Related Experiment Video
Updated: Jul 26, 2026

Immuno-fluorescence Assay of Leptospiral Surface-exposed Proteins
Published on: July 1, 2011
Assessment of Listeria monocytogenes Surface Proteins Identified from Proteomics Analysis for Use as Diagnostic
Cathy X Y Zhang1,2, Brian W Brooks1, Hongsheng Huang1
1Ottawa Laboratory Fallowfield, Canadian Food Inspection Agencygrid.418040.9, Ottawa, Ontario, Canada.
Abstract:
The Gram-positive bacterium Listeria monocytogenes is an important pathogen that causes a foodborne illness with a high percentage of fatalities. Surface proteins, specifically expressed from a wide range of L. monocytogenes serotypes under selective enrichment culture conditions, can serve as targets for the detection and isolation of this pathogen using antibody-based methods. Among a number of surface proteins identified by mass spectrometry in a previous proteomic study, six candidates (annotated as LMOf2365_0148, LMOf2365_0312, LMOf2365_0546, LMOf2365_1883, LMOf2365_2111, and LMOf2365_2742) were selected here for investigating their expression in the bacterial cells cultured in vitro by raising rabbit polyclonal antibodies (PAbs) against the recombinant form of each candidate. These protein candidates contained regions conserved among various L. monocytogenes isolates but variable in other Listeria species. LMOf2365_0148, an uncharacterized protein with a LPXTG motif accountable for covalent linkage to the cell wall peptidoglycan, exhibited a strong reaction signal from anti-LMOf2365_0148 PAb binding to the cell surface, as detected by immunofluorescence microscopy. Further study, through the generation of a panel of mouse monoclonal antibodies (MAbs) to the recombinant LMOf2365_0148, showed that one of the MAbs, M3686, reacted to bacterial isolates belonging to all three lineages of L. monocytogenes under Health Canada's standard enrichment culture conditions (MFHPB-07 and MFHPB-30). These results demonstrated the potential of using LMOf2365_0148 as a surface biomarker, in conjunction with specific MAbs developed here, for the isolation and detection of L. monocytogenes from foods and food processing environments. IMPORTANCE Strains of Listeria monocytogenes are differentiated serologically into at least 13 serotypes and grouped phylogenetically into 4 distinct lineages (I, II, III, and IV). No single monoclonal antibody (MAb) reported to date is capable of binding to the surface of L. monocytogenes strains representing all the serotypes. This study assessed the expression of six surface proteins selected from a previous proteomic study and demonstrated that surface protein LMOf2365_0148 has the greatest potential as a surface biomarker. A panel of 24 MAbs to LMOf2365_0148 were assessed extensively, revealing that one of the MAbs, M3686, reacted to a wide range of L. monocytogenes isolates (lineage I, II, and III isolates) grown under standard enrichment culture conditions and thus led to the conclusion that LMOf2365_0148 is a useful novel surface biomarker for identifying, detecting, and isolating the pathogen from food and environmental samples.
Insights
This study identifies a novel surface protein, LMOf2365_0148, in Listeria monocytogenes. A specific antibody, M3686, can detect this protein across multiple L. monocytogenes lineages, aiding in pathogen detection.
Area of Science:
- Microbiology
- Immunology
- Food Safety
Background:
- Listeria monocytogenes is a dangerous foodborne pathogen with high fatality rates.
- Surface proteins of L. monocytogenes can be targeted for detection and isolation.
- Previous proteomic studies identified potential surface protein candidates.
Purpose of the Study:
- To investigate the expression of six candidate surface proteins in L. monocytogenes.
- To develop and characterize antibodies for specific L. monocytogenes surface proteins.
- To evaluate LMOf2365_0148 as a potential biomarker for pathogen detection.
Main Methods:
- Recombinant expression of six candidate surface proteins.
- Generation of rabbit polyclonal antibodies (PAbs) against candidate proteins.
- Immunofluorescence microscopy to detect surface protein expression.
- Development of mouse monoclonal antibodies (MAbs) against LMOf2365_0148.
- Testing MAb reactivity against L. monocytogenes isolates from different lineages.
Main Results:
- LMOf2365_0148 showed strong surface expression via immunofluorescence.
- One MAb, M3686, reacted with L. monocytogenes isolates from lineages I, II, and III.
- The reactivity of M3686 was confirmed under standard food enrichment conditions.
Conclusions:
- LMOf2365_0148 is a promising surface biomarker for L. monocytogenes.
- The MAb M3686 demonstrates broad reactivity across L. monocytogenes lineages.
- This biomarker and antibody combination can improve pathogen detection and isolation from food and environmental samples.

