Evidence map›Paper›PMID 42151817›Full record

ArticleBMC microbiology2026

Characterization of two exoU

Yi Yan, Lvxin Qian, Xiaoqin Feng, Furong Zhang, Min Tang, Huan Chen, Ying Li, Luhua Zhang

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yi Yan *The School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Lvxin Qian *The School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Xiaoqin FengThe School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Furong ZhangDepartment of Clinical Laboratory, Pengzhou People's Hospital, Chengdu, Sichuan, China.
Min TangDepartment of Clinical Laboratory, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Huan ChenThe School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Ying LiThe School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China. Lying1019@swmu.edu.cn.
Luhua ZhangThe School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China. zhluhua@swmu.edu.cn.

Funding

National Natural Science Foundation of China 82302576
6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa is a major cause of acute nosocomial infections, as well as chronic respiratory infections associated with cystic fibrosis (CF). In chronic lung infections, P. aeruginosa populations typically exhibit extensive phenotypic variation, a trait linked to their need to undergo pathoadaptive mutations to counteract host-derived selective pressures.

methodsIn this study, two clonally related P. aeruginosa isolates, SCPA07 and SCPA08, were identified to coexist in a single bronchoalveolar lavage fluid (BALF) sample from a patient with bacterial pneumonia. Whole-genome sequencing (WGS) was conducted to characterize their genetic background, as well as antimicrobial resistance and virulence gene profiles. A comprehensive analysis of phylogenetic relationships and comparative genomic features of the two isolates was conducted using a panel of bioinformatics tools. Their antimicrobial resistance mechanisms were elucidated via gene sequence analysis and quantitative reverse-transcription PCR (qRT-PCR). A series of phenotypic experiments, including growth, biofilm formation, environmental stress, and virulence assays, and others were performed to characterize their phenotypic traits.

resultsAntimicrobial susceptibility assay showed that both strains were carbapenem-non-susceptible (defined as intermediate or resistant according to the Clinical and Laboratory Standards Institute (CLSI) guidelines). Genomic analysis revealed that they are 'hypermutator' strains and harbor both the exoS and exoU virulence genes, indicating an increased propensity for persistent host infection and high virulence potential. Both strains harbored mutations in oprD, and exhibited elevated expression of AmpC β-lactamase and the efflux pump MexB, which most likely contributed to their non-susceptibility to carbapenems. Despite harboring nucleotide variations at only ten genetic loci, these two strains exhibited distinct phenotypic traits: SCPA07 showed rapid growth, strong biofilm formation, high virulence, and growth advantages under iron limitation and serum stress; in contrast, its variant SCPA08 had slow growth, poor motility, reduced pyocyanin production, low virulence, and increased tolerance to the host antimicrobials human cathelicidin LL-37 and hydrogen peroxide (H

conclusionsThis study elucidates the divergent adaptive evolutionary strategies of a single exoS

Indexed as

CarbapenemsLungPneumonia, BacterialPseudomonas aeruginosaPseudomonas InfectionsAnti-Bacterial AgentsBacterial ProteinsBacterial ToxinsBiofilmsBronchoalveolar Lavage FluidDrug Resistance, BacterialGenome, BacterialHumansMicrobial Sensitivity TestsPhylogenyVirulenceAnti-Bacterial AgentsBacterial ProteinsBacterial ToxinsCarbapenemspseudomonas exoprotein A protein, Pseudomonas aeruginosaVirulence FactorsCarbapenem-non-susceptibleexoUHigh virulenceHypermutatorPseudomonas aeruginosa

Identifiers

PMID42151817
PMCPMC13352818

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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.