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猪布鲁氏菌脂多糖O抗原在小鼠巨噬细胞吞噬体形成及抑制吞噬体-溶酶体融合中的作用

Role of the Brucella suis lipopolysaccharide O antigen in phagosomal genesis and in inhibition of phagosome-lysosome fusion in murine macrophages.

作者信息

Porte Françoise, Naroeni Aroem, Ouahrani-Bettache Safia, Liautard Jean-Pierre

机构信息

Institut National de la Santé et de la Recherche Médicale U-431, Montpellier, France.

出版信息

Infect Immun. 2003 Mar;71(3):1481-90. doi: 10.1128/IAI.71.3.1481-1490.2003.

Abstract

Brucella species are gram-negative, facultative intracellular bacteria that infect humans and animals. These organisms can survive and replicate within a membrane-bound compartment inside professional and nonprofessional phagocytic cells. Inhibition of phagosome-lysosome fusion has been proposed as a mechanism for intracellular survival in both cell types. However, the molecular mechanisms and the microbial factors involved are poorly understood. Smooth lipopolysaccharide (LPS) of Brucella has been reported to be an important virulence factor, although its precise role in pathogenesis is not yet clear. In this study, we show that the LPS O side chain is involved in inhibition of the early fusion between Brucella suis-containing phagosomes and lysosomes in murine macrophages. In contrast, the phagosomes containing rough mutants, which fail to express the O antigen, rapidly fuse with lysosomes. In addition, we show that rough mutants do not enter host cells by using lipid rafts, contrary to smooth strains. Thus, we propose that the LPS O chain might be a major factor that governs the early behavior of bacteria inside macrophages.

摘要

布鲁氏菌属是革兰氏阴性兼性胞内细菌,可感染人类和动物。这些微生物能够在专职和非专职吞噬细胞内的膜结合区室中存活并繁殖。吞噬体 - 溶酶体融合的抑制被认为是这两种细胞类型中胞内存活的一种机制。然而,其中涉及的分子机制和微生物因子仍知之甚少。布鲁氏菌的光滑脂多糖(LPS)已被报道为一种重要的毒力因子,尽管其在发病机制中的精确作用尚不清楚。在本研究中,我们表明LPS O侧链参与抑制鼠巨噬细胞中含猪布鲁氏菌的吞噬体与溶酶体的早期融合。相反,含有粗糙突变体(无法表达O抗原)的吞噬体则迅速与溶酶体融合。此外,我们还表明,与光滑菌株相反,粗糙突变体不通过脂筏进入宿主细胞。因此,我们认为LPS O链可能是控制巨噬细胞内细菌早期行为的主要因素。

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