Evidence map›Paper›PMID 42627004›Full record

ArticleChemistry & biodiversity2026

The Antimycobacterial Activity, Toxicity and Chemical Composition of South African Propolis.

Nyiko F Mzimba, Efficient N Ncube, Elliasu Y Salifu, Alvaro Viljoen, Bhavna Gordhan, Bavesh Kana, Sandy van Vuuren

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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

7 authors.

Nyiko F MzimbaDepartment of Pharmacy and Pharmacology, Faculty of Health Sciences, University of the Witwatersrand, Parktown, South Africa.ORCID https://orcid.org/0000-0002-1203-1862
Efficient N NcubeDepartment of Pharmaceutical Sciences, Faculty of Science, Tshwane University of Technology, Pretoria, South Africa.ORCID https://orcid.org/0000-0001-6278-3774
Elliasu Y SalifuDepartment of Pharmaceutical Sciences, Faculty of Science, Tshwane University of Technology, Pretoria, South Africa.ORCID https://orcid.org/0000-0001-8713-5001
Alvaro ViljoenDepartment of Pharmaceutical Sciences, Faculty of Science, Tshwane University of Technology, Pretoria, South Africa.ORCID https://orcid.org/0000-0002-6810-2981
Bhavna GordhanFaculty of Health Sciences, Infectious Diseases and Oncology Research Institute (IDORI), School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
Bavesh KanaFaculty of Health Sciences, Infectious Diseases and Oncology Research Institute (IDORI), School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
Sandy van VuurenDepartment of Pharmacy and Pharmacology, Faculty of Health Sciences, University of the Witwatersrand, Parktown, South Africa.ORCID https://orcid.org/0000-0002-4859-1845

Funding

Faculty of Research Committee Individual Research GrantNational Research FoundationOppenheimer Memorial TrustSouth African Medical Research Councilthe University of the Witwatersrand Postgraduate Scholarship
6 · The paper itself

Abstract

Global research has explored the antimicrobial properties of propolis; however, the antimycobacterial activity of South African (SA) propolis has been neglected. This study evaluated 109 propolis samples collected from eight SA provinces where the antimycobacterial activity, chemical composition and toxicity was evaluated. Samples were tested using a broth microdilution assay against various Mycobacterium strains (M. fortuitum ATCC 6841, M. gordonae ATCC 14470 and M. smegmatis ATCC 14468) and the pathogenic M. tuberculosis H37Rv strain. A multi-step approach combining ultra-performance liquid chromatography/ mass spectrometry (UPLC-MS) profiling, high-performance thin-layer chromatography (HPTLC) bio-autography, brine shrimp toxicity testing and molecular docking was employed on eight bio-active and eight non-active propolis samples. Two samples (GP68 and EC77B) demonstrated promising activity, with MICs ranging from 49-195 µg/mL against non-tuberculous strains and 125 µg/mL against M. tuberculosis. Chemometric and bio-autography analyses identified flavonoids and related compounds, including pinocembrin, galangin, chrysin and pinobanksin compounds as major contributors to activity. Both samples were non-toxic at concentrations (1 mg/mL at 24 h; 0.5 mg/mL at 48 h). Molecular docking indicated favourable binding to key M. tuberculosis targets involved in cell wall biosynthesis (DprE1) and transcription (RNAP). This study demonstrates that selected SA-derived propolis samples show strong antimycobacterial potential.

Indexed as

Anti-Bacterial AgentsAntitubercular AgentsMycobacteriumPropolisAnimalsArtemiaChromatography, High Pressure LiquidFlavanonesFlavonoidsMicrobial Sensitivity TestsMolecular Docking SimulationSouth AfricaAnti-Bacterial AgentsAntitubercular AgentsFlavanonesFlavonoidspinocembrinPropolisbiological Activitychromatographymolecular dockingmycobacteriapropolis

Identifiers

PMID42627004
PMCPMC13495129

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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.