Prophage-associated virulence factors in pathogenic Neisseria species
Prophage-associated virulence factors in pathogenic Neisseria species
批准号:
7531795
负责人:
Anna C. Karls
金额:
$7.38万
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:
2007-12-01 至 2011-05-31
关键词:
Acute suppurative arthritis due to bacteriaAffectBacteriaBacteriophagesBiological AssayBloodBlood - brain barrier anatomyBlood CirculationBrainCase StudyCell membraneChromosomesCyclophosphamideDNADNA Insertion ElementsDevelopmentDiseaseDisease ProgressionElementsEndocarditisEndothelial CellsEpithelialEpitheliumExcisionExhibitsGenesGenetic RecombinationGenital systemGenomeGoalsGonorrheaGrowthHomologous GeneHumanIncidenceIndividualInfectionInflammationInflammatory ResponseInvestigationLysogenyMeasuresMediatingMeningitisMeningococcal InfectionsMental RetardationMorbidity - disease rateMovementMucous MembraneNeisseriaNeisseria gonorrhoeaeNeisseria meningitidisPathogenesisPelvic Inflammatory DiseasePenetrationPlayProcessProphagesProtein SecretionProteinsPublic HealthQualifyingQuantitative Reverse Transcriptase PCRRegulationReplication InitiationResearchRoleSepsisSeptic ShockSepticemiaSerogroup B Neisseria meningitidisSignal TransductionSiteSpecificityStagingStreamSurface AntigensSurvivorsSystemTestingTight JunctionsToxinTransposaseVaccinesVibrio choleraeVirulenceVirulence FactorsWorkZot proteinantimicrobialchemotherapydeafnessdesignexperiencemortalitypathogenresponsetherapeutic vaccine
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
The long-term goal of this research is to identify virulence factors that may be targeted for the design of effective vaccines and therapeutics for Neisseria gonorrhoeae (gonococci, GC), which causes gonorrhoeae and pelvic inflammatory disease, and Neisseria meningitidis (meningococci, MC), which causes septicemia and meningitis. The objective of this R03 application is to examine the role of the meningococcal disease-associated (MDA) prophage in the pathogenesis of GC and MC. The MDA prophage, which is found at multiple loci on the GC and MC genomes, encodes a potential toxin that is a homologue of the Vibrio cholera CTX prophage zonular occulens toxin (Zot) that alters epithelial and endothelial tight junctions. Thus, the MDA prophage Zot proteins in GC and MC have the potential to be involved in inflammation, sepsis, and/or invasion of the blood-brain barrier. The insertion (and excision) of the MDA phage DNA into the host chromosome to establish lysogeny and possible excision to initiation replication may be mediated by the transposase of the ISNgo2/3 elements, which are part of the phage genome. Defining the mechanism for the movement of the phage DNA is essential to understanding the role of the phage in GC and MC pathogenesis. The specific aims are to: 1. Determine the activities of the meningococcal and gonococcal Zot proteins, and 2. Define the role of the ISNgo2/3 transposase, Irg, in directing insertion and/or excision of MDAphi DNA and controlling zot expression in MC and GC. Experimental approaches will include assays for zonular occludens toxin activity for Zot from MC and GC on epithelial and brain microvascular endothelial cell membranes; quantitative reverse transcriptase PCR to measure expression of zot and irg under different growth conditions; and quantitative PCR to detect movement and replication of MDAphi.
This work is relevant to public health because there is no effective vaccine for Neisseria gonnorrhoeae or for the most prevalent serogroup (B) of Neisseria meningitidis in the U.S. The annual U.S. incidence of gonococcal disease is 130 in 100,000, while the incidence of meningococcal disease is 1 in 100,000. Despite the use of chemotherapeutics, 10-40% of invasive meningococcal infections are fatal and 10-15% of survivors have serious sequelae, including mental retardation and deafness.
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会议论文
Prophage-associated virulence factors in pathogenic Neisseria species
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批准号:7918663
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项目类别:
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资助金额:$6.98万
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财政年份:2009
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负责人:Anna C. Karls
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依托单位:
Prophage-associated virulence factors in pathogenic Neisseria species
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批准号:7385356
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项目类别:
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资助金额:$7.38万
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财政年份:2007
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负责人:Anna C. Karls
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依托单位:
SITE-SPECIFIC DNA INVERSION IN MORAXELLA LACUNATA
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批准号:2187331
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项目类别:
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资助金额:$10.72万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
SITE-SPECIFIC DNA INVERSION IN MORAXELLA LACUNATA
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批准号:2459496
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项目类别:
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资助金额:$11.37万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
SITE-SPECIFIC DNA INVERSION IN MORAXELLA LACUNATA
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批准号:3469121
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项目类别:
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资助金额:$10.54万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
SITE-SPECIFIC DNA INVERSION IN MORAXELLA LACUNATA
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批准号:2187330
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项目类别:
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资助金额:$10.27万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
NOVEL MECHANISMS FOR DNA INVERSION AND TRANSPOSITION
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批准号:6689002
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项目类别:
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资助金额:$21.29万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
NOVEL MECHANISMS FOR DNA INVERSION AND TRANSPOSITION
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批准号:6627185
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项目类别:
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资助金额:$21.29万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
SITE-SPECIFIC DNA INVERSION IN MORAXELLA LACUNATA
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批准号:2187332
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项目类别:
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资助金额:$11.04万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
NOVEL MECHANISMS FOR DNA INVERSION AND TRANSPOSITION
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批准号:6287225
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项目类别:
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资助金额:$20.46万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
NOVEL MECHANISMS FOR DNA INVERSION AND TRANSPOSITION
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批准号:6490062
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项目类别:
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资助金额:$21.29万
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财政年份:1993
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负责人:Anna C. Karls
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依托单位:
海外基金