Protection against Streptococcus equi infection by monoclonal antibodies against an M-like protein.
Abstract: We have developed an in vivo passive transfer assay using mice to identify monoclonal antibodies (mAbs) which offer protection against Streptococcus equi infection. The assay was developed using serum antibodies collected from horses convalescing from strangles. In this study, we show that a preparation of M-like protein, acid-extracted from S. equi, affords 80% protection to mice immunized with it. A number of mouse mAbs directed against a preparation of M-like protein were then assessed for their ability to passively protect mice against challenge with a lethal dose of the bacteria. Two mAbs, 1D10 and 2A6, were shown to be highly protective. It was also demonstrated, by means of a competitive enzyme immunoassay, that these mAbs recognized different epitopes in the preparation. Examination of a dose-response curve for mAbs 1D10 and 2A6 revealed that optimal levels of protection were achieved using 1 mg of either 1D10 or 2A6, or 0.5 mg 1D10 and 0.5 mg 2A6 given together. Immunological reactivity of these mAbs with a preparation of M-like protein showed that the antigens they recognized were comparable in size to some of the antigens recognized by convalescent horse serum antibodies. The role of immunoglobulin isotype in conferring protection is discussed.
Publication Date: 1991-09-01 PubMed ID: 1721084DOI: 10.1099/00221287-137-9-2125Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research article explores the protection offered against Streptococcus equi infection by using monoclonal antibodies (mAbs) against an M-like protein. The study identified two specific mAbs, 1D10 and 2A6, capable of providing significant protection against a lethal dose of the bacteria.
Research Methodology
- The researchers developed a passive transfer assay in mice as a mode of identifying mAbs which could provide protection against Streptococcus equi, a bacterium causing equine strangles, an infectious, contagious disease in horses.
- The assay used serum antibodies harvested from horses which were recovering from strangles. These antibodies were then introduced to mice.
- They also applied a preparation of an M-like protein, extracted from S. equi, on the mice. They observed it provided 80% protection to the mice against the infection.
Findings
- The team assessed a number of mouse mAbs that were directed against a preparation of M-like protein for their protective ability against a lethal dose of the bacteria.
- Two mAbs, designated 1D10 and 2A6, were found to be highly protective.
- Through a competitive enzyme immunoassay, it was shown that these antibodies recognized different epitopes or antigen binding sites in the preparation.
- Further examination of the dose-response curve for mAb 1D10 and 2A6 indicated that optimal protection levels were achieved with either 1 mg of 1D10 or 2A6, or a combination of 0.5 mg of 1D10 and 0.5 mg of 2A6.
Additional Observations and Inferences
- The immunological reactivity of mAbs 1D10 and 2A6 with the M-like protein preparation revealed that the antigens they recognized were similar in size to some of the antigens recognized by the antibodies from the convalescent horse serum.
- This might suggest that these antibodies target the same antigens that are recognized by the immune system during natural infection, potentially making them efficacious therapeutic options.
- The role of immunoglobulin isotype, a class of antibody that differs in their type of heavy chain, in providing protection was also discussed as a topic of further study. Isotype may play a role in the specificity and overall effectiveness of the targeted immune response.
Significance of Research
- This study contributes to the ongoing efforts in developing effective antibody-based therapies against bacterial infections, specifically Streptococcus equi. It provides insight into how specific mAbs could potentially be used to guard against detrimental bacterial infections in not only horses, but potentially other animals or even humans.
- The results could be instrumental in the development of targeted vaccinations and therapies by aiding our understanding of how these antibodies interact with their specific antigens.
Cite This Article
APA
Jean-François MJ, Poskitt DC, Turnbull SJ, Macdonald LM, Yasmeen D.
(1991).
Protection against Streptococcus equi infection by monoclonal antibodies against an M-like protein.
J Gen Microbiol, 137(9), 2125-2133.
https://doi.org/10.1099/00221287-137-9-2125 Publication
Researcher Affiliations
- Commonwealth Serum Laboratories, Research and Development Division, Parkville, Victoria, Australia.
MeSH Terms
- Animals
- Antibodies, Monoclonal / immunology
- Antibodies, Monoclonal / therapeutic use
- Antigens, Bacterial / immunology
- Bacterial Outer Membrane Proteins
- Bacterial Proteins / immunology
- Carrier Proteins
- Electrophoresis, Polyacrylamide Gel
- Epitopes
- Hemagglutination
- Horse Diseases / immunology
- Horse Diseases / microbiology
- Horse Diseases / prevention & control
- Horses
- Immunization, Passive
- Mice
- Streptococcal Infections / immunology
- Streptococcal Infections / prevention & control
- Streptococcal Infections / veterinary
Citations
This article has been cited 4 times.- Timoney JF, Suther P, Velineni S, Artiushin SC. The Antiphagocytic Activity of SeM of Streptococcus equi Requires Capsule.. J Equine Sci 2014;25(2):53-6.
- Fan H, Wang Y, Tang F, Lu C. Determination of the mimic epitope of the M-like protein adhesin in swine Streptococcus equi subsp. zooepidemicus.. BMC Microbiol 2008 Oct 7;8:170.
- Bisno AL, Collins CM, Turner JC. M proteins of group C streptococci isolated from patients with acute pharyngitis.. J Clin Microbiol 1996 Oct;34(10):2511-5.
- Boschwitz JS, Timoney JF. Inhibition of C3 deposition on Streptococcus equi subsp. equi by M protein: a mechanism for survival in equine blood.. Infect Immun 1994 Aug;62(8):3515-20.
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