Evidence map›Paper›PMID 39106212›Full record

ReviewGut microbes

Phage lysins for intestinal microbiome modulation: current challenges and enabling techniques.

Iris Pottie, Roberto Vázquez Fernández, Tom Van de Wiele, Yves Briers

Abstract readReview
In one paragraph

Review in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  16. [Phage endolysins-a novel class of antibacterial agents with a wide range of applications].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2025
    Review
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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

4 authors.

Iris PottieLaboratory of Applied Biotechnology, Department of Biotechnology, Ghent University, Gent, Belgium.ORCID 0000-0003-4023-8737
Roberto Vázquez FernándezLaboratory of Applied Biotechnology, Department of Biotechnology, Ghent University, Gent, Belgium.ORCID 0000-0002-7919-552X
Tom Van de WieleCenter for Microbial Ecology and Technology (CMET), Faculty of Bioscience Engineering, Ghent University, Gent, Belgium.
Yves BriersLaboratory of Applied Biotechnology, Department of Biotechnology, Ghent University, Gent, Belgium.ORCID 0000-0001-7723-1040

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The importance of the microbiota in the intestinal tract for human health has been increasingly recognized. In this perspective, microbiome modulation, a targeted alteration of the microbial composition, has gained interest. Phage lysins, peptidoglycan-degrading enzymes encoded by bacteriophages, are a promising new class of antibiotics currently under clinical development for treating bacterial infections. Due to their high specificity, lysins are considered microbiome-friendly. This review explores the opportunities and challenges of using lysins as microbiome modulators. First, the high specificity of endolysins, which can be further modulated using protein engineering or targeted delivery methods, is discussed. Next, obstacles and possible solutions to assess the microbiome-friendliness of lysins are considered. Finally, lysin delivery to the intestinal tract is discussed, including possible delivery methods such as particle-based and probiotic vehicles. Mapping the hurdles to developing lysins as microbiome modulators and identifying possible ways to overcome these hurdles can help in their development. In this way, the application of these innovative antimicrobial agents can be expanded, thereby taking full advantage of their characteristics.

Indexed as

BacteriophagesEndopeptidasesGastrointestinal MicrobiomeAnimalsAnti-Bacterial AgentsBacteriaBacterial InfectionsHumansPeptidoglycanProbioticsViral ProteinsAnti-Bacterial AgentsendolysinEndopeptidasesPeptidoglycanViral Proteinsantibioticdysbiosisendolysinmicrobiome modulationPhage lysin

Identifiers

PMID39106212
PMCPMC11305034

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.