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Vaccine2009; 27(36); 4923-4929; doi: 10.1016/j.vaccine.2009.06.042

Impact of immunization against SpyCEP during invasive disease with two streptococcal species: Streptococcus pyogenes and Streptococcus equi.

Abstract: Currently there is no licensed vaccine against the human pathogen Streptococcus pyogenes. The highly conserved IL-8 cleaving S. pyogenes cell envelope proteinase SpyCEP is surface expressed and is a potential vaccine candidate. A recombinant N-terminal part of SpyCEP (CEP) was expressed and purified. AntiCEP antibodies were found to neutralize the IL-8 cleaving activity of SpyCEP. CEP-immunized mice had reduced bacterial dissemination from focal S. pyogenes intramuscular infection and intranasal infection. We also identified a functional SpyCEP-homolog protease SeCEP, expressed by the equine pathogen Streptococcus equi, which was able to cleave both human and equine IL-8. CEP-immunized mice also demonstrated reduced bacterial dissemination from S. equi intramuscular infection. Therefore immunization against SpyCEP may provide protection against other streptococci species with homologous proteases.
Publication Date: 2009-06-27 PubMed ID: 19563892PubMed Central: PMC2759039DOI: 10.1016/j.vaccine.2009.06.042Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article explores the potential of using immunization against SpyCEP, a proteinase found in Streptococcus pyogenes, to protect against infection. The study found that antiCEP antibodies neutralized the IL-8 cleaving activity of SpyCEP, which reduced bacterial spread in mice. Interestingly, the findings also suggest that immunization against SpyCEP could potentially offer protection against other streptococcal species with similar proteases.

Introduction to the Research

  • At the present, there is no licensed vaccine against Streptococcus pyogenes, a harmful human pathogen.
  • This study investigated the potential of using a conserved proteinase called SpyCEP, found on the cell surface of S. pyogenes, as a vaccine candidate.

Study Methodology

  • The researchers created a recombinant, or genetically engineered, N-terminal part of SpyCEP, referred to as CEP.
  • They then purified this CEP for use in their study.

Results and Findings

  • It was found that antibodies against CEP (known as antiCEP antibodies) effectively neutralized the function of SpyCEP that cleaves IL-8, a protein responsible for attracting neutrophils, a type of white blood cell involved in fighting infections.
  • This neutralization activity thus limited the ability of the bacteria to spread within the host.
  • In mice, it was observed that immunization with CEP led to a reduction in bacterial dissemination from a local S. pyogenes infection, both when the bacterium was introduced via an intramuscular route and through an intranasal route.

Additional Findings

  • The researchers also identified a SpyCEP-equivalent, SeCEP, in Streptococcus equi, a pathogen commonly found in horses.
  • SeCEP was also found to cleave both human and equine IL-8.
  • Interestingly, mice immunized with CEP showed a reduced spread of S. equi infection as well.

Implications of the Research

  • These results suggest that immunizing against SpyCEP may have the broader potential of providing protection against other species of streptococci that express similar proteases.
  • The exploration of SpyCEP as a potential vaccine candidate holds promise in future immunization strategies against S. pyogenes and possibly a range of other streptococci bacteria.

Cite This Article

APA
Turner CE, Kurupati P, Wiles S, Edwards RJ, Sriskandan S. (2009). Impact of immunization against SpyCEP during invasive disease with two streptococcal species: Streptococcus pyogenes and Streptococcus equi. Vaccine, 27(36), 4923-4929. https://doi.org/10.1016/j.vaccine.2009.06.042

Publication

ISSN: 1873-2518
NlmUniqueID: 8406899
Country: Netherlands
Language: English
Volume: 27
Issue: 36
Pages: 4923-4929

Researcher Affiliations

Turner, Claire E
  • Department of Infectious Diseases & Immunity, Hammersmith Hospital, Du Cane Road, London, W12 0NN, United Kingdom.
Kurupati, Prathiba
    Wiles, Siouxsie
      Edwards, Robert J
        Sriskandan, Shiranee

          MeSH Terms

          • Amino Acid Sequence
          • Animals
          • Antibodies, Bacterial / immunology
          • Antigens, Bacterial / immunology
          • Colony Count, Microbial
          • Liver / microbiology
          • Mice
          • Molecular Sequence Data
          • Neutralization Tests
          • Peptide Hydrolases / immunology
          • Sequence Alignment
          • Spleen / microbiology
          • Streptococcal Infections / prevention & control
          • Streptococcal Infections / therapy
          • Streptococcal Vaccines / immunology
          • Streptococcus equi / immunology
          • Streptococcus pyogenes / immunology
          • Vaccines, Synthetic / immunology

          Grant Funding

          • BB/E52708X/1 / Biotechnology and Biological Sciences Research Council
          • G0800777 / Medical Research Council
          • Wellcome Trust

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