Institute for Food Safety and Hygiene, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
Foodborne Pathog Dis. 2010 Jul;7(7):775-83. doi: 10.1089/fpd.2009.0458.
The cold shock protein (Csp) family comprises small, highly conserved proteins that bind nucleic acids to modulate various bacterial gene expressions. In addition to cold adaptation functions, this group of proteins is thought to facilitate various cellular processes to promote normal growth and stress adaptation responses. Three proteins making up the Listeria monocytogenes Csp family (CspA, CspB, and CspD) promote both cold and osmotic stress adaptation functions in this bacterium. The contribution of these three Csps in the host cell invasion processes of L. monocytogenes was investigated based on human Caco-2 and murine macrophage in vitro cell infection models. The DeltacspB, DeltacspD, DeltacspAB, DeltacspAD, DeltacspBD, and DeltacspABD strains were all significantly impaired in Caco-2 cell invasion compared with the wild-type strain, whereas in the murine macrophage infection assay only, the double (DeltacspBD) and triple (DeltacspABD) csp mutants were also significantly impaired in cell invasion compared with the wild-type strain. The DeltacspBD and DeltacspABD mutants displayed the most severely impaired invasion phenotypes. The invasion ability of these two mutant strains was also further analyzed using cold-stress-exposed organisms. In both cell infection models a significant reduction in invasiveness was observed after cold stress exposure of Listeria organisms. The negative impact of cold stress on subsequent cell invasion ability was, however, more severe in cold-sensitive csp mutants (DeltacspBD and DeltacspABD) compared with the wild type. The impaired macrophage invasion and intracellular growth of DeltacspBD and DeltacspABD also led us to examine oxidative stress resistance capacity in these two mutant strains. Both strains also displayed higher oxidative stress sensitivity relative to the wild-type strain. Our data indicate that besides cold and osmotic stress adaptation roles, Csp family proteins also promote efficient host cell invasion and oxidative stress adaptation processes in L. monocytogenes.
冷休克蛋白(Csp)家族由小而高度保守的蛋白质组成,可结合核酸以调节各种细菌基因表达。除了适应寒冷的功能外,这群蛋白质被认为有助于促进各种细胞过程,以促进正常生长和应激适应反应。李斯特菌 Csp 家族的三种蛋白质(CspA、CspB 和 CspD)促进该细菌的冷应激和渗透压应激适应功能。基于人类 Caco-2 和鼠巨噬细胞体外细胞感染模型,研究了这三种 Csp 在李斯特菌宿主细胞入侵过程中的作用。与野生型菌株相比,DeltacspB、DeltacspD、DeltacspAB、DeltacspAD、DeltacspBD 和 DeltacspABD 菌株在 Caco-2 细胞入侵中均受到显著损害,而在鼠巨噬细胞感染试验中,只有双(DeltacspBD)和三(DeltacspABD)csp 突变株在细胞入侵中也明显受损与野生型菌株相比。DeltacspBD 和 DeltacspABD 突变株显示出最严重的入侵表型受损。还使用冷应激暴露的生物体进一步分析了这两个突变株的入侵能力。在两种细胞感染模型中,李斯特菌生物体冷应激暴露后观察到侵袭能力显著降低。然而,与野生型相比,冷敏感 csp 突变体(DeltacspBD 和 DeltacspABD)中冷应激对随后的细胞入侵能力的负面影响更为严重。DeltacspBD 和 DeltacspABD 对巨噬细胞的入侵和胞内生长的损害也促使我们检查这两个突变株的氧化应激抗性能力。与野生型菌株相比,这两个菌株对氧化应激的敏感性也更高。我们的数据表明,除了适应寒冷和渗透压的应激作用外,Csp 家族蛋白还促进李斯特菌有效入侵宿主细胞和适应氧化应激的过程。