Role of extracellular matrix proteins in Candida biofilm formation
Role of extracellular matrix proteins in Candida biofilm formation
批准号:
7849927
负责人:
Pranab Kumar Mukherjee
金额:
$19.63万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-01 至 2012-05-31
关键词:
Antifungal AgentsApplications GrantsArchitectureArtsBacteriaBiological AssayCandida albicansCarbohydratesCathetersCell surfaceConsultationsDNADataDatabasesDevelopmentDiagnosticEarly identificationEdetic AcidElectron MicroscopyExtracellular MatrixExtracellular Matrix ProteinsExtracellular ProteinFluorescence MicroscopyFungal Drug ResistanceGel ChromatographyGene DeletionGene TargetingGenesIn VitroInfectionKnowledgeLaser Scanning MicroscopyMALDI-TOF Mass SpectrometryMass Spectrum AnalysisMeasurementMedical DeviceMedical centerMentorsMetabolicMethodsMicrobial BiofilmsModelingMolecularMorphologyOryctolagus cuniculusPhasePlayPredispositionPreventionProductionProteinsProteomicsPublicationsResearch PersonnelResistanceRoleScanningSouthern BlottingSpottingsTechniquesTestingThe science of MycologyThickTwo-Dimensional Gel ElectrophoresisWeightbasecandida biofilmextracellularfollow-upfungusgel electrophoresisin vitro Modelin vivomicrobial communitymutantnoveltherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Candida albicans (CA) is the most commonly isolated fungus associated with biofilms [extracellular matrix (ECM)-encased microbial communities formed on indwelling medical devices which are resistant against commonly used antifungals. The carbohydrate-rich ECM is believe to play critical role in the biofilm forming ability of different bacteria, but its role in fungal biofilm formation and antifungal resistance has not been investigated. Therefore, obvious knowledge gaps exist in the study of fungal biofilm ECM. In Preliminary Studies, we: (1) standardized an EDTA-treatment based method to isolate ECM associated proteins from CA biofilm, (2) demonstrated that the levels of total carbohydrates (TC), total protein (TP), and extracellular DNA (eDNA) increase during biofilm development, (3) optimized a gel filtration method to isolate ECM proteins, (4) used traditional two-dimensional gel electrophoresis (2DGE) to identify 15 proteins differentially expressed in biofilm ECM, (5) used state-of-the-art technique of 2D difference in gel electrophoresis (DIGE) proteomics to demonstrate that 231 ECM proteins were differentially expressed in ECM of biofilm and planktonic CA. These analyses also showed 10 unique proteins to be expressed in ECM of biofilms eight in mature biofilms, and two in early phase biofilms. (6) Used preliminary mass spectrometry (MS) analyses to identify five differentially expressed proteins. Based on these Preliminary Data, we hypothesize that CA biofilm-specific ECM proteins play critical roles in biofilm formation and antifungal resistance. To test this hypothesis, in this grant application, we propose studies based on the following specific aims: Aim I. Determine the identity of proteins uniquely expressed in matrix of mature biofilms, using 2D-DIGE proteomics. Aim II. Construct isogenic mutant strains of C. albicans lacking the biofilm matrix-specific proteins. Aim III. Determine the effect of: (A) EDTA treatment of biofilms on their antifungal susceptibility, and (B) Targeted gene deletions on the ability of CA to form biofilms and the morphology, architecture, and antifungal susceptibility of these biofilms. The studies described in this proposal will allow us to identify biofilm-specific ECM proteins that are critical to Candida biofilm formation in vitro and in vivo, which may represent novel anti-biofilm therapeutic targets and/or diagnostic markers. Candida albicans (CA) is the most commonly isolated fungus associated with biofilms [extracellular matrix (ECM)-encased microbial communities formed on indwelling medical devices, which are resistant against commonly used antifungals. The studies described in this proposal will allow us to identify biofilm-specific ECM proteins that are critical to Candida biofilm formation in vitro, which may represent novel anti-biofilm therapeutic targets and/or diagnostic markers.
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DOI:
--
发表时间:
2014-06
期刊:
Journal of dental hygiene : JDH
影响因子:
--
作者:
[S. Ujaoney;J. Chandra;F. Faddoul;Maya Chane;Jing Wang;Louay Taifour;M. Mamtani;T. Thakre;H. Kulkarni;P. Mukherjee;M. Ghannoum]
通讯作者:
S. Ujaoney;J. Chandra;F. Faddoul;Maya Chane;Jing Wang;Louay Taifour;M. Mamtani;T. Thakre;H. Kulkarni;P. Mukherjee;M. Ghannoum
DOI:
10.1371/journal.ppat.1000713
发表时间:
2010-01-08
期刊:
PLoS pathogens
影响因子:
6.7
作者:
[Ghannoum MA, Jurevic RJ, Mukherjee PK, Cui F, Sikaroodi M, Naqvi A, Gillevet PM]
通讯作者:
Gillevet PM
DOI:
10.1155/2012/398207
发表时间:
2012
期刊:
Mediators of inflammation
影响因子:
4.6
作者:
[Rouabhia M, Semlali A, Chandra J, Mukherjee P, Chmielewski W, Ghannoum MA]
通讯作者:
Ghannoum MA
Gentian violet exhibits activity against biofilms formed by oral Candida isolates obtained from HIV-infected patients.
龙胆紫对从 HIV 感染者的口腔念珠菌分离株形成的生物膜具有活性。
DOI:
10.1128/aac.01601-10
发表时间:
2011
期刊:
Antimicrobial agents and chemotherapy
影响因子:
4.9
作者:
[Traboulsi,RanaS, Mukherjee,PranabK, Chandra,Jyotsna, Salata,RobertA, Jurevic,Richard, Ghannoum,MahmoudA]
通讯作者:
Ghannoum,MahmoudA
Biomarkers of Fusarium biofilm formation in vitro and in vivo
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批准号:8307794
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项目类别:
-
资助金额:$19.63万
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财政年份:2011
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负责人:Pranab Kumar Mukherjee
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依托单位:
Biomarkers of Fusarium biofilm formation in vitro and in vivo
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批准号:8190783
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项目类别:
-
资助金额:$23.55万
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财政年份:2011
-
负责人:Pranab Kumar Mukherjee
-
依托单位:
Role of extracellular matrix proteins in Candida biofilm formation
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批准号:7386259
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项目类别:
-
资助金额:$23.55万
-
财政年份:2009
-
负责人:Pranab Kumar Mukherjee
-
依托单位: