Defining mechanisms of microbe-microbe interactions in chronic wound infection
Defining mechanisms of microbe-microbe interactions in chronic wound infection
批准号:
10569495
负责人:
Carolyn Brook Ibberson
金额:
$10.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-02-09 至 2025-01-31
关键词:
AddressAffectAmericanAnimal ModelChronicCoculture TechniquesCommunitiesComplexConfocal MicroscopyDataDiseaseDisease OutcomeEconomic BurdenElectron TransportEnvironmentFermentationGene ExpressionGlobal ChangeGoalsHealthcare SystemsHumanIn SituIn VitroInfectionInvestigationMediatingMetabolicMetabolismMicrobeMolecularMusOrganismPathogenesisPhysiologyProcessPseudomonas aeruginosaRoleSeverity of illnessStaphylococcus aureusStructureSystemTechniquesTestingWorkWound InfectionWound modelsanalysis pipelineantibiotic tolerancechronic woundco-infectiondesignfitnessgenetic approachhealingimprovedin vitro Modelin vivoinhibitormicrobial communitymicroorganism interactionnext generation sequencingnovel therapeutic interventionopportunistic pathogenpathogenresponsesynergismtranscriptometranscriptome sequencingwound
中文摘要
项目摘要
金黄色葡萄球菌是世界范围内人类感染的主要原因。葡萄球菌调查
金黄色葡萄球菌的致病机制主要集中在单种感染和共感染微生物对金黄色葡萄球菌的影响。
金黄色葡萄球菌在感染过程中的生理学仍然研究不足,但至关重要。我最近的工作主要集中在
表征S.使用Next-在铜绿假单胞菌单一和合并感染期间观察金黄色葡萄球菌生理学
代测序技术。目前的应用程序逻辑上建立在这项工作,并侧重于
描述了S.金黄色葡萄球菌和慢性伤口感染中的共感染微生物。
本申请的总体目标是双重的:1)定义S.
金黄色葡萄球菌和共感染的微生物在感染(具体目标1);和2)扩大这些发现,
确定微生物-微生物相互作用对S.人类感染中的金黄色葡萄球菌生理学(特异性
目标2)。这项工作很可能会产生重要的发现,有助于我们了解潜在的
慢性多微生物感染中微生物-微生物相互作用的机制。
英文摘要
Project Summary
Staphylococcus aureus is a leading cause of human infection worldwide. Investigations into Staphylococcus
aureus pathogenesis have focused on mono-species infections and the impact of co-infecting microbes on S.
aureus physiology during infection remains understudied but critically important. My recent work has focused on
characterizing S. aureus physiology during mono- and co-infection with Pseudomonas aeruginosa using next-
generation sequencing techniques. The current application builds logically on this work and is focused on
characterizing the interactions between S. aureus and co-infecting microbes within chronic wound infections.
The overall goal of this application is two-fold: 1) to define the metabolic interactions that occur between S.
aureus and co-infecting microbes during infection (Specific Aim 1); and 2) to expand on these findings to
determine the impact of microbe-microbe interactions on S. aureus physiology within human infections (Specific
Aim 2). This work is likely to yield important discoveries that will aid in our understanding of the underlying
mechanisms of microbe-microbe interactions within chronic polymicrobial infections.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
Defining Microbial Community Functions in Chronic Human Infection with Metatranscriptomics.
用宏转录组学定义人类慢性感染中的微生物群落功能。
DOI:
10.1101/2023.06.06.543868
发表时间:
2023
期刊:
bioRxiv : the preprint server for biology
影响因子:
--
作者:
[Adekoya,AanuoluwaE, Kargbo,HoodyA, Ibberson,CarolynB]
通讯作者:
Ibberson,CarolynB
DOI:
10.1073/pnas.2212340119
发表时间:
2022-12-20
期刊:
Proceedings of the National Academy of Sciences of the United States of America
影响因子:
11.1
作者:
[]
通讯作者:
海外基金