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The Biofilm-Specific Antibiotic Resistance Gene ndvB Is Important for Expression of Ethanol Oxidation Genes in Pseudomonas aeruginosa Biofilms

机译:生物膜特异性抗生素抗性基因ndvB对于铜绿假单胞菌生物膜中乙醇氧化基因的表达很重要。

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摘要

Bacteria growing in biofilms are responsible for a large number of persistent infections and are often more resistant to antibiotics than are free-floating bacteria. In a previous study, we identified a Pseudomonas aeruginosa gene, ndvB, which is important for the formation of periplasmic glucans. We established that these glucans function in biofilm-specific antibiotic resistance by sequestering antibiotic molecules away from their cellular targets. In this study, we investigate another function of ndvB in biofilm-specific antibiotic resistance. DNA microarray analysis identified 24 genes that were responsive to the presence of ndvB. A subset of 20 genes, including 8 ethanol oxidation genes (ercS′, erbR, exaA, exaB, eraR, pqqB, pqqC, and pqqE), was highly expressed in wild-type biofilm cells but not in ΔndvB biofilms, while 4 genes displayed the reciprocal expression pattern. Using quantitative real-time PCR, we confirmed the ndvB-dependent expression of the ethanol oxidation genes and additionally demonstrated that these genes were more highly expressed in biofilms than in planktonic cultures. Expression of erbR in ΔndvB biofilms was restored after the treatment of the biofilm with periplasmic extracts derived from wild-type biofilm cells. Inactivation of ethanol oxidation genes increased the sensitivity of biofilms to tobramycin. Together, these results reveal that ndvB affects the expression of multiple genes in biofilms and that ethanol oxidation genes are linked to biofilm-specific antibiotic resistance.
机译:生物膜中生长的细菌是造成大量持续感染的原因,与自由漂浮细菌相比,它们对抗生素的抵抗力通常更高。在先前的研究中,我们鉴定了铜绿假单胞菌ndvB,该基因对于周质葡聚糖的形成很重要。我们通过隔离抗生素分子使其远离细胞靶标,确定了这些葡聚糖在生物膜特异性抗生素抗性中起作用。在这项研究中,我们调查了ndvB在生物膜特异性抗生素抗性中的另一功能。 DNA微阵列分析确定了对ndvB的存在有反应的24个基因。在野生型生物膜细胞中高表达了20个基因的子集,其中包括8个乙醇氧化基因(ercS',erbR,exaA,exaB,eraR,pqqB,pqqC和pqqE),而在ΔndvB生物膜中却没有表达,而显示了4个基因互惠表达模式。使用定量实时PCR,我们确认了乙醇氧化基因的ndvB依赖性表达,并进一步证明了这些基因在生物膜中的表达高于浮游生物。用衍生自野生型生物膜细胞的周质提取物处理生物膜后,恢复了ΔndvB生物膜中erbR的表达。乙醇氧化基因的失活增加了生物膜对妥布霉素的敏感性。总之,这些结果表明 ndvB 影响生物膜中多个基因的表达,并且乙醇氧化基因与生物膜特异性抗生素抗性相关。

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