مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

173
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

110
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Development of a rapid, one-step-visual method to detect Salmonella based on IC-LAMP method

Pages

  20-25

Abstract

 Background: Salmonella can cause serious human gastroenteritis and is frequently isolated from various food samples. The cell culturing, immunoassay, and polymerase chain reactions (PCR) are the current methods to detect such pathogenic agents. However, these methods are time-consuming and labor-intensive, and thus unavailable for rapid-monitoring of Salmonella. Aims: This study aimed to develop an immunocapture-loop-mediated isothermal amplification (IC-LAMP) for rapid and sensitive Detection of Salmonella. Methods: Salmonella was used as antigen to produce Monoclonal antibody (mAb) and mAbs were prepared via subcloning three times. The mAb 1B12 with high affinity was coated on the surface of the immuno-magnetic beads (IMBs) to capture Salmonella. The enriched products (IMBs-Salmonella) were used for LAMP using the special primers targeted the conserved invA gene of Salmonella. Results: The IC-LAMP was developed based on mAb 1B12 and LAMP. Targeting the conserved invA gene of Salmonella, the Detection time was shortened to 50 min from three days. If the reaction contains Salmonella, the green fluorescence and the trapezoidal strip can be clearly observed. Importantly, the method combines the specificity of antibody and LAMP with a Detection limit of 5 CFU/ml in artificially contaminated water and milk. The specificity of this method was demonstrated by testing other similar bacteria. The results indicate that the IC-LAMP reacts only with Salmonella and does not crossreact with other similar bacteria. Conclusion: The IC-LAMP assay developed here is a rapid, sensitive, one-step-visual method to screen for the presence of Salmonella in food samples. This method is faster than traditional PCR, LAMP, and other methods, and can be used as a primary screening method for the Detection.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    ZHANG, L., DU, X., CHEN, C., HAN, Q., CHEN, Q., ZHANG, M., XIA, X., SONG, Y., & ZHANG, J.. (2020). Development of a rapid, one-step-visual method to detect Salmonella based on IC-LAMP method. IRANIAN JOURNAL OF VETERINARY RESEARCH (IJVR), 21(1 (70)), 20-25. SID. https://sid.ir/paper/744616/en

    Vancouver: Copy

    ZHANG L., DU X., CHEN C., HAN Q., CHEN Q., ZHANG M., XIA X., SONG Y., ZHANG J.. Development of a rapid, one-step-visual method to detect Salmonella based on IC-LAMP method. IRANIAN JOURNAL OF VETERINARY RESEARCH (IJVR)[Internet]. 2020;21(1 (70)):20-25. Available from: https://sid.ir/paper/744616/en

    IEEE: Copy

    L. ZHANG, X. DU, C. CHEN, Q. HAN, Q. CHEN, M. ZHANG, X. XIA, Y. SONG, and J. ZHANG, “Development of a rapid, one-step-visual method to detect Salmonella based on IC-LAMP method,” IRANIAN JOURNAL OF VETERINARY RESEARCH (IJVR), vol. 21, no. 1 (70), pp. 20–25, 2020, [Online]. Available: https://sid.ir/paper/744616/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops

  • No record.





  • Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button