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Development of a Colony Lift Immunoassay To Facilitate Rapid Detection and Quantification of Escherichia coli O157:H7 from Agar Plates and Filter Monitor Membranes

机译:菌落提升免疫分析的发展以促进从琼脂平板和过滤器监测膜中快速检测和定量大肠杆菌O157:H7

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摘要

E. coli O157:H7 is a food-borne adulterant that can cause hemorrhagic ulcerative colitis and hemolytic uremic syndrome. Faced with an increasing risk of foods contaminated with E. coli O157:H7, food safety officials are seeking improved methods to detect and isolate E. coli O157:H7 in hazard analysis and critical control point systems in meat- and poultry-processing plants. A colony lift immunoassay was developed to facilitate the positive identification and quantification of E. coli O157:H7 by incorporating a simple colony lift enzyme-linked immunosorbent assay with filter monitors and traditional culture methods. Polyvinylidene difluoride (PVDF) membranes (Millipore, Bedford, Mass.) were prewet with methanol and were used to make replicates of every bacterial colony on agar plates or filter monitor membranes that were then reincubated for 15 to 18 h at 36 ± 1°C, during which the colonies not only remained viable but were reestablished. The membranes were dried, blocked with blocking buffer (Kirkegaard and Perry Laboratories [KPL], Gaithersburg, Md.), and exposed for 7 min to an affinity-purified horseradish peroxidase-labeled goat anti-E. coli O157 antibody (KPL). The membranes were washed, exposed to a 3,3′,5,5′-tetramethylbenzidine membrane substrate (TMB; KPL) or aminoethyl carbazole (AEC; Sigma Chemical Co., St. Louis, Mo.), rinsed in deionized water, and air dried. Colonies of E. coli O157:H7 were identified by either a blue (via TMB) or a red (via AEC) color reaction. The colored spots on the PVDF lift membrane were then matched to their respective parent colonies on the agar plates or filter monitor membranes. The colony lift immunoassay was tested with a wide range of genera in the family Enterobacteriaceae as well as different serotypes within the E. coli genus. The colony lift immunoassay provided a simple, rapid, and accurate method for confirming the presence of E. coli O157:H7 colonies isolated on filter monitors or spread plates by traditional culture methods. An advantage of using the colony lift immunoassay is the ability to test every colony serologically on an agar plate or filter monitor membrane simultaneously for the presence of the E. coli O157 antigen. This colony lift immunoassay has recently been successfully incorporated into a rapid-detection, isolation, and quantification system for E. coli O157:H7, developed in our laboratories for retail meat sampling.
机译:大肠杆菌O157:H7是一种食源性掺杂物,可引起出血性溃疡性结肠炎和溶血性尿毒症综合征。面对被O157:H7大肠杆菌污染的食品的风险不断增加,食品安全官员正在寻求改进的方法,以在肉类和家禽加工厂的危害分析和关键控制点系统中检测和分离O157:H7大肠杆菌。通过将简单的菌落提升酶联免疫吸附测定法与滤膜监测器和传统培养方法结合使用,开发了菌落提升免疫测定法,以促进对O157:H7大肠杆菌的阳性鉴定和定量。用甲醇对聚偏二氟乙烯(PVDF)膜(Millipore,Bedford,Mass。)进行预湿,并用于在琼脂平板或过滤器监控器膜上复制每个细菌菌落,然后将其在36±1°C下重新孵育15至18 h。 ,在此期间,殖民地不仅保持生存,而且得以重建。将膜干燥,用封闭缓冲液(Kirkegaard and Perry Laboratories [KPL],Gaithersburg,MD)封闭,并暴露于亲和纯化的辣根过氧化物酶标记的山羊抗E素7分钟。 O157抗体(KPL)。洗涤膜,使其暴露于3,3',5,5'-四甲基联苯胺膜底物(TMB; KPL)或氨乙基咔唑(AEC; Sigma Chemical Co.,St.Louis,MO),在去离子水中冲洗,并风干。大肠杆菌O157:H7的菌落通过蓝色(通过TMB)或红色(通过AEC)显色反应鉴定。然后将PVDF提升膜上的有色斑点与琼脂平板或滤膜监控器膜上的相应亲本菌落匹配。用肠杆菌科的广泛属以及大肠杆菌属中的不同血清型测试了菌落提升免疫测定法。菌落提升免疫测定法提供了一种简单,快速,准确的方法,用于确认通过传统培养方法在滤膜监控器或铺板上分离的大肠杆菌O157:H7菌落的存在。使用菌落提升免疫测定法的一个优势是能够同时在琼脂平板或过滤器监测膜上通过血清学方法检测每个菌落是否存在大肠杆菌O157抗原。该菌落提升免疫测定法最近已成功地整合到我们实验室中用于零售肉类采样的大肠杆菌O157:H7的快速检测,分离和定量系统中。

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