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产超广谱β-内酰胺酶(ESBL)的尿路致病性细菌在无效抗生素诱导的形态转变过程中与毒力相关基因的转录变化

Transcriptional Alterations of Virulence-Associated Genes in Extended Spectrum Beta-Lactamase (ESBL)-Producing Uropathogenic during Morphologic Transitions Induced by Ineffective Antibiotics.

作者信息

Demirel Isak, Rangel Ignacio, Petersson Ulrika, Persson Katarina, Kruse Robert

机构信息

School of Medical Sciences, Örebro UniversityÖrebro, Sweden.

Faculty of Medicine and Health, Inflammatory Response and Infection Susceptibility Centre, Örebro UniversityÖrebro, Sweden.

出版信息

Front Microbiol. 2017 Jun 13;8:1058. doi: 10.3389/fmicb.2017.01058. eCollection 2017.

Abstract

It is known that an ineffective antibiotic treatment can induce morphological shifts in uropathogenic (UPEC) but the virulence properties during these shifts remain to be studied. The present study examines changes in global gene expression patterns and in virulence factor-associated genes in an extended spectrum beta-lactamase (ESBL)-producing UPEC (ESBL019) during the morphologic transitions induced by an ineffective antibiotic and in the presence of human primary bladder epithelial cells. Microarray results showed that the different morphological states of ESBL019 had significant transcriptional alterations of a large number of genes (Transition; 7%, Filamentation; 32%, and Reverted 19% of the entities on the array). All three morphological states of ESBL019 were associated with a decreased energy metabolism, altered iron acquisition systems and altered adhesion expression. In addition, genes associated with LPS synthesis and bacterial motility was also altered in all the morphological states. Furthermore, the transition state induced a significantly higher release of TNF-α from bladder epithelial cells compared to all other morphologies, while the reverted state was unable to induce TNF-α release. Our findings show that the morphological shifts induced by ineffective antibiotics are associated with significant transcriptional virulence alterations in ESBL-producing UPEC, which may affect survival and persistence in the urinary tract.

摘要

已知无效的抗生素治疗可诱导尿路致病性大肠杆菌(UPEC)发生形态转变,但这些转变过程中的毒力特性仍有待研究。本研究检测了产超广谱β-内酰胺酶(ESBL)的UPEC(ESBL019)在无效抗生素诱导的形态转变过程中以及在人原代膀胱上皮细胞存在的情况下,其整体基因表达模式和毒力因子相关基因的变化。微阵列结果显示,ESBL019的不同形态状态对大量基因有显著的转录改变(转变;阵列上7%的实体,丝状化;32%,回复;19%)。ESBL019的所有三种形态状态均与能量代谢降低、铁获取系统改变和黏附表达改变有关。此外,与脂多糖合成和细菌运动相关的基因在所有形态状态下也发生了改变。此外,与所有其他形态相比,转变状态诱导膀胱上皮细胞释放的肿瘤坏死因子-α(TNF-α)显著更高,而回复状态则无法诱导TNF-α释放。我们的研究结果表明,无效抗生素诱导的形态转变与产ESBL的UPEC中显著的转录毒力改变有关,这可能会影响其在尿路中的存活和持续存在。

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