作者: Chanida Kupradit , Sureelak Rodtong , Mariena Ketudat-Cairns
DOI: 10.1007/S11274-013-1394-1
关键词: Shigella boydii 、 16S ribosomal RNA 、 Salmonella 、 Listeria monocytogenes 、 Escherichia coli 、 Bacteria 、 Pathogenic bacteria 、 Shigella 、 Biology 、 Microbiology
摘要: A DNA macroarray was developed to provide the ability detect multiple foodborne pathogens in fresh chicken meat. Probes targeted 16S rRNA and genus- species-specific genes, including fimY, ipaH, prfA, uspA, were selected for specific detection of Salmonella spp., Shigella Listeria monocytogenes, Escherichia coli, respectively. The combination target gene amplification by PCR a our system able distinguish all bacteria from pure cultures with sensitivity 105 c.f.u. ml−1. also applied 10 meat samples. assay validation demonstrated that combining enrichment steps macroarray, 4 could be detected simultaneously L. monocytogenes boydii samples at least 3 initial contamination 25 g samples, advantages protocol are high accuracy time reduction when compared conventional culture. investigation cost effective modern oligonucleotide microarray techniques because there no expensive equipment required pathogens.