Lu Yan, Toma Claudia, Honma Yasuko, Iwanaga Masaaki
Department of Bacteriology, Faculty of Medicine, University of the Ryukyus, Uehara 207, 903-0215, Nishihara, Okinawa, Japan.
Diagn Microbiol Infect Dis. 2002 May;43(1):7-12. doi: 10.1016/s0732-8893(02)00363-2.
We developed a new practical method to identify enteropathogenic Escherichia coli (EPEC) by detecting the pathogenic factor, EspB. E. coli were cultured in Dulbecco's Modification of Eagle's Medium (DMEM), and EspB was detected in the culture supernatant by reversed passive latex agglutination (RPLA). All 63 E. coli strains harboring the eaeA gene encoding intimin were positive for RPLA, and all 25 strains without the eaeA gene were negative. Among these 63 eaeA-positive strains, 38 Shiga toxin-producing E. coli (STEC) produced Shiga toxin (Stx) under the same culture conditions (DMEM). Subtypes of EspB alpha, beta and gamma were antigenically cross-reactive to each other as determined by RPLA and Western blotting. A kit for Stx detection (RPLA) is commercially available and therefore this RPLA for detection of EspB could be a practical method to define EPEC in both clinical laboratories and the field.
我们开发了一种通过检测致病因子EspB来鉴定肠致病性大肠杆菌(EPEC)的新实用方法。大肠杆菌在杜氏改良伊格尔培养基(DMEM)中培养,通过反向被动乳胶凝集试验(RPLA)检测培养上清液中的EspB。所有63株携带编码紧密黏附素的eaeA基因的大肠杆菌菌株RPLA检测均为阳性,而所有25株无eaeA基因的菌株均为阴性。在这63株eaeA阳性菌株中,38株产志贺毒素大肠杆菌(STEC)在相同培养条件(DMEM)下产生志贺毒素(Stx)。通过RPLA和蛋白质印迹法确定,EspB的α、β和γ亚型在抗原上相互交叉反应。一种用于检测Stx的试剂盒(RPLA)已上市,因此这种用于检测EspB的RPLA可能是临床实验室和现场鉴定EPEC的实用方法。