Evidence map›Paper›PMID 41120835›Full record

ArticleBMC microbiology2025

Quorum quenching by endophytic Bacillus cereus AL1: a lactonase-based anti-virulence strategy against Pseudomonas aeruginosa.

Alaa A Fawzy, Marwa M Raafat, R Mahmoud, Omneya M Helmy

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Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

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4 · The record

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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.

Alaa A FawzyDepartment of Microbiology and Immunology, Faculty of Pharmacy, Future University in Egypt, Cairo, Egypt.
Marwa M RaafatDepartment of Microbiology and Immunology, Faculty of Pharmacy, Future University in Egypt, Cairo, Egypt. Marwa.Mahmoud@fue.edu.eg.ORCID 0000-0001-5614-5127
R MahmoudDepartment of Pharmacology, Toxicology and Supporting Science, College of Pharmacy- Al-Farahidi University, Baghdad, Iraq.
Omneya M HelmyMicrobiology and Immunology Department, Faculty of Pharmacy, Cairo University in Egypt, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa infections are often challenging to treat due to multiple drug resistance, besides the development of biofilms and a plethora of virulence factors regulated by quorum sensing. Quorum-quenching enzymes, such as N-acyl homoserine lactonases, represent a promising anti-virulence strategy by disrupting this signaling mechanism without exerting selective pressure, leading to resistance. This study aimed to screen endophyte and epiphyte isolates for lactonase activity and evaluate their potential to inhibit virulence in Pseudomonas aeruginosa.

resultsFifty-two bacterial isolates (42 endophyte and 10 epiphyte) were isolated from ten plants. The aiiA gene encoding lactonase enzyme was detected in 11 endophytes and one epiphyte isolate, among which nine showed complete degradation (100%) of the quorum sensing signal molecule N-hexanoyl-L-homoserine lactone. The partially purified lactonase enzyme from the endophyte Bacillus cereus AL1 isolate exhibited significant anti-virulence activity, reducing biofilm formation, swarming motility, and pyocyanin production against Pseudomonas aeruginosa PAO1 and clinical Pseudomonas aeruginosa isolates. Sequence alignment of the Bacillus cereus AL1 lactonase protein revealed close similarity to the homologous lactonase from Bacillus cereus. The quorum quenching activity of the partially purified lactonase AL1 provided protection in a Galleria mellonella infection model.

conclusionThe study highlights the potential of Bacillus cereus AL1 lactonase as an effective anti-virulence agent against Pseudomonas aeruginosa without the pressure for resistance development.

Indexed as

Bacillus cereusBacterial ProteinsCarboxylic Ester HydrolasesEndophytesPseudomonas aeruginosaQuorum SensingAnimalsAnti-Bacterial AgentsBiofilmsMetalloendopeptidasesPseudomonas InfectionsPyocyanineVirulenceVirulence FactorsAiiA protein, BacillusAnti-Bacterial AgentsBacterial ProteinsCarboxylic Ester HydrolasesMetalloendopeptidasesN-acyl homoserine lactonasePyocyanineVirulence FactorsBacillus cereusBiofilmEndophytesEpiphytesLactonasePseudomonas aeruginosaQuorum quenching

Identifiers

PMID41120835
PMCPMC12539043

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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.