Evidence map›Paper›PMID 27021321›Full record

ArticleAntimicrobial agents and chemotherapy2016

Efficacy of Artilysin Art-175 against Resistant and Persistent Acinetobacter baumannii.

Valerie Defraine, Joris Schuermans, Barbara Grymonprez, Sander K Govers, Abram Aertsen, Maarten Fauvart, Jan Michiels, Rob Lavigne, Yves Briers

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 142 citations in OpenAlex.

  1. Review
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  5. Enhancing the Antibacterial Activity of Endolysin againstJournal of microbiology and biotechnology · 2026
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19 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Valerie DefraineCentre of Microbial and Plant Genetics, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.
Joris SchuermansLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Barbara GrymonprezLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Sander K GoversLaboratory of Food Microbiology, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.
Abram AertsenLaboratory of Food Microbiology, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.
Maarten FauvartCentre of Microbial and Plant Genetics, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.
Jan MichielsCentre of Microbial and Plant Genetics, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.
Rob LavigneLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Yves BriersLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium Laboratory of Applied Biotechnology, Department of Applied Biosciences, Ghent University, Ghent, Belgium yves.briers@ugent.be.ORCID 0000-0001-7723-1040
KU Leuven · BEGhent University · BEIMEC · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteriophage-encoded endolysins have shown promise as a novel class of antibacterials with a unique mode of action, i.e., peptidoglycan degradation. However, Gram-negative pathogens are generally not susceptible due to their protective outer membrane. Artilysins overcome this barrier. Artilysins are optimized, engineered fusions of selected endolysins with specific outer membrane-destabilizing peptides. Artilysin Art-175 comprises a modified variant of endolysin KZ144 with an N-terminal fusion to SMAP-29. Previously, we have shown the high susceptibility of Pseudomonas aeruginosa to Art-175. Here, we report that Art-175 is highly bactericidal against stationary-phase cells of multidrug-resistant Acinetobacter baumannii, even resulting in a complete elimination of large inocula (≥10(8) CFU/ml). Besides actively dividing cells, Art-175 also kills persisters. Instantaneous killing of A. baumannii upon contact with Art-175 could be visualized after immobilization of the bacteria in a microfluidic flow cell. Effective killing of a cell takes place through osmotic lysis after peptidoglycan degradation. The killing rate is enhanced by the addition of 0.5 mM EDTA. No development of resistance to Art-175 under selection pressure and no cross-resistance with existing resistance mechanisms could be observed. In conclusion, Art-175 represents a highly active Artilysin against both A. baumannii and P. aeruginosa, two of the most life-threatening pathogens of the order Pseudomonadales.

Indexed as

Acinetobacter baumanniiAcinetobacter InfectionsAnti-Bacterial AgentsCathelicidinsDrug Resistance, Multiple, BacterialEdetic AcidEndopeptidasesHumansMicrobial Sensitivity TestsMicrofluidic Analytical TechniquesPseudomonas aeruginosaRecombinant Fusion ProteinsAnti-Bacterial AgentsArt-175CathelicidinsEdetic AcidendolysinEndopeptidasesRecombinant Fusion Proteins

Identifiers

PMID27021321
PMCPMC4879360
OpenAlexW2320694902

What OpenQuestion holds

Textmetadata
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.