Combatting Quinolone Antimicrobial Resistance
Combatting Quinolone Antimicrobial Resistance
批准号:
8322046
负责人:
LYNN ZECHIEDRICH
金额:
$38.73万
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:
2004-03-15 至 2014-07-31
关键词:
AccountingAffectAnimal ModelAntimicrobial ResistanceBacteriaBacterial InfectionsBioinformaticsBiological AvailabilityClinicClinicalComplexDataDatabasesDrug Delivery SystemsDrug resistanceEmerging Communicable DiseasesEscherichia coliEscherichia coli drug resistanceEvolutionFluoroquinolonesFoundationsFrequenciesFundingGene DeletionGenesGeneticGenomicsGoalsGram-Negative BacteriaHealthHealth Insurance Portability and Accountability ActHomologous GeneHospitalsHumanHypoxiaIn VitroIndividualKnowledgeLaboratoriesLeadMarketingMeasuresMedical centerMiningMolecularMonitorMulti-Drug ResistanceMutationPathway interactionsPatient CarePatientsPatternPeriod AnalysisPharmaceutical PreparationsPhysiciansPlasmidsPositioning AttributePredispositionProtocols documentationPumpQuinolonesRegulationResearch InfrastructureResearch PersonnelResistanceReverse TranscriptionRoleRouteTechnologyTexasTopoisomeraseToxic effectTranscriptTranslational ResearchUnited StatesVariantVisitWorkantimicrobial drugclinical phenotypecombatcost effectivedata managementdesignefflux pumpfluoroquinolone resistancemutantnext generationnovel therapeuticspathogenpreventquinolone resistanceresearch studyresistance mechanismresistance mutation
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Fluoroquinolones are the most frequently prescribed antimicrobial agents in the United States. Fluoroquinolone- and multidrug-resistant bacteria are emerging infectious disease agents of worldwide concern and E. coli is an important human pathogen and excellent model organism. The long-term goals of the Zechiedrich laboratory are to determine how bacteria respond to and resist antimicrobial agents and to use this knowledge both to prolong the usefulness of current drugs and to aid in the design of new therapeutic protocols to help prevent and combat fluoroquinolone- and multidrug-resistant bacterial infections. The goals of this competing renewal proposal are to determine the (i) regulation, (ii) cellular roles, and (iii) molecular mechanisms of the multidrug efflux pumps, and the (iv) genetic alterations and (v) selection mechanisms that cause increased drug MICs in patient isolates. With thousands of characterized and uncharacterized fluoroquinolone- and multidrug-resistant E. coli patient isolates and the accompanying patient data, >9 million patient visits/year in the Texas Medical Center, and the strength of the combined expertise of the investigators, the goals will be achieved with the following Specific Aims: (1) Understand the interplay between and molecular mechanisms of the efflux pumps important for fluoroquinolone-resistance in E. coli; and (2) Identify molecular mechanisms, mutant selection mechanisms, and genetic pathways to fluoroquinolone- and multidrug-resistance in E. coli clinical isolates. These Specific Aims will be achieved by three highly inter-related approaches: (i) A molecular approach will determine the transcriptional relationships among the fluoroquinolone efflux pumps and their regulators using quantitative reverse- transcription PCR first in defined mutant strains and then in fluoroquinolone-resistant E. coli clinical isolates; (ii) A computational approach will uncover evolutionarily related regions of the efflux pumps indicative of functionality; and (iii) A genomic approach using cost effective sequencing technologies will identify relevant heritable variations that correlate with the drug-resistance of the clinical isolates. These approaches are tied together using bioinformatics and data management infrastructures. PUBLIC HEALTH RELEVANCE: With few new antimicrobial agents being developed, we must work to preserve those used currently. Excellent bioavailability, low toxicity and, in general, low resistance frequency, make the fluoroquinolones an important drug class to maintain in the physician's arsenal. Results from the proposed translational research will aid in the prescription practices of physicians and in the design of new therapeutic protocols to combat drug-resistant bacterial infections.
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Repurposed Transcriptomic Data Reveal Small Viral RNA Produced by Influenza Virus during Infection in Mice.
重新利用的转录组数据揭示了流感病毒在小鼠感染过程中产生的小病毒 RNA。
DOI:
10.1371/journal.pone.0165729
发表时间:
2016
期刊:
PloS one
影响因子:
3.7
作者:
[Koire,Amanda, Gilbert,BrianE, Sucgang,Richard, Zechiedrich,Lynn]
通讯作者:
Zechiedrich,Lynn
DOI:
10.1093/nar/gkp041
发表时间:
2009-02
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Liu Z, Deibler RW, Chan HS, Zechiedrich L]
通讯作者:
Zechiedrich L
DOI:
10.1371/journal.pone.0180800
发表时间:
2017
期刊:
PloS one
影响因子:
3.7
作者:
[Bodine TJ, Evangelista MA, Chang HT, Ayoub CA, Samuel BS, Sucgang R, Zechiedrich L]
通讯作者:
Zechiedrich L
Editorial comment to genome-wide transcriptome analysis of fluoroquinolone resistance in clinical isolates of Escherichia coli.
对大肠杆菌临床分离株氟喹诺酮耐药性的全基因组转录组分析的编辑评论。
DOI:
10.1111/j.1442-2042.2012.02996.x
发表时间:
2012
期刊:
International journal of urology : official journal of the Japanese Urological Association
影响因子:
--
作者:
[Zechiedrich,Lynn]
通讯作者:
Zechiedrich,Lynn
DOI:
10.1038/gt.2010.123
发表时间:
2011-03
期刊:
Gene therapy
影响因子:
5.1
作者:
[]
通讯作者:
共 8 条
Harnessing Supercoiling to Regulate DNA Activity
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批准号:10482361
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项目类别:
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资助金额:$40.0万
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财政年份:2021
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负责人:LYNN ZECHIEDRICH
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依托单位:
Harnessing Supercoiling to Regulate DNA Activity
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批准号:10205924
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项目类别:
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资助金额:$40.0万
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财政年份:2021
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依托单位:
Harnessing Supercoiling to Regulate DNA Activity
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批准号:10705655
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项目类别:
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资助金额:$40.0万
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财政年份:2021
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依托单位:
Harnessing Supercoiling to Regulate DNA Activity
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批准号:10798577
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项目类别:
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资助金额:$6.44万
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财政年份:2021
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负责人:LYNN ZECHIEDRICH
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依托单位:
Molecular Mechanisms Underlying Fluoroquinolone Susceptibility and Resistance
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批准号:8941338
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项目类别:
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资助金额:$38.04万
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财政年份:2015
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负责人:LYNN ZECHIEDRICH
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依托单位:
S2: Molecular Mechanisms Underlying Fluoroquinolone Susceptibility and Resistance
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批准号:9539894
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项目类别:
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资助金额:$4.66万
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财政年份:2015
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负责人:LYNN ZECHIEDRICH
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依托单位:
Molecular Mechanisms Underlying Fluoroquinolone Susceptibility and Resistance
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批准号:9276741
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项目类别:
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资助金额:$38.04万
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财政年份:2015
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负责人:LYNN ZECHIEDRICH
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依托单位:
Molecular Mechanisms Underlying Fluoroquinolone Susceptibility and Resistance
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批准号:9276456
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项目类别:
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资助金额:$16.59万
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财政年份:2015
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依托单位:
TOPOISOMERASES
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资助金额:$0.87万
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财政年份:2008
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负责人:LYNN ZECHIEDRICH
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依托单位:
TOPOISOMERASES
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资助金额:$1.62万
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财政年份:2007
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资助金额:$1.63万
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财政年份:2006
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负责人:LYNN ZECHIEDRICH
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依托单位:
TOPOISOMERASES
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项目类别:
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资助金额:$1.51万
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财政年份:2005
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负责人:LYNN ZECHIEDRICH
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依托单位:
Combatting Quinolone Antimicrobial Resistance
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批准号:7894910
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项目类别:
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资助金额:$38.38万
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财政年份:2004
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负责人:LYNN ZECHIEDRICH
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依托单位:
COMBATTING QUINOLONE ANTIMICROBIAL RESISTANCE
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批准号:6729491
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项目类别:
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资助金额:$33.86万
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财政年份:2004
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负责人:LYNN ZECHIEDRICH
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依托单位:
Combatting Quinolone Antimicrobial Resistance
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批准号:8227067
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项目类别:
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资助金额:$38.73万
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财政年份:2004
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负责人:LYNN ZECHIEDRICH
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依托单位:
Combatting Quinolone Antimicrobial Resistance
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批准号:7649731
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资助金额:$38.38万
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财政年份:2004
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依托单位:
TOPOISOMERASES
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资助金额:$1.85万
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负责人:LYNN ZECHIEDRICH
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COMBATTING QUINOLONE ANTIMICROBIAL RESISTANCE
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资助金额:$33.86万
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财政年份:2004
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COMBATTING QUINOLONE ANTIMICROBIAL RESISTANCE
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批准号:7060019
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项目类别:
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资助金额:$33.07万
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财政年份:2004
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负责人:LYNN ZECHIEDRICH
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COMBATTING QUINOLONE ANTIMICROBIAL RESISTANCE
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资助金额:$32.11万
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负责人:LYNN ZECHIEDRICH
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依托单位:
海外基金