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评价 eazyplex SuperBug CRE 检测试剂盒在检测克雷伯氏菌属和铜绿假单胞菌属的β-内酰胺酶基因中的应用。

Evaluation of eazyplex SuperBug CRE Test for Beta-Lactamase Genes Detection in Klebsiella spp. and P. aeruginosa Strains.

机构信息

Department of Microbiology, Ludwik Rydygier Collegium Medicum, Nicolaus Copernicus University, 9 M. Sklodowska-Curie Street, 85-094, Bydgoszcz, Poland.

出版信息

Curr Microbiol. 2020 Jan;77(1):99-103. doi: 10.1007/s00284-019-01806-5. Epub 2019 Nov 14.

Abstract

The multi-drug resistance of Gram-negative rods is one of the most important issues of present medicine. In recent years, more and more strains resistant to the majority or to all possible therapeutic options have been isolated-especially Klebsiella spp. and Pseudomonas spp. representatives. It is very important to detect strains with these phenotypes as quickly and reliably as possible. The aim of the study was to evaluate the usefulness of eazyplex SuperBug CRE test (Amplex Diagnostics) for the detection of the most important beta-lactam resistance genes. eazyplex SuperBug CRE test is based on the loop-mediated isothermal amplification (LAMP) method, and detects genes for the following beta-lactamases: KPC, NDM-1, VIM, OXA-48, CTX-M1, CTX-M9 and OXA-181. The study involved 87 strains. For all of the positive strains in the LAMP method, additional PCR were performed to increase the spectrum of ESBLs detected by the genes encoding for enzymes belonging to TEM and SHV families. The results obtained by the tested method and standard PCR were consistent for all Klebsiella spp. strains. The discrepancy between the evaluated test and PCR results was observed for one P. aeruginosa strain. The eazyplex SuperBug CRE test can be used for quick detection of the most important beta-lactam resistance mechanisms amongst Gram-negative rods.

摘要

革兰氏阴性杆菌的多药耐药性是当今医学的最重要问题之一。近年来,越来越多的菌株对大多数或所有可能的治疗选择产生了耐药性,尤其是克雷伯氏菌属和假单胞菌属的代表菌株。尽快、可靠地检测具有这些表型的菌株非常重要。本研究旨在评估eazyplex SuperBug CRE 测试(Amplex Diagnostics)在检测最重要的β-内酰胺类耐药基因方面的有用性。eazyplex SuperBug CRE 测试基于环介导等温扩增(LAMP)方法,可检测以下β-内酰胺酶的基因:KPC、NDM-1、VIM、OXA-48、CTX-M1、CTX-M9 和 OXA-181。本研究涉及 87 株菌株。对于 LAMP 方法中的所有阳性菌株,均进行了额外的 PCR 以增加 TEM 和 SHV 家族编码酶所检测的 ESBLs 的谱。所测试方法和标准 PCR 的结果对所有克雷伯氏菌属菌株均一致。在一株铜绿假单胞菌菌株中观察到评估测试和 PCR 结果之间的差异。eazyplex SuperBug CRE 测试可用于快速检测革兰氏阴性杆菌中最重要的β-内酰胺类耐药机制。

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