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      Molecular Epidemiology of Kaposi’s Sarcoma-Associated Herpes Virus, and Risk Factors in HIV-infected Patients in Tehran, 2014

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          Abstract

          Background

          Kaposi’s sarcoma (KS) remains the most common malignancy among HIV-infected patients. Human herpesvirus type-8 (HHV-8) is regarded as the infectious etiological agent of Kaposi’s sarcoma (KSHV). Diagnostic procedures associated with KSHV are not routinely performed in HIV-infected subjects.

          Objectives

          The main objective of this study is to obtain information on KSHV epidemiology in Iranian HIV-infected individuals.

          Patients and Methods

          In the present cross-sectional study, 109 patients with established HIV infection, who visited a governmental and referral center for HIV screening in Tehran (Tehran west health center (TWHC)) between May 2014 and July 2015 were enrolled according to the convenience sample strategy. After peripheral blood collection, isolation of plasma and peripheral blood mononuclear cell (PBMC) compartments, DNA extraction was performed. KSHV DNA was analyzed by nested polymerase chain reaction (nested PCR) using primers from ORF-26 (virus minor capsid).

          Results

          Among all 109 HIV-infected patients, 67 (61.5%) were male, with an age range of 2 - 64 years (mean ± standard deviation 35.8 ± 13.3). KSHV DNA was found in PBMC and plasma samples of six (5.5%) and four (3.6%) patients, respectively.

          Conclusions

          This study revealed a considerable prevalence of KSHV DNA, during latent and lytic phases, among HIV-infected patients. Risk factors for KSHV infection acquisition and concurrent. 0+infection with HIV were also evaluated. Diagnosis of KSHV in the group could be helpful for prognosis of Kaposi’s sarcoma and clinical management.

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          Most cited references35

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          Molecular Cloning : A Laboratory Manual

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            Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma.

            Representational difference analysis was used to isolate unique sequences present in more than 90 percent of Kaposi's sarcoma (KS) tissues obtained from patients with acquired immunodeficiency syndrome (AIDS). These sequences were not present in tissue DNA from non-AIDS patients, but were present in 15 percent of non-KS tissue DNA samples from AIDS patients. The sequences are homologous to, but distinct from, capsid and tegument protein genes of the Gammaherpesvirinae, herpesvirus saimiri and Epstein-Barr virus. These KS-associated herpesvirus-like (KSHV) sequences appear to define a new human herpesvirus.
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              Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

              A thermostable DNA polymerase was used in an in vitro DNA amplification procedure, the polymerase chain reaction. The enzyme, isolated from Thermus aquaticus, greatly simplifies the procedure and, by enabling the amplification reaction to be performed at higher temperatures, significantly improves the specificity, yield, sensitivity, and length of products that can be amplified. Single-copy genomic sequences were amplified by a factor of more than 10 million with very high specificity, and DNA segments up to 2000 base pairs were readily amplified. In addition, the method was used to amplify and detect a target DNA molecule present only once in a sample of 10(5) cells.
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                Author and article information

                Journal
                Iran Red Crescent Med J
                Iran Red Crescent Med J
                10.5812/ircmj
                Kowsar
                Iranian Red Crescent Medical Journal
                Kowsar
                2074-1804
                2074-1812
                19 June 2016
                November 2016
                : 18
                : 11
                : e32603
                Affiliations
                [1 ]Department of Virology, Iran University of Medical Sciences, Tehran, IR Iran
                [2 ]Middle East Liver Diseases (MELD) Center, Tehran, IR Iran
                [3 ]HIV Laboratory of National Center, Deputy of Health, Iran University of Medical Sciences, Tehran, IR Iran
                [4 ]Department of Virology, Pasteur Institute of Iran, Tehran, IR Iran
                Author notes
                [* ]Corresponding Author: Maryam Esghaei, Department of Virology, Iran University of Medical Sciences, Tehran, IR Iran. Tel: +98-2186703014, E-mail: Esghaei.m@ 123456iums.ac.ir
                Article
                10.5812/ircmj.32603
                5292624
                f5c48666-be5a-4461-a6aa-dfdeaccaf98d
                Copyright © 2016, Iranian Red Crescent Medical Journal

                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.

                History
                : 23 August 2015
                : 26 October 2015
                : 24 November 2015
                Categories
                Research Article

                Medicine
                herpesvirus 8,human,hiv,sarcoma,kaposi,nested pcr
                Medicine
                herpesvirus 8, human, hiv, sarcoma, kaposi, nested pcr

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