Outer membrane protein A (OmpA) may be used as a novel target to enrich and detect Escherichia coli in milk samples

多克隆抗体 大肠杆菌 免疫磁选 细菌 生物 重组DNA 细菌外膜 检出限 色谱法 肠杆菌科 微生物学 分子生物学 食品科学 化学 抗体 基因 生物化学 遗传学
作者
Yichen Tian,Kaiqing Yang,Yaoqiang Shi,Jinyang Zhang,Qinqin Han,Xueshan Xia,Yuzhu Song
出处
期刊:Journal of Dairy Science [Elsevier BV]
卷期号:105 (4): 2849-2857 被引量:6
标识
DOI:10.3168/jds.2021-20974
摘要

In recent years, food safety incidents caused by Escherichia coli have occurred and have endangered human health. Due to the complex matrix of milk samples and the long pretreatment time, the existing methods cannot quickly detect E. coli in milk samples. It is necessary to enrich the E. coli in the complex matrix to improve the detection sensitivity. The E. coli outer membrane protein A (OmpA) is widely present on the cell membrane of E. coli and may be used as a new target to enrich E. coli. In this study, the purified recombinant OmpA protein was used to immunize BALB/c mice to produce polyclonal antibody. Immunomagnetic beads were combined with the polyclonal antibody to enrich the E. coli in the artificially contaminated milk samples. The products of immunoprecipitation were further used for PCR assay. The bacteria in the PCR sample can be pre-enriched, and the limit of detection is 10 × 100 cfu/mL, which is about 100 times more sensitive than samples not processed by this method. Then, the artificially contaminated milk, coffee, juice, and soybean milk samples were tested separately, and it was found that the E. coli gene could be amplified. The whole analysis time was about 120 min, including the enrichment of bacteria and the detection of eluate. We found that OmpA combined with immunomagnetic beads was more efficient, fast, and convenient than the conventional method. Bacteria can be enriched more efficiently without extracting genomic DNA and culturing bacteria. Therefore, this method has potential value for improving the detection sensitivity and shortening the detection time of E. coli in food samples.
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