首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Controlling persister cells of Pseudomonas aeruginosa PDO300 by (Z)-4-bromo-5-(bromomethylene)-3-methylfuran-2(5H)-one
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Controlling persister cells of Pseudomonas aeruginosa PDO300 by (Z)-4-bromo-5-(bromomethylene)-3-methylfuran-2(5H)-one

机译:通过(Z)-4-溴-5-(溴甲基)-3-甲基呋喃-2(5h) - 酮(Z)-4-溴-5-(溴亚甲基)-3-甲基呋喃-2(5H) - 控制抗铜绿假单胞菌PDO300的渗漏细胞

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摘要

Pseudomonas aeruginosa is a major pathogen causing chronic pulmonary infections; for example, 80% of cystic fibrosis patients get infected by this bacterium as the disease progresses. Such chronic infections are challenging because P. aeruginosa exhibits high-level tolerance to antibiotics by forming biofilms (multicellular structures attached to surfaces), by entering dormancy and forming antibiotic tolerant persister cells, and by conversion to the mucoid phenotype. Recently, we reported that a synthetic quorum sensing inhibitor, (Z)-4-bromo-5-(bromomethylene)-3-methylfuran-2(5H)-one (BF8), can sensitize both planktonic and biofilm-associated persister cells of P. aeruginosa PAO1 to antibiotics at the concentrations non-inhibitory to its growth. In this study, we further characterized the effects of this compound on the mucoid strain P. aeruginosa PDO300. BF8 was found to reduce persistence during the growth of PDO300 and effectively kill the persister cells isolated from PDO300 cultures. In addition to planktonic cells, BF8 was also found to inhibit biofilm formation of PDO300 and reduce associated persistence. These findings broaden the activities of this class of compounds and indicate that BF8 also has other targets in P. aeruginosa in addition to quorum sensing.
机译:假单胞菌铜绿假单胞菌是一种主要病原体,导致慢性肺部感染;例如,随着疾病的进展,80%的囊性纤维化患者受到这种细菌的感染。这种慢性感染是具有挑战性的,因为P.铜绿假单胞菌通过形成休眠和形成抗生素耐受性泄漏细胞,通过形成生物膜(用与表面附着的多细胞结构)表现出对抗生素的高水平耐受性,并通过转化为粘液表型。最近,我们报道了一种合成法定批量传感抑制剂(Z)-4-溴-5-(溴甲基)-3-甲基呋喃-2(5H) - One(BF8)可以敏化浮游生物和生物膜相关的抗静电细胞P.铜绿假单胞菌Pao1对浓度的抗生素不抑制其生长。在这项研究中,我们进一步表征了该化合物对粘液菌株P.铜绿假单胞菌PDO300的影响。发现BF8在PDO300的生长过程中减少持续性,并有效地杀死从PDO300培养物中分离的渗漏细胞。除浮游细胞外,还发现BF8抑制PDO300的生物膜形成并减少相关的持久性。这些发现扩大了这类化合物的活动,并表明BF8还具有在Quorum感测的铜绿假单胞菌中具有其他靶点。

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