Zenk Sebastian F, Jantsch Jonathan, Hensel Michael
Infektionsbiologische Abteilung, Universitätsklinikum Erlangen, Erlangen, Germany.
J Immunol. 2009 Aug 15;183(4):2697-707. doi: 10.4049/jimmunol.0900937. Epub 2009 Jul 22.
In contrast to nonpathogenic bacteria, the Gram-negative pathogen Salmonella enterica is not eradicated, but persists in murine dendritic cells (DC). The molecular basis of this phenotype is unknown. We set out to characterize bacterial and DC functions that are involved in Salmonella persistence. Our data prove that neither bacterial nor host cell de novo protein biosynthesis is required for Salmonella persistence in DC. We identified the Salmonella O-Ag of the LPS of Salmonella as an important factor for controlling the intracellular fate of Salmonella in DC. A Salmonella strain with entirely absent O-Ag showed an increased rate of uptake by DC, altered intracellular processing, and increased degradation, and also boosted the activation of immune functions of DC. These novel findings demonstrate that in addition to the multiple functions of the bacterial LPS in adaptation to the intestinal environment and protection against innate immune function, this molecule also has an important role in interaction of Salmonella with DC.
与非致病性细菌不同,革兰氏阴性病原体肠炎沙门氏菌不会被根除,而是会在小鼠树突状细胞(DC)中持续存在。这种表型的分子基础尚不清楚。我们着手表征参与沙门氏菌持续存在的细菌和DC功能。我们的数据证明,沙门氏菌在DC中持续存在既不需要细菌也不需要宿主细胞从头合成蛋白质。我们确定沙门氏菌脂多糖(LPS)的O抗原是控制沙门氏菌在DC内细胞命运的重要因素。一株完全缺失O抗原的沙门氏菌菌株显示出被DC摄取的速率增加、细胞内加工改变、降解增加,并且还增强了DC免疫功能的激活。这些新发现表明,除了细菌LPS在适应肠道环境和抵御先天免疫功能方面的多种功能外,该分子在沙门氏菌与DC的相互作用中也具有重要作用。