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多黏菌素或头孢他啶/阿维巴坦耐药肺炎克雷伯菌引起的血流感染的新选择。

New options for bloodstream infections caused by colistin- or ceftazidime/avibactam-resistant Klebsiella pneumoniae.

机构信息

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Int J Antimicrob Agents. 2021 Dec;58(6):106458. doi: 10.1016/j.ijantimicag.2021.106458. Epub 2021 Oct 25.

Abstract

Concerns regarding carbapenem-resistant Klebsiella pneumoniae (CR-Kp), especially in bloodstream infections (BSIs), are continuing to increase worldwide. Several novel agents with activity against BSI CR-Kp have been approved or are in late-stage clinical development. In this study, the antibacterial effects of ceftazidime/avibactam (CZA), aztreonam/avibactam (AZA), meropenem/vaborbactam (MEV), imipenem-cilastatin/relebactam (ICR) and eravacycline (ERV) against three colistin-resistant CR-Kp (COLR-Kp) and four CZA-resistant CR-Kp (CZAR-Kp) were tested by time-kill assay. Klebsiella pneumoniae ATCC® BAA-1705TM was used as a control strain. Two COLR-Kp isolates carried the blaKPC-2 gene and four CAZR-Kp isolates carried metallo-β-lactamase genes. The results revealed that ERV resulted in re-growth of seven tested isolates. CZA and MEV showed a bactericidal effect against isolates harbouring blaKPC-2. ICR reduced the population of six isolates to >5 log10 CFU/mL compared with the initial count. AZA showed a bactericidal effect (>5 log10 CFU/mL) against seven isolates and a bacteriostatic effect (<3 log10 CFU/mL) against one CZAR-Kp isolate. Therefore, AZA and ICR are effective therapeutic candidates for COLR-Kp and CZAR-Kp isolates.

摘要

全球范围内,人们对碳青霉烯类耐药肺炎克雷伯菌(CR-Kp)的担忧持续增加,尤其是血流感染(BSI)。几种对 CR-Kp 引起的 BSI 具有活性的新型药物已获得批准或处于临床开发后期。在这项研究中,通过时间杀伤试验检测了头孢他啶/阿维巴坦(CZA)、氨曲南/阿维巴坦(AZA)、美罗培南/沃巴坦(MEV)、亚胺培南-西司他丁/雷利巴坦(ICR)和依拉环素(ERV)对 3 株黏菌素耐药 CR-Kp(COLR-Kp)和 4 株 CZA 耐药 CR-Kp(CZAR-Kp)的抗菌作用。肺炎克雷伯菌 ATCC® BAA-1705TM 被用作对照菌株。2 株 COLR-Kp 分离株携带 blaKPC-2 基因,4 株 CZAR-Kp 分离株携带金属β-内酰胺酶基因。结果显示,ERAV 导致 7 株受试分离株重新生长。CZA 和 MEV 对携带 blaKPC-2 的分离株表现出杀菌作用。与初始计数相比,ICR 将 6 株分离株的数量减少到>5log10 CFU/mL。AZA 对 7 株分离株表现出杀菌作用(>5log10 CFU/mL),对 1 株 CZAR-Kp 分离株表现出抑菌作用(<3log10 CFU/mL)。因此,AZA 和 ICR 是治疗 COLR-Kp 和 CZAR-Kp 分离株的有效候选药物。

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