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Characterisation of hepatitis C virus recombination in Cameroon using non-specific next generation sequencing.

Abstract:
The importance of recombination for the evolution and genetic diversity of the hepatitis C virus (HCV) is currently uncertain. Only a small number of inter-genotypic recombinants have been so far identified, and each has core and envelope genes classified as genotype 2. Here we investigate two putative genotype 4/1 recombinants from southern Cameroon using a number of approaches, including standard Sanger sequencing, genotype-specific PCR amplification, and non-HCV specific Illumina RNAseq sequencing. Recombination between genotypes 1 and 4 is confirmed in both samples and the parental lineages of each recombinant belong to HCV subtypes that are co-circulating at high prevalence in Cameroon. Using the RNAseq approach we obtained a complete genome for one sample, which contained a recombination breakpoint at the E2/P7 gene junction. We developed and applied a new method, called Deep SimPlot, that can be used to visualise and identify viral recombination directly from the short sequence reads created by next-generation sequencing in conjunction with a consensus sequence.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1128/jcm.00483-15

Authors


Publisher:
American Society for Microbiology
Journal:
Journal of Clinical Microbiology More from this journal
Volume:
53
Issue:
10
Pages:
3155-3164
Publication date:
2015-01-01
DOI:
EISSN:
1098-660X
ISSN:
0095-1137


Language:
English
Pubs id:
pubs:535876
UUID:
uuid:44353acc-eda8-4197-a787-885de7057aee
Local pid:
pubs:535876
Source identifiers:
535876
Deposit date:
2015-08-07
ARK identifier:

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