Genome-wide association to Staphylococcus carriage
Genome-wide association to Staphylococcus carriage
批准号:
8306913
负责人:
ERIC L BROWN
金额:
$61.82万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2014-06-30
关键词:
AbscessAffectAllelesAmishAnteriorAntibiotic ResistanceAntibioticsBacterial InfectionsBiologicalCessation of lifeClinicalCollaborationsCommunitiesCountyDNA Microarray ChipData AnalysesDevelopmentDiabetes MellitusDiseaseDisease susceptibilityEndocarditisEpidemiologyFranceGenesGeneticGenetic Predisposition to DiseaseGenetic VariationGenomeGenotypeGenus staphylococcusHaemophilus influenzaeHealthHumanHuman GeneticsImmune responseIncidenceIndividualInfectionInfectious Skin DiseasesInformaticsInterventionInvestigationLaboratoriesLettersLightMarylandMediatingMethicillin ResistanceMethodsMexican AmericansMinorModalityNatureNon-Insulin-Dependent Diabetes MellitusNoseOrganismPathway interactionsPatientsPersonsPneumoniaPopulationPredispositionPrevention strategyProceduresProcessProteinsRecording of previous eventsResistanceRiskRoleSNP genotypingSamplingSeveritiesSkinStaphylococcus aureusStatistical MethodsStreptococcus pneumoniaeSwabSymptomsTestingTexasTimeUnited StatesUniversitiesVaccine DesignVariantVestibuleVirulence Factorsbasecomputer sciencediabeticfollow-upgene interactiongenome wide association studygenome-wideimprovedinnovationmedical schoolsmethicillin resistant Staphylococcus aureusnon-diabeticnovelpathogenpublic health relevanceresistant strainsuccesstreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Staphylococcus aureus is an opportunistic pathogen that colonizes the skin (primarily the anterior nasal vestibule) of as many as 1 out 4 individuals without causing clinical disease symptoms. Humans are either persistently or intermittently colonized or never colonized with S. aureus i.e., defined as carriers, intermittent carriers or non-carriers. An individual's carriage status affects their likelihood of becoming infected and the nature of their immune response by S. aureus exposure. In addition, carriage status affects the severity of the infection(s) that range from minor skin infections to lethal infections associated with abscess formation, endocarditis and pneumonia. Certain antibiotics are available for the treatment of S. aureus-mediated disease, but the number of antibiotic-resistant strains is increasing rapidly. S. aureus is one of the most common causes of modern bacterial infections, in part due to increasing resistance to antibiotics and the recent emergence of infections caused by Community-Associated MRSA strains (CA-MRSA). In 2005, there were 94,360 invasive cases of MRSA in the United States, 18,650 resulted in death (incidence rate of 31.8/100,000 persons) much higher than S. pneumoniae and H. influenzae. The changing epidemiology of infections caused by S. aureus and increased antibiotic resistance necessitates the development of novel treatment modalities. Host susceptibility to S. aureus carriage status is at least partially under the control of underlying genetic factors. Their identification would provide targets for developing intervention strategies e.g., identification of novel pathways associated with carriage or genes associated with susceptibility will allow for the development of new interventions to eliminate carriage or treat infections. We will shortly complete genome-wide genotyping on 1000 nondiabetic and 1000 Type-2 diabetic Mexican-Americans from Starr County, Texas using the Affymetrix 6.0 platform. We have recently piloted procedures for determining carriage strains in this population and propose to determine S. aureus carriage status for 800 of the controls and 600 of diabetes cases for whom we will have nearly 1 million SNPs and 1 million copy number variants to carry out the proposed studies. Identification of these SNPs/genes will improve risk prediction and shed light on novel biological pathways bridging health and disease. It will also allow determining the role/interaction of Type-2 diabetes and S. aureus carriage/disease susceptibility. Success of genome-wide association studies depends on innovative and rigorous data analysis and replication in independent samples. We will use a combination of computer science- based informatics and statistical methods to prioritize genes and regions for follow-up. Understanding the genetics of susceptibility or resistance to this organism shall significantly accelerate and improve vaccine design strategies e.g., identification of novel pathways associated with carriage or genes associated with susceptibility will allow for the development of new interventions to eliminate carriage or treat infections.
PUBLIC HEALTH RELEVANCE: Community-acquired S. aureus infections are a growing problem and the increasing number of antibiotic resistant strains is limiting available treatment options. This proposal aims to develop an understanding of the human genetic components associated with S. aureus carriage as means of identifying novel genes or pathways associated with carriage/disease. This information may then be used to develop novel treatment and prevention strategies.
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会议论文
Microbiome and Worsening Glycemia Among Mexican Americans in Starr County, Texas
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批准号:9469119
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项目类别:
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资助金额:$65.34万
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财政年份:2017
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负责人:ERIC L BROWN
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依托单位:
Microbiome and Worsening Glycemia Among Mexican Americans in Starr County, Texas
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批准号:9977172
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项目类别:
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资助金额:$60.98万
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财政年份:2017
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负责人:ERIC L BROWN
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依托单位:
Genome-wide association to Staphylococcus carriage
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批准号:8099018
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项目类别:
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资助金额:$65.97万
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财政年份:2010
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负责人:ERIC L BROWN
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依托单位:
Genome-wide association to Staphylococcus carriage
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批准号:8502236
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项目类别:
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资助金额:$42.64万
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财政年份:2010
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负责人:ERIC L BROWN
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依托单位:
Genome-wide association to Staphylococcus carriage
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批准号:7987960
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项目类别:
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资助金额:$63.44万
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财政年份:2010
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负责人:ERIC L BROWN
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H.Pylori Infection in Hispanic Children: Immune response pathway SNP pattterns
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批准号:7917868
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项目类别:
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资助金额:$4.14万
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财政年份:2009
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负责人:ERIC L BROWN
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依托单位:
Catalytic Antibodies To Staphylococcus Aureus: Identification and Characterizatio
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批准号:7914338
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项目类别:
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资助金额:$22.5万
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财政年份:2009
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负责人:ERIC L BROWN
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依托单位:
H.Pylori Infection in Hispanic Children: Immune response pathway SNP pattterns
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批准号:7459079
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项目类别:
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资助金额:$18.82万
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财政年份:2007
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负责人:ERIC L BROWN
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依托单位:
海外基金