Salmonella polymicrobial interactions
Salmonella polymicrobial interactions
批准号:
8264043
负责人:
Brian M Ahmer
金额:
$8.05万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-05-15 至 2013-04-30
关键词:
Aeromonas hydrophilaAnatomyAnimal ModelAnimalsAntibiotic TherapyAntibioticsBacteriaBacterial InfectionsBolus InfusionDetectionDiseaseDoseEcologyEngineeringEpidemicFamily suidaeFarming environmentFecesGastrointestinal tract structureGenesGoalsHomologous GeneHumanIn VitroIndividualInfectionInfection preventionIntestinesLaboratory miceLactonesLeadLibrariesLocationMeasuresMethodsMicrobeModelingMolecularMusMutagenesisNamesNutrientOrganismOutputPhenotypePhysiologyPlayPopulationProbioticsProcessProductionRegulonRiskRoleSalmonellaSalmonella entericaSalmonella infectionsSchemeScreening procedureSignaling MoleculeSiteSystemTechnologyTestingTimeTurtlesValidationVirus DiseasesVitaminsWorkYersiniaYersinia enterocoliticaYersinia infectionsabstractingbasedesignfitnessgenetic selectionin vivoindexinginsightmembermouse modelmutantnovelpathogenpathogenic bacteriapreventresearch studysuccesstransmission process
中文摘要
摘要正常的微生物群为宿主提供必需的营养和维生素,也使病原微生物很难定植。众所周知,某些病毒感染可促进继发性细菌感染。然而,细菌在促进其他细菌感染方面所起的作用尚未得到很好的研究。我们已经确定沙门氏菌编码一种名为SdiA的LuxR同源物,可以检测宿主中其他致病菌的信号分子。到目前为止,我们已经确定沙门氏菌可以在海龟中检测到嗜水气单胞菌,在小鼠和猪中检测到小肠结肠炎耶尔森菌。沙门氏菌在猪体内检测耶尔森氏菌信号分子的能力导致沙门氏菌脱落的大量增加。在一项单独的研究中,最近观察到感染小肠结肠炎耶尔森菌的猪被肠道沙门氏菌定植的风险增加。鉴于沙门氏菌是世界上最重要的病原体之一,确定导致这种有机体传播的参数是很重要的。在这项工作中,将确定耶尔森氏菌感染增加沙门氏菌定殖宿主并从宿主中脱落的能力的程度。我们将检验沙门氏菌感染剂量、沙门氏菌脱落量和沙门氏菌脱落持久性的假设,这些假设在某种程度上取决于沙门氏菌检测耶尔森菌合成ahl的能力。将确定每个sdiA调节成员在这些表型中的作用。此外,基于阵列的转座子筛选将用于鉴定新的沙门氏菌基因,以利用共感染。这些基因将被解析为sdiA依赖和不依赖组,其中sdiA依赖组将进一步分类,以确定它们是sdiA调控的新成员还是与sdiA协同作用的基因。的相关性。宿主的正常菌群在预防细菌感染中起着非常重要的作用。病原体绕过或超越正常微生物群的机制在很大程度上是未知的。在这个提议中,我们假设一种方法是利用另一种病原体的成功。了解病原体相互作用以及与正常微生物群相互作用的机制将有助于深入了解病原体宿主范围以及疾病和流行病的生态学。这将有利于抗生素和益生菌的合理设计和使用。
英文摘要
DESCRIPTION (provided by applicant): Salmonella polymicrobial interactions Abstract The normal microbiota provide essential nutrients and vitamins to the host and also make it very difficult for pathogenic microbes to colonize. It is well known that certain viral infections can facilitate secondary bacterial infections. However, the role that bacteria play in facilitating other bacterial infections is not well studied. We have determined that Salmonella encodes a LuxR homolog named SdiA that can detect the signaling molecules of other pathogenic bacteria in the host. To date, we have determined that Salmonella can detect Aeromonas hydrophila in turtles and Yersinia enterocolitica in mice and pigs. The ability of Salmonella to detect the signaling molecules of Yersinia in pigs led to a large increase in Salmonella shedding. In a separate study it was recently observed that swine infected with Yersinia enterocolitica are at increased risk to be colonized with Salmonella enterica. Given that Salmonella is one of the world's most significant pathogens, it is important to determine the parameters that lead to transmission of this organism. In this work, the extent to which a Yersinia infection increases the ability of Salmonella to colonize a host and be shed from that host will be determined. We will test the hypotheses that the infectious dose for Salmonella, the amount of Salmonella shed, and the persistence of Salmonella shedding are altered in a manner dependent upon the ability of Salmonella to detect the AHLs synthesized by Yersinia. The role of individual sdiA regulon members in each of these phenotypes will be determined. Additionally, array-based transposon screening will be used to identify novel Salmonella genes required to take advantage of coinfections. These genes will be parsed into sdiA- dependent and -independent groups, with the sdiA-dependent group being further categorized as to whether they are new members of the sdiA regulon or genes that act synergistically with sdiA. Relevance. The normal microbiota of the host play a very important role in preventing bacterial infections. The mechanisms by which pathogens circumvent or outcompete the normal microbiota are largely unknown. In this proposal we hypothesize that one method is to take advantage of another pathogen's success. Understanding the mechanisms by which pathogens interact with each other and with the normal microbiota will provide insights into pathogen host range and the ecology of disease and epidemics. This will facilitate the rational design and use of antibiotics and probiotics.
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会议论文
Microbial ecology of the inflamed intestine
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批准号:10462602
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项目类别:
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资助金额:$70.6万
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财政年份:2018
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负责人:Brian M Ahmer
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Salmonella-specific therapeutics
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批准号:9764264
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Salmonella-specific therapeutics
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批准号:10215469
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资助金额:$63.53万
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负责人:Brian M Ahmer
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Microbial ecology of the inflamed intestine
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批准号:10227082
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资助金额:$70.6万
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财政年份:2018
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负责人:Brian M Ahmer
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Microbial ecology of the inflamed intestine
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批准号:9789832
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资助金额:$70.6万
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财政年份:2018
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负责人:Brian M Ahmer
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Salmonella, colonization resistance, and fructose-asparagine
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批准号:8966010
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项目类别:
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资助金额:$49.66万
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财政年份:2014
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依托单位:
Salmonella, colonization resistance, and fructose-asparagine
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批准号:9184529
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项目类别:
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资助金额:$49.66万
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财政年份:2014
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负责人:Brian M Ahmer
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依托单位:
Coordination of metabolism and virulence during infection
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批准号:8214355
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项目类别:
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资助金额:$38.69万
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财政年份:2011
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负责人:Brian M Ahmer
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依托单位:
Coordination of metabolism and virulence during infection
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批准号:8582536
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项目类别:
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资助金额:$49.06万
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财政年份:2011
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负责人:Brian M Ahmer
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依托单位:
Coordination of metabolism and virulence during infection
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批准号:8374104
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项目类别:
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资助金额:$40.98万
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财政年份:2011
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负责人:Brian M Ahmer
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依托单位:
Salmonella polymicrobial interactions
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批准号:8063534
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项目类别:
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资助金额:$50.06万
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财政年份:2008
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负责人:Brian M Ahmer
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依托单位:
Salmonella polymicrobial interactions
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批准号:8259465
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项目类别:
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资助金额:$58.03万
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财政年份:2008
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负责人:Brian M Ahmer
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依托单位:
Salmonella polymicrobial interactions
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批准号:7527342
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项目类别:
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资助金额:$50.51万
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财政年份:2008
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负责人:Brian M Ahmer
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依托单位:
Salmonella polymicrobial interactions
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批准号:7808091
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项目类别:
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资助金额:$57.86万
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财政年份:2008
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负责人:Brian M Ahmer
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依托单位:
Salmonella polymicrobial interactions
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批准号:7623026
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项目类别:
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资助金额:$59.73万
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财政年份:2008
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负责人:Brian M Ahmer
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依托单位:
Detection of Mixed Microbial Communities by Salmonella
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项目类别:
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资助金额:$22.12万
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财政年份:2001
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负责人:Brian M Ahmer
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依托单位:
Detection of mixed microbial communities by Salmonella
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资助金额:$30.0万
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财政年份:2001
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负责人:Brian M Ahmer
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依托单位:
Detection of Mixed Microbial Communities by Salmonella
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批准号:6362006
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项目类别:
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资助金额:$19.85万
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财政年份:2001
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负责人:Brian M Ahmer
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依托单位:
Detection of Mixed Microbial Communities by Salmonella
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批准号:6632478
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项目类别:
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资助金额:$22.13万
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财政年份:2001
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负责人:Brian M Ahmer
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依托单位:
Detection of Mixed Microbial Communities by Salmonella
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批准号:6742401
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项目类别:
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资助金额:$22.13万
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财政年份:2001
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负责人:Brian M Ahmer
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依托单位:
海外基金