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基于多克隆抗体的免疫分析检测方法可检测到人类和环境样本中大肠杆菌产生的七种志贺毒素 2 亚型。

A polyclonal antibody based immunoassay detects seven subtypes of Shiga toxin 2 produced by Escherichia coli in human and environmental samples.

机构信息

Western Regional Research Center, Agricultural Research Service, United States Department of Agriculture (USDA), Albany, California, United States of America.

出版信息

PLoS One. 2013 Oct 16;8(10):e76368. doi: 10.1371/journal.pone.0076368. eCollection 2013.

Abstract

BACKGROUND

Shiga toxin-producing Escherichia coli (STEC) are frequent causes of severe human diseases ranging from diarrhea to hemolytic uremic syndrome. The existing strategy for detection of STEC relies on the unique sorbitol-negative fermentation property of the O157 strains, the most commonly identified serotype has been E. coli O157. It is becoming increasingly evident, however, that numerous non-O157 STEC serotypes also cause outbreaks and severe illnesses. It is necessary to have new methods that are capable of detecting all STEC strains.

METHODS AND FINDINGS

Here we describe the development of a sandwich ELISA assay for detecting both O157 and non-O157 STECs by incorporating a novel polyclonal antibody (pAb) against Stx2. The newly established immunoassay was capable of detecting Stx2a spiked in environmental samples with a limit of detection between 10 and 100 pg/mL in soil and between 100 and 500 pg/mL in feces. When applied to 36 bacterial strains isolated from human and environmental samples, this assay detected Stx2 in all strains that were confirmed to be stx2-positive by real-time PCR, demonstrating a 100% sensitivity and specificity.

CONCLUSIONS

The sandwich ELISA developed in this study will enable any competent laboratory to identify and characterize Stx2-producing O157 and non-O157 strains in human and environmental samples, resulting in rapid diagnosis and patient care. The results of epitope mapping from this study will be useful for further development of a peptide-based antibody and vaccine.

摘要

背景

产志贺毒素大肠杆菌(STEC)是引起人类严重疾病的常见原因,从腹泻到溶血尿毒综合征不等。目前用于检测 STEC 的策略依赖于 O157 株的独特山梨醇阴性发酵特性,最常见的鉴定血清型为大肠杆菌 O157。然而,越来越明显的是,许多非 O157 STEC 血清型也会引起暴发和严重疾病。有必要开发新的方法来检测所有 STEC 菌株。

方法和发现

在这里,我们描述了通过结合针对 Stx2 的新型多克隆抗体(pAb)开发用于检测 O157 和非 O157 STEC 的夹心 ELISA 测定法。新建立的免疫测定法能够检测到环境样品中添加的 Stx2,其在土壤中的检测限为 10 至 100pg/ml,在粪便中的检测限为 100 至 500pg/ml。当应用于从人和环境样品中分离出的 36 株细菌菌株时,该测定法通过实时 PCR 证实了所有被确认为 stx2 阳性的菌株均检测到 Stx2,具有 100%的敏感性和特异性。

结论

本研究中开发的夹心 ELISA 将使任何有能力的实验室能够识别和表征人类和环境样本中的产志贺毒素 O157 和非 O157 菌株,从而实现快速诊断和患者护理。本研究中从表位映射得到的结果将有助于进一步开发基于肽的抗体和疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4927/3797811/57001b807d8f/pone.0076368.g001.jpg

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