Staphylococcus aureus biofilms: in vitro and in vivo studies
Staphylococcus aureus biofilms: in vitro and in vivo studies
批准号:
8074921
负责人:
Mark E Shirtliff
金额:
$35.69万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-06-01 至 2013-05-31
关键词:
Animal ModelAntibodiesAntigensBacillus (bacterium)Cessation of lifeChronicClostridiumCommunitiesDataDevelopmentDisinfectionEvaluationExcisionGene ExpressionGene Expression ProfileGene ProteinsGenus staphylococcusGlycocalyxGoalsGrowthHospitalizationHumanImmune systemImmunizationImplantIn VitroInfectionInfection preventionInflammatory ResponseInterferonsInterleukin-12JointsLaboratoriesListeriaMass Spectrum AnalysisMediatingMedical DeviceMicrobeMicrobial BiofilmsModelingMolecularMorbidity - disease rateNatureOryctolagus cuniculusPatientsPhagocytesPhasePhysiologicalProductionProteinsProteomeProteomicsResearchResearch PersonnelResolutionStaphylococcus aureusStreptococcusSuperantigensSurfaceSystemTNF geneTimeToxinTwo-Dimensional Gel ElectrophoresisUnited StatesVirulence Factorsadaptive immunityantimicrobial drugcapsulecell mediated immune responsecytokineimplantationin vivomicrobialmortalitynovelpreventprogramsprotective efficacyquorum sensingresponseretinal rodsstandard caretwo-dimensionalvaccine development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Staphylococcus aureus is a gram positive, ubiquitous bacterial species, with the predominant reservoir in nature being humans. The increased use of implanted medical devices such as intramedullary rods, screws, plates, and artificial joints has provided a physiological niche for microbes to cause infections. While a number of bacterial species may cause microbial fouling of indwelling medical devices, S. aureus causes a majority of these infections, producing high chronicity, morbidity, and mortality. One of the important mechanisms by which S. aureus is able to cause persistent infections on indwelling medical devices is through colonizing and synthesizing a "slime" layer, termed the glycocalyx or biofilm. This layer prevents infection resolution by antimicrobial agents and host phagocytic cells. Once an implant is colonized and chronic infection ensues, the standard treatment option is implant removal. This proposal seeks to identify S. aureus gene products with upregulated production in biofilms using two dimensional (2D) gel electrophoresis. Selected up-regulated proteins will then be evaluated, first, for their ability to be recognized by the host immune system during an in vivo biofilm infection, and second, for their protective efficacy in preventing infections in an implant-associated infection model in rabbits. The data generated here may contribute to the eventual development of a vaccine against S. aureus biofilms infections in humans. In addition, this proposal will also contribute to a more complete understanding of the bacterial factors involved in S. aureus biofilm formation and maturation. This understanding will enable one to create novel materials, surfaces, and/or disinfection strategies that resist or eliminate staphylococcal fouling and biofilm formation. Also, the proteome will be compared to transcriptome DMA microarray studies already completed in the Pi's laboratory in order to determine the global interrelation between gene expression and protein production for S. aureus biofilms grown under flow, thereby allowing staphylococci to be understood at a new level. Lastly, the results obtained in the evaluation of S. aureus biofilm formation may be used as a model for the biofilm formation by other closely related gram positive bacterial species, including Streptococcus spp., Listeria spp., Clostridium spp. and Bacillus spp.
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DOI:
10.2217/fmb.14.64
发表时间:
2014
期刊:
Future microbiology
影响因子:
3.1
作者:
[McConoughey SJ, Howlin R, Granger JF, Manring MM, Calhoun JH, Shirtliff M, Kathju S, Stoodley P]
通讯作者:
Stoodley P
DOI:
10.1111/j.1574-695x.2010.00708.x
发表时间:
2010-08
期刊:
FEMS immunology and medical microbiology
影响因子:
--
作者:
[Harro JM, Peters BM, O'May GA, Archer N, Kerns P, Prabhakara R, Shirtliff ME]
通讯作者:
Shirtliff ME
Bacterial biofilms and periprosthetic infections.
细菌生物膜和假体周围感染。
DOI:
10.2106/jbjs.2223
发表时间:
2013
期刊:
The Journal of bone and joint surgery. American volume
影响因子:
--
作者:
[Arnold,WilliamV, Shirtliff,MarkE, Stoodley,Paul]
通讯作者:
Stoodley,Paul
DOI:
10.1007/s11033-011-0676-7
发表时间:
2011-11
期刊:
Molecular biology reports
影响因子:
2.8
作者:
[Xu Z, Li L, Shi L, Shirtliff ME]
通讯作者:
Shirtliff ME
DOI:
10.1016/j.foodres.2011.04.042
发表时间:
2012-07-01
期刊:
FOOD RESEARCH INTERNATIONAL
影响因子:
8.1
作者:
[Xu, Zhenbo, Li, Lin, Chu, Jin, Peters, Brian M., Harris, Megan L., Li, Bing, Shi, Lei, Shirtliff, Mark E.]
通讯作者:
Shirtliff, Mark E.
共 7 条
Staphylococcus aureus biofilms: in vitro and in vivo studies
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批准号:8116811
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项目类别:
-
资助金额:$31.95万
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财政年份:2010
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负责人:Mark E Shirtliff
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依托单位:
Staphylococcus aureus biofilms: in vitro and in vivo studies
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批准号:7618784
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项目类别:
-
资助金额:$36.42万
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财政年份:2007
-
负责人:Mark E Shirtliff
-
依托单位:
Staphylococcus aureus biofilms: in vitro and in vivo studies
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批准号:7890454
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项目类别:
-
资助金额:$36.06万
-
财政年份:2007
-
负责人:Mark E Shirtliff
-
依托单位:
Staphylococcus aureus biofilms: in vitro and in vivo studies
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批准号:7320471
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项目类别:
-
资助金额:$37.13万
-
财政年份:2007
-
负责人:Mark E Shirtliff
-
依托单位:
Staphylococcus aureus biofilms: in vitro and in vivo studies
-
批准号:7423938
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项目类别:
-
资助金额:$36.42万
-
财政年份:2007
-
负责人:Mark E Shirtliff
-
依托单位:
海外基金