MOLECULAR ANALYSIS OF T. DENTICOLA-HOST INTERACTIONS
MOLECULAR ANALYSIS OF T. DENTICOLA-HOST INTERACTIONS
批准号:
6784713
负责人:
J CHRISTOPHER FENNO
金额:
$24.08万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-04-15 至 2006-07-31
关键词:
Treponema infectionbacterial cytopathogenic effectbacterial geneticsbacterial proteinsdental plaqueenzyme complexepitope mappingextracellular matrixgene expressiongenetic librarygenetic regulatory elementhost organism interactionhuman tissueimmunologic assay /testlaboratory rabbitmembrane proteinsmolecular pathologymutantnucleic acid sequenceperiodontium disorderpolymerase chain reactionprotein structure functiontissue /cell culturevirulenceyeast two hybrid system
中文摘要
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英文摘要
DESCRIPTION: The predominance of spirochetes in subgingival plaque associated
with severe periodontal lesions suggests an important role in periodontal
pathogenesis. The goal of this research is to characterize interactions of
Treponema denticola with subgingival tissues at the molecular level. By
focusing on analysis of surface-expressed proteins that directly affect host
cells, insights will be gained into mechanisms of periodontal cytopathology.
The major outer membrane protein (Msp) of T. denticola binds to cells and ECM
components, and has pore-forming cytotoxic activity. Msp is genetically
conserved in many oral spirochetes, yet shows considerable inter-strain
heterogeneity, suggesting that it is an important immunogen. The overall
hypothesis is that Msp is a significant virulence determinant in periodontal
disease, and is a key component of an outer membrane protein complex mediating
interactions of the spirochete with subgingival tissue.
Specific Aims of the proposed research, and the individual hypotheses to be
tested are: 1) to characterize T. denticola proteins associated with Msp
expression. Outer membrane components other than Msp are required for native
Msp expression and assembly of the native outer membrane complex. Isogenic
mutants and recombinant expression systems will be used to characterize these
processes. 2) to identify immunodominant and functional domains of Msp.
Antigenic heterogeneity of Msp is a factor in host antibody recognition of oral
spirochetes. Archived serum samples will be screened for reactivity with
specific Msps. Genes encoding novel Msps will be identified in patient plaque
samples. 3) to characterize the role of Msp in cytopathic cellular responses to
T. denticola. The ability of parent and msp mutant strains to bind host cells,
ECM and serum components, and to activate pro-inflammatory cellular responses
will be assayed. A putative Msp receptor identified on epithelial cell surfaces
will be characterized.
These studies, which involve both genetic and biochemical analyses, are
intended to contribute significantly to the understanding of microbe-host
interactions in the etiology of periodontal diseases, and to basic knowledge of
the molecular biology of pathogenic spirochetes.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
Expression of Treponema denticola oligopeptidase B in Escherichia coli.
齿垢密螺旋体寡肽酶 B 在大肠杆菌中的表达。
DOI:
10.1007/s00284-003-4168-4
发表时间:
2004
期刊:
Current microbiology.
影响因子:
--
作者:
[Lee,SiYoung, Fenno,JChristopher]
通讯作者:
Fenno,JChristopher
Characterization of Treponema denticola pyrF encoding orotidine-5'-monophosphate decarboxylase.
编码乳清苷-5-单磷酸脱羧酶的密螺旋体pyrF的表征。
DOI:
10.1111/j.1574-6968.2006.00589.x
发表时间:
2007
期刊:
FEMS microbiology letters
影响因子:
2.1
作者:
[Capone,RicardoF, Ning,Yu, Pakulis,Nora, Alhazzazi,Turki, ChristopherFenno,J]
通讯作者:
ChristopherFenno,J
Analysis of a unique interaction between the complement regulatory protein factor H and the periodontal pathogen Treponema denticola.
补体调节蛋白 H 因子与牙周病原体齿垢密螺旋体之间独特相互作用的分析。
DOI:
10.1128/iai.01544-08
发表时间:
2009
期刊:
Infection and immunity
影响因子:
3.1
作者:
[McDowell,JohnV, Huang,Bernice, Fenno,JChristopher, Marconi,RichardT]
通讯作者:
Marconi,RichardT
Oral Treponema Surface Proteins: Host Cell Interactions
-
批准号:9096755
-
项目类别:
-
资助金额:$60.81万
-
财政年份:2015
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Oral Treponema Surface Proteins: Host Cell Interactions
-
批准号:8941164
-
项目类别:
-
资助金额:$64.12万
-
财政年份:2015
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Treponema - Host Cell and Tissue Interactions
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批准号:10366859
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项目类别:
-
资助金额:$61.88万
-
财政年份:2015
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Treponema - Host Cell and Tissue Interactions
-
批准号:10551350
-
项目类别:
-
资助金额:$59.53万
-
财政年份:2015
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Oral Treponema Surface Proteins: Host Cell Interactions
-
批准号:9274236
-
项目类别:
-
资助金额:$67.34万
-
财政年份:2015
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Treponomics: enhanced tools for genetic manipulation in spirochetes
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批准号:8489671
-
项目类别:
-
资助金额:$21.4万
-
财政年份:2013
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Treponomics: enhanced tools for genetic manipulation in spirochetes
-
批准号:8719805
-
项目类别:
-
资助金额:$19.43万
-
财政年份:2013
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Surface protein complexes of oral treponemes: assembly and host cell interactions
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批准号:7826782
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项目类别:
-
资助金额:$38.63万
-
财政年份:2009
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Surface protein complexes of oral treponemes: assembly and host cell interactions
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批准号:7464047
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项目类别:
-
资助金额:$36.58万
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财政年份:2009
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Choline phosphotransferase-dependent phospholipid synthesis in Treponema
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批准号:7509591
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项目类别:
-
资助金额:$26.6万
-
财政年份:2008
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
Choline phosphotransferase-dependent phospholipid synthesis in Treponema
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批准号:7640752
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项目类别:
-
资助金额:$15.2万
-
财政年份:2008
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
MOLECULAR ANALYSIS OF T. DENTICOLA-HOST INTERACTIONS
-
批准号:6498089
-
项目类别:
-
资助金额:$24.08万
-
财政年份:2001
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
MOLECULAR ANALYSIS OF T. DENTICOLA-HOST INTERACTIONS
-
批准号:6332416
-
项目类别:
-
资助金额:$25.24万
-
财政年份:2001
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
MOLECULAR ANALYSIS OF T. DENTICOLA-HOST INTERACTIONS
-
批准号:6628523
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项目类别:
-
资助金额:$24.08万
-
财政年份:2001
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
The OppA PEPTIDE Permease HOMOLOGUE OF ORAL SPIROCHETES
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批准号:6379961
-
项目类别:
-
资助金额:$3.79万
-
财政年份:2000
-
负责人:J CHRISTOPHER FENNO
-
依托单位:
OPPA PEPTIDE HOMOLOGUE OF ORAL SPIROCHETES
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批准号:6133526
-
项目类别:
-
资助金额:$3.79万
-
财政年份:2000
-
负责人:J CHRISTOPHER FENNO
-
依托单位: