Detection of Shiga toxin-producing Escherichia coli O26, O45, O103, O111, O113, O121, O145, and O157 serogroups by multiplex polymerase chain reaction of the wzx gene of the O-antigen gene cluster |
| |
Authors: | DebRoy Chitrita Roberts Elisabeth Valadez Angela M Dudley Edward G Cutter Catherine N |
| |
Affiliation: | E. coli Reference Center, Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, Wiley Lane, University Park, PA 16802, USA. rcd3@psu.edu |
| |
Abstract: | O-antigens on the surface of Escherichia coli are important virulence factors that are targets of both the innate and adaptive immune system and play a major role in pathogenicity. O-antigens that are responsible for antigenic specificity of the strain determine the O-serogroup. E. coli O26, O45, O103, O111, O113, O121, O145, and O157 have been the most commonly identified O-serogroups associated with Shiga toxin-producing E. coli (STEC) implicated in outbreaks of human illness all over the world. A multiplex polymerase chain reaction assay was developed to simultaneously detect the eight STEC O-serogroups targeting the wzx (O-antigen-flippase) genes of all O-antigen gene clusters. The sensitivity of the multiplex polymerase chain reaction was found to be 10 colony forming units for each O-group when enriched in broth and 100 colony forming units when enriched in artificially inoculated apple juice diluted with tryptic soy broth for 16?h at 37°C. The method can be used for detecting STEC O-groups simultaneously and may be exploited for improving the safety of food products. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|