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2013 年至 2017 年全球临床实验室分离的革兰氏阴性杆菌对依拉环素的活性。

Activity of Eravacycline against Gram-Negative Bacilli Isolated in Clinical Laboratories Worldwide from 2013 to 2017.

机构信息

IHMA Europe Sàrl, Monthey, Switzerland

Tetraphase Pharmaceuticals, Watertown, Massachusetts, USA.

出版信息

Antimicrob Agents Chemother. 2020 Feb 21;64(3). doi: 10.1128/AAC.01699-19.

Abstract

Eravacycline is a novel, fully synthetic fluorocycline antibiotic developed for the treatment of serious infections, including those caused by multidrug-resistant (MDR) pathogens. Here, we evaluated the activities of eravacycline and comparator antimicrobial agents against a global collection of frequently encountered clinical isolates of Gram-negative bacilli. The CLSI broth microdilution method was used to determine MIC data for isolates of ( = 13,983), ( = 2,097), ( = 1,647), and ( = 1,210) isolated primarily from respiratory, intra-abdominal, and urinary specimens by clinical laboratories in 36 countries from 2013 to 2017. Susceptibilities were interpreted using both CLSI and EUCAST breakpoints. Multidrug-resistant (MDR) isolates were defined by resistance to agents from ≥3 different antimicrobial classes. The MICs ranged from 0.25 to 1 μg/ml for and were 1 μg/ml for and 2 μg/ml for , , and Eravacycline's potency was up to 4-fold greater than that of tigecycline against genera/species of , , and The MICs for five of six individual genera/species of and were within 2-fold of the MICs for their respective subsets of MDR isolates, while the MDR subpopulation of spp. demonstrated 4-fold higher MICs. Eravacycline demonstrated potent activity against the majority of clinical isolates of Gram-negative bacilli, including MDR isolates, collected over a 5-year period. This study further underscores the potential benefit of eravacycline in the treatment of infections caused by MDR Gram-negative pathogens.

摘要

依拉环素是一种新型全合成氟环素类抗生素,用于治疗严重感染,包括由多重耐药(MDR)病原体引起的感染。在此,我们评估了依拉环素和对照抗菌药物对来自 36 个国家的临床实验室在 2013 年至 2017 年间分离的革兰氏阴性杆菌的全球常见临床分离株的活性。CLSI 肉汤微量稀释法用于确定 ( = 13983)、 ( = 2097)、 ( = 1647)和 ( = 1210)的分离株的 MIC 数据,这些分离株主要来自呼吸道、腹腔和尿液标本。使用 CLSI 和 EUCAST 折点解释敏感性。多药耐药(MDR)分离株定义为对来自≥3 种不同抗菌药物类别的药物耐药。 对 和 的 MIC 范围为 0.25 至 1μg/ml,对 和 的 MIC 为 1μg/ml,对 和 的 MIC 为 2μg/ml。与替加环素相比,依拉环素对 、 和 属/种的效力高 4 倍。六种 和 属/种中的五种的单个属/种的 MIC 与各自 MDR 分离株的 MIC 相差 2 倍以内,而 种的 MDR 亚群的 MIC 高 4 倍。依拉环素对革兰氏阴性杆菌的大多数临床分离株具有强大的 活性,包括在 5 年内收集的 MDR 分离株。本研究进一步强调了依拉环素在治疗由 MDR 革兰氏阴性病原体引起的感染方面的潜在益处。

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