice, C.M., Stapleton, J.T., and Simmonds, P. 2013. Expanded classification of hepatitis C virus into 7 genotypes and 67 subtypes, updated criteria assignment web resource Hepatology (in press, pdf available here)