Identification of EPEC and non-EPEC serotypes in the EPEC O serogroups by PCR-RFLP analysis of the fliC gene

被引:15
|
作者
Botelho, BA
Bando, SY
Trabulsi, LR
Moreira, CA
机构
[1] Univ Sao Paulo, Inst Ciencias Biol, Dept Immunol, BR-05550890 Sao Paulo, Brazil
[2] Inst Butantan, Lab Especial Microbiol, BR-05503900 Sao Paulo, Brazil
关键词
EPEC O serogroups; fliC gene; PCR-RFLP; SSCP;
D O I
10.1016/S0167-7012(03)00010-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Polymerase chain reaction-restriction fragment length polymorphisin (PCR-RFLP) analysis of the flagellin gene (fliC) was performed in 233 strains of enteropathogenic Escherichia coli (EPEC) O serogroups for determining their flagellar antigen (H) status. The serological detection of flagellin is the basis for the H-codes typing system in E. coli. Thus, it is impossible to serotype nonmotile bacteria (i.e. to assign H-codes). Twenty-eight fliC restriction patterns were obtained for motile (H2, H4, H6, H7, H8, F19, H10, H11, H12, H18, H21, H27, H32, H34, H35, H40 and H51) and nonmotile serotypes (H-). Each motile serotype was characterized by one or two fliC specific restriction patterns. The only exception was serogroup O128ab, where a common restriction pattern was found for serotypes O128ab:H2 and O128ab:H35, even after digestion with RsaI, AluI and Sau3AI endonucleases. These two serotypes were, however, discriminated by single strand conformation polymorphisin (SSCP) analysis of RsaI restriction fragments. Nonmotile strains showed fliC restriction patterns identical to some known H serotypes. The PCR-R-FLP analysis of fliC gene proved to be a useful method for identifying the H variants in motile and nonmotile EPEC O serogrOUPS. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
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