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Enzyme-linked synthetic oligonucleotide probes: non-radioactive detection of enterotoxigenic Escherichia coli in faecal specimens

机译:酶联合成寡核苷酸探针:粪便标本中的非放射性检测产肠毒素的大肠杆菌

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Synthetic oligonucleotides, complementary to unique sequences in the heat stable enterotoxin gene of Escherichia coli specific for humans, were prepared with a 30-atom spacer arm and a 3′ terminal sulfhydryl group which was coupled to bromoacetyl-derivatized alkaline phosphatase. The resulting direct enzyme-linked oligonucleotide probes, containing one enzyme molecule per oligonucleotide, successfully diagnosed enterotoxigenic Escherichia coli in clinical specimens by using a modified colony hybridization method and a colorimetric assay. The procedure is rapid, simple and reliable with a sensitivity equivalent to that using 5′-terminally labelled [32P]-oligo-nucleotide probes. The results indicate that the enzyme-labelled oligonucleotide probes should be applicable to the routine diagnosis of enterotoxigenic Escherichia coli and possess the potential for the detection of other microbial pathogens.
机译:合成的寡核苷酸与人类特异的大肠杆菌热稳定肠毒素基因中的独特序列互补,具有30个原子的间隔臂和一个3'末端巯基,并与溴乙酰基衍生的碱性磷酸酶偶联。所得的直接酶联寡核苷酸探针每个寡核苷酸包含一个酶分子,通过使用改良的菌落杂交法和比色法成功地诊断出临床标本中的产肠毒素大肠杆菌。该过程快速,简单且可靠,灵敏度与使用5'-末端标记的[ 32 P]-寡核苷酸探针的灵敏度相同。结果表明,酶标记的寡核苷酸探针应适用于产肠毒素大肠杆菌的常规诊断,并具有检测其他微生物病原体的潜力。

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