• DocumentCode
    3332695
  • Title

    Development of a 6 Plex PCR for Simultaneous Detection of Salmonella Enteritidis and Shiga Toxin-Producing Escherichia coli O157

  • Author

    Wang, Yuexia ; Suo, Biao

  • Author_Institution
    Coll. of Life Sci., Henan Agric. Univ., Zhengzhou, China
  • fYear
    2011
  • fDate
    10-12 May 2011
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Salmonella enterica Enteritidis and shiga toxin-producing Escherichia coli O157 are important pathogens that could contaminate food or drinking water. A 6-plex PCR assay was developed to achieve an effective detection and identification of them. After thorough optimization of amplification system, the multiplex PCR assay could specifically and sensitively detect and identify target pathogens. The limits in were approximately 48 and 52 genomic DNA copies from S. enterica Enteritidis ATCC 13076 and E. coli O157:H7 ATCC 43895, respectively. The 6-plex PCR assay is a rapid and reliable method, and have a great potential in effectively screening single or multiple pathogens occurrences in various food or environmental samples.
  • Keywords
    food safety; 6 plex PCR; Salmonella enterica Enteritidis; amplification system optimization; drinking water contamination; food contamination; pathogens; shiga toxin-producing Escherichia coli O157; Bioinformatics; DNA; Genomics; Microorganisms; Multiplexing; Pathogens; Strain;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
  • Conference_Location
    Wuhan
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-5088-6
  • Type

    conf

  • DOI
    10.1109/icbbe.2011.5780810
  • Filename
    5780810