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达氟沙星和萘甲唑啉对支原体和其他种属的活性。

Activity of Delafloxacin and Finafloxacin against Mycoplasma hominis and Species.

机构信息

Department of Clinical Laboratory, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Key Laboratory of Precision Medicine in Diagnosis and Monitoring Research of Zhejiang Province, Hangzhou, China.

出版信息

Microbiol Spectr. 2022 Jun 29;10(3):e0009922. doi: 10.1128/spectrum.00099-22. Epub 2022 May 9.

Abstract

The activity of two new fluoroquinolones, delafloxacin and finafloxacin, were evaluated against and spp. The MICs of delafloxacin, finafloxacin, and two classical fluoroquinolones (moxifloxacin and levofloxacin) were tested against 29 and 67 spp. isolates using the broth microdilution method. The molecular mechanisms underlying fluoroquinolone resistance were also investigated. Delafloxacin exhibited low MICs against and spp., including the levofloxacin-resistant isolates. For , delafloxacin showed low MIC value of 1 μg/mL (MIC range, <0.031 -1 μg/mL) compared to 8 μg/mL for finafloxacin, 16 μg/mL for moxifloxacin, and 32 μg/mL for levofloxacin. For and , delafloxacin had low MIC values (, 2 μg/mL; , 4 μg/mL) compared to 16 -32 μg/mL for finafloxacin, 16 μg/mL for moxifloxacin, and 32 - >32 μg/mL for levofloxacin. The two mutations GyrA S153L and ParC S91I were commonly identified in fluoroquinolone-resistant , and ParC S83L was the most frequent mutation identified in fluoroquinolone-resistant spp. Delafloxacin displayed lower MICs against fluoroquinolone-resistant isolates of both and spp. that have mutations in the quinolone resistance determining regions (QRDRs) than the two classical fluoroquinolones. Delafloxacin is a promising fluoroquinolone with low MICs against fluoroquinolone-resistant and spp. Our study confirms the potential clinical use of delafloxacin in treating antimicrobial-resistant and spp. infections. Fluoroquinolone resistance in Mycoplasma hominis and spp. is on the rise globally, which has compromised the efficacy of the currently available antimicrobial agents. This study evaluated the antimicrobial activity of two new fluoroquinolones, delafloxacin and finafloxacin, for the first time, against and spp. clinical isolates. Delafloxacin and finafloxacin displayed different antimicrobial susceptibility profiles against and spp. . Delafloxacin was found to be more effective against and spp. than three classical fluoroquinolones (finafloxacin, moxifloxacin, and levofloxacin). Finafloxacin displayed activity similar to moxifloxacin but superior to levofloxacin against and spp. Our findings demonstrate that delafloxacin is a promising fluoroquinolone with outstanding activity against fluoroquinolone-resistant and spp.

摘要

两种新型氟喹诺酮类药物,德拉沙星和非奈沙星的活性被评估用于治疗 和 种。使用肉汤微量稀释法测试了德拉沙星、非奈沙星和两种经典氟喹诺酮类药物(莫西沙星和左氧氟沙星)对 29 株 和 67 株 种分离株的 MIC。还研究了氟喹诺酮类耐药的分子机制。德拉沙星对 和 种,包括左氧氟沙星耐药株,表现出低 MICs。对于 ,与 8μg/ml 的非奈沙星、16μg/ml 的莫西沙星和 32μg/ml 的左氧氟沙星相比,德拉沙星的 MIC 值较低,为 1μg/ml(MIC 范围,<0.031-1μg/ml)。对于 和 ,与 16-32μg/ml 的非奈沙星、16μg/ml 的莫西沙星和 32- >32μg/ml 的左氧氟沙星相比,德拉沙星的 MIC 值较低( ,2μg/ml; ,4μg/ml)。在氟喹诺酮类耐药 中,常见的突变是 GyrA S153L 和 ParC S91I,在氟喹诺酮类耐药 种中,最常见的突变是 ParC S83L。与两种经典氟喹诺酮类药物相比,德拉沙星对喹诺酮耐药决定区(QRDRs)突变的 和 种氟喹诺酮类耐药分离株的 MICs 较低。德拉沙星是一种很有前途的氟喹诺酮类药物,对氟喹诺酮类耐药的 和 种具有较低的 MICs。我们的研究证实了德拉沙星在治疗抗微生物药物耐药的 和 种感染方面的潜在临床应用。全球范围内,人型支原体和 种的氟喹诺酮类耐药性呈上升趋势,这削弱了现有抗菌药物的疗效。本研究首次评估了两种新型氟喹诺酮类药物,德拉沙星和非奈沙星,对 和 种临床分离株的抗菌活性。德拉沙星和非奈沙星对 和 种的抗菌敏感性不同。与三种经典氟喹诺酮类药物(非奈沙星、莫西沙星和左氧氟沙星)相比,德拉沙星对 和 种的作用更强。非奈沙星对 和 种的活性与莫西沙星相似,但优于左氧氟沙星。我们的研究结果表明,德拉沙星是一种很有前途的氟喹诺酮类药物,对氟喹诺酮类耐药的 和 种具有出色的活性。

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