Patra G, Sylvestre P, Ramisse V, Thérasse J, Guesdon J L
Laboratoire de Prédéveloppement des Sondes, Institut Pasteur, Paris, France.
FEMS Immunol Med Microbiol. 1996 Oct;15(4):223-31. doi: 10.1111/j.1574-695X.1996.tb00088.x.
A 277-bp long DNA fragment, Ba813, was isolated from an avirulent Bacillus anthracis strain 7700 genomic library. Two oligonucleotides derived from the Ba813 sequence were used as primers in polymerase chain reaction tests on genomic DNA from 28 Bacillus anthracis and from 33 heterologous bacteria strains. A specific, 152-bp long DNA fragment was amplified only when Bacillus anthracis DNA was used as the target. The amplified product was analysed by non-radioactive sandwich hybridisation in microtiter plates using two oligonucleotides. The capture oligonucleotide C1 was covalently linked onto aminated wells of microtiter plates. The detection oligonucleotide D3 was labelled with biotine. The hybrid molecules were detected by avidine conjugated with alkaline phosphatase and chromogenic substrate. Amplification of Ba813 sequence may provide the basis for rapid and reliable assay for the detection and identification of Bacillus anthracis.
从无毒炭疽芽孢杆菌菌株7700的基因组文库中分离出一段277个碱基对长的DNA片段Ba813。以源自Ba813序列的两条寡核苷酸作为引物,对28株炭疽芽孢杆菌和33株异源细菌菌株的基因组DNA进行聚合酶链反应检测。仅以炭疽芽孢杆菌DNA为模板时,可扩增出一条特异性的152个碱基对长的DNA片段。使用两条寡核苷酸,通过微孔板中的非放射性夹心杂交对扩增产物进行分析。捕获寡核苷酸C1共价连接到微孔板的胺化孔上。检测寡核苷酸D3用生物素标记。通过与碱性磷酸酶和显色底物偶联的抗生物素蛋白检测杂交分子。Ba813序列的扩增可为快速、可靠地检测和鉴定炭疽芽孢杆菌提供基础。