S GORDONII AS A VECTOR FOR P GINGIVALIS FIMBRILLIN
S GORDONII AS A VECTOR FOR P GINGIVALIS FIMBRILLIN
批准号:
2372351
负责人:
Ashu Sharma
金额:
$16.85万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-20 至 2000-09-19
关键词:
Bacteroides gingivalis Streptococcus antibiotics antigen antibody reaction bacterial proteins bactericidal immunity biotechnology drug design /synthesis /production genetic strain implant laboratory rat microorganism interaction microorganism mass culture oral bacteria periodontium disorder pilus recombinant DNA transfection virulence
中文摘要
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英文摘要
DESCRIPTION (Adapted from the investigator's Abstract): The broad,
long-term goal of this project is to develop a system for continuous
production of biologically active factors which block mucosal infections.
The applicant proposes the development of genetically engineered strains of
the commensal organism, Streptococcus gordonii, which expresses
Porphyromonas gingivalis fimbrillin polypeptides capable of blocking
adherence, and of inducing a protective immune response. The specific aims
are: (1) to further characterize the expression system recently developed
in our laboratory for P. gingivalis fimbrillin on the surface of S.
gordonii; (2) to optimize a secretion system in S. gordonii for the
production of P. gingivalis fimbrillin; and (3) to test these genetically
engineered strains of S. gordonii in the rat model of periodontal disease
for reduction of colonization with P. gingivalis and for protection against
destructive periodontitis. S. gordonii was selected since it is a
non-pathogenic commensal organism, universally found in the human oral
cavity, and strains have been genetically engineered to express foreign
antigens. P. gingivalis is an important pathogen in a well-established
model of mucosal infection, periodontal disease, and its fimbrillin subunit
was selected since it has been cloned and sequenced. Furthermore, P.
gingivalis fimbrillin domains involved in adherence and in the immune
response have been determined. Recombinant S. gordonii strains have been
generated that express biologically active domains of fimbrillin and have
shown that they are able to generate fimbrillin-specific immune response in
rats following oral colonization as well as after parenteral immunization.
Rats infected with P. gingivalis were selected as a model of mucosal
infection in which to study the early steps in the disease process, namely
adherence and colonization, since it is well characterized and provides a
useful model to assess in vivo efficacy of a genetically engineered
commensal organism producing factors which interfere with virulence.
Therefore, studies are proposed to generate recombinant strains of S.
gordonii able to either secrete or surface express important fimbrillin
peptides, and capable of modulating P. gingivalis infection in a rat model
of periodontal disease. Such genetically engineered strains of S. gordonii
expressing fimbrillin peptides may be used as a vaccine against P.
gingivalis infection, and as a model to study this novel approach to
vaccines for other mucosal infections. The model can also be used for
evaluating the utility of continuously expressed biologically active
molecules by commensal organisms, directed to block colonization and other
key early stages in the pathogenesis of mucosal infections.
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Tannerella forsythia intercations with host cells and other bacteria
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Tannerella forsythia intercations with host cells and other bacteria
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S GORDONII AS A VECTOR FOR P GINGIVALIS FIMBRILLIN
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