| Literature DB >> 25473152 |
Maria Victoria Preciado1, Pamela Valva1, Alejandro Escobar-Gutierrez1, Paula Rahal1, Karina Ruiz-Tovar1, Lilian Yamasaki1, Carlos Vazquez-Chacon1, Armando Martinez-Guarneros1, Juan Carlos Carpio-Pedroza1, Salvador Fonseca-Coronado1, Mayra Cruz-Rivera1.
Abstract
Hepatitis C virus (HCV) infection represents an important public health problem worldwide. Reduction of HCV morbidity and mortality is a current challenge owned to several viral and host factors. Virus molecular evolution plays an important role in HCV transmission, disease progression and therapy outcome. The high degree of genetic heterogeneity characteristic of HCV is a key element for the rapid adaptation of the intrahost viral population to different selection pressures (e.g., host immune responses and antiviral therapy). HCV molecular evolution is shaped by different mechanisms including a high mutation rate, genetic bottlenecks, genetic drift, recombination, temporal variations and compartmentalization. These evolutionary processes constantly rearrange the composition of the HCV intrahost population in a staging manner. Remarkable advances in the understanding of the molecular mechanism controlling HCV replication have facilitated the development of a plethora of direct-acting antiviral agents against HCV. As a result, superior sustained viral responses have been attained. The rapidly evolving field of anti-HCV therapy is expected to broad its landscape even further with newer, more potent antivirals, bringing us one step closer to the interferon-free era.Entities:
Keywords: Clinical outcome; Drug resistance; Evolution; Hepatitis C virus; Phylogenetics
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Year: 2014 PMID: 25473152 PMCID: PMC4239486 DOI: 10.3748/wjg.v20.i43.15992
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742