Cargando…
Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population
Epstein-Barr virus (EBV) is associated with Burkitt’s lymphoma (BL), and in regions of sub-Saharan Africa where endemic BL is common, both the EBV Type 1 (EBV-1) and EBV Type 2 strains (EBV-2) are found. Little is known about genetic variation of EBV strains in areas of sub-Saharan Africa. In the pr...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416826/ https://www.ncbi.nlm.nih.gov/pubmed/25933165 http://dx.doi.org/10.1371/journal.pone.0125420 |
_version_ | 1782369288326217728 |
---|---|
author | Simbiri, Kenneth O. Smith, Nicholas A. Otieno, Richard Wohlford, Eric E. M. Daud, Ibrahim I. Odada, Sumba P. Middleton, Frank Rochford, Rosemary |
author_facet | Simbiri, Kenneth O. Smith, Nicholas A. Otieno, Richard Wohlford, Eric E. M. Daud, Ibrahim I. Odada, Sumba P. Middleton, Frank Rochford, Rosemary |
author_sort | Simbiri, Kenneth O. |
collection | PubMed |
description | Epstein-Barr virus (EBV) is associated with Burkitt’s lymphoma (BL), and in regions of sub-Saharan Africa where endemic BL is common, both the EBV Type 1 (EBV-1) and EBV Type 2 strains (EBV-2) are found. Little is known about genetic variation of EBV strains in areas of sub-Saharan Africa. In the present study, spontaneous lymphoblastoid cell lines (LCLs) were generated from samples obtained from Kenya. Polymerase chain reaction (PCR) amplification of the EBV genome was done using multiple primers and sequenced by next-generation sequencing (NGS). Phylogenetic analyses against the published EBV-1 and EBV-2 strains indicated that one sample, LCL10 was closely related to EBV-2, while the remaining 3 LCL samples were more closely related to EBV-1. Moreover, single nucleotide polymorphism (SNP) analyses showed clustering of LCL variants. We further show by analysis of EBNA-1, BLLF1, BPLF1, and BRRF2 that latent genes are less conserved than lytic genes in these LCLs from a single geographic region. In this study we have shown that NGS is highly useful for deciphering detailed inter and intra-variations in EBV genomes and that within a geographic region different EBV genetic variations can co-exist, the implications of which warrant further investigation. The findings will enhance our understanding of potential pathogenic variants critical to the development and maintenance of EBV-associated malignancies. |
format | Online Article Text |
id | pubmed-4416826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44168262015-05-07 Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population Simbiri, Kenneth O. Smith, Nicholas A. Otieno, Richard Wohlford, Eric E. M. Daud, Ibrahim I. Odada, Sumba P. Middleton, Frank Rochford, Rosemary PLoS One Research Article Epstein-Barr virus (EBV) is associated with Burkitt’s lymphoma (BL), and in regions of sub-Saharan Africa where endemic BL is common, both the EBV Type 1 (EBV-1) and EBV Type 2 strains (EBV-2) are found. Little is known about genetic variation of EBV strains in areas of sub-Saharan Africa. In the present study, spontaneous lymphoblastoid cell lines (LCLs) were generated from samples obtained from Kenya. Polymerase chain reaction (PCR) amplification of the EBV genome was done using multiple primers and sequenced by next-generation sequencing (NGS). Phylogenetic analyses against the published EBV-1 and EBV-2 strains indicated that one sample, LCL10 was closely related to EBV-2, while the remaining 3 LCL samples were more closely related to EBV-1. Moreover, single nucleotide polymorphism (SNP) analyses showed clustering of LCL variants. We further show by analysis of EBNA-1, BLLF1, BPLF1, and BRRF2 that latent genes are less conserved than lytic genes in these LCLs from a single geographic region. In this study we have shown that NGS is highly useful for deciphering detailed inter and intra-variations in EBV genomes and that within a geographic region different EBV genetic variations can co-exist, the implications of which warrant further investigation. The findings will enhance our understanding of potential pathogenic variants critical to the development and maintenance of EBV-associated malignancies. Public Library of Science 2015-05-01 /pmc/articles/PMC4416826/ /pubmed/25933165 http://dx.doi.org/10.1371/journal.pone.0125420 Text en © 2015 Simbiri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Simbiri, Kenneth O. Smith, Nicholas A. Otieno, Richard Wohlford, Eric E. M. Daud, Ibrahim I. Odada, Sumba P. Middleton, Frank Rochford, Rosemary Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title | Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title_full | Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title_fullStr | Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title_full_unstemmed | Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title_short | Epstein–Barr Virus Genetic Variation in Lymphoblastoid Cell Lines Derived from Kenyan Pediatric Population |
title_sort | epstein–barr virus genetic variation in lymphoblastoid cell lines derived from kenyan pediatric population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416826/ https://www.ncbi.nlm.nih.gov/pubmed/25933165 http://dx.doi.org/10.1371/journal.pone.0125420 |
work_keys_str_mv | AT simbirikennetho epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT smithnicholasa epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT otienorichard epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT wohlfordericem epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT daudibrahimi epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT odadasumbap epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT middletonfrank epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation AT rochfordrosemary epsteinbarrvirusgeneticvariationinlymphoblastoidcelllinesderivedfromkenyanpediatricpopulation |