Sana Saleem1, Amjad Ali2, Bushra Khubaib3, Madiha Akram4, Zareen Fatima5, Muhammad Idrees6. 1. Division of Molecular Virology and Molecular Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan. Electronic address: sanacemb@yahoo.com. 2. Molecular Virology laboratory, Centre for Applied Molecular Biology (CAMB) University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan. Electronic address: amjad.camb@pu.edu.pk. 3. Division of Molecular Virology and Molecular Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan; Department of Biotechnology, Lahore College for Women University, Lahore, Pakistan. Electronic address: bushra_khubaib@yahoo.com. 4. Division of Molecular Virology and Molecular Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan; Department of Biotechnology, Lahore College for Women University, Lahore, Pakistan. Electronic address: akrammadiha12@yahoo.com. 5. Division of Molecular Virology and Molecular Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan; Bioinformatics & Biotechnology, International Islamic University, Sector H-10, New Campus, Islamabad, Pakistan. Electronic address: zfa_11@hotmail.com. 6. Division of Molecular Virology and Molecular Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 87-West Canal Bank Road Thokar Niaz Baig, Lahore, Pakistan; Vice Chancellor Hazara University Mansehra, Khyber Pakhtunkhwa, Pakistan. Electronic address: idrees.camb@pu.edu.pk.
Abstract
BACKGROUND: In Pakistan, HCV disease is considered a major public health issue with about 10-17 million people suffering with this infection and rate is increasing every day without any hindrance. The currently available Pyrosequencing approach used to analyze complex viral genomes as it can determine minor variants. It is crucial to understand viral evolution and quasispecies diversity in complex viral strains. OBJECTIVES: To assess genetic diversity in patients with HCV using Next Generation Sequencing (NGS) and compare nucleotide diversity of genotype 3a with respect to other genotypes. STUDY DESIGN: Intra-host viral diversity of HCV was determined using NGS from 13 chronically HCV infected individuals. NGS of three different regions (E2 (HVR1), NS3 and NS5B) of HCV-3a allowed for a comprehensive analysis of the viral population. RESULT: Phylogenetic analysis of different HCV genes revealed great variability within the Pakistani population. The average nucleotide diversity for HVR1, NS3 and NS5B was 0.029, 0.011 and 0.010 respectively. CONCLUSION: Our findings clearly indicate that patient-2 greater quasispecies heterogeneity than other patients of same genotype-3a using phylogenetic and one step network analyses. Initially phylogenetic analysis of these three genes showed that genotype 3a samples have greater genetic diversity. However, no significant difference was determined when nucleotide variability of genotype 3a compared with other genotypes (1a, 1b, 2a & 4a).
BACKGROUND: In Pakistan, HCV disease is considered a major public health issue with about 10-17 million people suffering with this infection and rate is increasing every day without any hindrance. The currently available Pyrosequencing approach used to analyze complex viral genomes as it can determine minor variants. It is crucial to understand viral evolution and quasispecies diversity in complex viral strains. OBJECTIVES: To assess genetic diversity in patients with HCV using Next Generation Sequencing (NGS) and compare nucleotide diversity of genotype 3a with respect to other genotypes. STUDY DESIGN: Intra-host viral diversity of HCV was determined using NGS from 13 chronically HCV infected individuals. NGS of three different regions (E2 (HVR1), NS3 and NS5B) of HCV-3a allowed for a comprehensive analysis of the viral population. RESULT: Phylogenetic analysis of different HCV genes revealed great variability within the Pakistani population. The average nucleotide diversity for HVR1, NS3 and NS5B was 0.029, 0.011 and 0.010 respectively. CONCLUSION: Our findings clearly indicate that patient-2 greater quasispecies heterogeneity than other patients of same genotype-3a using phylogenetic and one step network analyses. Initially phylogenetic analysis of these three genes showed that genotype 3a samples have greater genetic diversity. However, no significant difference was determined when nucleotide variability of genotype 3a compared with other genotypes (1a, 1b, 2a & 4a).