Evidence map›Paper›PMID 38864495›Full record

ArticleMicrobial biotechnology2024

LysJEP8: A promising novel endolysin for combating multidrug-resistant Gram-negative bacteria.

Jose Vicente Carratalá, Neus Ferrer-Miralles, Elena Garcia-Fruitós, Anna Arís

Abstract read
In one paragraph

Article in Microbial biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Microbes Saving Lives and Reducing Suffering.Microbial biotechnology · 2025
    Article
  7. Review
  8. Article
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.

Jose Vicente CarrataláInstitute of Biotechnology and Biomedicine, Autonomous University of Barcelona, Barcelona, Spain.ORCID 0000-0001-6950-2939
Neus Ferrer-MirallesInstitute of Biotechnology and Biomedicine, Autonomous University of Barcelona, Barcelona, Spain.ORCID 0000-0003-2981-3913
Elena Garcia-FruitósDepartment of Ruminant Production, Institute of Agriculture and Agrifood Research and Technology (IRTA), Barcelona, Spain.ORCID 0000-0001-7498-4864
Anna ArísDepartment of Ruminant Production, Institute of Agriculture and Agrifood Research and Technology (IRTA), Barcelona, Spain.ORCID 0000-0001-7830-888X

Funding

Agència de Gestió d'Ajuts Universitaris i de Recerca SGR 01552Agencia Española de Investigación PID2019-107298RB-C21/AEI/10.13039/501100011033Agencia Española de Investigación PID2019-107298RB-C22/AEI/10.13039/501100011033CERCA Program (Generalitat de Catalunya)European Social FundMargarita Salas Grant 722713
6 · The paper itself

Abstract

Antimicrobial resistance (AMR) is an escalating global health crisis, driven by the overuse and misuse of antibiotics. Multidrug-resistant Gram-negative bacteria, such as Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae, are particularly concerning due to their high morbidity and mortality rates. In this context, endolysins, derived from bacteriophages, offer a promising alternative to traditional antibiotics. This study introduces LysJEP8, a novel endolysin derived from Escherichia phage JEP8, which exhibits remarkable antimicrobial activity against key Gram-negative members of the ESKAPE group. Comparative assessments highlight LysJEP8's superior performance in reducing bacterial survival rates compared to previously described endolysins, with the most significant impact observed against P. aeruginosa, and notable effects on A. baumannii and K. pneumoniae. The study found that LysJEP8, as predicted by in silico analysis, worked best at lower pH values but lost its effectiveness at salt concentrations close to physiological levels. Importantly, LysJEP8 exhibited remarkable efficacy in the disruption of P. aeruginosa biofilms. This research underscores the potential of LysJEP8 as a valuable candidate for the development of innovative antibacterial agents, particularly against Gram-negative pathogens, and highlights opportunities for further engineering and optimization to address AMR effectively.

Indexed as

Anti-Bacterial AgentsDrug Resistance, Multiple, BacterialEndopeptidasesGram-Negative BacteriaAcinetobacter baumanniiBacteriophagesBiofilmsHydrogen-Ion ConcentrationKlebsiella pneumoniaeMicrobial Sensitivity TestsMicrobial ViabilityPseudomonas aeruginosaAnti-Bacterial AgentsendolysinEndopeptidases

Identifiers

PMID38864495
PMCPMC11167605

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.