Surveillance genome sequencing to detect SARS-CoV-2 virus variants in Montana
Surveillance genome sequencing to detect SARS-CoV-2 virus variants in Montana
批准号:
10381357
负责人:
BRUCE E BOWLER
金额:
$70.45万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2022-07-31
关键词:
2019-nCoVAddressAffectAgeAreaCLIA certifiedCOVID-19 detectionCOVID-19 pandemicCOVID-19 patientCOVID-19 severityCOVID-19 testingCOVID-19 vaccineCenters for Disease Control and Prevention (U.S.)Centers of Research ExcellenceCommunitiesCountryDangerousnessDataData AnalysesDatabasesDisease OutbreaksEarly identificationEthnic OriginEvolutionFrequenciesGenbankGeneticGenetic RecombinationGenetic StructuresGenomeGenomicsGoalsGrantGuidelinesHealthHealthcareHospitalsHumanKnowledgeMolecularMolecular EvolutionMonitorMonoclonal Antibody TherapyMontanaPatientsPatternPediatric HospitalsPharmacogeneticsPhasePopulationPublic HealthResearchReservationsResistanceResourcesRouteRuralRural CommunitySARS-CoV-2 B.1.1.7SARS-CoV-2 B.1.351SARS-CoV-2 genomeSARS-CoV-2 transmissionSARS-CoV-2 variantSalish and Kootenai TribesSamplingScientistServicesSiteStructureTestingTimeTreatment EfficacyUnited StatesUniversitiesVariantViralVirulenceVirusadaptive immunitygenome analysisgenome sequencinghost-microbe interactionsinsightinterestmetropolitanneutralizing monoclonal antibodiesnovelnovel vaccinespandemic diseaseresearch clinical testingresponsesextrendtribal Nationtribal communitytribal healthunderserved communityvaccine efficacyvariants of concernviral transmissionwhole genome
中文摘要
项目总结
英文摘要
Project Summary
Montana is a state with large rural and Tribal Nations populations. Both groups have been underrepresented in
whole genome sequencing of SARS-CoV-2 variants and the state of Montana lags significantly behind the
country as a whole in sequencing data available from patients infected with SARS-CoV-2. Given the
emergence of dangerous SARS-CoV-2 variants with higher viral transmissibility and reduced response to
monoclonal antibody therapy and vaccine efficacy, lack of sequencing data is a critical problem for the
Montana state Department of Public Health and Human Services (DPHHS) in mounting an appropriate
response to the pandemic. Furthermore, sequencing data will be particularly important for understanding viral
transmission in Tribal Nations, which have been disproportionately affected by the pandemic. This supplement
to the Center for Biomolecular Structure and Dynamics COBRE grant will allow whole genome sequencing and
analysis of >3000 SARS-CoV-2 viruses isolated from patients in the state of Montana, including those living in
rural and Tribal communities. General sequencing results will be made publicly available, except Tribal
samples unless Tribal approval is given, through GenBank and GISAID to facilitate broader analysis of the
emergence of variants of concern (VOC) and variants of interest (VOI) in the United States and will be
communicated directly to the Montana DPHHS and participating Tribal Nations so that they can adjust their
responses to the pandemic. We take advantage of the CLIA-certified SARS-CoV-2 testing facility on the
University of Montana campus, our expertise in whole genome sequencing and our established relationships
with Tribal Nations in Montana to accomplish the goals of this SARS-CoV-2 sequencing supplement. The
analysis of these data will focus on three specific aims:
Specific Aim 1: What is the genetic structure of SARS-CoV-2 variants across Montana communities
and how does this variation compare to regional, national, and global SARS-CoV-2 diversity?
Specific Aim 2: Does the genetic composition of circulating SARS-CoV-2 variants differ between rural
versus metropolitan and Tribal versus non-Tribal communities in Montana?
Specific Aim 3: Are specific outbreaks associated with known or putative novel variants of interest
and/or concern?
Overall, the project will provide critical new insight into how more dangerous variants of SARS-CoV-2 arise and
spread in a rural state and among the disproportionately-effected Tribal Nations in Montana that will allow for
better response to the pandemic for these groups.
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细胞色素 c 可以形成明确的碳氢化合物结合袋。
DOI:
10.1021/jacs.6b10745
发表时间:
2016-12-28
期刊:
Journal of the American Chemical Society
影响因子:
15
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[McClelland LJ, Steele HB, Whitby FG, Mou TC, Holley D, Ross JB, Sprang SR, Bowler BE]
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卤代乙腈 - GeF4 配合物的结构和能量性质。
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发表时间:
2017
期刊:
Journal of molecular structure
影响因子:
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[Waller,AnnaW, Weiss,NicoleM, Decato,DanielA, Phillips,JamesA]
通讯作者:
Phillips,JamesA
Synthesis and Biological Evaluation of Trehalose-based Bi-aryl Derivatives as C-type Lectin Ligands.
海藻糖基联芳基衍生物作为 C 型凝集素配体的合成和生物学评价。
DOI:
10.1016/j.tet.2022.133241
发表时间:
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Tetrahedron
影响因子:
2.1
作者:
[Rasheed,OmerK, Buhl,Cassandra, Evans,JayT, Holley,David, Ryter,KendalT]
通讯作者:
Ryter,KendalT
DOI:
10.1002/elps.201600381
发表时间:
2017-03
期刊:
Electrophoresis
影响因子:
2.9
作者:
[Penny WM, Steele HB, Ross JB, Palmer CP]
通讯作者:
Palmer CP
DOI:
10.1021/acscatal.9b00744
发表时间:
2019-03
期刊:
ACS catalysis
影响因子:
12.9
作者:
[John E. A. Russell;Emily D. Entz;I. Joyce;Sharon R. Neufeldt]
通讯作者:
John E. A. Russell;Emily D. Entz;I. Joyce;Sharon R. Neufeldt
共 48 条
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