Analyzing pathogenic Vibrio parahaemolyticus-oyster interactions to prevent human disease
Analyzing pathogenic Vibrio parahaemolyticus-oyster interactions to prevent human disease
批准号:
9979077
负责人:
Ann M Stevens
金额:
$8.01万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-03-01 至 2022-02-28
关键词:
AcuteAdolescentAnimal ModelAnimalsAquacultureBacteriaBacterial ProteinsBacteriologyBedsBioinformaticsBiological ModelsBiologyCellsCenters for Disease Control and Prevention (U.S.)ClinicalConsumptionDetectionDevelopmentDiseaseEatingEcologyEnvironmental Risk FactorEpithelialEpitheliumExcisionFoodFood SafetyFoundationsFutureGastroenteritisGenesGeneticGoalsHarvestHealthHumanImmunocompromised HostIndividualInfectionInterventionLaboratoriesLeadLibrariesLifeLocationMethodsMissionModelingMolecularMorbidity - disease rateOystersPalliative CarePathogenicityPathologyPhasePlayPrevention strategyProductionPublic HealthRegulationResearchRoleRouteScientistSeafoodShellfishSiteSourceSystemSystemic infectionTestingTissuesUnited StatesUnited States National Institutes of HealthVibrioVibrio parahaemolyticusVirulenceWaterWorkanimal breedinganimal tissuebasedisorder preventioneconomic impactemerging human pathogenfood surveillancefoodborne illnessgastrointestinalgenetic approachgenome-widehuman diseasehuman morbidityhuman mortalityimprovedin vivoinfection rateinsightmethod developmentmicrobiomemortalitymutantnovelnovel strategiesopen woundpandemic diseasepathogenpathogenic bacteriapreventrisk minimizationtherapy developmenttransmission processtransposon sequencingundercooked
中文摘要
项目概要/摘要
副溶血性弧菌(VP)是导致海产品传播胃肠炎的主要原因,
大流行规模。在美国,它是CDC报告的新兴人类病原体,
发病率和死亡率。致病性VP菌株引起的疾病对全球
与人类健康有关的食品安全和可持续性。最常见的是,人类疾病预防
重点是检测和减少食物来源中的VP。尽管如此,人类VP感染率仍然是
升中国关于VP如何与其海洋动物宿主相互作用,人们知之甚少。更好地理解本
这种关系有可能导致开发方法,以防止细菌-动物宿主
结合和/或增强在人类食用之前从宿主去除细菌,从而减轻
人类疾病的发生。我们建议使用牡蛎,这是VP的天然宿主,也是VP的常见途径。
传播给人类,作为一个动物模型系统,以了解何时以及如何VP与他们相互作用。是
假设A)VP将定位于牡蛎的特定组织,B)特定基因对
VP在牡蛎上定居的能力。我们的合作研究小组加强了拟议的工作,
是由四名科学家组成,他们在分子细菌学、贝类水产养殖、动物病理学
和生物信息学方法。从这项研究中获得的新信息将导致一个更可靠的
基于实验室的牡蛎模型系统,将奠定基础,为今后的工作,建立的作用
环境因素,包括常驻微生物组、宿主遗传学和特定细菌基因产物
在副总统和牡蛎的互动中发挥作用。改进的牡蛎模型不仅适用于VP,而且适用于其他
致病性弧菌物种,导致改进的方法,以防止人类食源性疾病的收购。
英文摘要
Project Summary/Abstract
The bacterium Vibrio parahaemolyticus (VP) is a leading cause of seafood-borne gastroenteritis on a
pandemic scale. In the United States, it is a CDC-reportable emerging human pathogen with increasing annual
morbidity and mortality rates. Diseases caused by pathogenic VP strains have important implications for global
food safety and sustainability in relation to human health. Most commonly, human disease prevention has
focused on the detection and reduction of VP in food sources. Despite this, human VP infection rates are still
rising. Little is known about how VP interacts with its marine animal hosts. A better understanding of this
relationship has the potential to lead to the development of methods to either prevent bacterial-animal host
association and/or enhance bacterial removal from the host prior to human consumption, thereby mitigating the
occurrence of human disease. We propose to use oysters, a natural host of VP and a common route of
transmission to humans, as an animal model system to understand when and how VP interacts with them. It is
hypothesized that A) VP will localize to specific tissues in the oyster and B) specific genes will be critical for the
ability of VP to colonize oysters. The proposed work is strengthened by our collaborative research team, which
is comprised of four scientists with expertise in molecular bacteriology, shellfish aquaculture, animal pathology
and bioinformatics methods. The novel information gained from this research will lead to a more reliable
laboratory-based oyster model system that will lay the foundation for future work to establish the roles
environmental factors, including the resident microbiome, host genetics and specific bacterial gene products
play in VP-oyster interactions. The refined oyster model will be applicable not only for VP but for other
pathogenic Vibrio species, leading to improved methods to prevent human food-borne disease acquisition.
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