Induction of neutralizing antibodies in mice immunized with an amino-terminal polypeptide of Streptococcus mutans P1 protein produced by a recombinant Bacillus subtilis strain


Autoria(s): TAVARES, Milene B.; SILVA, Bruno M.; CAVALCANTE, Rafael C. M.; SOUZA, Renata D.; LUIZ, Wilson B.; PACCEZ, Juliano D.; CROWLEY, Paula J.; BRADY, L. Jeannine; FERREIRA, Luis C. S.; FERREIRA, Rita C. C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

The oral pathogen Streptococcus mutans expresses a surface protein, P1, which interacts with the salivary pellicle on the tooth surface or with fluid-phase saliva, resulting in bacterial adhesion or aggregation, respectively. P1 is a target of protective immunity. Its N-terminal region has been associated with adhesion and aggregation functions and contains epitopes recognized by efficacious antibodies. In this study, we used Bacillus subtilis, a gram-positive expression host, to produce a recombinant N-terminal polypeptide of P1 (P1(39-512)) derived from the S. mutans strain UA159. Purified P1(39-512) reacted with an anti-full-length P1 antiserum as well as one raised against intact S. mutans cells, indicating preserved antigenicity. Immunization of mice with soluble and heat-denatured P1(39-512) induced antibodies that reacted specifically with native P1 on the surface of S. mutans cells. The anti-P1(39-512) antiserum was as effective at blocking saliva-mediated aggregation of S. mutans cells and better at blocking bacterial adhesion to saliva-coated plastic surfaces compared with the anti-full-length P1 antiserum. In addition, adsorption of the anti-P1 antiserum with P1(39-512) eliminated its ability to block the adhesion of S. mutans cells to abiotic surfaces. The present results indicate that P1(39-512), expressed and purified from a recombinant B. subtilis strain, maintains important immunological features of the native protein and represents an additional tool for the development of anticaries vaccines.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional do Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

National Institute for Dental and Craniofacial Research

National Institute for Dental and Craniofacial Research[R01 DE13882]

Identificador

FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, v.59, n.2, p.131-142, 2010

0928-8244

http://producao.usp.br/handle/BDPI/28413

10.1111/j.1574-695X.2010.00669.x

http://dx.doi.org/10.1111/j.1574-695X.2010.00669.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

Fems Immunology and Medical Microbiology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #Streptococcus mutans #P1 protein #recombinant proteins #Bacillus subtilis #antibody responses #saliva-binding region #LOCAL PASSIVE-IMMUNIZATION #GRAM-POSITIVE BACTERIA #SALIVA-BINDING REGION #ANTIGEN-I/II FAMILY #RICH REPEAT DOMAIN #MONOCLONAL-ANTIBODIES #DENTAL-CARIES #ALANINE-RICH #SEROTYPE-C #MUCOSAL IMMUNIZATION #Immunology #Infectious Diseases #Microbiology
Tipo

article

original article

publishedVersion