首页> 外文期刊>Frontiers in Microbiology >Transcriptional Alterations of Virulence-Associated Genes in Extended Spectrum Beta-Lactamase (ESBL)-Producing Uropathogenic Escherichia coli during Morphologic Transitions Induced by Ineffective Antibiotics
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Transcriptional Alterations of Virulence-Associated Genes in Extended Spectrum Beta-Lactamase (ESBL)-Producing Uropathogenic Escherichia coli during Morphologic Transitions Induced by Ineffective Antibiotics

机译:在无效抗生素诱导的形态学转变过程中,产超广谱β-内酰胺酶(ESBL)产生致病性大肠杆菌的毒力相关基因的转录变化。

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It is known that an ineffective antibiotic treatment can induce morphological shifts in uropathogenic Escherichia coli (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.
机译:众所周知,无效的抗生素治疗可以诱导尿路致病性大肠杆菌(UPEC)发生形态变化,但是在这些变化过程中的毒力特性仍有待研究。本研究在无效的抗生素诱导的形态转换和人类原发性膀胱存在的情况下,研究了产生超广谱β-内酰胺酶(ESBL)的UPEC(ESBL019)中全局基因表达模式和毒力因子相关基因的变化上皮细胞。微阵列结果表明,ESBL019的不同形态状态对大量基因具有明显的转录改变(转换;阵列中7%,细丝形成; 32%还原了19%的实体)。 ESBL019的所有三种形态状态均与能量代谢降低,铁捕获系统改变和粘附表达改变有关。另外,与LPS合成和细菌运动相关的基因在所有形态学状态下也都发生了改变。此外,与所有其他形态相比,过渡状态诱导的膀胱上皮细胞释放的TNF-α明显更高,而恢复状态无法诱导TNF-α的释放。我们的发现表明,无效抗生素诱导的形态变化与产生ESBL的UPEC中明显的转录毒力变化有关,这可能会影响尿道的生存和持久性。

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