Host factors in determining resistance to cryptosporidiosis in cattle
Host factors in determining resistance to cryptosporidiosis in cattle
批准号:
BB/M012751/1
负责人:
Elisabeth Innes
金额:
$58.77万
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2015
资助国家:
英国
项目状态:
已结题
起止时间:
2015 至 --
中文摘要
隐孢子虫寄生虫是英国和全世界幼牛肠道疾病的最重要原因,也是导致人类婴儿腹泻的主要原因之一[1]。新生牛犊非常容易患上隐孢子虫病,严重腹泻和脱水导致严重发病率,死亡率报告也在增加。隐孢子虫病是一个难以控制的挑战,因为受感染的动物向环境中排放了数十亿个具有感染性的、长期存活的卵囊,这些卵囊是其他动物和人类的感染源。这种疾病已经成为吸牛场日益严重的问题,畜牧业领导人非常关注缺乏安全有效的治疗或疫苗来帮助预防和控制隐孢子虫病,并对这一提议给予了大力支持。我们对决定疾病结果的宿主-病原体相互作用的了解是有限的。新生小牛非常容易受到感染,经常表现出临床疾病,而年龄较大的小牛更具抵抗力。决定这种年龄相关性易感性的因素尚不清楚,该项目旨在通过应用新颖和创新的体内、体外和体外技术来详细研究宿主寄生虫在牛犊急性感染和康复期间的相互作用,以解决与隐孢子虫病抗性有关的宿主因素。限制我们提高对决定疾病抵抗力的因素的理解的一个限制因素是缺乏简单的研究系统来详细分析宿主寄生虫的相互作用。啮齿动物模型是公认的较差的隐孢子虫病临床疾病对照,体外培养隐孢子虫寄生虫的能力非常有限。该项目旨在通过利用体内和体外牛系统的组合来评估固有和适应性细胞免疫反应,并检查隐孢子虫与肠道上皮细胞的相互作用,以解决这些能力上的差距。此外,创新的3D牛肠器官体外培养系统将被应用于详细分析宿主寄生虫在牛肠上皮中的相互作用。来自实验研究的数据将通过与研究农场自然感染的牛犊获得的类似数据进行比较来验证。这一项目将为牛如何抵抗隐孢子虫寄生虫感染提供迄今最全面的探索。对宿主反应的详细说明将提供一个重要的知识平台,使人们能够开发疫苗以帮助预防疾病,并确定相关的生物标志物,使选择性育种方案能够提高复原力。此外,新的牛体外系统的开发将彻底改变我们研究宿主和病原体与隐孢子虫相互作用的能力,最大限度地减少使用动物模型的需要。该项目的成果将引起动物卫生行业、畜牧业生产者、环境和公共卫生工作者以及学术研究人员的兴趣。制定有效的控制战略将对动物生产的可持续效率、保障粮食安全、改善动物健康和福利、减少废物和环境污染以及改善公众和环境健康产生重大影响。[1]Streipen B(2013)自然503:189
英文摘要
Cryptosporidium parasites are the most important cause of enteric disease in young cattle in UK and worldwide and are also one of the leading causes of infant diarrhoea in humans [1]. Neonatal calves are very vulnerable to cryptosporidiosis resulting in significant morbidity due to severe diarrhoea and dehydration and there are increasing reports of mortality. Cryptosporidiosis is a challenge to control as infected animals shed billions of infective, long lived oocysts into the environment and these are a source of infection for other animals as well as people. The disease has emerged as an increasing problem in beef suckler units, and livestock industry leaders are very concerned about the lack of safe and effective treatments or vaccines available to help prevent and control cryptosporidiosis and have given their strong support for this proposal. Our understanding of the host-pathogen interactions that determine disease outcome is limited. Neonatal calves are very vulnerable to infection and often exhibit clinical disease, whereas older calves are more resistant. The factors involved in determining this age-related susceptibility are unclear and this project aims to address the host factors involved in resistance to cryptosporidiosis by applying novel and innovative in vivo, ex vivo and in vitro technologies to examine in detail the host parasite interaction during acute infection and recovery in calves.One of the constraints for improving our understanding of the factors that determine disease resistance has been the lack of simple research systems that permit the detailed analysis of host parasite interactions. The rodent model is an acknowledged poor comparator for clinical disease in cryptosporidiosis in particular, and the capability for culturing Cryptosporidium parasites in vitro is very limited. This project aims to tackle these gaps in capability by utilising a combination of in vivo and in vitro bovine systems to assess innate and adaptive cellular immune responses and examine the interaction of Cryptosporidium with gut epithelial cells. In addition, innovative 3D bovine gut organoid in vitro culture systems will be applied to enable a detailed analysis of host parasite interactions in the bovine gut epithelium. Data derived from the experimental studies will be validated by comparison to similar data obtained from naturally infected calves on a study farm.This project will provide the fullest exploration yet of how cattle resist infection with Cryptosporidium parasites. A detailed account of the host responses involved will provide an important knowledge platform that will enable the development of vaccines to aid disease prevention and the identification of relevant biomarkers that will enable selective breeding programmes to improve resilience. In addition, the development of novel in vitro bovine systems would revolutionise our capability to study host-pathogen interactions with Cryptosporidium minimising the need for use of animal models.Outputs from the project will be of interest to the animal health industry, livestock producers, environmental and public health workers and to academic researchers. The development of effective control strategies will have a significant impact on the sustainable efficiency of animal production, safeguard food security, improve animal health and welfare, reduce waste and environmental contamination and improve public and environmental health. [1] Streipen B (2013) Nature 503:189
期刊论文(10)
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DOI:
10.1186/s13567-017-0447-0
发表时间:
2017-08-11
期刊:
Veterinary research
影响因子:
4.4
作者:
[Thomson S, Hamilton CA, Hope JC, Katzer F, Mabbott NA, Morrison LJ, Innes EA]
通讯作者:
Innes EA
DOI:
10.1186/s13567-018-0547-5
发表时间:
2018-07-03
期刊:
Veterinary research
影响因子:
4.4
作者:
[Hamilton CA, Young R, Jayaraman S, Sehgal A, Paxton E, Thomson S, Katzer F, Hope J, Innes E, Morrison LJ, Mabbott NA]
通讯作者:
Mabbott NA
DOI:
10.1186/s13071-015-1107-8
发表时间:
2015-10-01
期刊:
Parasites & vectors
影响因子:
3.2
作者:
[Hotchkiss EJ, Gilray JA, Brennan ML, Christley RM, Morrison LJ, Jonsson NN, Innes EA, Katzer F]
通讯作者:
Katzer F
Genetic diversity and shedding profiles for Cryptosporidium parvum in adult cattle and their calves.
DOI:
10.1016/j.crpvbd.2021.100027
发表时间:
2021
期刊:
Current research in parasitology & vector-borne diseases
影响因子:
--
作者:
[Shaw HJ, Armstrong C, Uttley K, Morrison LJ, Innes EA, Katzer F]
通讯作者:
Katzer F
MOESM5 of Development of in vitro enteroids derived from bovine small intestinal crypts
MOESM5 牛小肠隐窝体外肠类的开发
DOI:
10.6084/m9.figshare.6740006
发表时间:
2018
期刊:
影响因子:
--
作者:
[Hamilton C]
通讯作者:
Hamilton C
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