Inorganic Antimicrobials in Exocrine Fluids
Inorganic Antimicrobials in Exocrine Fluids
批准号:
7344841
负责人:
MICHAEL T ASHBY
金额:
$14.56万
依托单位:
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:
2007-02-01 至 2010-01-31
关键词:
AddressAnimal ModelAreaAtherosclerosisBiocideBiological AssayBiologyBioreactorsBuffersCellsCellular StructuresChemicalsChemistryChloride IonChloridesChronicCommitCommunicable DiseasesComplexCredentialingCystic FibrosisDefense MechanismsDevelopmentDiffusionDiseaseEnvironmentEnzymesEscherichia coliEuropeanExhibitsFundingFutureGeneticGingivaGingival Crevicular FluidGoalsGrantHealthHeterogeneityHost DefenseHumanHuman ResourcesHypochloriteHypochlorous AcidHypochlorous AcidsIn SituIndividualInfectionInflammatoryKineticsLaboratoriesLibrariesLifeLiquid substanceMammalian CellMethodsMicrobeMicrobial BiofilmsMicrobiologyModelingOSCN-Operating SystemOralOral cavityOrganismOxidation-ReductionPathway interactionsPeriodontitisPeroxidasePeroxidasesPhysiologicalPlayPropertyProtocols documentationRadiationRangeReactionReproducibilityResearchResearch PersonnelRoleSalivaSeedsStudentsSulfhydryl CompoundsSurveysSuspension substanceSuspensionsSystemTechniquesTestingThiocyanatesTimeTimeLineTissuesTrainingUnited States National Institutes of HealthWorkXerostomiaantimicrobialattenuationbasechemical kineticshypothiocyanitein vivointerfacialkillingsoral bacteriaoral infectionoxidationreaction raterepairedresearch studyresponsestemsynergismthiocyanatetool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this R21 project is to contribute to an understanding of the efficacies of hypohalite host defense factors toward pathogenic oral bacteria. Within the oral cavity, hypochlorite (OCI-) and hypothiocyanite (OSCN-) are produced by enzymes. Nevertheless, we have discovered a facile non-enzymic pathway that produces hypothiocyanite by oxidation of thiocyanate (SCN-) with hypochlorous acid (HOCI), a reaction that preserves the oxidizing equivalents of hypochlorite by transferring them to hypothiocyanite, a more discriminate biocide that is not lethal to mammalian cells. Remarkably little is known about the biocidal mechanisms of the hypohalites, due in part to their extraordinary reactivities and the fact that they produce cascades of derivative reactive intermediates with largely unknown physiologic properties. In addition to the complexities of the dynamic chemistry, the issue of biocidal mechanisms is further complicated by the heterogeneity of the oral cavity, where complex biofilms develop in chemically distinct environments. Recent studies have suggested that the genetic response of E. coli is different for the hypochlorite as compared to the hypothiocyanite system. Given that hypochlorite and hypothiocyanite apparently control spatially distinct regions of the oral cavity, but interracial regions near the gingival margin likely exhibit a concentration gradient of these hypohalites, we posit that these two biocides act in concert. The Specific Aims of this project are: 1) to develop protocols for assessing the biocidal efficacies of the hypochlorite and hypothiocyanite chemical systems and selected secondary derivatives toward a library of oral bacteria (and some controls); and 2) employing this protocol and the same library of oral bacteria, investigate synergistic effects of the primary and secondary biocides. These goals will be achieved through the application of whole-cell chemical-quench-flow and the introduction of chemical insults (some generated in real time) vis-a-vis a bioreactor system. We note that all of the experiments we describe in this R21 application involve planktonic cultures, which we believe is a logical first step before tackling the complexities of heterogeneous systems. Nevertheless, the methods that will be developed are expected to be adaptable to future studies that will include mixed-cultures and heterogeneous systems (including biofilms). Long-range Benefit: An understanding of the capacity of human defense mechanisms to control pathogenic oral microbes is essential for the improvement of therapies for oral infectious diseases. The ultimate objective of our research is the development of specific approaches to reduce pathogenic flora without altering the normal commensal (non-injurious) flora of the oral cavity.
期刊论文(12)
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DOI:
10.1021/ja0770532
发表时间:
2007-12
期刊:
Journal of the American Chemical Society
影响因子:
15
作者:
[P. Nagy;Xiaoguang Wang;K. Lemma;M. Ashby]
通讯作者:
P. Nagy;Xiaoguang Wang;K. Lemma;M. Ashby
Catabolite control protein A controls hydrogen peroxide production and cell death in Streptococcus sanguinis.
分解代谢控制蛋白 A 控制血链球菌中过氧化氢的产生和细胞死亡。
DOI:
10.1128/jb.01131-10
发表时间:
2011
期刊:
Journal of bacteriology
影响因子:
3.2
作者:
[Zheng,Lanyan, Chen,Zhijun, Itzek,Andreas, Ashby,Michael, Kreth,Jens]
通讯作者:
Kreth,Jens
DOI:
10.1021/bi902089w
发表时间:
2010-03-09
期刊:
Biochemistry
影响因子:
2.9
作者:
[Xulu BA, Ashby MT]
通讯作者:
Ashby MT
DOI:
10.1021/tx800195n
发表时间:
2008-10
期刊:
Chemical research in toxicology
影响因子:
4.1
作者:
[Xiaoguang Wang;M. Ashby]
通讯作者:
Xiaoguang Wang;M. Ashby
Reactive sulfur species: kinetics and mechanism of the hydrolysis of cysteine thiosulfinate ester.
活性硫物质:半胱氨酸硫代亚磺酸酯水解的动力学和机制。
DOI:
10.1021/tx700168z
发表时间:
2007
期刊:
Chemical research in toxicology
影响因子:
4.1
作者:
[Nagy,Peter, Ashby,MichaelT]
通讯作者:
Ashby,MichaelT
Inorganic Antimicrobials in Exocrine Fluids
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批准号:7196380
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项目类别:
-
资助金额:$24.02万
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财政年份:2007
-
负责人:MICHAEL T ASHBY
-
依托单位:
海外基金