首页> 外文期刊>Journal of food protection >Modified immunoliposome sandwich assay for the detection of Escherichia coli O157:H7 in apple cider.
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Modified immunoliposome sandwich assay for the detection of Escherichia coli O157:H7 in apple cider.

机译:改良的免疫脂质体夹心测定法,用于检测苹果酒中的大肠杆菌O157:H7。

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Detection of Escherichia coli O157:H7 in fruit juices such as apple cider is necessary for diagnosis of infection and epidemiological investigations. However, inhibitors in the apple cider, such as endogenous polyphenols and acids, often decrease the sensitivity of PCR assays and immunoassays, thus routinely requiring laborious cell separation steps to increase the sensitivity. In the current study, polyethylene glycol (PEG)-derivatized liposomes encapsulating sulforhodamine B were tagged with anti-E. coli O157:H7 antibodies and used in an immunoliposome sandwich assay for the detection of E. coli O157:H7 in apple cider. Even without prior separation, this assay can detect E. coli O157:H7 in apple cider samples inoculated with as few as 1 CFU/ml after an 8-h enrichment period. The lower limit of detection in pure cultures without enrichment was 7 x 10(3) CFU/ml (280 CFU/40-microl sample). PEGylated immunoliposomes are suitable as an analytical reagent for the detection of E. coli O157:H7 in fruit juices containing polyphenols.
机译:检测果汁(例如苹果酒)中的大肠杆菌O157:H7对诊断感染和进行流行病学调查非常必要。但是,苹果酒中的抑制剂(例如内源多酚和酸)通常会降低PCR分析和免疫分析的灵敏度,因此通常需要费力的细胞分离步骤来提高灵敏度。在当前的研究中,封装磺基若丹明B的聚乙二醇(PEG)衍生的脂质体用抗E标签。大肠杆菌O157:H7抗体,用于免疫脂质体夹心分析,用于检测苹果酒中的大肠杆菌O157:H7。即使没有事先分离,该测定法也可以在富集8小时后以低至1 CFU / ml的浓度对苹果酒样品中的大肠杆菌O157:H7进行检测。在不富集的纯培养物中,检测下限为7 x 10(3)CFU / ml(280 CFU / 40微升样品)。聚乙二醇化的免疫脂质体适合作为分析试剂,用于检测含有多酚的果汁中的大肠杆菌O157:H7。

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