Evidence map›Paper›PMID 33758343›Full record

ArticleScientific reports2021

OMN6 a novel bioengineered peptide for the treatment of multidrug resistant Gram negative bacteria.

Shira Mandel, Janna Michaeli, Noa Nur, Isabelle Erbetti, Jonathan Zazoun, Livia Ferrari, Antonio Felici, Moshe Cohen-Kutner, Niv Bachnoff

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% of its field
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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Drug-resistantClinical microbiology reviews · 2025
    Pooled it
  2. Review
  3. Article
  4. Membrane-Focused Strategies AgainstAntibiotics (Basel, Switzerland) · 2026
    Review
  5. Review
  6. [New antimicrobial substances to combat increasing resistance].Innere Medizin (Heidelberg, Germany) · 2026
    Review
  7. Advances of Antimicrobial Peptides in the Treatment of Multidrug-Resistant Bacteria.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Microorganisms · 2025
    Review
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  18. Article
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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

9 authors at 2 institutions in 2 countries.

Shira MandelOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel.
Janna MichaeliOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel.
Noa NurOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel.
Isabelle ErbettiEvotec Anti-Infective, Department of Microbiology Discovery, Aptuit (Verona) S.R.L., an Evotec Company, via A. Fleming 4, 37135, Verona, Italy.
Jonathan ZazounOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel.
Livia FerrariEvotec Anti-Infective, Department of Microbiology Discovery, Aptuit (Verona) S.R.L., an Evotec Company, via A. Fleming 4, 37135, Verona, Italy.
Antonio FeliciEvotec Anti-Infective, Department of Microbiology Discovery, Aptuit (Verona) S.R.L., an Evotec Company, via A. Fleming 4, 37135, Verona, Italy.
Moshe Cohen-KutnerOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel.
Niv BachnoffOmnix Medical Ltd., High-Tech Village, Givat-Ram Campus, 9270401, Jerusalem, Israel. niv@omnixmedical.com.
Aptuit (Italy) · ITOmni Sciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New antimicrobial agents are urgently needed, especially to eliminate multidrug resistant Gram-negative bacteria that stand for most antibiotic-resistant threats. In the following study, we present superior properties of an engineered antimicrobial peptide, OMN6, a 40-amino acid cyclic peptide based on Cecropin A, that presents high efficacy against Gram-negative bacteria with a bactericidal mechanism of action. The target of OMN6 is assumed to be the bacterial membrane in contrast to small molecule-based agents which bind to a specific enzyme or bacterial site. Moreover, OMN6 mechanism of action is effective on Acinetobacter baumannii laboratory strains and clinical isolates, regardless of the bacteria genotype or resistance-phenotype, thus, is by orders-of-magnitude, less likely for mutation-driven development of resistance, recrudescence, or tolerance. OMN6 displays an increase in stability and a significant decrease in proteolytic degradation with full safety margin on erythrocytes and HEK293T cells. Taken together, these results strongly suggest that OMN6 is an efficient, stable, and non-toxic novel antimicrobial agent with the potential to become a therapy for humans.

Indexed as

Acinetobacter baumanniiAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial Outer MembraneDrug Resistance, Multiple, BacterialPore Forming Cytotoxic ProteinsProtein EngineeringProtein StabilityAnti-Bacterial AgentsAntimicrobial Cationic Peptidescecropin APore Forming Cytotoxic Proteins

Identifiers

PMID33758343
PMCPMC7988117
OpenAlexW3137303799

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.