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Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array

BACKGROUND: Infectious agents are estimated to play a causative role in approximately 20% of cancers worldwide. Viruses, notably the Epstein-Barr virus (EBV), are associated with 10-15% of B-cell lymphomas and are found at a higher frequency in immunosuppressed patients. In this study, we screened h...

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Autores principales: Tellez, Joseph, Jaing, Crystal, Wang, Jun, Green, Ralph, Chen, Mingyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310026/
https://www.ncbi.nlm.nih.gov/pubmed/25635226
http://dx.doi.org/10.1186/s40364-014-0024-x
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author Tellez, Joseph
Jaing, Crystal
Wang, Jun
Green, Ralph
Chen, Mingyi
author_facet Tellez, Joseph
Jaing, Crystal
Wang, Jun
Green, Ralph
Chen, Mingyi
author_sort Tellez, Joseph
collection PubMed
description BACKGROUND: Infectious agents are estimated to play a causative role in approximately 20% of cancers worldwide. Viruses, notably the Epstein-Barr virus (EBV), are associated with 10-15% of B-cell lymphomas and are found at a higher frequency in immunosuppressed patients. In this study, we screened human lymphoma tissues using a novel Lawrence Livermore Microbial Detection Array (LLMDA), a comprehensive detection system that contains probes for all sequenced viruses and bacteria. This technology has been applied to identify pathogen-associated diseases. RESULTS: We evaluated samples from 58 cases with various lymphoid tissue disorders using LLMDA. These included 30 B-cell lymphomas (9 indolent and 21 aggressive type), 2 T-cell lymphomas and 2 NK/T cell lymphomas, 4 plasmacytomas as well as 8 specimens of benign lymphoid tissue. Five of 21 high-grade B-cell lymphomas were positive for Epstein-Barr virus-encoded small RNA (EBER+), while all the indolent B-cell lymphomas were EBER-. Similarly, both NK/T cell lymphomas were EBER+, and the benign tissues were EBER-. We also screened 10 cases of post-transplant lymphoproliferative disorder (PTLD). Five of these cases (4 B-cell lymphomas and 1 NK/T cell lymphoma) were EBER+, and the remaining five cases were EBER-. CONCLUSIONS: We have confirmed the reliability of the LLMDA methods by detecting EBV in EBV-positive lymphomas while observing no false-positive results in EBV-negative lymphomas. The LLMDA technique provides a sensitive and alternative method for identifying known viral pathogen associated with tumors and may prove useful for future clinical identification of novel cancer-associated viral pathogens.
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spelling pubmed-43100262015-01-30 Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array Tellez, Joseph Jaing, Crystal Wang, Jun Green, Ralph Chen, Mingyi Biomark Res Methodology BACKGROUND: Infectious agents are estimated to play a causative role in approximately 20% of cancers worldwide. Viruses, notably the Epstein-Barr virus (EBV), are associated with 10-15% of B-cell lymphomas and are found at a higher frequency in immunosuppressed patients. In this study, we screened human lymphoma tissues using a novel Lawrence Livermore Microbial Detection Array (LLMDA), a comprehensive detection system that contains probes for all sequenced viruses and bacteria. This technology has been applied to identify pathogen-associated diseases. RESULTS: We evaluated samples from 58 cases with various lymphoid tissue disorders using LLMDA. These included 30 B-cell lymphomas (9 indolent and 21 aggressive type), 2 T-cell lymphomas and 2 NK/T cell lymphomas, 4 plasmacytomas as well as 8 specimens of benign lymphoid tissue. Five of 21 high-grade B-cell lymphomas were positive for Epstein-Barr virus-encoded small RNA (EBER+), while all the indolent B-cell lymphomas were EBER-. Similarly, both NK/T cell lymphomas were EBER+, and the benign tissues were EBER-. We also screened 10 cases of post-transplant lymphoproliferative disorder (PTLD). Five of these cases (4 B-cell lymphomas and 1 NK/T cell lymphoma) were EBER+, and the remaining five cases were EBER-. CONCLUSIONS: We have confirmed the reliability of the LLMDA methods by detecting EBV in EBV-positive lymphomas while observing no false-positive results in EBV-negative lymphomas. The LLMDA technique provides a sensitive and alternative method for identifying known viral pathogen associated with tumors and may prove useful for future clinical identification of novel cancer-associated viral pathogens. BioMed Central 2014-12-05 /pmc/articles/PMC4310026/ /pubmed/25635226 http://dx.doi.org/10.1186/s40364-014-0024-x Text en © Tellez et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Tellez, Joseph
Jaing, Crystal
Wang, Jun
Green, Ralph
Chen, Mingyi
Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title_full Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title_fullStr Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title_full_unstemmed Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title_short Detection of Epstein-Barr virus (EBV) in human lymphoma tissue by a novel microbial detection array
title_sort detection of epstein-barr virus (ebv) in human lymphoma tissue by a novel microbial detection array
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310026/
https://www.ncbi.nlm.nih.gov/pubmed/25635226
http://dx.doi.org/10.1186/s40364-014-0024-x
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