Iron Acquisition From Host Proteins in S. pyogenes
Iron Acquisition From Host Proteins in S. pyogenes
批准号:
7407996
负责人:
ZEHAVA EICHENBAUM
金额:
$20.3万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-05-01 至 2011-04-30
关键词:
ATP-Binding Cassette TransportersAffinityAttenuatedBacteriaBindingBiochemical GeneticsBiological AssayBiologyCell physiologyCodeComplexCuesDefectDiseaseElectron TransportEnvironmentEnzymesFamilyGenesGeneticGoalsGram-Positive BacteriaGrowthHemeHeme IronHemeproteinsHemoglobinHemolysinHomeostasisHumanImmunoprecipitationIn VitroInfectionInvadedInvestigationIronLaboratoriesLigandsMediatingMembrane ProteinsModelingMolecularMusMutagenesisNamesOperonParasitesPathway interactionsPhasePhysiologyPolymerase Chain ReactionProcessProductionProteinsRoleSiderophoresSite-Directed MutagenesisSolidSourceStagingStreptococcusStreptococcus pyogenesStructureSurfaceSystemTestingVirulenceZebrafishcatalystcrosslinkheme-binding proteinin vivoiron metabolismmutantnovelpathogenreceptorreceptor bindinguptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The long-term goal of this project is to increase the understanding of the physiology and virulence of the human pathogen Streptococcus pyogenes. This investigation is specifically concerned with the molecular mechanisms used by S. pyogenes to obtain iron during infection. Most bacteria require iron, which serves as a catalyst for electron transfer and is an essential component of many important enzymes. The vast majority of iron in the mammalian body is sequestered by high affinity proteins, resulting in an environment that is essentially free of unbound iron, which in turn presents a challenge to invading bacteria that need iron for growth. Heme and heme-compounds are valuable sources of iron for the hemolytic Streptococcus. Yet, the mechanisms used by S. pyogenes and related pathogens to capture and transport heme or iron are not well characterized. Genetic studies done in this laboratory identified two iron-regulated operons named sia (for Streptococcal Iron Acquisition) and sit (for Streptococcal Iron Transport) that are involved in the utilization of hemoglobin. The first specific aim dissects the function of the sia and the sit operons and their role in S. pyogenes physiology. Genetic and biochemical analysis that includes mutant characterization and employs in vivo binding and transport assays will be used. The second specific aim analyzes the operon role in virulence; studies will be conducted in zebrafish and mice infection models. The third specific aim analyzes the structure and function of surface receptors involved in hemoprotein utilization. Substrate recognition and heme or iron capture will be investigated by in vitro binding assays; site-directed mutagenesis and arbitrary PCR mutagenesis will be used to identify functional receptor domains. The interactions between different receptor components will be studied with solid phase binding assays, cross-linking, and immunoprecipitation. Iron acquisition from host hemoproteins is likely to have important implications on the physiology and virulence of S. pyogenes, an obligate human parasite. The proposed characterization of iron acquisition in S. pyogenes will advance our understanding of this important pathogen, and will add to the understanding of the process of iron uptake in other Gram-positive bacteria, many of which are important human pathogens.
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DOI:
10.1016/j.abb.2013.08.009
发表时间:
2013-10
期刊:
Archives of biochemistry and biophysics
影响因子:
3.9
作者:
[Mahamoudou Ouattara;A. Pennati;Darius J. Devlin;Ya-Shu Huang;G. Gadda;Z. Eichenbaum]
通讯作者:
Mahamoudou Ouattara;A. Pennati;Darius J. Devlin;Ya-Shu Huang;G. Gadda;Z. Eichenbaum
DOI:
10.1093/infdis/jir149
发表时间:
2011-06
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
[Ya-Shu Huang;M. Fisher;Ziyad Nasrawi;Z. Eichenbaum]
通讯作者:
Ya-Shu Huang;M. Fisher;Ziyad Nasrawi;Z. Eichenbaum
DOI:
10.1099/mic.0.28075-0
发表时间:
2005-11
期刊:
Microbiology
影响因子:
1.5
作者:
[Griselle E Montañez;M. Neely;Z. Eichenbaum]
通讯作者:
Griselle E Montañez;M. Neely;Z. Eichenbaum
DOI:
10.1111/j.1365-2958.2010.07367.x
发表时间:
2010-11
期刊:
Molecular microbiology
影响因子:
3.6
作者:
[Ouattara M, Cunha EB, Li X, Huang YS, Dixon D, Eichenbaum Z]
通讯作者:
Eichenbaum Z
DOI:
10.1016/j.jinorgbio.2015.10.016
发表时间:
2016-05
期刊:
Journal of inorganic biochemistry
影响因子:
3.9
作者:
[Akbas N, Draganova EB, Block DR, Sook BR, Chan YF, Zhuo J, Eichenbaum Z, Rodgers KR, Dixon DW]
通讯作者:
Dixon DW
Impact of Heme During Group A Streptococcus Infection
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批准号:10825476
-
项目类别:
-
资助金额:$64.72万
-
财政年份:2023
-
负责人:ZEHAVA EICHENBAUM
-
依托单位:
Examining SecA as a Potential Target for Treating Gram-positive Bacteria
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批准号:8913328
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项目类别:
-
资助金额:$44.4万
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财政年份:2014
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负责人:ZEHAVA EICHENBAUM
-
依托单位:
Iron Acquisition From Host Proteins in S. pyogenes
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批准号:7224930
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项目类别:
-
资助金额:$20.69万
-
财政年份:2004
-
负责人:ZEHAVA EICHENBAUM
-
依托单位:
Iron Acquisition From Host Proteins in S. pyogenes
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批准号:6835437
-
项目类别:
-
资助金额:$24.33万
-
财政年份:2004
-
负责人:ZEHAVA EICHENBAUM
-
依托单位:
Iron Acquisition From Host Proteins in S. pyogenes
-
批准号:7054137
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项目类别:
-
资助金额:$21.31万
-
财政年份:2004
-
负责人:ZEHAVA EICHENBAUM
-
依托单位:
Iron Acquisition From Host Proteins in S. pyogenes
-
批准号:6891287
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项目类别:
-
资助金额:$21.83万
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财政年份:2004
-
负责人:ZEHAVA EICHENBAUM
-
依托单位:
海外基金