Infection and Immunity, January 2001, p. 622-625, Vol. 69, No. 1
Department of Microbial Pathogenesis and
Vaccine Research, Division of Microbiology, GBF-German Research
Centre for Biotechnology, D-38124 Braunschweig, Germany
Received 19 July 2000/Returned for modification 12 September
2000/Accepted 12 October 2000
Fibronectin-binding protein I (SfbI) represents a major adhesin of
Streptococcus pyogenes. Mice were intranasally immunized with recombinant proteins spanning different portions of SfbI to
identify the minimal fragment able to elicit a protective response against a lethal challenge with S. pyogenes. The strongest
cellular responses and the highest levels of antigen-specific secretory immunoglobulin A (IgA) were detected in mice immunized with the fibronectin-binding region of SfbI. In contrast, animals vaccinated with a polypeptide spanning the aromatic and proline-rich regions showed the highest titers and fastest IgG response in serum.
Vaccination with either SfbI without a membrane anchor and signal
peptide or a polypeptide encompassing its fibronectin-binding regions resulted in efficient protection against heterologous challenge (60%
and 80%, respectively), whereas the use of a polypeptide lacking this
region conferred marginal protection (10%) with respect to the control
group (0%). These results demonstrate that the fibronectin-binding
region of SfbI is a promising candidate antigen for developing
anti-S. pyogenes vaccines.
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.622-625.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Characterization of the Domain of Fibronectin-Binding Protein I
of Streptococcus pyogenes Responsible for Elicitation of
a Protective Immune Response
*
Corresponding author. Mailing address: Vaccine Research
Group, Department of Microbial Pathogenesis and Vaccine Research, Division of Microbiology, GBF-German Research Centre for Biotechnology, Mascheroder Weg 1, D-38124 Braunschweig, Germany. Phone:
(49-531)6181558. Fax: (49-531)6181411. E-mail: cag{at}gbf.de.
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