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Mixed Infections Unravel Novel HCV Inter-Genotypic Recombinant Forms Within the Conserved IRES Region

Overview
Journal Viruses
Publisher MDPI
Specialty Microbiology
Date 2024 Apr 27
PMID 38675902
Authors
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Abstract

Hepatitis C virus (HCV) remains a significant global health challenge, affecting millions of people worldwide, with chronic infection a persistent threat. Despite the advent of direct-acting antivirals (DAAs), challenges in diagnosis and treatment remain, compounded by the lack of an effective vaccine. The HCV genome, characterized by high genetic variability, consists of eight distinct genotypes and over ninety subtypes, underscoring the complex dynamics of the virus within infected individuals. This study delves into the intriguing realm of HCV genetic diversity, specifically exploring the phenomenon of mixed infections and the subsequent detection of recombinant forms within the conserved internal ribosome entry site (IRES) region. Previous studies have identified recombination as a rare event in HCV. However, our findings challenge this notion by providing the first evidence of 1a/3a (and vice versa) inter-genotypic recombination within the conserved IRES region. Utilizing advanced sequencing methods, such as deep sequencing and molecular cloning, our study reveals mixed infections involving genotypes 1a and 3a. This comprehensive approach not only confirmed the presence of mixed infections, but also identified the existence of recombinant forms not previously seen in the IRES region. The recombinant sequences, although present as low-frequency variants, open new avenues for understanding HCV evolution and adaptation.

References
1.
Smith D, Mellor J, Jarvis L, Davidson F, Kolberg J, Urdea M . Variation of the hepatitis C virus 5' non-coding region: implications for secondary structure, virus detection and typing. The International HCV Collaborative Study Group. J Gen Virol. 1995; 76 ( Pt 7):1749-61. DOI: 10.1099/0022-1317-76-7-1749. View

2.
Laporte J, Malet I, Andrieu T, Thibault V, Toulme J, Wychowski C . Comparative analysis of translation efficiencies of hepatitis C virus 5' untranslated regions among intraindividual quasispecies present in chronic infection: opposite behaviors depending on cell type. J Virol. 2000; 74(22):10827-33. PMC: 110962. DOI: 10.1128/jvi.74.22.10827-10833.2000. View

3.
Forton D, Karayiannis P, Mahmud N, Taylor-Robinson S, Thomas H . Identification of unique hepatitis C virus quasispecies in the central nervous system and comparative analysis of internal translational efficiency of brain, liver, and serum variants. J Virol. 2004; 78(10):5170-83. PMC: 400349. DOI: 10.1128/jvi.78.10.5170-5183.2004. View

4.
Noppornpanth S, Lien T, Poovorawan Y, Smits S, Osterhaus A, Haagmans B . Identification of a naturally occurring recombinant genotype 2/6 hepatitis C virus. J Virol. 2006; 80(15):7569-77. PMC: 1563718. DOI: 10.1128/JVI.00312-06. View

5.
Kalinina O, Norder H, Magnius L . Full-length open reading frame of a recombinant hepatitis C virus strain from St Petersburg: proposed mechanism for its formation. J Gen Virol. 2004; 85(Pt 7):1853-1857. DOI: 10.1099/vir.0.79984-0. View