Phage-ELISA for ultrasensitive detection of Salmonella enteritidis

Mangmang Shen1, Chang Ni1, Jiasheng Yuan1

  • 1College of Veterinary Medicine, Institute of Comparative Medicine, Yangzhou University, Yangzhou 225009, China. zhou_xin@126.com.

The Analyst
|January 16, 2025
PubMed

Insights

Researchers developed a sensitive phage-ELISA for detecting Salmonella enteritidis. This method uses single-chain variable fragment (scFv) phage display technology for enhanced pathogen identification.

Area of Science:

  • Biotechnology
  • Immunology
  • Microbiology

Background:

  • M13 phage displaying single-chain variable fragments (scFv) are crucial for constructing antibody libraries.
  • Phage display facilitates the identification of antibodies with high specificity and affinity.

Purpose of the Study:

  • To construct an scFv phage display library targeting "Salmonella enteritidis" (strain C50041).
  • To develop a highly sensitive phage-ELISA for detecting "Salmonella enteritidis".

Main Methods:

  • Immunization of mice with "Salmonella enteritidis" and extraction of splenic cells.
  • Construction of the C50041-M13-scFv library and biopanning to isolate high-affinity clones.
  • Expression and validation of scFv-4 antibody and development of a phage-ELISA using HRP-conjugated antibodies.

Main Results:

  • A high-affinity phage clone (C50041-scFv-4) targeting "Salmonella enteritidis" was successfully isolated.
  • The derived scFv antibody (scFv-4) demonstrated high specificity and affinity for the target bacteria.
  • The developed phage-ELISA achieved a sensitivity of 10^4 CFU mL^-1, surpassing traditional ELISA by one order of magnitude.

Conclusions:

  • The study successfully established a robust scFv phage display library and a highly sensitive phage-ELISA for "Salmonella enteritidis" detection.
  • The phage-ELISA offers broad applicability for detecting various pathogens, including bacteria and viruses.
  • This technology provides an improved platform for sensitive and specific pathogen detection.