Published in:
Liver International, 43 (2023) 4, Seite 794-804
Language:
English
DOI:
10.1111/liv.15517
ISSN:
1478-3231;
1478-3223
Origination:
Footnote:
Description:
AbstractBackground and AimsHepatitis E virus is a major cause of acute hepatitis worldwide and can progress to chronicity in immunocompromised individuals. Various virus–host recombination events have been reported in the hypervariable region of the hepatitis E virus genome, but the patterns of assembly and selection remain unclear.MethodsTo gain further insight into viral evolution, we assessed the presence of low abundance variants in 16 samples from individuals with acute or chronic infection using a targeted next‐generation sequencing approach.ResultsIn seven samples, different variants with insertions and/or deletions were identified. Among them, eight insertions originating either from human genes or from the hepatitis E virus genome. Five different deletions could be identified. The amino acid composition of sequences with insertions showed a higher frequency of lysine and a lower abundance of proline, and additionally acetylation and ubiquitination sites were more frequent than in hepatitis E virus wild‐type sequences.ConclusionsThese findings suggest that the nucleotide composition of insertions and sites for post‐translational modification may contribute to recombination events. Although the impact of low‐level hepatitis E virus variants is uncertain, our results highlight the importance of a highly sensitive next‐generation sequencing approach to capture the full diversity of hypervariable region.