1Department of Biology, Shahed University, Tehran, IR Iran
2Department of Biology, Imam Hussein University, Tehran, IR Iran
*Corresponding Author: Department of Biology, Faculty of Science, Shahed University, Tehran-Qom Freeway, Opposite Imam Khomeini's shrine, Tehran, IR Iran., slmousavi@shahed.ac.ir. Email: slmousavi@shahed.ac.ir
Archives of Clinical Infectious Diseases:Vol. 4, issue 2; 97-103
Published online:Apr 30, 2009
Article type:Research Article
How to Cite:Mousavi SL, Rasooli I, Nazarian S, Amani J. Simultaneous Detection of Escherichia Coli O157:H7, Toxigenic Vibrio Cholerae, and Salmonella Typhimurium by Multiplex PCR. Arch Clin Infect Dis. 2009;4(2):. doi:
Abstract
Background:
Escherichia coli O157:H7, Vibrio cholerae, and Salmonella typhimurium are pathogenic bacteria found in contaminated water and food. No assay method is currently available on simultaneous detection or identification of all the three pathogens. Our aim was to develop a rapid and reliable method for this purpose.
Materials and methods:
A protocol for sample collection, and a PCR procedure was designed specifically for the assay. Selected fragments of 239 bp, 432 bp, and 360 bp for E. coli O157 lipopolysaccharide (LPS) gene (rfbE), V. cholera toxin gene (ctx), and Salmonella typhimurium putative cytoplasmic protein gene (STM4497), respectively, were amplified from the extracted bacterial DNA samples in a single tube by multiplex PCR. The multiplex PCR products were analyzed by gel electrophoresis.
Results:
All unknown samples were verifiably identified. The assay was sensitive enough to detect and identify as few as 100 cells of E. coli O157:H7, V. cholerae and Salmonella typhimurium. The presence of other bacteria did not interfere with the analysis.
Conclusion:
This assay is a specific and reliable tool which allows cost-effective detection of all three bacterial pathogens in one reaction tube.
Alishahi A, Imani Fooladi AA, Fallah Mehrabadi J, Mahmoodzadeh Hosseini H. Facile and Rapid Detection of Vibrio cholerae by Multiplex PCR Based on ompU, ctxA, and toxR Genes. Jundishapur J Microbiol. 2013;6(10):e7933. doi: https://doi.org/10.5812/jjm.7933
He P, Yan Y, Zhu G, Zhu Z, Chen Z. Development and Evaluation of a Multiplex Fluorescence PCR for Salmonella Virulence Genes Analysis. Jundishapur J Microbiol. 2024;17(3):e144579. doi: https://doi.org/10.5812/jjm-144579
Mousavi SL, Salimiyan J, Karimi Rahgerdi A, Amani J, Nazarian S, et al. A rapid and specific PCR–ELISA for detecting Salmonella typhi. Arch Clin Infect Dis. 2006;1(3):e93386. doi:
Resendiz-Nava C, Esquivel-Hernandez Y, Alcaraz-Gonzalez A, Castaneda-Serrano P, Nava GM. PCR Assays Based on invA Gene Amplification are not Reliable for Salmonella Detection. Jundishapur J Microbiol. 2019;12(2):e68764. doi: https://doi.org/10.5812/jjm.68764