MODULATION OF HOST SIGNALING FUNCTIONS BY YERSINIA YOPS
MODULATION OF HOST SIGNALING FUNCTIONS BY YERSINIA YOPS
批准号:
6349865
负责人:
James B Bliska
金额:
$27.47万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-02-01 至 2005-01-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (Adapted from the Applicant's Abstract): The human-pathogenic
Yersinia spp. (Y. pestis, Y. enterocolitica, and Y. pseudotuberculosis) are
responsible for a range of diseases including diarrhea, mesenteric
lymphadenitis, and bubonic plague. These bacteria invade into and colonize the
lymphatic organs of humans and a variety of animal hosts. Colonization of a
host by Yersinia requires the function of a plasmid-encoded contact-dependent
type III secretion system. This type III system translocates a set of toxic
proteins known as Yops into host cells. The Yops impair normal host cell
signaling functions, resulting in inhibition of phagocytosis, suppression of
cytokine synthesis, and induction of apoptosis. The long-term goal of this
grant is to understand how Yops modulate host cell signaling functions. The
investigators will focus their studies primarily on YopH, a protein tyrosine
phosphatase that inhibits phagocytosis, and YopJ, a protein that prevents
cytokine synthesis and induces apoptosis. The first specific aim is to carry
out a structure/function analysis of an amino-terminal domain in YopH that
mediates translocation and substrate recognition. A combination of biophysical
and genetic approaches will be used to achieve this goal. The second specific
aim is to examine the mechanism of substrate recognition by YopH inside host
cells. Animal and cultured cell infection assays will be used to study the
behavior of genetically-altered YopH proteins in vivo. The third specific aim
is to analyze the interaction of YopJ with host target proteins and to
elucidate its mechanism action. Mutant forms of YopJ unable to bind target
proteins will be generated and analyzed for biological activity in animal and
cultured cell infection assays. The possibility that other Yops modulate the
activities of mitogen-activated protein kinases in host cells will also be
explored. As type III secretion pathways are important virulence determinants
in a large number of bacterial pathogens, and the Yops provide an extremely
powerful system to study pathogen interference with host signaling functions,
these studies will aid the development of new strategies to combat a variety
infectious diseases.
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Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:9898220
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项目类别:
-
资助金额:$36.55万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:8369546
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项目类别:
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资助金额:$39.01万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:8646872
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项目类别:
-
资助金额:$39.24万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:9056447
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项目类别:
-
资助金额:$39.26万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:9308272
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项目类别:
-
资助金额:$35.96万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:10604531
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项目类别:
-
资助金额:$41.56万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:8461104
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项目类别:
-
资助金额:$36.77万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Regulation of host innate and adaptive immunity by bacterial type III effectors
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批准号:10708101
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项目类别:
-
资助金额:$43.14万
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财政年份:2012
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负责人:James B Bliska
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依托单位:
Development of mAb immunotherapy for genetically modified plague
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批准号:8230241
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项目类别:
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资助金额:$41.13万
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财政年份:2011
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负责人:James B Bliska
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依托单位:
Development of mAb immunotherapy for genetically modified plague
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批准号:7670796
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项目类别:
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资助金额:$38.44万
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财政年份:2009
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负责人:James B Bliska
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依托单位:
Bacterial Pathogenesis and Therapeutics
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批准号:7706281
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项目类别:
-
资助金额:$18.05万
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财政年份:2008
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负责人:James B Bliska
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依托单位:
Intracellular Survival Determinants of Yersinia pestis
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批准号:6730790
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项目类别:
-
资助金额:$40.5万
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财政年份:2003
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负责人:James B Bliska
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依托单位:
Microarray Analysis of Plague-Induced Apoptosis
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批准号:6571445
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项目类别:
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资助金额:$11.29万
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财政年份:2002
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负责人:James B Bliska
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依托单位:
Microarray Analysis of Plague-Induced Apoptosis
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批准号:6659051
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项目类别:
-
资助金额:$11.29万
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财政年份:2002
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负责人:James B Bliska
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依托单位:
Intracellular survival determinants of Yersinia pestis
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批准号:6511514
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项目类别:
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资助金额:$7.53万
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财政年份:2001
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负责人:James B Bliska
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依托单位:
Intracellular survival determinants of Yersinia pestis
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批准号:6414642
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项目类别:
-
资助金额:$7.53万
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财政年份:2001
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负责人:James B Bliska
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依托单位:
Intracellular survival determinants of Yersinia pestis
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批准号:6632429
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项目类别:
-
资助金额:$7.53万
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财政年份:2001
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负责人:James B Bliska
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依托单位:
MODULATION OF HOST SIGNALING FUNCTIONS BY YERSINIA YOPS
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批准号:6046118
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项目类别:
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资助金额:$26.63万
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财政年份:2000
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负责人:James B Bliska
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依托单位:
Modulation of Host Signaling Functions by Yersinia Yops
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批准号:8105589
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项目类别:
-
资助金额:$38.73万
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财政年份:2000
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负责人:James B Bliska
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依托单位:
MODULATION OF HOST SIGNALING FUNCTIONS BY YERSINIA YOPS
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批准号:6689569
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项目类别:
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资助金额:$30.02万
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财政年份:2000
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负责人:James B Bliska
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依托单位:
海外基金