Genetic adaptation in Campylobacter: mechanisms and impacts on human health
Genetic adaptation in Campylobacter: mechanisms and impacts on human health
批准号:
7896746
负责人:
JOHN E LINZ
金额:
$18.25万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-21 至 2011-06-30
关键词:
AddressAreaCampylobacterCampylobacter jejuniCessation of lifeDataDevelopmentDiseaseDisease ReservoirsDomestic FowlsFrequenciesFundingGastrointestinal tract structureGenesGeneticGenetic VariationGoalsGrantHealthHumanInterleukin-10MeasuresMethodsModelingMusMutationPatternPlayRoleadaptive immunitycostfoodborne pathogenhuman diseasepreventpublic health relevance
中文摘要
描述(由申请人提供):食源性病原体空肠弯曲杆菌(CJ)每年导致250万至300万人患病,约100人死亡,估计成本在16亿至62亿美元之间。家禽是由希杰病毒引起的人类疾病的主要宿主。我们的长期目标是通过在两个方面制定有效的控制战略来预防人类疾病:a)生物防治剂,以减少家禽疾病库的发展;B)增强先天或适应性免疫以减少人类殖民。在此之前,我们证实了所有被分析的CJ菌株都能在Ross 308肉鸡中定植,而只有一小部分菌株能在C57BL/6J IL10(-/-)小鼠中定植,C57BL/6J IL10(-/-)小鼠是我们的人类疾病模型。在定植过程中,CJ在肉鸡胃肠道中的遗传多样性扩大,而在小鼠胃肠道中的遗传多样性严重减少。我们还证明了这两种不同的遗传适应方法促进了CJ随后在小鼠中的定植。我们的中心假设是,家禽中的遗传适应在CJ随后在小鼠中定植和引起疾病的能力中起关键作用。为了验证这一假设,我们将完成以下具体目标:1)通过分析偶然性基因的突变频率和模式,研究肉鸡和小鼠遗传多样性产生的机制;2)阻断肉鸡的遗传适应,并分析对小鼠后续定殖和致病能力的影响。了解家禽中CJ人类疾病储存库的发展将对与这种食源性病原体相关的人类疾病产生重大的积极影响。公共卫生相关性:食源性病原体空肠弯曲杆菌(CJ)每年导致250万至300万例人类疾病病例,约100人死亡,估计成本在16亿至62亿美元之间。家禽是由希杰病毒引起的人类疾病的主要宿主。我们的长期目标是通过在两个方面制定有效的控制战略来预防人类疾病:a)生物防治剂,以减少家禽疾病库的发展;B)增强先天或适应性免疫以减少人类殖民。
英文摘要
DESCRIPTION (provided by applicant): The food borne pathogen Campylobacter jejuni (CJ) causes between 2.5 and 3 million human disease cases and approximately 100 deaths annually at an estimated cost of between 1.6 and 6.2 billion dollars. Poultry is the major reservoir for human disease caused by CJ. Our long term goal is to prevent human illness by developing effective control strategies in two areas: a) bio-control agents to reduce disease reservoir development in poultry; b) enhance innate or adaptive immunity to reduce human colonization. Previously we demonstrated that all CJ strains analyzed colonize Ross 308 broilers while only a small number of these strains colonize C57BL/6J IL10 (-/-) mice, our model for human disease. During colonization, CJ genetic diversity expands in the broiler GI tract while genetic diversity is severely reduced in the mouse GI tract. We also demonstrated that these two dissimilar methods of genetic adaptation promote subsequent colonization of mice by CJ. Our central hypothesis is that genetic adaptation in poultry plays a key role in the ability of CJ subsequently to colonize and cause disease in mice. To address this hypothesis, we will accomplish the following Specific Aims: 1) study the mechanisms for generating genetic diversity in broilers and mice by analyzing the frequency and pattern of mutation in contingency genes; 2) block genetic adaptation in broilers and analyze the impact on subsequent ability to colonize and cause disease in mice. An understanding of CJ human disease reservoir development in poultry will result in a major positive impact on human illness associated with this food borne pathogen. PUBLIC HEALTH RELEVANCE: The food borne pathogen Campylobacter jejuni (CJ) causes between 2.5 and 3 million human disease cases and approximately 100 deaths annually at an estimated cost of between 1.6 and 6.2 billion dollars. Poultry is the major reservoir for human disease caused by CJ. Our long term goal is to prevent human illness by developing effective control strategies in two areas: a) bio-control agents to reduce disease reservoir development in poultry; b) enhance innate or adaptive immunity to reduce human colonization.
期刊论文(2)
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会议论文
Genetic adaptation in Campylobacter: mechanisms and impacts on human health
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批准号:7627897
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项目类别:
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资助金额:$17.76万
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AFLATOXIN B1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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RAS GENES AND REGULATION OF CELLULAR MORPHOGENESIS
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RAS GENES AND REGULATION OF CELLULAR MORPHOGENESIS
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Aflatoxin B1 biosynthesis in Aspergillus parasiticus
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Aflatoxin B1 biosynthesis in Aspergillus parasiticus
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ALFLATOXIN B1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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AFLATOXIN B1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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AFLATOXIN B-1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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Aflatoxin B1 biosynthesis in Aspergillus parasiticus
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Elimination of dietary aflatoxin to prevent liver cancer
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AFLATOXIN B1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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RAS GENES AND REGULATION OF CELLULAR MORPHOGENESIS
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Aflatoxin B1 biosynthesis in Aspergillus parasiticus
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AFLATOXIN B-1 BIOSYNTHESIS IN ASPERGILLUS PARASITICUS
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