Evidence map›Paper›PMID 42158020›Full record

ReviewBiochemistry research international2026

Animal Venom Pharmacological Resources: Exploiting Bioactive Peptides to Target Multi-Drug-Resistant Bacteria.

Rima Jaber, César Mattei, Claudine Accary, Rabih Roufayel, Ziad Abi Khattar, Ziad Fajloun

Abstract readReview
In one paragraph

Review in Biochemistry research international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Rima JaberLaboratory of Applied Biotechnology (LBA3B), Azm Center for Research in Biotechnology and Its Applications, EDST, Lebanese University, 1300, Tripoli, Lebanon, ul.edu.lb.ORCID https://orcid.org/0009-0008-3016-3886
César MatteiUniversity of Angers, INSERM U1083, CNRS UMR 6015, MITOVASC, SFR ICAT, F-49000, Angers, France, univ-angers.fr.ORCID https://orcid.org/0000-0002-2214-2611
Claudine AccaryFaculty of Health Sciences, University of Balamand, Al-Kourah P.O. Box 100, Tripoli, 1300, Lebanon, balamand.edu.lb.ORCID https://orcid.org/0009-0004-7240-4685
Rabih RoufayelCollege of Engineering and Technology, American University of the Middle East, Egaila, 54200, Kuwait, aum.edu.kw.ORCID https://orcid.org/0000-0002-4595-1104
Ziad Abi KhattarFaculty of Medicine and Medical Sciences, University of Balamand, Kalhat P.O. Box 100, Tripoli, Lebanon, balamand.edu.lb.ORCID https://orcid.org/0000-0003-4386-7467
Ziad FajlounLaboratory of Applied Biotechnology (LBA3B), Azm Center for Research in Biotechnology and Its Applications, EDST, Lebanese University, 1300, Tripoli, Lebanon, ul.edu.lb.ORCID https://orcid.org/0000-0002-6502-3110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The escalating rise of multi-drug-resistant (MDR) bacterial strains significantly threatens global health, creating a "silent pandemic" prompted by natural selection, gene mutation, and horizontal gene transfer. This crisis is worsened by the deficit in the development of new treatments, necessitating the innovative discovery of new potent antibacterial agents. Objective: This review examines animal venom, a complex mixture of an evolutionary array of bioactive molecules, as an important emergent source of broad-spectrum antimicrobial peptides (AMPs), creating potential drug templates for next-generation therapeutics. Results: We highlight numerous identified AMPs from various venomous taxa, including scorpions, snakes, spiders, frogs, bees, and wasps, characterized by their bactericidal activity against both Gram-positive and Gram-negative bacteria. They exhibit diverse mechanisms of action, characterized by rapid membrane disruption models, biofilm inhibition, bacterial enzyme dysregulation, immunomodulatory effects, and the control of intracellular targets. These bioresources serve as a structural base for the development of analogs with enhanced potency, higher selectivity, and less systemic toxicity. We also discuss repurposing strategies applied to the native AMPs, the potential application of nanoparticle technologies and the usage of computational methods. Conclusion: These advanced approaches accelerate the examination of large databases to optimize structure-function characteristics, providing a roadmap for the development of future potential antimicrobial treatments derived from the rich reservoir of animal venom bioactive molecules.

Indexed as

animal venomsantibiotic resistance crisisantimicrobial peptidesantisepsisrational molecular designstructural bioinformatics

Identifiers

PMID42158020
PMCPMC13181146

What OpenQuestion holds

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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.