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Superinfection and cure of infected cells as mechanisms for hepatitis C virus adaptation and persistence.


ABSTRACT: RNA viruses exist as a genetically diverse quasispecies with extraordinary ability to adapt to abrupt changes in the host environment. However, the molecular mechanisms that contribute to their rapid adaptation and persistence in vivo are not well studied. Here, we probe hepatitis C virus (HCV) persistence by analyzing clinical samples taken from subjects who were treated with a second-generation HCV protease inhibitor. Frequent longitudinal viral load determinations and large-scale single-genome sequence analyses revealed rapid antiviral resistance development, and surprisingly, dynamic turnover of dominant drug-resistant mutant populations long after treatment cessation. We fitted mathematical models to both the viral load and the viral sequencing data, and the results provided strong support for the critical roles that superinfection and cure of infected cells play in facilitating the rapid turnover and persistence of viral populations. More broadly, our results highlight the importance of considering viral dynamics and competition at the intracellular level in understanding rapid viral adaptation. Thus, we propose a theoretical framework integrating viral and molecular mechanisms to explain rapid viral evolution, resistance, and persistence despite antiviral treatment and host immune responses.

SUBMITTER: Ke R 

PROVIDER: S-EPMC6065014 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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Superinfection and cure of infected cells as mechanisms for hepatitis C virus adaptation and persistence.

Ke Ruian R   Li Hui H   Wang Shuyi S   Ding Wenge W   Ribeiro Ruy M RM   Giorgi Elena E EE   Bhattacharya Tanmoy T   Barnard Richard J O RJO   Hahn Beatrice H BH   Shaw George M GM   Perelson Alan S AS  

Proceedings of the National Academy of Sciences of the United States of America 20180709 30


RNA viruses exist as a genetically diverse quasispecies with extraordinary ability to adapt to abrupt changes in the host environment. However, the molecular mechanisms that contribute to their rapid adaptation and persistence in vivo are not well studied. Here, we probe hepatitis C virus (HCV) persistence by analyzing clinical samples taken from subjects who were treated with a second-generation HCV protease inhibitor. Frequent longitudinal viral load determinations and large-scale single-genom  ...[more]

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