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Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon

Human rotavirus remains a major cause of gastroenteritis worldwide despite the availability of effective vaccines. In this study, we investigated the genetic diversity of rotaviruses circulating in Lebanon. We genetically characterized the VP4 and VP7 genes encoding the outer capsid proteins of 132...

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Autores principales: Harastani, Houda H., Reslan, Lina, Sabra, Ahmad, Ali, Zainab, Hammadi, Moza, Ghanem, Soha, Hajar, Farah, Matar, Ghassan M., Dbaibo, Ghassan S., Zaraket, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054381/
https://www.ncbi.nlm.nih.gov/pubmed/32174920
http://dx.doi.org/10.3389/fimmu.2020.00317
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author Harastani, Houda H.
Reslan, Lina
Sabra, Ahmad
Ali, Zainab
Hammadi, Moza
Ghanem, Soha
Hajar, Farah
Matar, Ghassan M.
Dbaibo, Ghassan S.
Zaraket, Hassan
author_facet Harastani, Houda H.
Reslan, Lina
Sabra, Ahmad
Ali, Zainab
Hammadi, Moza
Ghanem, Soha
Hajar, Farah
Matar, Ghassan M.
Dbaibo, Ghassan S.
Zaraket, Hassan
author_sort Harastani, Houda H.
collection PubMed
description Human rotavirus remains a major cause of gastroenteritis worldwide despite the availability of effective vaccines. In this study, we investigated the genetic diversity of rotaviruses circulating in Lebanon. We genetically characterized the VP4 and VP7 genes encoding the outer capsid proteins of 132 rotavirus-associated gastroenteritis specimens, previously identified in hospitalized children (<5 years) from 2011 to 2013 in Lebanon. These included 43 vaccine-breakthrough specimens and the remainder were from non-vaccinated subjects. Phylogenetic analysis of VP4 and VP7 genes revealed distinct clustering compared to the vaccine strains, and several substitutions were identified in the antigenic epitopes of Lebanese specimens. No unique changes were identified in the breakthrough specimens compared to non-breakthroughs that could explain the occurrence of infection in vaccinated children. Further, we report the emergence of a rare P[8] OP354-like strain with a G9 VP7 in Lebanon, possessing high genetic variability in their VP4 compared to vaccine strains. Therefore, human rotavirus strains circulating in Lebanon and globally have accumulated numerous substitutions in their antigenic sites compared to those currently used in the licensed vaccines. The successful spread and continued genetic drift of these strains over time might undermine the effectiveness of the vaccines. The effect of such changes in the antigenic sites on vaccine efficacy remains to be assessed.
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spelling pubmed-70543812020-03-13 Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon Harastani, Houda H. Reslan, Lina Sabra, Ahmad Ali, Zainab Hammadi, Moza Ghanem, Soha Hajar, Farah Matar, Ghassan M. Dbaibo, Ghassan S. Zaraket, Hassan Front Immunol Immunology Human rotavirus remains a major cause of gastroenteritis worldwide despite the availability of effective vaccines. In this study, we investigated the genetic diversity of rotaviruses circulating in Lebanon. We genetically characterized the VP4 and VP7 genes encoding the outer capsid proteins of 132 rotavirus-associated gastroenteritis specimens, previously identified in hospitalized children (<5 years) from 2011 to 2013 in Lebanon. These included 43 vaccine-breakthrough specimens and the remainder were from non-vaccinated subjects. Phylogenetic analysis of VP4 and VP7 genes revealed distinct clustering compared to the vaccine strains, and several substitutions were identified in the antigenic epitopes of Lebanese specimens. No unique changes were identified in the breakthrough specimens compared to non-breakthroughs that could explain the occurrence of infection in vaccinated children. Further, we report the emergence of a rare P[8] OP354-like strain with a G9 VP7 in Lebanon, possessing high genetic variability in their VP4 compared to vaccine strains. Therefore, human rotavirus strains circulating in Lebanon and globally have accumulated numerous substitutions in their antigenic sites compared to those currently used in the licensed vaccines. The successful spread and continued genetic drift of these strains over time might undermine the effectiveness of the vaccines. The effect of such changes in the antigenic sites on vaccine efficacy remains to be assessed. Frontiers Media S.A. 2020-02-26 /pmc/articles/PMC7054381/ /pubmed/32174920 http://dx.doi.org/10.3389/fimmu.2020.00317 Text en Copyright © 2020 Harastani, Reslan, Sabra, Ali, Hammadi, Ghanem, Hajar, Matar, Dbaibo and Zaraket. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Harastani, Houda H.
Reslan, Lina
Sabra, Ahmad
Ali, Zainab
Hammadi, Moza
Ghanem, Soha
Hajar, Farah
Matar, Ghassan M.
Dbaibo, Ghassan S.
Zaraket, Hassan
Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title_full Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title_fullStr Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title_full_unstemmed Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title_short Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
title_sort genetic diversity of human rotavirus a among hospitalized children under-5 years in lebanon
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054381/
https://www.ncbi.nlm.nih.gov/pubmed/32174920
http://dx.doi.org/10.3389/fimmu.2020.00317
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