Evidence map›Paper›PMID 32174920›Full record

ArticleFrontiers in immunology2020

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

Houda H Harastani, Lina Reslan, Ahmad Sabra, Zainab Ali, Moza Hammadi, Soha Ghanem, Farah Hajar, Ghassan M Matar, Ghassan S Dbaibo, Hassan Zaraket

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
0.5field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 3 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  4. Human Riboviruses: A Comprehensive Study.Journal of molecular evolution · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Houda H HarastaniFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Lina ReslanFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Ahmad SabraFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Zainab AliFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Moza HammadiFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Soha GhanemFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Farah HajarFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Ghassan M MatarFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Ghassan S DbaiboFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
Hassan ZaraketFaculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.
American University of Beirut · LB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Child, HospitalizedGenetic VariationAmino Acid SequenceAntigens, ViralCapsid ProteinsChild, PreschoolEpitopesFemaleGastroenteritisGlycosylationHumansInfantLebanonMaleModels, MolecularPhylogenyAntigens, ViralCapsid ProteinsEpitopesRNA, ViralVaccines, AttenuatedViral VaccinesVP4 protein, RotavirusVP7 protein, Rotavirusbreakthroughcapsid proteinsdiversityhuman rotavirusRotarixRotaTeqvaccine

Identifiers

PMID32174920
PMCPMC7054381
OpenAlexW3007902428

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.