Bacterial chitinases as new virulence factors

细菌几丁质酶作为新的毒力因子

基本信息

项目摘要

DESCRIPTION (provided by applicant): Recently, we discovered that a secreted chitinase of Legionella pneumophila, the agent of Legionnaires' disease, promotes the persistence of the bacterium in the lungs of experimentally infected mice. In vitro experiments then documented that the L. pneumophila chitinase (ChiA) promotes growth in lung epithelial cells but not in macrophages. Taken together, these data are the first demonstration of a chitinase, a type of enzyme that is traditionally viewed as only being relevant in chitin-containing environmental niches, acting like a virulence factor. Thus, we hypothesize that bacterial chitinases represent a new class of virulence factor. To explore this hypothesis, we will further investigate the role of chitinase in L. pneumophila intracellular infection of lung cells as well as test for the first time the importance of a chitinase in the virulence of a second intracellular pathogen, Listeria monocytogenes. More specifically, we will determine the intracellular location of and trafficking patterns influenced by ChiA and begin to ascertain the effects of ChiA on the lung inflammatory response. For the Listeria experiments, new chitinase mutants will be constructed and then, after confirmation of their loss of chitinase activity and their in vitro growth characteristics, tested in murine models of listeriosis. The proposed studies will i) increase our understanding of the pathogenesis of Lp, which is an important public health concern within the US and throughout the world, ii) examine for the first time the role of chitinase in the pathogenesis of L. monocytogenes, an organism that is also an important public health concern, iii) expand our appreciation of bacterial intracellular infection and the novel role that a chitinase can have in it, iv) have implications for numerous other environmental pathogens that also express chitinases, and iv) offer potential new targets for disease diagnosis, treatment, or prevention. PUBLIC HEALTH RELEVANCE: We recently discovered that the secreted chitinase of Legionella pneumophila promotes bacterial persistence in the lungs of experimentally infected mice. From this novel finding, we hypothesize that microbial chitinases, which have traditionally been viewed as being relevant only in environmental niches, actually represent a new class of virulence factor and therefore are potential new targets for antimicrobial therapy. To explore this hypothesis, we will further investigate the role of chitinase in L. pneumophila intracellular infection of lung cells as well as test for the first time the importance of chitinases in the virulence of a second intracellular pathogen, Listeria monocytogenes.
描述(由申请人提供):最近,我们发现嗜肺军团菌(军团病的病原体)分泌的几丁质酶可促进该细菌在实验感染小鼠肺部的持久存在。体外实验证明,嗜肺军团菌几丁质酶 (ChiA) 促进肺上皮细胞生长,但不促进巨噬细胞生长。总而言之,这些数据首次证明了几丁质酶,这种酶传统上被认为只与含有几丁质的环境利基相关,其作用类似于毒力因子。因此,我们假设细菌几丁质酶代表了一类新的毒力因子。为了探索这一假设,我们将进一步研究几丁质酶在嗜肺军团菌肺细胞内感染中的作用,并首次测试几丁质酶在第二种细胞内病原体单核细胞增生李斯特菌毒力中的重要性。更具体地说,我们将确定 ChiA 影响的细胞内位置和运输模式,并开始确定 ChiA 对肺部炎症反应的影响。对于李斯特菌实验,将构建新的几丁质酶突变体,然后在确认其几丁质酶活性丧失及其体外生长特性后,在李斯特菌病小鼠模型中进行测试。拟议的研究将 i) 增加我们对 Lp 发病机制的了解,这是美国和全世界的一个重要的公共卫生问题,ii) 首次研究几丁质酶在单核细胞增生李斯特菌发病机制中的作用, iii) 扩大我们对细菌细胞内感染以及几丁质酶在其中的新作用的认识,iv) 对许多也表达几丁质酶的其他环境病原体有影响,以及iv) 为疾病诊断、治疗或预防提供潜在的新目标。公共健康相关性:我们最近发现,嗜肺军团菌分泌的几丁质酶可促进实验感染小鼠肺部细菌的持久存在。根据这一新发现,我们假设微生物几丁质酶(传统上被认为仅与环境生态位相关)实际上代表了一类新的毒力因子,因此是抗菌治疗的潜在新靶点。为了探索这一假设,我们将进一步研究几丁质酶在嗜肺军团菌肺细胞内感染中的作用,并首次测试几丁质酶在第二种细胞内病原体单核细胞增生李斯特氏菌毒力中的重要性。

项目成果

期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Stenotrophomonas maltophilia strains replicate and persist in the murine lung, but to significantly different degrees.
嗜麦芽寡养单胞菌菌株在小鼠肺部复制并持续存在,但程度显着不同。
  • DOI:
  • 发表时间:
    2011-07
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Rouf, Ruella;Karaba, Sara M;Dao, Jenny;Cianciotto, Nicholas P
  • 通讯作者:
    Cianciotto, Nicholas P
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NICHOLAS P CIANCIOTTO其他文献

NICHOLAS P CIANCIOTTO的其他文献

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{{ truncateString('NICHOLAS P CIANCIOTTO', 18)}}的其他基金

Stenotrophomonas maltophilia TfcA and TfcB: Antibacterial T4SS effectors from an emerging human pathogen
嗜麦芽寡养单胞菌 TfcA 和 TfcB:来自新兴人类病原体的抗菌 T4SS 效应子
  • 批准号:
    10661253
  • 财政年份:
    2023
  • 资助金额:
    $ 18.98万
  • 项目类别:
Rethinking Legionella pneumophila type IV pili and their roles in intracellular infection
重新思考嗜肺军团菌 IV 型菌毛及其在细胞内感染中的作用
  • 批准号:
    10738431
  • 财政年份:
    2023
  • 资助金额:
    $ 18.98万
  • 项目类别:
Mucinases as Emerging Players in Legionella pneumophila Pathogenesis
粘蛋白酶作为嗜肺军团菌发病机制中的新兴参与者
  • 批准号:
    10643053
  • 财政年份:
    2023
  • 资助金额:
    $ 18.98万
  • 项目类别:
Siderophores of Legionella pneumophila
嗜肺军团菌的铁载体
  • 批准号:
    10172838
  • 财政年份:
    2018
  • 资助金额:
    $ 18.98万
  • 项目类别:
Virulence Mechanisms of the Emerging Pathogen Stenotrophomonas maltophilia
新兴病原体嗜麦芽寡养单胞菌的毒力机制
  • 批准号:
    8867607
  • 财政年份:
    2015
  • 资助金额:
    $ 18.98万
  • 项目类别:
CRISPR Cas genes and Legionella pneumophila infection
CRISPR Cas基因与嗜肺军团菌感染
  • 批准号:
    8733513
  • 财政年份:
    2013
  • 资助金额:
    $ 18.98万
  • 项目类别:
CRISPR Cas genes and Legionella pneumophila infection
CRISPR Cas基因与嗜肺军团菌感染
  • 批准号:
    8424733
  • 财政年份:
    2013
  • 资助金额:
    $ 18.98万
  • 项目类别:
Pyomelanin and Legionella pneumophila Infection
黑色素和嗜肺军团菌感染
  • 批准号:
    8076237
  • 财政年份:
    2010
  • 资助金额:
    $ 18.98万
  • 项目类别:
Pyomelanin and Legionella pneumophila Infection
黑色素和嗜肺军团菌感染
  • 批准号:
    7940261
  • 财政年份:
    2010
  • 资助金额:
    $ 18.98万
  • 项目类别:
Virulence Factors of Stenotrophomonas maltophilia
嗜麦芽寡养单胞菌的毒力因子
  • 批准号:
    7897600
  • 财政年份:
    2009
  • 资助金额:
    $ 18.98万
  • 项目类别:

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