Detection of EspB using reversed passive latex agglutination:: application to determination of enteropathogenic Escherichia coli

被引:13
作者
Lu, Y
Toma, C
Honma, Y
Iwanaga, M
机构
[1] Univ Ryukyus, Fac Med, Dept Bacteriol, Okinawa 9030215, Japan
[2] Fujita Hlth Univ, Sch Med, Dept Microbiol, Aichi 4701192, Japan
关键词
D O I
10.1016/S0732-8893(02)00363-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 (Six) 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 Six 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. (C) 2002 Elsevier Science Inc. All rights reserved.
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页码:7 / 12
页数:6
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