Roland F
Ann Microbiol (Paris). 1980 Jul-Aug;131B(1):1-10.
The enterotoxigenic Escherichia coli strain H-10407 (078-H11) of Evans, possessing a colonization factor antigen (CFA/I) and haemagglutinating in the presence of mannose, was tested as to its ability to cause haemagglutination in the presence of phenothiazines. The phenothiazines (chlorpromazine, thioridazine, prochlorperazine, triethylpiperazine, promethiazine and promazine) were able to inhibit E. coli haemagglutination when added to the complex E. coli-erythrocytes. The most potent inhibitors were prochlorperazine and thioridazine, which inhibited E. coli haemagglutination in 1 min at a concentration of 1.5 mg/ml. The less potent was promethazine that inhibited haemagglutination at 6 mg/ml. Once haemagglutination had occurred the phenothiazines were able to reverse it, to "unhood" the E. coli from the erythrocytes. Prochlorperazine at a concentration of 0.4 mg/ml could reverse haemagglutination after 1 h contact with the E. coli erythrocytes complex. E. coli H-10407 grown in the presence of phenothiazines lost its haemagglutinating activity. The resulting non haemagglutinating E. coli recovered its haemagglutinating activity when recultured in a prochlorperazine free medium.
埃文斯的产肠毒素大肠杆菌菌株H - 10407(O78 - H11),具有定植因子抗原(CFA/I)且在有甘露糖存在时能发生血凝,对其在有吩噻嗪存在时引起血凝的能力进行了测试。当将吩噻嗪(氯丙嗪、硫利达嗪、丙氯拉嗪、三乙哌嗪、异丙嗪和丙嗪)添加到大肠杆菌 - 红细胞复合物中时,它们能够抑制大肠杆菌的血凝。最有效的抑制剂是丙氯拉嗪和硫利达嗪,它们在浓度为1.5毫克/毫升时1分钟内就能抑制大肠杆菌的血凝。效力稍弱的是异丙嗪,它在浓度为6毫克/毫升时能抑制血凝。一旦发生血凝,吩噻嗪能够使其逆转,使大肠杆菌从红细胞上“解离”。浓度为0.4毫克/毫升的丙氯拉嗪在与大肠杆菌 - 红细胞复合物接触1小时后能够逆转血凝。在有吩噻嗪存在的情况下生长的大肠杆菌H - 10407失去了其血凝活性。当在无丙氯拉嗪的培养基中再次培养时,产生的非血凝性大肠杆菌恢复了其血凝活性。