Key result
Phylogenetic analysis of HCV genomes identifies 4 novel naturally occurring inter-subtype recombinants with NS5B breakpoints.
Why the study?
Recombination in Hepatitis C virus is considered rare, and further investigation is needed to identify novel recombination events.
The identification of four novel naturally occurring inter-subtype recombinants in HCV suggests that while recombination is rare, it warrants further investigation.
Novel HCV inter-subtype recombinants identified; leaves open prevalence, transmissibility, and antiviral implications requiring further study.
Recombination in Hepatitis C virus (HCV) is considered to be rare. In this study, we performed a phylogenetic analysis of 1278 full-length HCV genome sequences to identify potential recombination events. Nine inter-genotype recombinants were identified, all of which have been previously reported. This confirms the rarity of inter-genotype HCV recombinants. The analysis also identified five inter-subtype recombinants, four of which are documented for the first time (EU246930, EU246931, EU246932, and EU246937). Specifically, the latter represent four different novel recombination types (6a/6o, 6e/6o, 6e/6h, and 6n/6o), and this was well supported by seven independent methods embedded in RDP. The breakpoints of the four novel HCV recombinants are located within the NS5B coding region and were different from all previously reported breakpoints. While the locations of the breakpoints identified by RDP were not identical, they are very close. Our study suggests that while recombination in HCV is rare, this warrants further investigation.
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Shi et al. (2012) studied Hepatitis C Virus (n=1,278). Phylogenetic analysis was evaluated on Identification of novel HCV recombinants. Phylogenetic analysis of 1,278 full-length HCV genomes identified four novel naturally occurring inter-subtype recombinants (6a/6o, 6e/6o, 6e/6h, and 6n/6o) with breakpoints in the NS5B region.
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