Literature DB >> 27449600

Naturally occurring NS3 resistance-associated variants in hepatitis C virus genotype 1: Their relevance for developing countries.

Natalia Echeverría1, Gabriela Betancour1, Fabiana Gámbaro1, Nelia Hernández2, Pablo López2, Daniela Chiodi2, Adriana Sánchez2, Susana Boschi3, Alvaro Fajardo1, Martín Sóñora1, Gonzalo Moratorio1, Juan Cristina1, Pilar Moreno4.   

Abstract

Hepatitis C virus (HCV) is a major cause of global morbidity and mortality, with an estimated 130-150 million infected individuals worldwide. HCV is a leading cause of chronic liver diseases including cirrhosis and hepatocellular carcinoma. Current treatment options in developing countries involve pegylated interferon-α and ribavirin as dual therapy or in combination with one or more direct-acting antiviral agents (DAA). The emergence of resistance-associated variants (RAVs) after treatment reveals the great variability of this virus leading to a great difficulty in developing effective antiviral strategies. Baseline RAVs detected in DAA treatment-naïve HCV-infected patients could be of great importance for clinical management and outcome prediction. Although the frequency of naturally occurring HCV NS3 protease inhibitor mutations has been addressed in many countries, there are only a few reports on their prevalence in South America. In this study, we investigated the presence of RAVs in the HCV NS3 serine protease region by analysing a cohort of Uruguayan patients with chronic hepatitis C who had not been treated with any DAAs and compare them with the results found for other South American countries. The results of these studies revealed that naturally occurring mutations conferring resistance to NS3 inhibitors exist in a substantial proportion of Uruguayan treatment-naïve patients infected with HCV genotype 1 enrolled in these studies. The identification of these baseline RAVs could be of great importance for patients' management and outcome prediction in developing countries.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  DAAs; HCV variability; Resistance-associated variants

Mesh:

Substances:

Year:  2016        PMID: 27449600     DOI: 10.1016/j.virusres.2016.07.008

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  7 in total

1.  Internal Disequilibria and Phenotypic Diversification during Replication of Hepatitis C Virus in a Noncoevolving Cellular Environment.

Authors:  Elena Moreno; Isabel Gallego; Josep Gregori; Adriana Lucía-Sanz; María Eugenia Soria; Victoria Castro; Nathan M Beach; Susanna Manrubia; Josep Quer; Juan Ignacio Esteban; Charles M Rice; Jordi Gómez; Pablo Gastaminza; Esteban Domingo; Celia Perales
Journal:  J Virol       Date:  2017-04-28       Impact factor: 5.103

2.  Synergistic lethal mutagenesis of hepatitis C virus.

Authors:  Isabel Gallego; María Eugenia Soria; Josep Gregori; Ana I de Ávila; Carlos García-Crespo; Elena Moreno; Ignacio Gadea; Jaime Esteban; Ricardo Fernández-Roblas; Juan Ignacio Esteban; Jordi Gómez; Josep Quer; Esteban Domingo; Celia Perales
Journal:  Antimicrob Agents Chemother       Date:  2019-09-30       Impact factor: 5.191

3.  The outcome of re-treatment of relapsed hepatitis C virus infection in a resource-limited setting.

Authors:  Gina Gamal Naguib; Tari George Michael; Yehia Elshazly; Maha Magdy Wahdan; Aya Mostafa; Ossama Ashraf Ahmed; Hany Dabbous; Heba Ismail Saad Aly; Mohamed Kamal Shaker; Hosam Samir Elbaz; Magdy El-Serafy; Wahid Doss; Sherief Abd-Elsalam; Manal Hamdy El-Sayed
Journal:  Virusdisease       Date:  2021-07-27

4.  Pipeline for specific subtype amplification and drug resistance detection in hepatitis C virus.

Authors:  María Eugenia Soria; Josep Gregori; Qian Chen; Damir García-Cehic; Meritxell Llorens; Ana I de Ávila; Nathan M Beach; Esteban Domingo; Francisco Rodríguez-Frías; María Buti; Rafael Esteban; Juan Ignacio Esteban; Josep Quer; Celia Perales
Journal:  BMC Infect Dis       Date:  2018-09-03       Impact factor: 3.090

5.  Prevalence and Factors Related to Natural Resistance-Associated Substitutions to Direct-Acting Antivirals in Patients with Genotype 1 Hepatitis C Virus Infection.

Authors:  Isabella Esposito; Sebastián Marciano; Leila Haddad; Omar Galdame; Alejandra Franco; Adrián Gadano; Diego Flichman; Julieta Trinks
Journal:  Viruses       Date:  2018-12-21       Impact factor: 5.048

6.  Assessing in vivo mutation frequencies and creating a high-resolution genome-wide map of fitness costs of Hepatitis C virus.

Authors:  Kaho H Tisthammer; Caroline Solis; Faye Orcales; Madu Nzerem; Ryan Winstead; Weiyan Dong; Jeffrey B Joy; Pleuni S Pennings
Journal:  PLoS Genet       Date:  2022-05-02       Impact factor: 6.020

7.  Pretreatment Hepatitis C Virus NS5A/NS5B Resistance-Associated Substitutions in Genotype 1 Uruguayan Infected Patients.

Authors:  Fabián Aldunate; Natalia Echeverría; Daniela Chiodi; Pablo López; Adriana Sánchez-Cicerón; Alvaro Fajardo; Martín Soñora; Juan Cristina; Nelia Hernández; Pilar Moreno
Journal:  Dis Markers       Date:  2018-08-14       Impact factor: 3.434

  7 in total

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