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急性炎症的遗传决定因素调控沙门氏菌感染,并在特定小鼠品系中调节Slc11a1基因(原Nramp1)的作用。

Genetic determinants of acute inflammation regulate Salmonella infection and modulate Slc11a1 gene (formerly Nramp1) effects in selected mouse lines.

作者信息

Borrego Andrea, Peters Luciana Carla, Jensen José Ricardo, Ribeiro Orlando Garcia, Koury Cabrera Wafa Hanna, Starobinas Nancy, Seman Michel, Ibañez Olga Martinez, De Franco Marcelo

机构信息

Laboratório de Imunogenética - Instituto Butantan, Av. Vital Brasil, 1500, São Paulo, SP 05503900, Brazil.

出版信息

Microbes Infect. 2006 Oct;8(12-13):2766-71. doi: 10.1016/j.micinf.2006.08.005. Epub 2006 Sep 7.

Abstract

Two lines of mice selected to produce maximal (AIRmax) or minimal (AIRmin) acute inflammatory reactions (AIR) differ in their susceptibility to infection by Salmonella enterica serotype Typhimurium (S. Typhimurium). The LD(50) for AIRmax mice is 1000 times higher than that observed for AIRmin mice, and higher frequencies of Slc11a1 alleles (known to confer either resistance (R) or high susceptibility (S) to S. Typhimurium) were consistently found in AIRmax and AIRmin mouse lines, respectively. In order to evaluate the effect of the quantitative trait loci (QTL) segregated in AIRmax and AIRmin mice on Slc11a1 dependent susceptibility to S. Typhimurium, the R and S alleles were fixed in homozygosity in AIRmax and AIRmin backgrounds by genotype assisted breedings. These new lines were named AIRmax(RR), AIRmax(SS), AIRmin(RR), and AIRmin(SS). Acute inflammation of Slc11a1(RR) animals was more severe in comparison to their Slc11a1(SS) counterparts, implicating Slc11a1 (or other linked genes) in AIR regulation. The LD(50) of S. Typhimurium was 800-times higher for AIRmax(SS) than for AIRmin(SS), demonstrating that AIR QTL can act as modifiers of the Slc11a1(SS) susceptibility gene. Four microsatellite markers for S. Typhimurium susceptibility QTL described in other mouse lines showed specific allele fixation in AIRmax or AIRmin mice, suggesting that these chromosomal regions also segregate with inflammatory phenotypes.

摘要

为产生最大(AIRmax)或最小(AIRmin)急性炎症反应(AIR)而选择的两系小鼠,对鼠伤寒沙门氏菌(S. Typhimurium)感染的易感性存在差异。AIRmax小鼠的半数致死剂量(LD(50))比AIRmin小鼠高1000倍,并且在AIRmax和AIRmin小鼠品系中分别持续发现了较高频率的Slc11a1等位基因(已知该等位基因赋予对鼠伤寒沙门氏菌的抗性(R)或高易感性(S))。为了评估在AIRmax和AIRmin小鼠中分离的数量性状基因座(QTL)对Slc11a1依赖性鼠伤寒沙门氏菌易感性的影响,通过基因型辅助育种在AIRmax和AIRmin背景中将R和S等位基因纯合固定。这些新的品系被命名为AIRmax(RR)、AIRmax(SS)、AIRmin(RR)和AIRmin(SS)。与它们的Slc11a1(SS)对应物相比,Slc11a1(RR)动物的急性炎症更严重,这表明Slc11a1(或其他连锁基因)参与AIR调节。AIRmax(SS)的鼠伤寒沙门氏菌LD(50)比AIRmin(SS)高800倍,表明AIR QTL可作为Slc11a1(SS)易感基因的修饰因子。在其他小鼠品系中描述的四个鼠伤寒沙门氏菌易感性QTL的微卫星标记在AIRmax或AIRmin小鼠中显示出特定的等位基因固定,表明这些染色体区域也与炎症表型分离。

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