Evidence map›Paper›PMID 40143333›Full record

ArticleViruses2025

Genomic Insights into Neglected Orthobunyaviruses: Molecular Characterization and Phylogenetic Analysis.

Safiétou Sankhe, Idrissa Dieng, Mouhamed Kane, Amadou Diallo, Ndeye Awa Ndiaye, Ndeye Marieme Top, Moussa Dia, Ousmane Faye, Amadou Alpha Sall, Oumar Faye and 4 more

Abstract read
In one paragraph

Article in Viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

14 authors.

Safiétou SankheVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0001-8559-2161
Idrissa DiengVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0002-8584-5592
Mouhamed KaneVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0009-0009-6489-7244
Amadou DialloEpidemiology, Clinical Research and Data Science Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0002-8584-9972
Ndeye Awa NdiayeVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.
Ndeye Marieme TopEpidemiology, Clinical Research and Data Science Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.
Moussa DiaVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0009-0008-9911-0176
Ousmane FayeVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.
Amadou Alpha SallVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.
Oumar FayeVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0002-3478-1322
Pape Mbacke SembeneAnimal Biology Department, Faculty of Sciences and Techniques, Cheikh Anta Diop University of Dakar, Dakar BP 5005, Senegal.
Cheikh LoucoubarEpidemiology, Clinical Research and Data Science Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0002-9582-4197
Martin FayeVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0003-3207-6344
Moussa Moise DiagneVirology Department, Institut Pasteur de Dakar, Dakar BP 220, Senegal.ORCID 0000-0001-5461-5623

Funding

Africa Pathogen Genomics Initiative funds 4306-22-EIPHLSSGENOMICSAgence Française de Développement CZZ3209
6 · The paper itself

Abstract

Orthobunyaviruses are a diverse group of segmented RNA viruses with significant but underexplored public and veterinary health implications. This study provides a genomic, phylogenetic, and ecological analysis of neglected Orthobunyaviruses using next-generation sequencing and computational predictions. We identified unique phylogenetic relationships, with Tanga virus forming a distinct lineage linked to zoonotic, human-associated, or non-vertebrate viruses across segments. GC content analysis revealed segment-specific patterns: higher GC content in the S segment suggests genomic stability and immune evasion, while lower GC content in the L segment reflects host-vector adaptation. Phylogenetic ties to well-characterized pathogenic viruses, such as Ilesha virus with Cache Valley virus and Bwamba virus with California encephalitis virus, indicate potential neurotropism. Ingwavuma virus clustered with Oropouche virus, suggesting risks of systemic febrile illnesses. Within the Simbu serogroup, Sango and Sabo viruses show teratogenic risks to livestock. Vector and host predictions implicate rodents, artiodactyls, and primates in Orthobunyavirus transmission, emphasizing complex ecological dynamics and zoonotic potential. These findings advance the understanding of Orthobunyavirus diversity, linking genomic features to pathogenicity and ecological adaptation, while providing a foundation for future surveillance and intervention strategies targeting these neglected viruses.

Indexed as

Bunyaviridae InfectionsGenome, ViralOrthobunyavirusPhylogenyAnimalsBase CompositionGenomicsHigh-Throughput Nucleotide SequencingHumansZoonosesgenomic characterizationneglected Orthobunyavirusesphylogeneticsvector-borne diseaseszoonotic potential

Identifiers

PMID40143333
PMCPMC11945402

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.