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DESCRIPTION (provided by applicant): Renal lithiasis, or kidney stones, and associated complications are a major burden on our health care system affecting 8.8% of the population in the United States. Oxalate is a simple organic acid widely consumed by humans and is also a constituent in 80% of all kidney stones. Many adults host intestinal oxalate-degrading bacteria, which can degrade oxalate and significantly reduce the amount circulating in the blood. Individuals who do not host oxalate-degrading bacteria can acquire them and the benefits they confer, as probiotic supplements. However, these probiotics are often lost in the intestines over time, and a high oxalate diet is required for their maintenance. The mechanisms driving the loss of probiotic oxalate-degrading bacteria on a low oxalate diet represents a considerable gap in our understanding of the gut microbiome and is a challenge for the successful treatment of hyperoxaluria. My long-term goal is to understand the mechanisms that facilitate the persistent colonization of bacteria in the gut and develop effective probiotics to treat oxalate-related illnes. The overall objectives of this application are to use molecular techniques such as metagenomics and qPCR to identify the mechanisms behind the loss of oxalate-degrading bacteria inoculated into a host. We hypothesize that the oxalate-degrading function is supported by the metabolic activity of the non- degrading proportion of the gut microbiota. Three specific aims are proposed to test this hypothesis: (1) Determine the persistence of the oxalate-degrading community on variable oxalate loads; (2) Identify the unique metabolic pathways and microbial taxa that are present in persistent oxalate-degrading microbiota; and (3) Quantify the differences in the relative expression of genes encoding for oxalate-sensitive anion-transport proteins in animals with or without natural communities of oxalate-degrading bacteria. Completion of the specific aims will identify the mechanisms facilitating the persistence and loss of oxalate-degrading communities in the gut. Outcomes will have a positive impact by identifying the molecular mechanisms that lead to the persistence and loss of oxalate-degrading bacteria, which is an important step in making oxalate-degrading bacteria a viable treatment for hyperoxaluria.
期刊论文(11)
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Evolutionary irony: evidence that 'defensive' plant spines act as a proximate cue to attract a mammalian herbivore.
进化的讽刺:有证据表明“防御性”植物刺是吸引哺乳动物草食动物的直接线索。
DOI: 10.1111/oik.02004
发表时间: 2015
期刊: Oikos (Copenhagen, Denmark)
影响因子: --
作者: [Kohl,KevinD, Miller,AaronW, Dearing,MDenise]
通讯作者: Dearing,MDenise
Microbial Community Transplant Results in Increased and Long-Term Oxalate Degradation.
微生物群落移植会导致草酸盐降解和长期降解。
DOI: 10.1007/s00248-016-0800-2
发表时间: 2016-08
期刊: MICROBIAL ECOLOGY
影响因子: 3.6
作者: [Miller, Aaron W., Oakeson, Kelly F., Dale, Colin, Dearing, M. Denise]
通讯作者: Dearing, M. Denise
Draft Genome Sequence of an Oxalate-Degrading Strain of Clostridium sporogenes from the Gastrointestinal Tract of the White-Throated Woodrat (Neotoma albigula).
来自白喉林鼠(Neotoma albigula)胃肠道的产孢梭菌草酸盐降解菌株的基因组序列草案。
DOI: 10.1128/genomea.00392-16
发表时间: 2016
期刊: Genome announcements
影响因子: --
作者: [Oakeson,KellyF, Miller,Aaron, Dale,Colin, Dearing,Denise]
通讯作者: Dearing,Denise
Commentary: Loss of Function Dysbiosis Associated with Antibiotics and High Fat, High Sugar Diet
评论:与抗生素和高脂肪、高糖饮食相关的功能丧失、生态失调
DOI: 10.29245/2689-9981/2019/3.1141
发表时间: 2019
期刊: Journal of infectiology
影响因子: --
作者: [Aaron W. Miller]
通讯作者: Aaron W. Miller
The role of acetogenic, methanogenic, and sulfate-reducing bacteria in oxalate metabolism and hyperoxaluria
  • 批准号:
    10617252
  • 项目类别:
  • 资助金额:
    $45.18万
  • 财政年份:
    2020
  • 负责人:
    Aaron W Miller
  • 依托单位:
The role of acetogenic, methanogenic, and sulfate-reducing bacteria in oxalate metabolism and hyperoxaluria
  • 批准号:
    10366042
  • 项目类别:
  • 资助金额:
    $46.31万
  • 财政年份:
    2020
  • 负责人:
    Aaron W Miller
  • 依托单位:
Mechanisms facilitating the persistent colonization of oxalate-degrading bacteria
  • 批准号:
    8831275
  • 项目类别:
  • 资助金额:
    $5.33万
  • 财政年份:
    2014
  • 负责人:
    Aaron W Miller
  • 依托单位:
Mechanisms facilitating the persistent colonization of oxalate-degrading bacteria
  • 批准号:
    8996474
  • 项目类别:
  • 资助金额:
    $5.8万
  • 财政年份:
    2014
  • 负责人:
    Aaron W Miller
  • 依托单位:
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