Evidence map›Paper›PMID 41645084›Full record

ArticleBMC infectious diseases2026

MARVpred: machine learning prediction of inhibitors targeting Marburg virus Gene 4 Small ORF protein.

Eugene Lamptey, Gabriel Anyaele, Harry Arthur, Thaddeus Adjadeh, Dorothy Sagoe, George Hanson, Endalkachew Girma, Olaitan I Awe

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Eugene Lamptey *West African Center for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana. lampteyeugene8@gmail.com.ORCID http://orcid.org/0009-0002-3354-1500
Gabriel Anyaele *Department of Biomedical Engineering, School of Engineering Sciences, University of Ghana, Accra, Ghana.ORCID http://orcid.org/0009-0004-5094-5835
Harry ArthurDepartment of Biomedical Engineering, School of Engineering Sciences, University of Ghana, Accra, Ghana.ORCID http://orcid.org/0009-0007-5987-9143
Thaddeus AdjadehDepartment of Biomedical Engineering, School of Engineering Sciences, University of Ghana, Accra, Ghana.ORCID http://orcid.org/0009-0006-3777-3631
Dorothy SagoeDepartment of Biomedical Engineering, School of Engineering Sciences, University of Ghana, Accra, Ghana.ORCID http://orcid.org/0009-0003-2015-3282
George Hanson *Department of Parasitology, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana.ORCID http://orcid.org/0009-0007-2720-9102
Endalkachew GirmaArmauer Hansen Research Institute, Addis Ababa, Ethiopia. endalkgirma21@gmail.com.ORCID http://orcid.org/0000-0002-6004-1109
Olaitan I AweInstitute for Genomic Medicine Research, West Hartford, CT, USA. laitanawe@gmail.com.ORCID http://orcid.org/0000-0002-4257-3611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Marburg virus (MARV), responsible for severe hemorrhagic fevers with mortality rates as high as 90%, remains a significant public health threat. This study employs machine learning to identify inhibitors targeting the MARV Gene 4 Small ORF protein, crucial for the virus's replication and immune evasion. The Gene 4 Small ORF protein is pivotal in taking over the host's cellular mechanisms, facilitating unchecked viral replication and significant immune system disruption. Effective targeting of this protein holds promise for mitigating the viral lifecycle and entry, potentially curbing the severity of the disease outbreaks. A dataset from PubChem, including 301,745 compounds, was utilized to train models like Random Forest (RF), Gradient Boosting Machines (GBM), CatBoost (CB), AdaBoost (AB), and Logistic Regression (LR). The activity outcomes were classified with integers active as 1 and inactive as 0, followed by molecular descriptor generation using RDKit and PaDEL. The models were trained on an 80:20 split and validated on a novel dataset to ensure robustness, with performance metrics such as accuracy and AUC-ROC guiding evaluation. Morgan fingerprints outperformed PubChem fingerprints, achieving higher accuracy (76%), precision (80%), and ROC-AUC (84%). Among the machine learning models evaluated, RF and GBM were the best performers, with RF achieving the highest specificity (83%) and ROC-AUC (0.84). Validation on new datasets further confirmed the effectiveness of these models, with RF and GBM demonstrating strong predictive reliability for identifying potential inhibitors of the Marburg virus. A Web Application known as MARVpred was developed to predict the activity of compounds with anti-MARV properties from the ChEMBL database. MARVpred is freely accessible online (https://igmr.org/software/marvpred). This study signifies a critical step forward in the computational prediction of viral inhibitors, offering a valuable tool for accelerating the development of Marburg virus therapeutics.

Indexed as

Antiviral AgentsMachine LearningMarburgvirusViral ProteinsBoosting Machine Learning AlgorithmsClassification AlgorithmsHumansMarburg Virus DiseaseOpen Reading FramesPrediction AlgorithmsPredictive Learning ModelsRandom ForestAntiviral AgentsViral ProteinsArtificial intelligenceDrug discoveryGene 4 Small ORF proteinMachine learningMarburg virus disease (MVD)Marburg virus (MARV)

Identifiers

PMID41645084
PMCPMC12973574

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.