Polymorphic membrane proteins of Chlamydia trachomatis
Polymorphic membrane proteins of Chlamydia trachomatis
批准号:
6572647
负责人:
RU-CHING HSIA
金额:
$31.68万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-05-01 至 2005-04-30
关键词:
Chlamydia trachomatis adolescence (12-20) antibody bacterial genetics bacterial proteins clinical research confocal scanning microscopy enzyme linked immunosorbent assay gene expression genetic polymorphism human subject immunoelectron microscopy interview longitudinal human study membrane proteins microorganism culture polymerase chain reaction questionnaires sexually transmitted diseases young adult human (21-34)
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Chlamydial polymorphic membrane proteins (Pmps) are a newly identified family of Chlamydia-specific membrane proteins, whose role in chlamydial biology and pathogenesis is unknown. Genomic analysis of the prop family of C. pneumoniae has revealed frameshift mutations, deletions and gene duplications. Studies of the larger pmp families of C. pneumoniae and C. psittaci have also revealed that Pmp proteins are expressed in vitro, that some can be detected at the elementary body surface, and that some are dominant antigens during infection and may be targets for vaccine design. The emerging evidence is consistent with a role of the prop gene family in pathogenesis and immune evasion. The purpose of this project is to characterize the smallest pmp gene family identified to date: the 9-member family of C. trachomatis. In preliminary studies using the 9 partially purified recombinant Pmps as target antigens, I have observed differential Pmp-specific antibody responses in archived sera from patients with pelvic inflammatory disease. This analysis will be expanded through cross-sectional and longitudinal comparisons of Pmp-specific responses in a well-characterized patient population with genital C. trachomatis infection. This analysis may identify direct relationships between Pmp-specific responses and disease outcome. A second focus of this project will be to identify and characterize genetic and molecular determinants of Pmp expression in C. trachomatis. Polymorphisms will be identified and compared in the pmp families of selected study isolates. Experiments will be performed to characterize developmental patterns of pmp expression in these isolates. Using a panel of Pmp-specific monoclonal and polyclonal antibodies generated in this project, I will examine Pmp protein expression and eventual translocation to the surface of the outer membrane along development and at the single cell level using laser scanning confocal fluorescence microscopy.
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DOI:
10.1111/j.1462-5822.2011.01598.x
发表时间:
2011-07
期刊:
Cellular microbiology
影响因子:
3.4
作者:
[Carrasco JA, Tan C, Rank RG, Hsia RC, Bavoil PM]
通讯作者:
Bavoil PM
DOI:
10.1111/j.1462-5822.2009.01389.x
发表时间:
2010-02
期刊:
Cellular microbiology
影响因子:
3.4
作者:
[Tan C, Hsia RC, Shou H, Carrasco JA, Rank RG, Bavoil PM]
通讯作者:
Bavoil PM
Kinematics of intracellular chlamydiae provide evidence for contact-dependent development.
细胞内衣原体的运动学为接触依赖性发育提供了证据。
DOI:
10.1128/jb.00293-09
发表时间:
2009
期刊:
Journal of bacteriology
影响因子:
3.2
作者:
[Wilson,DavidP, Whittum-Hudson,JudithA, Timms,Peter, Bavoil,PatrikM]
通讯作者:
Bavoil,PatrikM
A novel co-infection model with Toxoplasma and Chlamydia trachomatis highlights the importance of host cell manipulation for nutrient scavenging.
弓形虫和沙眼衣原体的新型共感染模型强调了宿主细胞操作对于营养物清除的重要性。
DOI:
10.1111/cmi.12060
发表时间:
2013
期刊:
Cellular microbiology
影响因子:
3.4
作者:
[Romano,JuliaD, deBeaumont,Catherine, Carrasco,JoseA, Ehrenman,Karen, Bavoil,PatrikM, Coppens,Isabelle]
通讯作者:
Coppens,Isabelle
Cryo Upgrade of UMB EM Core Facility
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批准号:7794116
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项目类别:
-
资助金额:$42.07万
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财政年份:2010
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负责人:RU-CHING HSIA
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依托单位: