[酶联免疫吸附试验(ELISA)检测肠出血性大肠杆菌(EHEC)菌株脂多糖抗体在胃肠道疾病患者和溶血性尿毒症综合征患者中的有效性评价]。

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引用次数: 0

摘要

肠出血性大肠杆菌(EHEC)是一种重要的人畜共患食源性和水源性病原体,可引起人类腹泻和严重溶血性尿毒症综合征(HUS)。该研究的目的是评估酶免疫测定ELISA在胃肠道疾病患者和溶血性尿毒症综合征患者中检测肠出血性大肠杆菌脂多糖(LPS)抗体的有效性。材料与方法:采用基于lps的酶联免疫吸附试验对526例胃肠道疾病患者、26例溶血性尿毒综合征患者和74例不同细菌性肠胃炎感染患者的血清进行筛选。采用改良的Boivin法获得EHEC血清群O26、O103、O104、O111、O121、O145和O157的LPS抗原。此外,为了确定临界值,对122名健康人的血清进行了检测。用大肠杆菌O14细胞提取物吸附去除肠杆菌科共同抗原(ECA)抗体。结果:胃肠疾病患者不同肠出血性大肠杆菌血清中LPS抗体的阳性率普遍较低。此外,一些阳性结果的解释是困难的事实,许多血清学相互作用。特别是在不同细菌性肠胃炎患者血清中发现了许多交叉反应。该研究还表明,在大多数情况下,ECA抗体的吸收对ELISA中观察到的交叉反应没有显著影响。另一方面,在溶血性尿毒综合征患者中,5例患者检测到大肠杆菌O26的LPS抗原抗体水平很高,4例患者检测到大肠杆菌O157, 3例患者检测到大肠杆菌O104和O145, 2例患者检测到大肠杆菌O111。对6例溶血性尿毒综合征患者相隔2-3周的配对血清的抗体水平分析显示,对LPS抗原的抗体水平迅速下降。结论:脂多糖抗原酶联免疫吸附试验对肠出血性大肠杆菌感染有较好的诊断价值。由于交叉反应的可能性,需要基于产生维罗毒素的大肠杆菌的重组蛋白开发更特异性的抗原。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Evaluation of usefulness of the enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to lipopolysaccharides of Enterohemorrhagic Escherichia coli (EHEC) strains in patients with gastrointestinal disorders and patients with hemolytic uremic syndrome].

Introduction: Enterohemorrhagic Escherichia coli (EHEC) strains are an important zoonotic food-borne and waterborne pathogens causing diarrhea and the severe hemolytic uremic syndrome (HUS) in humans. The aim of the study was to evaluate the usefulness of enzyme immunoassay ELISA for detection of antibodies to the lipopolysaccharides (LPS) of EHEC in patients with gastrointestinal disorders and patients with hemolytic-uremic syndrome.

Material and methods: Sera obtained from 526 patients with gastrointestinal disorders, 26 patients with HUS and 74 patients with different bacterial gastroenteritis infections were screened by an LPS-based ELISA. The LPS antigens of EHEC belonging to serogroups O26, O103, O104, O111, O121, O145, and O157 were obtained by modified Boivin's method. Additionally, to determine the cut-off level, the 122 sera from healthy people were tested. Cellular extract from E. coli O14 were used to remove by absorption antibodies to the Enterobacteriaceae Common Antigen (ECA).

Results: Generally, seroprevalence of antibodies to the LPS of different EHEC serogroups in patients with gastrointestinal disorders was low. Additionally, interpretation of the some positive results was difficult to the fact of many serological mutual interactions. Particularly a lot of cross-reactions were seen in the group of sera obtained from patients with different bacterial gastroenteritis infections. The study showed also that in most cases the absorption of antibodies to the ECA had no significant effect on the cross-reactions observed in ELISA. On the other hand, the very high level of antibodies to the LPS antigen of E. coli O26 was found in 5 patients, to E. coli O157 in 4 patients, to E. coli O104 and O145 in 3 patients and E. coli O111 in 2 patients with HUS. Analysis of antibody levels in paired sera taken 2-3 weeks apart obtained from six HUS patients showed a rapid decline of antibody levels to the LPS antigens.

Conclusions: The results showed the usefulness of the ELISA with lipopolysaccharides antigens to serodiagnosis of infection caused by EHEC. Due to the possibility of cross- -reaction there is a need to develop more specific antigens, based on the recombinant proteins of verotoxin-producing Escherichia coli.

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