Evidence map›Paper›PMID 42828604›Full record

ReviewWorld journal of microbiology & biotechnology2026

An in-depth review on antimicrobial efficacy of melittin in vivo.

Hamed Memariani, Mojtaba Memariani, Mohammadali Mazloumi

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In one paragraph

Review in World journal of microbiology & biotechnology, 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

3 authors.

Hamed MemarianiDepartment of Molecular Virology, Pasteur Institute of Iran, Tehran, Iran.ORCID http://orcid.org/0000-0003-1026-140X
Mojtaba MemarianiDepartment of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran. memaryani@gmail.com.ORCID http://orcid.org/0000-0002-4964-3117
Mohammadali MazloumiDepartment of Medical Biotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences (TUMS), Tehran, Iran. ma.mazlomi@gmail.com.ORCID http://orcid.org/0000-0001-5370-3111

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The past couple of decades have witnessed growing interest in the therapeutic potential of melittin, the main peptide constituent of honeybee venom. Given the rapid growth of in vivo studies investigating the antimicrobial efficacy of melittin and the absence of a thorough review devoted to this subject, a critical evaluation of the literature has become both necessary and opportune. This review commences with a brief overview of the structural characteristics and biological properties of melittin, followed by an evaluation of the in vivo evidence supporting its antibacterial, antifungal, antiprotozoal, and antiviral activities. The limitations of the available studies are also considered, and future research priorities are identified to guide the continued development and clinical translation of this multifunctional peptide. Evidence indicates that melittin can reduce microbial burdens in selected experimental infection models and modulate inflammatory responses. However, the magnitude and nature of these effects vary according to the pathogen, infection model, host context, administration route, dose, and formulation. The continued development of melittin as a therapeutic candidate will require a multidisciplinary strategy. Further efforts should be made to develop biocompatible delivery platforms, including inorganic nanomaterials, polymeric carriers, lipid-based systems, and hydrogels. Additionally, combination therapies with conventional antimicrobial agents or other antimicrobial peptides should be explored. Overall, melittin represents a promising anti-infective candidate, although further studies are required to define its therapeutic window, pharmacokinetic and biodistribution profiles, long-term safety, immunogenicity, and appropriate delivery strategies.

Indexed as

Anti-Infective AgentsMelittenAnimalsAnti-Bacterial AgentsAntimicrobial PeptidesBacteriaHumansAnti-Bacterial AgentsAnti-Infective AgentsAntimicrobial PeptidesMelittenAnimal modelsInfectionInflammationMelittinWound

Identifiers

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Registered trials

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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.