L. monocytogenes cells or the equivalent LLO produced by 4 to 61 cells on average in separate titration trials. Total assay processing and analysis time was approximately 30 mins. The assay has demonstrated the ability to detect 6 species of Listeria as desired by the USDA’s Food Safety Inspection Service (FSIS). The portable system was designed to be used primarily with surface swab samples from fomites, but it can also be used to assess enrichment cultures. The minimal time to detect a positive enrichment culture in our hands from an initial 10 cell inoculum in 200?ml of broth has been 8?h post-incubation at 37?°C in shaker flask cultures. An optional automated magnetic bead assay processing and wash device capable of simultaneously processing 6 samples with low and consistent fluorescence background for higher volume central laboratories is also described." />
Development of a Fluorescent Enzyme-Linked DNA Aptamer-Magnetic Bead Sandwich Assay and Portable Fluorometer for Sensitive and Rapid Listeria Detection
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  • 作者:John G. Bruno ; Taylor Phillips ; Tiffany Montez ; Adrian Garcia…
  • 关键词:Amplex red ; Aptamer ; Assay ; Listeria ; Listeriolysin ; Magnetic bead ; Portable ; Resazurin ; SELEX
  • 刊名:Journal of Fluorescence
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:25
  • 期:1
  • 页码:173-183
  • 全文大小:3,771 KB
  • 参考文献:1. Abu Al-Soud W, Radstr?m P (1998) Capacity of nine thermostable DNA polymerases to mediate DNA amplification in the presence of PCR-inhibiting samples. Appl Environ Microbiol 64:3748-753
    2. Allerberger F, Wagner M (2010) Listeriosis: a resurgent foodborne infection. Clin Microbiol Infect 16:16-3 CrossRef
    3. Bae YM, Baek SY, Lee SY (2012) Resistance of pathogenic bacteria on the surface of stainless steel depending on attachment form and efficacy of chemical sanitizers. Int J Food Microbiol 153:465-73 CrossRef
    4. Bielecki J (1994) Association of listeriolysin O with the cell surface of / Listeria monocytogenes. Acta Microbiol Pol 43:279-89
    5. Birmingham CL, Canadien V, Kaniuk NA, Steinberg BE, Higgins DE, Brumell JH (2008) Listeriolysin O allows / Listeria monocytogenes replication in macrophage vacuoles. Nature 451:350-54 CrossRef
    6. Border PM, Howard JJ, Plastow GS, Siggens KW (1990) Detection of / Listeria species and / Listeria monocytogenes using polymerase chain reaction. Lett Appl Microbiol 11:158-62 CrossRef
    7. Bruno JG, Carrillo MP, Phillips T, Andrews CJ (2010) A novel screening method for competitive FRET-aptamers applied to / E. coli assay development. J Fluoresc 20:1211-223 CrossRef
    8. Bruno JG, Phillips T, Carrillo MP, Crowell R (2009) Plastic-adherent DNA aptamer-magnetic bead and quantum dot sandwich assay for / Campylobacter detection. J Fluoresc 19:427-35 CrossRef
    9. Bruno JG, Richarte AM, Phillips T, Savage AA, Sivils JC, Greis A, Mayo M (2014) Development of a fluorescent enzyme-linked DNA aptamer-magnetic bead sandwich assay and portable fluorometer for sensitive and rapid / Leishmania detection in sandflies. J Fluoresc 24:267-77 CrossRef
    10. Centers for Disease Control and Prevention (2011) Multistate outbreak of listeriosis associated with Jensen Farms cantaloupe–United States, August-September 2011. MMWR Morb Mortal Week Rep 60:1357-358
    11. Churchill RLT, Lee H, Hall JC (2006) Detection of / Listeria monocytogenes and the toxin listeriolysin O in food. J Microbiol Methods 64:141-70 CrossRef
    12. Duan N, Wu S, Chen X, Huang Y, Xia Y, Ma X, Wang Z (2013) Selection and characterization of aptamers against / Salmonella Typhimurium using whole-bacterium SELEX. J Agric Food Chem In Press
    13. Duan N, Wu S, Zhu C, Ma X, Wang Z, Yu Y, Jiang Y (2012) Dual-color upconversion fluorescence and aptamer-functionalized magnetic nanoparticles-based bioassay for the simultaneous detection of / Salmonella typhimurium and / Staphylococcus aureus. Anal Chim Acta 723:1- CrossRef
    14. Dwivedi HP, Smiley RD, Jaykus LA (2010) Selection and characterization of DNA aptamers with binding selectivity to / Campylobacter jejuni using whole-cell SELEX. Appl Microbiol Biotechnol 87:2323-334 CrossRef
    15. Gómez D, Ari?o A, Carrami?ana JJ, Rota C, Yangüela J (2012) Comparison of sampling procedures for recovery of / Listeria monocytogenes from stainless steel food contact surfaces. J Food Prot 75:1077-082 CrossRef
    16. Goodridge LD, Bledar B (2011) Phage-based biocontrol strategies to reduce foodborne pathogens in foods. Bacteriophage 1:130-37 CrossRef
    17. Gründling A, Burrack LS, Bouwer HGA, Higgin DE (2004) / Listeria monocytogenes regulated flagellar motility gene expression through MogR, a transcriptional repressor required for virulence. Proc Natl Acad Sci U S A 101:12318-2323
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Biomedicine
    Biophysics and Biomedical Physics
    Biotechnology
    Biochemistry
    Analytical Chemistry
  • 出版者:Springer Netherlands
  • ISSN:1573-4994
文摘
A fluorescent DNA aptamer-magnetic bead sandwich assay was developed to detect listeriolysin O (LLO) protein from pathogenic Listeria bacteria using a peroxidase-linked system, Amplex Ultra Red (AUR; derivatized resazurin) substrate, and a custom-designed handheld fluorometer. The assay is highly sensitive with demonstrated limits of detection (LODs) in the range of 4 to 61-em class="a-plus-plus">L. monocytogenes cells or the equivalent LLO produced by 4 to 61 cells on average in separate titration trials. Total assay processing and analysis time was approximately 30 mins. The assay has demonstrated the ability to detect 6 species of Listeria as desired by the USDA’s Food Safety Inspection Service (FSIS). The portable system was designed to be used primarily with surface swab samples from fomites, but it can also be used to assess enrichment cultures. The minimal time to detect a positive enrichment culture in our hands from an initial 10 cell inoculum in 200?ml of broth has been 8?h post-incubation at 37?°C in shaker flask cultures. An optional automated magnetic bead assay processing and wash device capable of simultaneously processing 6 samples with low and consistent fluorescence background for higher volume central laboratories is also described.

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