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快速碳青霉烯失活法(rCIM)评估:一种用于产碳青霉烯酶肠杆菌科的表型筛选试验。

Evaluation of the rapid carbapenem inactivation method (rCIM): a phenotypic screening test for carbapenemase-producing Enterobacteriaceae.

机构信息

Research Unit EA7361 'Structure, dynamic, function and expression of broad spectrum β-lactamases', Faculty of Medicine, Université Paris-Sud, Université Paris-Saclay, Le Kremlin-Bicêtre, France.

Department of Bacteriology-Hygiene, Bicêtre Hospital, Assistance Publique - Hôpitaux de Paris, Le Kremlin-Bicêtre, France.

出版信息

J Antimicrob Chemother. 2018 Apr 1;73(4):900-908. doi: 10.1093/jac/dkx519.

Abstract

OBJECTIVES

Fast and accurate diagnostic tests to identify carbapenemase-producing Enterobacteriaceae (CPE) are mandatory for proper antimicrobial therapy and implementing infection control measures. Here, we have developed a rapid Carbapenem Inactivation Method (rCIM) for CPE detection.

METHODS

The rCIM consists of the incubation of a potential carbapenemase producer with meropenem discs and use of the resulting supernatant to challenge a susceptible indicator strain. Growth of the indicator strain is monitored using a nephelometer. The performances of the rCIM were compared with the CIM and Carba NP tests using a collection of 113 well-characterized carbapenem-resistant enterobacterial isolates, including 85 carbapenemase producers and 28 non-carbapenemase producers. In addition, rCIM was compared with the Carba NP test and PCR sequencing in a prospective analysis of 101 carbapenem-resistant enterobacterial isolates addressed to the French National Reference Center for Antimicrobial Resistance in July 2017.

RESULTS AND DISCUSSION

The rCIM correctly identified 84/85 carbapenemase producers and 28/28 non-carbapenemase producers, yielding a sensitivity of 99% and a specificity of 100%, slightly higher than the CIM and Carba NP test. In the prospective validation study, the rCIM showed a sensitivity and specificity of 97% and 95%, respectively. Two cephalosporinase-hyperproducing Enterobacter cloacae gave false-positive results, whereas an IMI-17-producing Enterobacter asburiae gave a false-negative result. The result was, however, positive when the isolate was grown on selective antibiotic-containing media.

CONCLUSIONS

The rCIM is a rapid (less than 3 h), cheap and accurate test for the detection of CPEs, which can be implemented in low-resource settings, making it a useful tool for microbiology laboratories.

摘要

目的

快速准确的诊断试验可用于鉴定产碳青霉烯酶肠杆菌科(CPE),这对于合理的抗菌治疗和实施感染控制措施是必要的。在此,我们开发了一种快速碳青霉烯酶失活法(rCIM)用于 CPE 的检测。

方法

rCIM 由可能产生碳青霉烯酶的菌与美罗培南纸片孵育组成,然后使用产生的上清液去挑战敏感的指示菌株。用浊度计监测指示菌株的生长情况。采用收集的 113 株特征明确的耐碳青霉烯肠杆菌分离株,包括 85 株碳青霉烯酶产生菌和 28 株非碳青霉烯酶产生菌,对 rCIM 的性能与 CIM 和 Carba NP 试验进行了比较。此外,在 2017 年 7 月向法国国家抗菌药物耐药性参考中心提交的 101 株耐碳青霉烯肠杆菌的前瞻性分析中,rCIM 与 Carba NP 试验和 PCR 测序进行了比较。

结果与讨论

rCIM 正确鉴定了 84/85 株碳青霉烯酶产生菌和 28/28 株非碳青霉烯酶产生菌,其敏感性为 99%,特异性为 100%,略高于 CIM 和 Carba NP 试验。在前瞻性验证研究中,rCIM 的敏感性和特异性分别为 97%和 95%。两株高产头孢菌素酶的阴沟肠杆菌产生了假阳性结果,而一株产 IMI-17 的爱氏柠檬酸杆菌产生了假阴性结果。然而,当在含有选择性抗生素的培养基上培养时,结果为阳性。

结论

rCIM 是一种快速(<3 小时)、廉价且准确的 CPE 检测方法,可在资源有限的环境中实施,是微生物学实验室的有用工具。

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