Evidence map›Paper›PMID 41463785›Full record

ReviewAntibiotics (Basel, Switzerland)2025

Recent Advances in Endolysin Engineering.

Mackenzie Aitken, Gayan Abeysekera, Craig Billington, Renwick C J Dobson

Abstract readReview
In one paragraph

Review in Antibiotics (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Domain shuffling of endolysin LysKB317 to controlBiotechnology reports (Amsterdam, Netherlands) · 2026
    Article
  5. Article
  6. Article
  7. Phage-Derived Endolysins TargetingAntibiotics (Basel, Switzerland) · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

4 authors.

Mackenzie AitkenBiomolecular Interaction Centre, School of Biological Sciences, University of Canterbury, Christchurch 8041, New Zealand.ORCID 0009-0003-7669-0562
Gayan AbeysekeraBiomolecular Interaction Centre, School of Biological Sciences, University of Canterbury, Christchurch 8041, New Zealand.
Craig BillingtonHealth Security Group, PHF Science, Christchurch 8041, New Zealand.ORCID 0000-0003-3433-4220
Renwick C J DobsonBiomolecular Interaction Centre, School of Biological Sciences, University of Canterbury, Christchurch 8041, New Zealand.ORCID 0000-0002-5506-4939

Funding

Marsden Fund from Government funding, administered by the Royal Society Te Apārangi MFP-ESR2401
6 · The paper itself

Abstract

Antimicrobial resistance threatens a new "dark age" in medical practice. Chronic antibiotic overuse has driven the rise in antimicrobial resistance and promoted the emergence of multidrug-resistant organisms. To address this problem, researchers have developed new approaches. Antimicrobials derived from bacteriophage, which are viruses that target bacteria, are promising candidates. Amongst these candidates, bacteriophage enzymes used in the viral replication cycle are of significant interest. Specifically, endolysins are used by bacteriophage to lyse the bacterial cell wall, leading to structural collapse and cell lysis. Researchers are increasingly applying these proteins externally to multidrug-resistant organisms as a novel antimicrobial treatment. Following this increased interest, many studies have presented protein engineering methods to further enhance the effectiveness of endolysins as antimicrobials. These methods include attachment of membrane-permeabilizing peptides, domain-swapping, and catalytic-site modification. Recent advances in all three fields have seen the implementation of tools like novel in silico design pipelines and library-based screening methods. This review summarizes these recent advances in the rapidly developing field of endolysin engineering and discusses potential future directions in this field.

Indexed as

antibioticantimicrobial resistanceendolysinmulti-drug-resistant organismprotein engineering

Identifiers

PMID41463785
PMCPMC12730064

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.