Evidence map›Paper›PMID 40087577›Full record

ArticleBMC microbiology2025

Characterization of AI-2/LuxS quorum sensing system in antibiotic resistance, pathogenicity of non carbapenemase-producing carbapenem-resistant Escherichia coli.

Xiaohong Xu, Meili Cai, Huishan Lai, Siyan Lian, Liping Hu, Yingping Cao

Abstract read
In one paragraph

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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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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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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5 · Who and what money

Authors and funding

6 authors.

Xiaohong Xu *Department of Laboratory Medicine, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China.
Meili Cai *Department of Laboratory Medicine, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China.
Huishan LaiDepartment of Laboratory Medicine, Fujian Tingzhou Hospital, Longyan, 366300, People's Republic of China.
Siyan LianDepartment of Laboratory Medicine, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China.
Liping HuDepartment of Laboratory Medicine, Xiamen Chang Gung Hospital Hua Qiao University, Xiamen, P. R. China. hulipinglhj@163.com.
Yingping CaoDepartment of Laboratory Medicine, Fujian Medical University Union Hospital, Fuzhou, 350001, People's Republic of China. caoyingping@aliyun.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a quorum sensing system, LuxS/AI-2 is closely associated with bacterial growth, biofilm formation, and virulence. As yet, it is not known how the luxS is associated with a diverse array of physiological activities in non- carbapenemase producing carbapenem resistant Escherichia coli (non-CP-CREC). The purpose of this study is to explore the characterization of AI-2/LuxS quorum sensing system in antibiotic resistance, pathogenicity of non-CP-CREC.

methodsA total of five non-CP-CREC isolates that did not have ompC and ompF deletions were collected from various clinical samples from January 2021 to December 2023. RT-qPCR was used to detect genes expression of luxS, acrA, acrB, tolC, mdtB, mdtC, mdtE, mdtF, ompA, ompX, IL-8, IL-6, and TNF-α. Homologous recombination was used to create the luxS knockout strain. Transcriptome sequencing was utilized to analyze gene expression changes before and after the luxS knockout. Biofilm formation was detected using crystal violet staining. Antimicrobial susceptibility test was used to determine drug resistance. Bacterial growth curves were used to detect the influence of the luxS on bacterial growth. A cell infection assay was used to detect the impact of the luxS on bacterial adhesion and the inflammatory response it induces.

resultsOur results indicated that the expression of the luxS was significantly elevated in non-CP-CREC strains compared to the carbapenem antibiotics sensitive E. coli (CSEC), with CREC229 exhibiting the most pronounced difference. Consequently, CREC229 was chosen for the development of the luxS knockout strain (CREC229△luxS). The deletion of the luxS did not impact the growth of non-CP-CREC. RNA sequencing analysis revealed that 82 genes were differentially expressed, with notable alterations observed in genes associated with biofilm formation regulation and outer membrane proteins in the ΔluxS strain. Our transcriptomic results show that the expression of bssS associated with biofilm formation is significantly reduced in the ΔluxS strain, which in turn reduces its capacity for biofilm formation. In addition, the luxS deletion increased the expression of adhesion-related genes, such as ompA and ompX, enhanced HCT-8 adherence to CREC229, and promoted the secretion of the inflammatory cytokine IL-6. In terms of bacterial resistance, the deletion of luxS increased the sensitivity of non-CP-CRECs to aminoglycoside antibiotics.

conclusionsLuxS/AI-2 quorum sensing systems can alter pathogenicity and resistance in several ways.

Indexed as

Bacterial ProteinsCarbapenem-Resistant EnterobacteriaceaeCarbon-Sulfur LyasesEscherichia coliHomoserineLactonesQuorum SensingAnti-Bacterial Agentsbeta-LactamasesBiofilmsCarbapenemsEscherichia coli InfectionsGene Expression Regulation, BacterialHumansMicrobial Sensitivity TestsVirulenceAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsCarbon-Sulfur LyasesHomoserineLactonesLuxS protein, BacteriaN-octanoylhomoserine lactoneBiofilm formationIL-6LuxS/AI-2Non-CP-CRECQuorum sensing systems

Identifiers

PMID40087577
PMCPMC11909908

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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.