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Monoclonal antibodies that react with live Listeria spp
R Torensma1, M J Visser, C J Aarsman
1Eijkman-Winkler Laboratory for Medical Microbiology, University Hospital Utrecht, The Netherlands.
Applied and Environmental Microbiology
|August 1, 1993
Summary
Seven new monoclonal antibodies (MAbs) targeting Listeria spp. were developed. MAb 55-23 showed broad reactivity, while others displayed varied patterns, highlighting potential for Listeria detection.
Area of Science:
- Immunology
- Microbiology
- Biotechnology
Background:
- Listeria species are significant foodborne pathogens.
- Accurate and sensitive detection methods are crucial for public health.
- Monoclonal antibodies (MAbs) offer specificity in diagnostic assays.
Purpose of the Study:
- To develop and characterize monoclonal antibodies (MAbs) for detecting live Listeria species.
- To evaluate the reactivity and specificity of these MAbs against various Listeria strains and other bacteria.
- To compare antibody performance using different immunoassay formats.
Main Methods:
- Development of seven monoclonal antibodies (MAbs) against Listeria spp.
- Testing MAb reactivity with live Listeria strains representing different serotypes.
- Comparative analysis of MAb performance using magnetic immunoluminescence assay and whole-cell enzyme-linked immunosorbent assay (ELISA).
- Western blot analysis to assess MAb reactivity with specific antigens.
Main Results:
- Two immunoglobulin M (IgM) and five immunoglobulin G (IgG) MAbs were generated.
- MAb 55-23 demonstrated broad reactivity against 148 out of 157 Listeria strains tested.
- Specific MAbs showed reactivity towards particular serotypes (e.g., 4b, 1/2a).
- Significant differences in MAb reactivity were observed between magnetic immunoluminescence and whole-cell ELISA.
- Minimal cross-reactivity was noted with Streptococcus spp., but not with Bacillus spp., E. coli, or Citrobacter sp.
- MAbs 55-23, 55-44, and 34-9 showed reactivity in Western blot assays.
Conclusions:
- The developed MAbs, particularly MAb 55-23, show promise for the specific detection of Listeria species.
- Assay format significantly impacts MAb performance, necessitating careful selection for diagnostic applications.
- Further characterization is needed to fully understand the antigenic targets and optimize MAb utility.