https://doi.org/10.5812/hepatmon.6133

Phylogenetic Analysis of Torque Teno Virus in Hepatitis C Virus Infected Patients in Shiraz

authors:

avatar Azra Kenar Koohi 1 , avatar Mehrdad Ravanshad ORCID 2 , * , avatar Manouchehr Rasouli 3 , avatar Shahab Falahi 4 , avatar Ashraf Baghban 1

Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, IR Iran
Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, ravanshad@modares.ac.ir, IR Iran
Alborzi Clinical Microbiology Research Center, Nemazee Hospital, IR Iran
Department of Microbiology, School of Medicine, Ilam University of Medical Sciences, IR Iran
Hepatitis Monthly: Vol.12, issue 7; 437-441
article type: Research Article
received: April 20, 2012
accepted: May 1, 2012

How To Cite Koohi A, Ravanshad M, Rasouli M, Falahi S, Baghban A. Phylogenetic Analysis of Torque Teno Virus in Hepatitis C Virus Infected Patients in Shiraz. Hepat Mon. 2012;12(7): 437-441. https://doi.org/10.5812/hepatmon.6133.

Abstract

Background: Torque teno virus (TTV) was the first human Circoviridae detected in a Japanese patient with unknown hepatitis in 1997. Subsequently, several studies performed to evaluate different aspects of Torque teno virus pathogenesis.
Objectives: The present study aimed to determine dominant genotype of Torque teno virus in chronic hepatitis disease using 5?-UTR sequence among patients infected by hepatitis C virus in Shiraz – Iran.
Patients and Methods: The study conducted in 240 patients with chronic hepatitis C from Prof. Alborzi Clinical Microbiology Research Center. The presence of Torque teno virus DNA and its genotype in plasma was assessed by nested polymerase chain reaction using two primer sets for 5?-UTR and N22 regions. Phylogenetic analysis was performed based on 5?-UTR region.
Results: DNA of Torque teno virus was detected in 220 out of 240 (92 %) patients with chronic hepatitis C by the use of 5?-UTR primer based PCR method and in 12 out of 240 (5%) by the use of N22 primer. Based on phylogenetic analysis it was shown that the Dominant genotype in this study was 11. Genotypes 1, 3, 17, and 22 were also detected. Some sequences could not be classified to a specific genotype.
Conclusions: The prevalence of Torque teno virus DNA in patients with chronic hepatitis C disease by the use of 5?-UTR primer appeared to be higher compared to that revealed by N22 primer. We observed five genotypes among hepatitis C chronic patients in our study.


Implication for health policy/practice/research/medical education:
TTV virus had been showed to be associated with hepatitis in human and since the virus is very diverse, detection, phylogenetic analysis is of concern. Current investigation focused on detection the virus based on N22 region which is widely used as well as 5’-UTR which have been showed to have more sensitivity and also phylogenetic analysis of circulating TTV among HCV infected patients was performed.
Please cite this paper as:
Kenar Koohi A , Ravanshad M, Rasouli M, Falahi S, Baghban A. Phylogenetic Analysis of Torque Teno Virus in Hepatitis C Virus Infected Patients From Shiraz. Hepat Mon. 2012;12(7):437-41. DOI: 10.5812/hepatmon.6133

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