Hepatitis C Viral Heterogeneity Based on Core Gene and an Attempt to Design Small Interfering RNA Against Strains Resistant to Interferon in Rawalpindi, Pakistan

AUTHORS

Sobia Kanwal 1 , Tariq Mahmood 2 , *

1 Faculty of Biological Sciences, Quaid-i-Azam University, Pakistan

2 Faculty of Biological Sciences, Quaid-i-Azam University, [email protected], Pakistan

How to Cite: Kanwal S, Mahmood T. Hepatitis C Viral Heterogeneity Based on Core Gene and an Attempt to Design Small Interfering RNA Against Strains Resistant to Interferon in Rawalpindi, Pakistan, Hepat Mon. Online ahead of Print ; 12(6):398-407. doi: 10.5812/hepatmon.6184.

ARTICLE INFORMATION

Hepatitis Monthly: 12 (6); 398-407
Article Type: Research Article
Received: May 1, 2012
Accepted: May 22, 2012
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Abstract

Background: Global prevalence of Hepatitis C Virus (HCV) infection corresponds to about 130 million HCV positive patients worldwide. The only drug that effectively reduces viral load is interferon-α (IFN-α) and currently combination of IFN and ribavirin is the choice for treatment.
Objectives: The present study is aimed to resolve the genotypes based on core gene that might affect the response to interferon therapy. Furthermore an attempt was made to propose a powerful therapeutic approach by designing the siRNA from sequences of the same patients who remain resistant to IFN in this study.
Patients and Methods: To achieve the objectives, a sequence analysis was performed in five HCV ELISA positive subjects who have completed IFN treatment. Neighbor Joining (NJ) method was used to study the evolutionary relationship. Atomic models were predicted using online software PROCHECK and i- TASSER.
Results: Two new genotypes were reported for the first time namely 4a from suburban region of Rawalpindi and 6e from all over the Pakistan. According to Ramachandran plot, satisfactory atomic model was considered useful for further studies, i.e. to calculate HCV genotypes conservation at structural level, to find out critical binding sites for drug
designing, or to silence those binding sites by using appropriate siRNA. Single siRNA can be used to inhibit HCV RNA synthesis against genotype 3 and 4, as the predicted siRNA were originated from the same domain in studied HCV core region in both genotypes.
Conclusions: We can conclude that any change or mutation in core region might be the cause of HCV strains to resist against IFN therapy. Therefore, further understanding of the complex mechanism involved in disrupting viral response to therapy would facilitate the development of more effective therapeutic regimens. Additionally, a single designed siRNA can be used as an alternative for current therapy against more than one resistant HCV genotypes.


Implication for health policy/practice/research/medical education:
This study investigates the role of genetic heterogenity of hepatitis C virus in IFn resistance and detected 2 new genotypes 4a and 6e in Pakistani population. Besides this an alternative therapeutic tool siRNA is presented to be used against HCV instead of IFn. This research work will be informative and useful for those who are involved in medical prevention and therapy to chronic hepatitis C.
Please cite this paper as:
Kanwal S, Mahmood T. Hepatitis C Viral Heterogeneity Based on Core Gene and an Attempt to Design Small Interfering RNA Against Strains Resistant to Interferon in Rawalpindi, Pakistan. Hepat Mon. 2012;12(6): 398-407. DoI: 10.5812/hepatmon.6184

Copyright © 2012 Kowsar Corp. All rights reserved.


Keywords

Interferons Small interfering RNA (siRNA) Hepatitis C

© 0, Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

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