Ye L Y, Lan F H, Zhu Z Y, Chen X M, Ye X L
East Hospital, Fujian, Peoples' Republic of China.
J Diarrhoeal Dis Res. 1993 Mar;11(1):38-40.
Two oligonucleotide primers were used in a polymerase chain reaction (PCR) procedure to amplify a region of the invasive-associated locus (ial) of Shigella and enteroinvasive Escherichia coli (EIEC). Detection of the amplified product can be done by agarose gel electrophoresis, which is specific and sensitive enough for routine diagnosis of these two pathogens. PCR is done using DNA extracted directly from faeces. The procedure can be completed in 7 h. These findings demonstrate a novel method for rapid, sensitive, specific, and simple diagnosis of diarrhoea caused by Shigella and EIEC.
在聚合酶链反应(PCR)过程中使用了两种寡核苷酸引物,以扩增志贺氏菌和肠侵袭性大肠杆菌(EIEC)的侵袭相关基因座(ial)区域。扩增产物的检测可通过琼脂糖凝胶电泳进行,该方法对这两种病原体的常规诊断具有足够的特异性和敏感性。PCR使用直接从粪便中提取的DNA进行。该过程可在7小时内完成。这些发现证明了一种用于快速、灵敏、特异且简单诊断志贺氏菌和EIEC引起的腹泻的新方法。