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Development and Characterization of Mouse Monoclonal Antibodies Specific for Clostridiodes (Clostridium) difficile Lipoteichoic Acid
- Source :
- ACS Chemical Biology. 15:1050-1058
- Publication Year :
- 2020
- Publisher :
- American Chemical Society (ACS), 2020.
-
Abstract
- Clostridiodes (Clostridium) difficile is an anaerobic Gram-positive, spore-forming nosocomial, gastrointestinal pathogen causing C. difficile-associated disease with symptoms ranging from mild cases of antibiotic-associated diarrhea to fatal pseudomembranous colitis. We developed murine monoclonal antibodies (mAbs) specific for a conserved cell surface antigen, lipoteichoic acid (LTA)of C. difficile. The mAbs were characterized in terms of their thermal stability, solubility, and their binding to LTA by surface plasmon resonance and competitive ELISA. Synthetic LTA molecules were prepared in order to better define the minimum epitope required to mimic the natural antigen, and three repeat units of the polymer were required for optimal recognition. One of the murine mAbs was chimerized with human constant region domains and was found to recognize the target antigen identically to the mouse version. These mAbs may be useful as therapeutics (standalone, in conjunction with known antitoxin approaches, or as delivery vehicles for antibody drug conjugates targeting the bacterium), as diagnostic agents, and in infection control applications.
- Subjects :
- 0301 basic medicine
biology
010405 organic chemistry
Chemistry
medicine.drug_class
General Medicine
Pseudomembranous colitis
Clostridium difficile
Monoclonal antibody
01 natural sciences
Biochemistry
Epitope
0104 chemical sciences
Microbiology
03 medical and health sciences
030104 developmental biology
Antigen
biology.protein
medicine
Molecular Medicine
Lipoteichoic acid
Antibody
Antitoxin
Subjects
Details
- ISSN :
- 15548937 and 15548929
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- ACS Chemical Biology
- Accession number :
- edsair.doi.dedup.....e007aaae88b69d3678f4bca5a4f06124
- Full Text :
- https://doi.org/10.1021/acschembio.0c00066