Exploitation of virulent/avirulent strain comparison to detect pathogen & host factors critical to the pathogenesis of bovine mastitis due to S.uberis

利用强毒/无毒菌株比较来检测病原体

基本信息

  • 批准号:
    BB/E018173/2
  • 负责人:
  • 金额:
    $ 168.61万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2007
  • 资助国家:
    英国
  • 起止时间:
    2007 至 无数据
  • 项目状态:
    已结题

项目摘要

Bacterial infection of the udder of dairy cows results in a disease named mastitis. This disease is the most common infectious disease in farmed animals; around one million cases occur each year in the UK. Mastitis occurs in all milk producing species; it is painful, occasionally life threatening and results in the loss of milk production or the production of milk that is unfit for human consumption. The disease is currently controlled only by the rigorous attention to the hygiene of dairy cows and the large scale use of antibiotics. Despite these measures cattle still become infected. Now, rather than the infection spreading from cow to cow, infection comes only from sources of bacteria in the environment (fields, straw bedding etc). One bacterium which is a common cause of this disease world wide and which is often present in high numbers in the environment is Streptococcus uberis (Strep uberis). In this research project we intend to identify parts of the Strep uberis that allows it to infect the cow's udder and in so doing identify those parts of the bacterium that should be used to make effective vaccines. We will do this by comparing versions of this bacterium that are able to cause disease (virulent) with others that cannot (avirulent). We will identify the differences between virulent and avirulent Strep uberis, in some instances, by comparing all the genes present in each and looking for those which occur only in the virulent type. In other instances, we will identify the proteins that virulent Strep uberis have on their surface and release into their surroundings and see which ones are missing from the avirulent Strep uberis. By identifying proteins that are produced only by the virulent type we will be able to produce a list of proteins that may have a part to play in causing this disease. Each protein we identify is produced from a single gene in Strep uberis; therefore we can determine which proteins are essential to cause mastitis by inactivating the gene that produces the particular protein and asking the question: Is the new form of Strep uberis, lacking that particular gene/protein, still able to cause disease? To do this we have to try and infect dairy cattle with the new form of the bacterium. This is done under strictly monitored conditions to ensure that we use the least number of animals possible to obtain the correct results. We will be able to identify a number of proteins from Strep uberis that are essential for disease and these will become components of vaccines to prevent this painful condition. We also intend to use the virulent and avirulent types of Strep uberis to help us identify what happens during disease and to identify any parts of the immune response of the dairy cow that can be altered to prevent disease. After infection with bacteria, animals including humans respond by producing messages in the form of chemicals. These are responsible for the way the infected animal responds to that infection and can result in many features associated with the disease. In the case of mastitis, these chemical messages are responsible such things as attracting specific types of white blood cells from the circulating blood into the mammary gland and for inducing the swelling that leads to pain associated the disease. However, we do not understand which messages control which parts of the response and therefore we do not know which ones are helpful to the control of disease and which contribute to the disease itself. As we now have the possibility of creating infections with avirulent Strep uberis, which do not subsequently result in disease, we can compare the messages produced by the host in response to both virulent and avirulent types of this bacterium. The differences will allow us to identify which responses are associated with disease and which are not. This information could subsequently be used to develop drugs that interfere with the chemical messages and reduce the level of disease.
奶牛乳房的细菌感染导致一种名为乳腺炎的疾病。这种疾病是养殖动物中最常见的传染病;在英国每年发生约100万例。乳腺炎发生在所有产奶物种中;它是痛苦的,偶尔危及生命,并导致产奶量损失或产奶量不适合人类消费。目前只有严格注意奶牛的卫生和大规模使用抗生素才能控制这种疾病。尽管采取了这些措施,牛仍然受到感染。现在,感染不是在奶牛之间传播,而是只来自环境中的细菌来源(田地,稻草垫料等)。一种细菌是世界范围内这种疾病的常见原因,并且经常大量存在于环境中,该细菌是尿链球菌(Strep urethra)。在这个研究项目中,我们打算确定链球菌的部分,使其能够感染奶牛的乳房,并在这样做,确定这些部分的细菌,应该用来制造有效的疫苗。我们将通过比较这种细菌的版本,能够引起疾病(有毒)和其他不能(无毒)。在某些情况下,我们将通过比较每种链球菌中存在的所有基因并寻找仅在强毒型中出现的基因来确定强毒和无毒链球菌之间的差异。在其他情况下,我们将确定有毒的链球菌表面上的蛋白质并释放到周围环境中,看看无毒的链球菌中缺少哪些蛋白质。通过鉴定仅由毒性类型产生的蛋白质,我们将能够产生一系列可能在引起这种疾病中发挥作用的蛋白质。我们鉴定的每种蛋白质都是由链球菌中的一个基因产生的;因此,我们可以通过灭活产生特定蛋白质的基因并提出以下问题来确定哪些蛋白质是引起乳腺炎所必需的:缺乏特定基因/蛋白质的新形式的链球菌是否仍然能够引起疾病?要做到这一点,我们必须尝试用这种新形式的细菌感染奶牛。这是在严格监控的条件下进行的,以确保我们使用尽可能少的动物来获得正确的结果。我们将能够从链球菌中鉴定出许多对疾病至关重要的蛋白质,这些蛋白质将成为预防这种痛苦状况的疫苗的组成部分。我们还打算使用有毒和无毒类型的链球菌来帮助我们确定疾病期间发生了什么,并确定奶牛免疫反应的任何部分,可以改变以预防疾病。在感染细菌后,包括人类在内的动物会以化学物质的形式产生信息。这些是受感染动物对感染的反应方式,并可能导致与疾病相关的许多特征。在乳腺炎的情况下,这些化学信息负责将特定类型的白色血细胞从循环血液中吸引到乳腺中,并引起肿胀,导致与疾病相关的疼痛。然而,我们不知道哪些信息控制了反应的哪些部分,因此我们不知道哪些信息有助于控制疾病,哪些信息有助于疾病本身。由于我们现在有可能用无毒力的链球菌感染,随后不会导致疾病,我们可以比较宿主对这种细菌的毒性和无毒力类型的反应产生的信息。这些差异将使我们能够确定哪些反应与疾病有关,哪些与疾病无关。这些信息随后可用于开发干扰化学信息并降低疾病水平的药物。

项目成果

期刊论文数量(5)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Sortase anchored proteins of Streptococcus uberis play major roles in the pathogenesis of bovine mastitis in dairy cattle.
  • DOI:
    10.1051/vetres/2010036
  • 发表时间:
    2010-09
  • 期刊:
  • 影响因子:
    4.4
  • 作者:
    Leigh JA;Egan SA;Ward PN;Field TR;Coffey TJ
  • 通讯作者:
    Coffey TJ
Vru (Sub0144) controls expression of proven and putative virulence determinants and alters the ability of Streptococcus uberis to cause disease in dairy cattle.
  • DOI:
    10.1099/mic.0.055863-0
  • 发表时间:
    2012-06
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Egan SA;Ward PN;Watson M;Field TR;Leigh JA
  • 通讯作者:
    Leigh JA
Virulence related sequences; insights provided by comparative genomics of Streptococcus uberis of differing virulence.
毒力相关的序列;通过不同毒力的Uberis链球菌的比较基因组学提供的见解。
  • DOI:
    10.1186/s12864-015-1512-6
  • 发表时间:
    2015-04-23
  • 期刊:
  • 影响因子:
    4.4
  • 作者:
    Hossain M;Egan SA;Coffey T;Ward PN;Wilson R;Leigh JA;Emes RD
  • 通讯作者:
    Emes RD
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James Leigh其他文献

Contribution of occupational risk factors to the global burden of disease— a summary of findings 1
职业风险因素对全球疾病负担的影响——调查结果摘要 1
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    M. Fingerhut;Tim Driscoll;Deborah Imel Nelson;L. Punnett;A. Pruss;Kyle Steenland;James Leigh
  • 通讯作者:
    James Leigh
The incidence of malignant mesothelioma in Australia 1982-1988.
1982-1988 年澳大利亚恶性间皮瘤的发病率。
  • DOI:
  • 发表时间:
    1991
  • 期刊:
  • 影响因子:
    3.5
  • 作者:
    James Leigh;Carlos F. Corvalán;Ashraf Grimwood;Geoffrey Berry;David A. Ferguson;Rebecca Thompson
  • 通讯作者:
    Rebecca Thompson
DNA adducts in coal miners: association with exposures to diesel engine emissions.
煤矿工人的 DNA 加合物:与柴油发动机排放物暴露的关联。
Contribution of occupational risk factors to the global burden of disease
职业危险因素对全球疾病负担的影响
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    M. Fingerhut;Tim Driscoll;D. ImelNelson;M. Concha;L. Punnett;A. Pruss;Kyle Steenland;James Leigh;Carlos F. Corvalán
  • 通讯作者:
    Carlos F. Corvalán
Localized Merkel cell carcinoma treatment considerations: a response to the forty-year experience at the Peter MacCallum cancer centre
  • DOI:
    10.1186/s12885-024-12443-y
  • 发表时间:
    2024-06-03
  • 期刊:
  • 影响因子:
    3.400
  • 作者:
    James Leigh;Kurt Gebauer
  • 通讯作者:
    Kurt Gebauer

James Leigh的其他文献

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{{ truncateString('James Leigh', 18)}}的其他基金

Prediction of phenotype from genotype with respect to bacterial infection
根据细菌感染的基因型预测表型
  • 批准号:
    BB/T001933/1
  • 财政年份:
    2019
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant
The role of sortase-anchored proteins in the virulence of Streptococcus uberis
分选酶锚定蛋白在乳房链球菌毒力中的作用
  • 批准号:
    S19514/3
  • 财政年份:
    2007
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant
Exploitation of virulent/avirulent strain comparison to detect pathogen & host factors critical to the pathogenesis of bovine mastitis due to S.uberis
利用强毒/无毒菌株比较来检测病原体
  • 批准号:
    BB/E018173/1
  • 财政年份:
    2007
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant
The role of sortase-anchored proteins in the virulence of Streptococcus uberis
分选酶锚定蛋白在乳房链球菌毒力中的作用
  • 批准号:
    S19514/2
  • 财政年份:
    2006
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant

相似海外基金

Exploitation of virulent/avirulent strain comparison to detect pathogen & host factors critical to the pathogenesis of bovine mastitis due to S.uberis
利用强毒/无毒菌株比较来检测病原体
  • 批准号:
    BB/E018114/1
  • 财政年份:
    2008
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant
Exploitation of virulent/avirulent strain comparison to detect pathogen & host factors critical to the pathogenesis of bovine mastitis due to S.uberis
利用强毒/无毒菌株比较来检测病原体
  • 批准号:
    BB/E018173/1
  • 财政年份:
    2007
  • 资助金额:
    $ 168.61万
  • 项目类别:
    Research Grant
The early inflammatory response to virulent and avirulent influenza viruses
对强毒力和无毒力流感病毒的早期炎症反应
  • 批准号:
    nhmrc : 400226
  • 财政年份:
    2006
  • 资助金额:
    $ 168.61万
  • 项目类别:
    NHMRC Project Grants
Developing Avirulent Rabies Virus Vaccines
开发无毒狂犬病病毒疫苗
  • 批准号:
    7478393
  • 财政年份:
    2002
  • 资助金额:
    $ 168.61万
  • 项目类别:
Developing Avirulent Rabies Virus Vaccines
开发无毒狂犬病病毒疫苗
  • 批准号:
    7900063
  • 财政年份:
    2002
  • 资助金额:
    $ 168.61万
  • 项目类别:
Developing Avirulent Rabies Virus Vaccines
开发无毒狂犬病病毒疫苗
  • 批准号:
    7318256
  • 财政年份:
    2002
  • 资助金额:
    $ 168.61万
  • 项目类别:
Developing Avirulent Rabies Virus Vaccines
开发无毒狂犬病病毒疫苗
  • 批准号:
    7653592
  • 财政年份:
    2002
  • 资助金额:
    $ 168.61万
  • 项目类别:
VIRULENT TO AVIRULENT CONVERSION OF L. PNEUMOPHILA
嗜肺军团菌从毒力到无毒的转化
  • 批准号:
    3140274
  • 财政年份:
    1988
  • 资助金额:
    $ 168.61万
  • 项目类别:
VIRULENT TO AVIRULENT CONVERSION OF L. PNEUMOPHILA
嗜肺军团菌从毒力到无毒的转化
  • 批准号:
    3140270
  • 财政年份:
    1988
  • 资助金额:
    $ 168.61万
  • 项目类别:
VIRULENT TO AVIRULENT CONVERSION OF L. PNEUMOPHILA
嗜肺军团菌从毒力到无毒的转化
  • 批准号:
    3140273
  • 财政年份:
    1988
  • 资助金额:
    $ 168.61万
  • 项目类别:
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