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在MOLF/Ei小鼠中,Tlr5与鼠伤寒沙门氏菌感染的易感性无主要关联。

Tlr5 is not primarily associated with susceptibility to Salmonella Typhimurium infection in MOLF/Ei mice.

作者信息

Angers Isabelle, Sancho-Shimizu Vanessa, Descoteaux Albert, Gewirtz Andrew T, Malo Danielle

机构信息

Department of Human Genetics, McGill University, Montreal, Quebec, Canada H3G 1A4.

出版信息

Mamm Genome. 2006 May;17(5):385-97. doi: 10.1007/s00335-005-0132-x.

DOI:10.1007/s00335-005-0132-x
PMID:16688529
Abstract

The extreme susceptibility to infection with Salmonella Typhimurium of wild-derived MOLF/Ei mice has been linked to one genomic region on Chromosome 1 (Ity3). A member of the Toll-like receptors family, Tlr5, located on distal Chromosome 1, was previously shown to be a candidate gene for Ity3 based on expression studies and sequencing analysis. The candidacy of Tlr5 as a Salmonella-susceptibility gene was evaluated functionally by comparing Tlr5 C57BL/6J and MOLF/Ei alleles in vitro and in vivo. In vitro studies showed that the MOLF/Ei Tlr5 allele is more transcriptionally active when the gene is removed from its natural genomic environment. This observation was supported by in vivo studies in B6.MOLF-Ity3 congenic mice that showed that mice homozygous for the MOLF/Ei allele at Ity3, including Tlr5, had an increased response to flagellin as measured by IL-6 and CXCL-1 secretion in the serum compared with parental MOLF/Ei mice. Despite the fact that both MOLF/Ei and B6.MOLF-Ity/Ity3 mice are more susceptible to Salmonella Typhimurium infection than B6.MOLF-Ity mice, they exhibit a different phenotype with respect to Tlr5 expression and Tlr5 signaling, supporting the prediction that Tlr5 is not primarily involved in the disease phenotype underlying the Ity3 locus in MOLF/Ei mice.

摘要

野生来源的MOLF/Ei小鼠对鼠伤寒沙门氏菌感染极度易感,这与1号染色体上的一个基因组区域(Ity3)有关。Toll样受体家族的成员Tlr5位于1号染色体远端,基于表达研究和测序分析,它先前被认为是Ity3的候选基因。通过在体外和体内比较Tlr5 C57BL/6J和MOLF/Ei等位基因,对Tlr5作为沙门氏菌易感基因的候选资格进行了功能评估。体外研究表明,当该基因从其自然基因组环境中去除时,MOLF/Ei Tlr5等位基因的转录活性更高。B6.MOLF-Ity3同源基因小鼠的体内研究支持了这一观察结果,该研究表明,在Ity3位点纯合MOLF/Ei等位基因(包括Tlr5)的小鼠,与亲代MOLF/Ei小鼠相比,血清中IL-6和CXCL-1分泌所测得的对鞭毛蛋白的反应增强。尽管MOLF/Ei和B6.MOLF-Ity/Ity3小鼠都比B6.MOLF-Ity小鼠更容易感染鼠伤寒沙门氏菌,但它们在Tlr5表达和Tlr5信号传导方面表现出不同的表型,这支持了Tlr5并非主要参与MOLF/Ei小鼠Ity3位点潜在疾病表型的预测。

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1
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J Immunol. 2006 Jun 1;176(11):6954-61. doi: 10.4049/jimmunol.176.11.6954.
2
Host susceptibility and clinical outcomes in toll-like receptor 5-deficient patients with typhoid fever in Vietnam.越南伤寒热患者中Toll样受体5缺陷宿主的易感性及临床结局
J Infect Dis. 2005 Apr 1;191(7):1068-71. doi: 10.1086/428593. Epub 2005 Feb 28.
3
In vitro and ex vivo activation of the TLR5 signaling pathway in intestinal epithelial cells by a commensal Escherichia coli strain.
Involvement of Toll-like receptor 5 in the recognition of flagellated bacteria.Toll样受体5参与对鞭毛细菌的识别。
Proc Natl Acad Sci U S A. 2006 Aug 15;103(33):12487-92. doi: 10.1073/pnas.0605200103. Epub 2006 Aug 4.
共生大肠杆菌菌株对肠道上皮细胞中TLR5信号通路的体外和离体激活
J Biol Chem. 2004 Oct 8;279(41):42984-92. doi: 10.1074/jbc.M405410200. Epub 2004 Aug 9.
4
Toll-like receptor signalling.Toll样受体信号传导
Nat Rev Immunol. 2004 Jul;4(7):499-511. doi: 10.1038/nri1391.
5
Activation of transcription factor NF-kappaB requires ELKS, an IkappaB kinase regulatory subunit.转录因子NF-κB的激活需要ELKS,一种IκB激酶调节亚基。
Science. 2004 Jun 25;304(5679):1963-7. doi: 10.1126/science.1098387.
6
Flagellin promotes myeloid differentiation factor 88-dependent development of Th2-type response.鞭毛蛋白促进依赖髓样分化因子88的Th2型反应的发展。
J Immunol. 2004 Jun 1;172(11):6922-30. doi: 10.4049/jimmunol.172.11.6922.
7
Expression and subcellular distribution of toll-like receptors TLR4, TLR5 and TLR9 on the gastric epithelium in Helicobacter pylori infection.幽门螺杆菌感染时胃上皮细胞中Toll样受体TLR4、TLR5和TLR9的表达及亚细胞分布
Clin Exp Immunol. 2004 Jun;136(3):521-6. doi: 10.1111/j.1365-2249.2004.02464.x.
8
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J Immunol. 2004 Apr 15;172(8):5056-62. doi: 10.4049/jimmunol.172.8.5056.
9
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Cell Microbiol. 2004 Mar;6(3):235-42. doi: 10.1046/j.1462-5822.2004.00360.x.
10
Immunity to Salmonella from a dendritic point of view.从树突状细胞角度看沙门氏菌免疫
Cell Microbiol. 2004 Jan;6(1):1-11. doi: 10.1046/j.1462-5822.2003.00336.x.