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用于快速检测多粘菌素耐药性的RapidResa多粘菌素NP试验

RapidResa Polymyxin NP Test for Rapid Detection of Polymyxin Resistance in .

作者信息

Bouvier Maxime, Sadek Mustafa, Pomponio Stefano, D'Emidio Fernando, Poirel Laurent, Nordmann Patrice

机构信息

Medical and Molecular Microbiology, Faculty of Science and Medicine, University of Fribourg, 1700 Fribourg, Switzerland.

Swiss National Reference Center for Emerging Antibiotic Resistance (NARA), University of Fribourg, 1700 Fribourg, Switzerland.

出版信息

Antibiotics (Basel). 2021 May 11;10(5):558. doi: 10.3390/antibiotics10050558.

Abstract

A homemade and culture-based test, relying on the visual detection of the reduction of the resazurin reagent (a cell viability indicator), has been developed for the rapid detection of polymyxin resistance in . Here, we evaluated the industrial version of this test, the RapidResa Polymyxin NP test (Liofilchem, Italy). A well-characterized panel of 68 clinical strains (36 polymyxin-susceptible, 26 polymyxin-resistant , and 6 colistin-heteroresistant isolates) of worldwide origin was tested. All the colistin-susceptible isolates gave negative results according to the RapidResa Polymyxin NP test, except for a single isolate that gave a false-positive result. Out of the 26 colistin-resistant strains, 25 were correctly identified as colistin resistant using the RapidResa Polymyxin NP test. Only a single colistin-resistant strain gave a false-negative result. Additionally, the six colistin-heteroresistant isolates tested gave positive results. Altogether, the sensitivity and the specificity of the test were found to be 96% and 97%, respectively. The turn-around-time of this easy-to-perform test was 3-4h, which showed excellent reliability for identification of polymyxin resistance in . The RapidResa Polymyxin NP test allows a rapid differentiation between polymyxin-susceptible and -resistant isolates, which may contribute to optimization of the use of polymyxins for treating infections due to multidrug-resistant

摘要

一种基于培养的自制检测方法已被开发出来,该方法依靠可视检测刃天青试剂(一种细胞活力指示剂)的还原情况,用于快速检测[具体对象]中的多粘菌素耐药性。在此,我们评估了该检测方法的工业版本——RapidResa多粘菌素NP检测法(意大利Liofilchem公司)。我们检测了一组来自世界各地的68株临床[具体菌株](36株对多粘菌素敏感,26株对多粘菌素耐药,6株对黏菌素呈异质性耐药),这些菌株特征明确。根据RapidResa多粘菌素NP检测法,所有对黏菌素敏感的[具体菌株]分离株均给出阴性结果,但有一株分离株给出了假阳性结果。在26株对黏菌素耐药的[具体菌株]中,有25株通过RapidResa多粘菌素NP检测法被正确鉴定为对黏菌素耐药。只有一株对黏菌素耐药的[具体菌株]给出了假阴性结果。此外,所检测的6株对黏菌素呈异质性耐药的分离株均给出阳性结果。总体而言,该检测方法的灵敏度和特异性分别为96%和97%。这种易于操作的检测方法的周转时间为3 - 4小时,在鉴定[具体对象]中的多粘菌素耐药性方面显示出极佳的可靠性。RapidResa多粘菌素NP检测法能够快速区分对多粘菌素敏感和耐药的[具体菌株]分离株,这可能有助于优化多粘菌素在治疗耐多药[相关感染]中的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40d5/8150362/c1098709981e/antibiotics-10-00558-g001.jpg

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