首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >In Vitro Activity of Five Quinolones and Analysis of the Quinolone Resistance-Determining Regions of gyrA gyrB parC and parE in Ureaplasma parvum and Ureaplasma urealyticum Clinical Isolates from Perinatal Patients in Japan
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In Vitro Activity of Five Quinolones and Analysis of the Quinolone Resistance-Determining Regions of gyrA gyrB parC and parE in Ureaplasma parvum and Ureaplasma urealyticum Clinical Isolates from Perinatal Patients in Japan

机译:五种喹诺酮类药物的体外活性及日本围产期尿道炎小儿和解脲脲原体临床分离株中gyrAgyrBparC和parE的喹诺酮耐药性决定区域分析

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摘要

Ureaplasma spp. cause several disorders, such as nongonococcal urethritis, miscarriage, and preterm delivery with lung infections in neonates, characterized by pathological chorioamnionitis in the placenta. Although reports on antibiotic resistance in Ureaplasma are on the rise, reports on quinolone-resistant Ureaplasma infections in Japan are limited. The purpose of this study was to determine susceptibilities to five quinolones of Ureaplasma urealyticum and Ureaplasma parvum isolated from perinatal samples in Japan and to characterize the quinolone resistance-determining regions in the gyrA, gyrB, parC, and parE genes. Out of 28 clinical Ureaplasma strains, we isolated 9 with high MICs of quinolones and found a single parC gene mutation, resulting in the change S83L. Among 158 samples, the ParC S83L mutation was found in 37 samples (23.4%), including 1 sample harboring a ParC S83L–GyrB P462S double mutant. Novel mutations of ureaplasmal ParC (S83W and S84P) were independently found in one of the samples. Homology modeling of the ParC S83W mutant suggested steric hindrance of the quinolone-binding pocket (QBP), and de novo prediction of peptide structures revealed that the ParC S84P may break/kink the formation of the α4 helix in the QBP. Further investigations are required to unravel the extent and mechanism of antibiotic resistance of Ureaplasma spp. in Japan.
机译:脲原体引起多种疾病,例如非淋菌性尿道炎,流产和新生儿肺部感染早产,其特征在于胎盘中的病理性绒毛膜羊膜炎。尽管有关脲原体抗生素耐药性的报道正在增加,但日本有关喹诺酮耐药性脲原体感染的报道却很少。这项研究的目的是确定对日本围生期样品中分离出的五个解脲脲原体和小脲尿素喹诺酮类药物的敏感性,并表征gyrA,gyrB,parC和parE基因中喹诺酮耐药性决定区。在28株临床尿素体菌株中,我们分离出9株具有高MIC的喹诺酮类药物,发现一个parC基因突变,导致S83L发生了变化。在158个样本中,在37个样本(占23.4%)中发现了ParC S83L突变,其中1个样本携带了ParC S83L-GyrB P462S双突变体。在其中一个样品中独立发现了脲原体ParC的新突变(S83W和S84P)。对ParC S83W突变体的同源性建模表明,喹诺酮结合口袋(QBP)的空间位阻,并且从头对肽结构的预测表明,ParC S84P可能破坏/扭结QBP中α4螺旋的形成。需要进一步的研究,以揭示Ureaplasma spp的抗生素耐药性的程度和机制。在日本。

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