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囊性纤维化患者铜绿假单胞菌临床分离株中呋喃酮C-30群体感应淬灭和生长抑制的高度变异性。

High variability in quorum quenching and growth inhibition by furanone C-30 in Pseudomonas aeruginosa clinical isolates from cystic fibrosis patients.

作者信息

García-Contreras Rodolfo, Peréz-Eretza Berenice, Jasso-Chávez Ricardo, Lira-Silva Elizabeth, Roldán-Sánchez Jesús Alberto, González-Valdez Abigail, Soberón-Chávez Gloria, Coria-Jiménez Rafael, Martínez-Vázquez Mariano, Alcaraz Luis David, Maeda Toshinari, Wood Thomas K

机构信息

Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad Nacional Autónoma de México, 04510 México Departamento de Bioquímica, Instituto Nacional de Cardiología, Mexico City 14080, Mexico

Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad Nacional Autónoma de México, 04510 México.

出版信息

Pathog Dis. 2015 Aug;73(6):ftv040. doi: 10.1093/femspd/ftv040. Epub 2015 Jun 5.

DOI:10.1093/femspd/ftv040
PMID:26048733
Abstract

Pseudomonas aeruginosa colonizes the lungs of cystic fibrosis patients causing severe damage. This bacterium is intrinsically resistant to antibiotics and shows resistance against new antimicrobials and its virulence is controlled by the quorum-sensing response. Thus, attenuating its virulence by quorum quenching instead of inhibiting its growth has been proposed to minimize resistance; however, resistance against the canonical quorum quencher furanone C-30 can be achieved by mutations leading to increased efflux. In the present work, the effect of C-30 in the attenuation of the QS-controlled virulence factors elastase and pyocyanin was investigated in 50 isolates from cystic fibrosis patients. The results demonstrate that there is a high variability in the expression of both elastase and pyocyanin and that there are many naturally resistant C-30 strains. We report that the main mechanism of C-30 resistance in these strains was not due to enhanced efflux but a lack of permeability. Moreover, C-30 strongly inhibited the growth of several of the isolates studied, thus imposing high selective pressure for the generation of resistance.

摘要

铜绿假单胞菌定殖于囊性纤维化患者的肺部,造成严重损害。这种细菌对抗生素具有内在抗性,并且对新型抗菌药物也表现出抗性,其毒力受群体感应反应控制。因此,有人提出通过群体猝灭来减弱其毒力而非抑制其生长,以尽量减少抗性;然而,导致外排增加的突变可使细菌对典型的群体猝灭剂呋喃酮C-30产生抗性。在本研究中,我们对50株来自囊性纤维化患者的分离株,研究了C-30对群体感应控制的毒力因子弹性蛋白酶和绿脓菌素的减弱作用。结果表明,弹性蛋白酶和绿脓菌素的表达存在高度变异性,并且存在许多对C-30天然耐药的菌株。我们报告,这些菌株对C-30耐药的主要机制不是外排增强,而是通透性缺乏。此外,C-30强烈抑制了所研究的几种分离株的生长,从而对耐药性的产生施加了很高的选择压力。

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