Biocontainment Research Support Service(s) Core
生物防护研究支持服务核心
基本信息
- 批准号:10793830
- 负责人:
- 金额:$ 94.49万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-08-18 至 2028-07-31
- 项目状态:未结题
- 来源:
- 关键词:2019-nCoVAdvanced DevelopmentAerosolsAnimal ModelAnimalsAreaBiological AssayBlood Chemical AnalysisCOVID-19 pandemicCaviaCellsChemicalsCollaborationsCommunicable DiseasesCommunicationCommunitiesContainmentControlled EnvironmentCore FacilityCustomDataDedicationsDevelopmentDiagnosticEmerging Communicable DiseasesEnsureEquipmentEvaluationEventFamily suidaeFerretsFlow CytometryFundingGoalsGoatGrowthHamstersHuman ResourcesImageImmune responseImmunityImmunologyInfectionInfectious Diseases ResearchInhalation ExposureInvestmentsLaboratoriesMaintenanceManufacturerMethodologyMethodsMicrobiologyMicroscopyMissouriModelingMonitorMusMutant Strains MiceNational Institute of Allergy and Infectious DiseaseOryctolagus cuniculusPersonsProceduresProductivityPublic HealthRattusRecoveryReproducibilityResearchResearch PersonnelResearch SupportResource DevelopmentResourcesRouteSafetySamplingScientistSecureServicesSheepSpecialistSpeedStructureSystemTechnical ExpertiseTechnologyTimeTrainingTransgenic AnimalsTranslatingUnited States National Institutes of HealthUniversitiesViralWorkWorkforce Developmentbiodefensebiosafety level 3 facilitycytokineemerging pathogenexperienceexperimental studyhuman diseasehuman modelin vitro Assayinstrumentationmedical countermeasurenew outbreaknext generationnovelnovel vaccinespathogenpathogen exposurepathogenic bacteriapathogenic viruspre-clinicalpreclinical developmentpriority pathogenprogramsreal-time imagesrecruitresearch and developmentresponsevector transmission
项目摘要
Project Summary
Core 3: Biocontainment Research Support Services Core
The objective of the Biocontainment Research Support Services Core (BRSSC, Core 3) is to provide sustainable
research resources that facilitate the pre-clinical development of medical countermeasures against emerging
and re-emerging pathogens. To achieve this, the BRSSC provides world-class resources in the priority areas of
aerobiology, animal modeling, immunology, imaging, and microbiology for BSL-3 bacterial and viral pathogens.
The BRSSC serves the needs of MU as well as NIAID and the RBL-NBL network by focusing its capabilities to
provide technical expertise under BSL-3 containment for NIAID priority pathogens and the evaluation of novel
vaccines, treatments, and diagnostics. The BRSSC closely collaborates with other relevant Research Services
at MU, including but not limited to the NIH-funded Resource and Research Centers for Mutant Mouse, Rat, and
Swine to develop and refine novel transgenic animal models for priority pathogens such as SARS-CoV-2. The
technical staff of the BRSSC is a dedicated team for conducting and supporting experiments using advanced
technology, high-precision instrumentation on live samples. Added layers of primary and secondary containment
allow for safe handling and usage of the unique support services that are offered in the BRSSC. For example,
direct access from the vivarium to the class III glovebox and its inhalation exposure chamber eliminates the need
to move infected animals through corridors or other space that may expose people. In addition, there is a high-
speed cell sorter, housed within a manufacturer-supplied class II BSC, that allows recovery of live cells infected
with a BSL-3 pathogen for downstream analysis. The Lionheart fluorescent microscopy system allows real-time
imaging of environmentally-controlled live BSL-3 samples in multi-well format, and is useful for optimization of
viral growth conditions and other live and in vitro assays without need for pathogen inactivation. Further imaging
and other instrumentation available in the ABSL-3 allows for longitudinal monitoring of the infection, blood
chemistry and immune responses without need to chemically inactivate sample, thereby reducing time and
unwanted impact for the procedure. All of these examples illustrate the capabilities for safe conduct of BSL-3
research using advanced technology instrumentation that is available through the BRSSC. The collaborative
effort between the dedicated teams of Cores 1, 2 and 3 of this UC7 application combined with regular interactions
with the NIAID RBL-NBL network will maximize best practices and usage of these unique resources. To create
sustainability, the BRSSC is committed to training diverse technical professionals and scientists in BSL-3/ACL-
3/ABSL-3 research. Through management of the critical resources at the LIDR, the BRSSC helps advance the
development of novel medical countermeasures against BSL-3 pathogens.
项目摘要
核心3:生物遏制研究支持服务核心
生物遏制研究支持服务核心(BRSSC,核心3)的目标是提供可持续的
促进临床前发展应对新出现的医学对策的研究资源
以及重新出现的病原体。为了实现这一目标,BRSSC在以下优先领域提供世界级的资源
BSL-3细菌和病毒病原体的空气生物学、动物模型、免疫学、成像和微生物学。
BRSSC通过集中其能力来满足MU、NIAID和RBL-NBL网络的需求
为NIAID优先病原体提供BSL-3遏制下的技术专长,并对新的
疫苗、治疗和诊断。BRSSC与其他相关研究机构密切合作
在墨尔本大学,包括但不限于NIH资助的突变小鼠、大鼠和
开发和改进针对SARS-CoV-2等优先病原体的新型转基因动物模型。这个
BRSSC的技术人员是一支专门进行和支持实验的团队,使用先进的
技术,现场样品的高精度仪器。增加了一级和二级安全壳的层数
允许安全处理和使用BRSSC中提供的独特支持服务。例如,
从隔膜直接接触到III类手套盒及其吸入曝光室不需要
通过走廊或其他可能暴露人的空间移动受感染的动物。此外,还有一个很高的-
快速细胞分选机,安装在制造商提供的II类BSC中,允许恢复受感染的活细胞
与BSL-3病原体进行下游分析。狮心荧光显微镜系统允许实时
以多井形式对环境控制的BSL-3活体样品进行成像,并有助于优化
病毒生长条件和其他活的和体外的检测,不需要病原体灭活。进一步成像
和ABSL-3中提供的其他仪器允许纵向监测感染、血液
化学和免疫反应,无需对样品进行化学灭活,从而缩短了时间和
对手术造成不必要的影响。所有这些例子都说明了BSL-3的安全指挥能力
使用BRSSC提供的先进技术仪器进行研究。协作
此UC7应用程序的核心1、2和3的专用团队之间的工作与定期交互相结合
有了NIAID,RBL-NBL网络将最大限度地利用这些独特的资源和最佳实践。要创建
为了实现可持续发展,BRSSC致力于培训不同的技术专业人员和科学家,了解BSL-3/ACL-
3/ABSL-3研究。通过管理LIDR的关键资源,BRSSC帮助推进
针对BSL-3病原体的新型医学对策的开发。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Rachel M Olson其他文献
Activation of Heme Oxygenase Expression by Cobalt Protoporphyrin Treatment Prevents Pneumonic Plague Caused by Inhalation of Yersinia pestis
钴原卟啉处理激活血红素加氧酶表达可预防吸入鼠疫耶尔森氏菌引起的肺鼠疫
- DOI:
- 发表时间:
2020 - 期刊:
- 影响因子:4.9
- 作者:
Joshua L. Willix;Jacob L. Stockton;Rachel M Olson;P. Anderson;Deborah M Anderson - 通讯作者:
Deborah M Anderson
Polyphenol content and antioxidant capacity of eggplant skin
茄子皮多酚含量及抗氧化能力
- DOI:
- 发表时间:
2008 - 期刊:
- 影响因子:0
- 作者:
Rachel M Olson;Albert Teo;Ajay P. Singh;Devanand L. Luthria;G. Bañuelos;S. Pasakdee;N. Vorsa;T. Wilson - 通讯作者:
T. Wilson
Macrophage LTB4 drives efficient phagocytosis of Borrelia burgdorferi via BLT1 or BLT2[S]
巨噬细胞 LTB4 通过 BLT1 或 BLT2 驱动伯氏疏螺旋体的高效吞噬作用[S]
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:6.5
- 作者:
Yan Zhang;Rachel M Olson;Charles R. Brown - 通讯作者:
Charles R. Brown
Fractionation Techniques to Examine Effector Translocation.
检查效应器易位的分离技术。
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:0
- 作者:
Rachel M Olson;Deborah M Anderson - 通讯作者:
Deborah M Anderson
Rachel M Olson的其他文献
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