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Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters

The molecular diversity of Epstein–Barr virus (EBV) is exceptionally complex and based on the characterization of sequences coding for several viral genes. The aim of this study was to analyze the distribution of EBV types 1 and 2 and to characterize LMP1 variants in a cohort of 73 patients with inf...

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Autores principales: Zidovec-Lepej, Snjezana, Batovic, Margarita, Rozman, Marija, Bodulić, Kristian, Prtorić, Laura, Šokota, Ante, Nikcevic, Andrea, Simicic, Petra, Tešović, Goran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384830/
https://www.ncbi.nlm.nih.gov/pubmed/37513762
http://dx.doi.org/10.3390/pathogens12070915
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author Zidovec-Lepej, Snjezana
Batovic, Margarita
Rozman, Marija
Bodulić, Kristian
Prtorić, Laura
Šokota, Ante
Nikcevic, Andrea
Simicic, Petra
Tešović, Goran
author_facet Zidovec-Lepej, Snjezana
Batovic, Margarita
Rozman, Marija
Bodulić, Kristian
Prtorić, Laura
Šokota, Ante
Nikcevic, Andrea
Simicic, Petra
Tešović, Goran
author_sort Zidovec-Lepej, Snjezana
collection PubMed
description The molecular diversity of Epstein–Barr virus (EBV) is exceptionally complex and based on the characterization of sequences coding for several viral genes. The aim of this study was to analyze the distribution of EBV types 1 and 2 and to characterize LMP1 variants in a cohort of 73 patients with infectious mononucleosis (IM), as well as to investigate a possible association between viral diversity and relevant clinical parameters. Population-based sequencing of EBNA-2 gene showed the presence of EBV type 1 in all IM patients. Analysis of LMP1 gene found a restricted repertoire of LMP1 variants with the predominance of wild-type B95-8, China1, Mediterranean and North Carolina variants with the presence of more than one LMP1 variant in 16.4% of patients. Co-infections with different LMP1 variants were associated with significantly higher levels of C-reactive protein and lower levels of maximal neutrophil counts and minimal platelet count. The results of this study have shown a narrow repertoire of LMP1 variants and an exclusive presence of EBV type 1 in a cohort of IM from Croatia, suggesting a characteristic local molecular pattern of this virus. The clinical importance of distinct immunobiological features of IM patients with LMP1 variant co-infections needs to be investigated further.
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spelling pubmed-103848302023-07-30 Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters Zidovec-Lepej, Snjezana Batovic, Margarita Rozman, Marija Bodulić, Kristian Prtorić, Laura Šokota, Ante Nikcevic, Andrea Simicic, Petra Tešović, Goran Pathogens Article The molecular diversity of Epstein–Barr virus (EBV) is exceptionally complex and based on the characterization of sequences coding for several viral genes. The aim of this study was to analyze the distribution of EBV types 1 and 2 and to characterize LMP1 variants in a cohort of 73 patients with infectious mononucleosis (IM), as well as to investigate a possible association between viral diversity and relevant clinical parameters. Population-based sequencing of EBNA-2 gene showed the presence of EBV type 1 in all IM patients. Analysis of LMP1 gene found a restricted repertoire of LMP1 variants with the predominance of wild-type B95-8, China1, Mediterranean and North Carolina variants with the presence of more than one LMP1 variant in 16.4% of patients. Co-infections with different LMP1 variants were associated with significantly higher levels of C-reactive protein and lower levels of maximal neutrophil counts and minimal platelet count. The results of this study have shown a narrow repertoire of LMP1 variants and an exclusive presence of EBV type 1 in a cohort of IM from Croatia, suggesting a characteristic local molecular pattern of this virus. The clinical importance of distinct immunobiological features of IM patients with LMP1 variant co-infections needs to be investigated further. MDPI 2023-07-06 /pmc/articles/PMC10384830/ /pubmed/37513762 http://dx.doi.org/10.3390/pathogens12070915 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zidovec-Lepej, Snjezana
Batovic, Margarita
Rozman, Marija
Bodulić, Kristian
Prtorić, Laura
Šokota, Ante
Nikcevic, Andrea
Simicic, Petra
Tešović, Goran
Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title_full Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title_fullStr Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title_full_unstemmed Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title_short Distribution of Epstein–Barr Virus LMP1 Variants in Patients with Infectious Mononucleosis and Association with Selected Biochemical and Hematological Parameters
title_sort distribution of epstein–barr virus lmp1 variants in patients with infectious mononucleosis and association with selected biochemical and hematological parameters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384830/
https://www.ncbi.nlm.nih.gov/pubmed/37513762
http://dx.doi.org/10.3390/pathogens12070915
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