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本文引用的文献

1
Meropenem-Vaborbactam versus Ceftazidime-Avibactam for Treatment of Carbapenem-Resistant Infections.美罗培南-维巴坦与头孢他啶-阿维巴坦治疗碳青霉烯类耐药感染。
Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.02313-19.
2
CTX-M-33, a CTX-M-15 derivative conferring reduced susceptibility to carbapenems.CTX-M-33,一种对碳青霉烯类药物敏感性降低的CTX-M-15衍生物。
Antimicrob Agents Chemother. 2019 Sep 9;63(12). doi: 10.1128/AAC.01515-19. Epub 2019 Sep 16.
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Rapid immunochromatography-based detection of carbapenemase producers.基于快速免疫层析法检测碳青霉烯酶产生菌。
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Nitro-Carba test, a novel and simple chromogenic phenotypic method for rapid screening of carbapenemase-producing Enterobacteriaceae.硝基卡巴试验,一种新型且简单的显色表型方法,可快速筛选产碳青霉烯酶的肠杆菌科细菌。
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5
Phenotypic Detection of Carbapenemase-Producing Organisms from Clinical Isolates.从临床分离株中表型检测碳青霉烯酶产生菌。
J Clin Microbiol. 2018 Oct 25;56(11). doi: 10.1128/JCM.01140-18. Print 2018 Nov.
6
Unusual carbapenem resistant but ceftriaxone and cefepime susceptible isolated from a blood culture: Case report and whole-genome sequencing investigation.从血培养中分离出的对碳青霉烯类耐药但对头孢曲松和头孢吡肟敏感的罕见菌株:病例报告及全基因组测序研究
IDCases. 2017 Nov 23;11:9-11. doi: 10.1016/j.idcr.2017.11.007. eCollection 2018.
7
OXA-244-Producing Escherichia coli Isolates, a Challenge for Clinical Microbiology Laboratories.产 OXA-244 的大肠埃希菌分离株,对临床微生物学实验室的挑战。
Antimicrob Agents Chemother. 2017 Aug 24;61(9). doi: 10.1128/AAC.00818-17. Print 2017 Sep.
8
Evaluation of the RAPIDEC® CARBA NP and β-CARBA® tests for rapid detection of Carbapenemase-producing Enterobacteriaceae.评估RAPIDEC® CARBA NP和β-CARBA®检测法对产碳青霉烯酶肠杆菌科细菌的快速检测效果。
Diagn Microbiol Infect Dis. 2017 Aug;88(4):293-297. doi: 10.1016/j.diagmicrobio.2017.05.006. Epub 2017 May 13.
9
Characterisation of OXA-244, a chromosomally-encoded OXA-48-like β-lactamase from Escherichia coli.对OXA-244的特性描述,一种来自大肠杆菌的染色体编码的OXA-48样β-内酰胺酶。
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10
Carbapenemase-producing Gram-negative bacteria: current epidemics, antimicrobial susceptibility and treatment options.产碳青霉烯酶革兰阴性菌:当前的流行情况、抗菌药物敏感性及治疗选择
Future Microbiol. 2015;10(3):407-25. doi: 10.2217/fmb.14.135.

用于快速检测和区分不同类别碳青霉烯酶的NitroSpeed-碳青霉烯酶检测试剂盒(Carba NP Test)

NitroSpeed-Carba NP Test for Rapid Detection and Differentiation between Different Classes of Carbapenemases in .

作者信息

Nordmann Patrice, Sadek Mustafa, Demord Anthony, Poirel Laurent

机构信息

Medical and Molecular Microbiology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland

INSERM European Unit (IAME), University of Fribourg, Fribourg, Switzerland.

出版信息

J Clin Microbiol. 2020 Aug 24;58(9). doi: 10.1128/JCM.00932-20.

DOI:10.1128/JCM.00932-20
PMID:32580949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7448648/
Abstract

A biochemical test (NitroSpeed-Carba NP test) was developed to identify carbapenemase production in and to discriminate between the different types of clinically significant carbapenemases (Ambler classes A, B, and D). It is based on two main features, namely, the hydrolysis by all β-lactamases, including carbapenemases of the nitrocefin substrate, and the capacity of ertapenem to prevent this hydrolysis for all β-lactamases except carbapenemases. Specific carbapenemase inhibitors of class A (avibactam, vaborbactam), class B (dipicolinic acid), and class D (avibactam) were used to inhibit the nitrocefin hydrolysis and to allow the identification of the carbapenemase types with a turnaround time of ca. 30 min. The test was evaluated with a collection of 248 clinical enterobacterial isolates, including 148 carbapenemase producers and 100 non-carbapenemase producers. Its overall sensitivity and specificity were 100% and 97%, respectively, including detection of all types of OXA-48-like carbapenemases. For the detection of the carbapenemase type, including strains that produce double carbapenemases, the sensitivity was 100%, 97%, and 100% for the detection of classes A, B, and D, respectively. This easy-to-implement test may contribute to optimization of the choice of the β-lactam/β-lactamase inhibitor combinations for treating infection due to carbapenemase producers.

摘要

开发了一种生化检测方法(NitroSpeed - Carba NP检测),用于鉴定碳青霉烯酶的产生,并区分不同类型具有临床意义的碳青霉烯酶(安布勒分类A、B和D类)。它基于两个主要特性,即所有β - 内酰胺酶(包括碳青霉烯酶)对头孢硝噻吩底物的水解作用,以及厄他培南对除碳青霉烯酶外的所有β - 内酰胺酶阻止这种水解的能力。使用A类(阿维巴坦、瓦博巴坦)、B类(吡啶 - 2,6 - 二甲酸)和D类(阿维巴坦)的特异性碳青霉烯酶抑制剂来抑制头孢硝噻吩的水解,并能够在约30分钟的周转时间内鉴定碳青霉烯酶类型。该检测方法用248株临床肠杆菌分离株进行了评估,其中包括148株碳青霉烯酶产生菌和100株非碳青霉烯酶产生菌。其总体敏感性和特异性分别为100%和97%,包括检测所有类型的OXA - 48样碳青霉烯酶。对于碳青霉烯酶类型的检测,包括产生双碳青霉烯酶的菌株,A类、B类和D类的检测敏感性分别为100%、97%和100%。这种易于实施的检测方法可能有助于优化治疗碳青霉烯酶产生菌引起的感染时β - 内酰胺/β - 内酰胺酶抑制剂组合的选择。