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      Detection of Epstein Barr Virus by Chromogenic In Situ Hybridization in cases of extra-hepatic biliary atresia

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          Abstract

          Introduction

          Extra-hepatic biliary atresia (EHBA) is an important cause of neonatal cholestasis. Several infectious agents have been proposed as etiologic factors such as Rotavirus and Reovirus. There is limited data on the role of Epstein Barr virus (EBV) infection in EHBA, so we decided to study the presence of EBV virus in a series of 16 proven EHBA cases by Chromogenic in situ hybridization (CISH) technique.

          Methods

          In the current study a total of 16 liver wedge biopsies of proven cases of EHBA were selected in a period of 4 years. CISH staining for EBV-encoded RNA (EBER) transcript was performed.

          Results

          The review of H&E-stained slides of liver biopsies revealed fibrosis and marked ductular proliferation. In CISH-stained slides, EBV trace was observed in hepatocytes in two cases and in biliary epithelium in one case of EHBA.

          Discussion

          Considering the association of hepatitis with the Epstein-Barr virus in later life, it is likely that EBV hepatitis and its complications occur in the neonatal/perinatal period. Since EHBA is a relatively rare disease, a similar study on wedge biopsies of this number of proven cases of EHBA has not been performed to date. Current observation proposes the need for a study of larger series and employing other methods for confirming the etiologic role of EBV in EHBA cases.

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          Most cited references19

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          Epstein-Barr virus infection.

          J I Cohen (2000)
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            PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules.

            DNA analogues are currently being intensely investigated owing to their potential as gene-targeted drugs. Furthermore, their properties and interaction with DNA and RNA could provide a better understanding of the structural features of natural DNA that determine its unique chemical, biological and genetic properties. We recently designed a DNA analogue, PNA, in which the backbone is structurally homomorphous with the deoxyribose backbone and consists of N-(2-aminoethyl)glycine units to which the nucleobases are attached. We showed that PNA oligomers containing solely thymine and cytosine can hybridize to complementary oligonucleotides, presumably by forming Watson-Crick-Hoogsteen (PNA)2-DNA triplexes, which are much more stable than the corresponding DNA-DNA duplexes, and bind to double-stranded DNA by strand displacement. We report here that PNA containing all four natural nucleobases hybridizes to complementary oligonucleotides obeying the Watson-Crick base-pairing rules, and thus is a true DNA mimic in terms of base-pair recognition.
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              Biliary atresia and reovirus type 3 infection.

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                Author and article information

                Journal
                Diagn Pathol
                Diagnostic Pathology
                BioMed Central
                1746-1596
                2008
                28 April 2008
                : 3
                : 19
                Affiliations
                [1 ]Pathology Department, Markaze Tebbi Koodakan (Children Hospital related to Tehran University of Medical Sciences), End of Keshavarz Boulevard, Tehran, Iran
                [2 ]Department of Pathology and Laboratory Medicine, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, Iran
                [3 ]Department of Gastro – Enterology, Markaze Tebbi Koodakan (Children Hospital related to Tehran University of Medical Sciences), End of Keshavarz Boulevard, Tehran, Iran
                [4 ]Infectious Disease Research Center, Markaze Tebbi Koodakan (Children Hospital related to Tehran University of Medical Sciences), End of Keshavarz Boulevard, Tehran, Iran
                Article
                1746-1596-3-19
                10.1186/1746-1596-3-19
                2424033
                18442403
                5aaf4e94-b5bf-416c-adff-ea199080f419
                Copyright © 2008 Mahjoub et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 7 February 2008
                : 28 April 2008
                Categories
                Research

                Pathology
                Pathology

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