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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Main Authors: Houda H. Harastani, Lina Reslan, Ahmad Sabra, Zainab Ali, Moza Hammadi, Soha Ghanem, Farah Hajar, Ghassan M. Matar, Ghassan S. Dbaibo, Hassan Zaraket
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2020.00317/full
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author Houda H. Harastani
Lina Reslan
Ahmad Sabra
Zainab Ali
Zainab Ali
Moza Hammadi
Moza Hammadi
Soha Ghanem
Soha Ghanem
Farah Hajar
Farah Hajar
Ghassan M. Matar
Ghassan M. Matar
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Hassan Zaraket
Hassan Zaraket
author_facet Houda H. Harastani
Lina Reslan
Ahmad Sabra
Zainab Ali
Zainab Ali
Moza Hammadi
Moza Hammadi
Soha Ghanem
Soha Ghanem
Farah Hajar
Farah Hajar
Ghassan M. Matar
Ghassan M. Matar
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Hassan Zaraket
Hassan Zaraket
author_sort Houda H. Harastani
collection DOAJ
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 doaj.art-267faf6f1e8a474091346357a2df648f2022-12-22T01:44:29ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-02-011110.3389/fimmu.2020.00317503497Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in LebanonHouda H. Harastani0Lina Reslan1Ahmad Sabra2Zainab Ali3Zainab Ali4Moza Hammadi5Moza Hammadi6Soha Ghanem7Soha Ghanem8Farah Hajar9Farah Hajar10Ghassan M. Matar11Ghassan M. Matar12Ghassan S. Dbaibo13Ghassan S. Dbaibo14Ghassan S. Dbaibo15Hassan Zaraket16Hassan Zaraket17Faculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Experimental Pathology, Immunology, and Microbiology, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, LebanonDepartment of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut, LebanonFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, LebanonDepartment of Experimental Pathology, Immunology, and Microbiology, Faculty of Medicine, American University of Beirut, Beirut, LebanonHuman 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.https://www.frontiersin.org/article/10.3389/fimmu.2020.00317/fullhuman rotaviruscapsid proteinsdiversityvaccinebreakthroughRotarix
spellingShingle Houda H. Harastani
Lina Reslan
Ahmad Sabra
Zainab Ali
Zainab Ali
Moza Hammadi
Moza Hammadi
Soha Ghanem
Soha Ghanem
Farah Hajar
Farah Hajar
Ghassan M. Matar
Ghassan M. Matar
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Ghassan S. Dbaibo
Hassan Zaraket
Hassan Zaraket
Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon
Frontiers in Immunology
human rotavirus
capsid proteins
diversity
vaccine
breakthrough
Rotarix
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 human rotavirus
capsid proteins
diversity
vaccine
breakthrough
Rotarix
url https://www.frontiersin.org/article/10.3389/fimmu.2020.00317/full
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