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Epithelial Glycoconjugates as Barriers against Enteric Infections

Epithelial Glycoconjugates as Barriers against Enteric Infections
上皮糖复合物作为肠道感染的屏障
批准号:
7738696
负责人:
LYNN BRY
金额:
$34.94万
依托单位:
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:
2009-09-15 至 2014-07-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Enteric infections remain a leading cause of morbidity and mortality in children under the age of five. Pathogens affecting this age group commonly use lectin-like adhesins to adhere to host glycoproteins and glycolipids expressed on small intestinal enterocytes and/or M cells. The expression patterns of these glycoconjugates can thus impact the host's underlying susceptibility to infection. A variety of factors including age, hormones, diet, and colonization with specific commensal microflora impacts epithelial glycoconjugate expression. We have shown that colonization of adult germ-free (gnotobiotic) with the commensal Bacteroides thetaiotaomicron induces a mature pattern by up-regulating enterocyte-specific expression of a 1,2 fucosyltransferase. Fucosyltransferases link fucose to terminal galactose and N-acetyl-glucosamine residues, and thereby mask potential ligands on epithelial surfaces. These data suggest that colonization with select commensals could be used to therapeutically stimulate beneficial changes in epithelial glycoconjugate expression in susceptible populations. This proposal will test the hypothesis that select microflora, notably B. thetaiotaomicron, stimulate the development of glycoconjugates on the apical surfaces of enterocytes and M cells that reduces the capacity of pathogenic bacteria, viruses and/or toxins to infect/intoxicate the intestinal epithelium. Aims 1 and 2 will determine the full impact of B. thetaiotaomicron on expression and accessibility of epithelial glycoconjugates in the small and large intestines. These aims are directly responsive to RFA HD 08-004 (Item 5) "Surveying glycoconjugates on the surface of enterocytes to discover oligosaccharides that may serves as ligands for pathogenic and non-pathogenic bacteria." Aim 3 will specifically test the proposed hypothesis using well-established mouse models of cholera toxin, ricin toxin, reovirus and Salmonella typhimurium infection.
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NMR-resolved dynamics of C. difficile metabolism
  • 批准号:
    10574895
  • 项目类别:
  • 资助金额:
    $8.95万
  • 财政年份:
    2022
  • 负责人:
    LYNN BRY
  • 依托单位:
Commensal control of C. difficile virulence
  • 批准号:
    10334540
  • 项目类别:
  • 资助金额:
    $67.37万
  • 财政年份:
    2021
  • 负责人:
    LYNN BRY
  • 依托单位:
Commensal control of C. difficile virulence
  • 批准号:
    10211712
  • 项目类别:
  • 资助金额:
    $74.84万
  • 财政年份:
    2021
  • 负责人:
    LYNN BRY
  • 依托单位:
Commensal control of C. difficile virulence
  • 批准号:
    10556405
  • 项目类别:
  • 资助金额:
    $67.37万
  • 财政年份:
    2021
  • 负责人:
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  • 依托单位:
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