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一种多重间接酶联免疫吸附试验,用于检测和区分大肠杆菌与其他肠杆菌科以及铜绿假单胞菌与其他非发酵葡萄糖菌。

A multiplexed, indirect enzyme-linked immunoassay for the detection and differentiation of E. coli from other Enterobacteriaceae and P. aeruginosa from other glucose non-fermenters.

机构信息

School of Public Health, Division of Infectious Disease and Vaccinology, University of California, Berkeley, CA 94720, USA.

Silver Lake Research Corporation, Azusa, CA 91702, USA.

出版信息

J Microbiol Methods. 2019 Mar;158:52-58. doi: 10.1016/j.mimet.2019.01.014. Epub 2019 Jan 29.

DOI:10.1016/j.mimet.2019.01.014
PMID:30708086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11675078/
Abstract

Gram-negative bacteria (GNB) are important causes of community (CA) and hospital (HA)- associated infections. Here we describe the development of an indirect ELISA (I-ELISA), which can be used to detect and differentiate the Enterobacteriaceae Escherichia coli, and glucose non-fermenter Pseudomonas aeruginosa from other GNB species. The I-ELISA utilizes six antibodies for bacterial speciation, which were grouped according to their bacterial targets; Enterobacteriaceae (SL-EntA and CH1810 mAb), Escherichia coli (SL-EcA and 6103-46 mAb), Pseudomonas aeruginosa (SL-PaA and SL-PaB). The six, anti-GNB antibodies were first screened against a panel of well-characterized clinical GNB isolates to optimize assay conditions and to determine individual antibody sensitivity and specificity. When tested against a diverse, blinded panel of 94 GNB clinical isolates, the I-ELISA exhibited the following sensitivity/specificity for each target: Enterobacteriaceae (94.4%/95%), E. coli (82.6%/88.7%), P. aeruginosa (83.3%/96%). An I-ELISA to detect and differentiate the most common GNB pathogens offers advantage in terms of simplicity over diagnostic tests currently used in most clinical settings.

摘要

革兰氏阴性菌(GNB)是引起社区(CA)和医院(HA)相关性感染的重要原因。在这里,我们描述了一种间接酶联免疫吸附试验(I-ELISA)的开发,该试验可用于检测和区分肠杆菌科的大肠杆菌和非发酵葡萄糖的铜绿假单胞菌与其他 GNB 物种。I-ELISA 利用六种用于细菌分类的抗体,这些抗体根据其细菌靶标进行分组;肠杆菌科(SL-EntA 和 CH1810 mAb)、大肠杆菌(SL-EcA 和 6103-46 mAb)、铜绿假单胞菌(SL-PaA 和 SL-PaB)。这六种抗 GNB 抗体首先针对一组经过充分表征的临床 GNB 分离株进行筛选,以优化测定条件并确定每种抗体的敏感性和特异性。当用 94 种不同的、盲目的 GNB 临床分离株进行测试时,I-ELISA 对每个靶标表现出以下敏感性/特异性:肠杆菌科(94.4%/95%)、大肠杆菌(82.6%/88.7%)、铜绿假单胞菌(83.3%/96%)。与大多数临床环境中目前使用的诊断检测相比,用于检测和区分最常见 GNB 病原体的 I-ELISA 在简单性方面具有优势。

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