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Phosphate starvation enhances phagocytosis of Mycobacterium bovis /BCG by macrophages

机译:磷酸盐饥饿通过巨噬细胞增强了肉毒杆菌/ BCG的吞噬作用

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Tuberculosis is an important health problem worldwide. The only available vaccine is M. bovis/BCG, an attenuated mycobacterium that activates the innate and the acquired immune system after being phagocytosed by macrophages and dendritic cells. Vaccination fails to prevent adult pulmonary tuberculosis although it may have a protective effect in childhood infection. Understanding how BCG interacts with macrophages and other immunocompetent cells is crucial to develop new vaccines. In this study we showed that macrophages phagocytose M. bovis/BCG bacilli with higher efficiency when they are cultured without phosphate. We isolated mycobacterial membranes to search for mycobacterial molecules that could be involved in these processes; by immunoblot, it was found that the plasma membranes of phosphate-deprived bacilli express the adhesins PstS-1, LpqH, LprG, and the APA antigen. These proteins are not detected in membranes of bacilli grown with usual amounts of phosphate. The interest of our observations is to show that under the metabolic stress implied in phosphate deprivation, mycobacteria respond upregulating adhesins that could improve their capacity to infect macrophages. These observations are relevant to understand how M. bovis/BCG induces protective immunity.
机译:结核病是全世界重要的健康问题。唯一可用的疫苗是M. Bovis / BCG,一个衰减的分枝杆菌,在巨噬细胞和树突细胞吞噬后激活先天和所获得的免疫系统。疫苗接种未能防止成人肺结核,尽管它可能对儿童感染可能具有保护作用。了解BCG如何与巨噬细胞相互作用,其他免疫合作细胞对于开发新疫苗至关重要。在这项研究中,我们展示巨噬细胞吞噬细胞芽孢杆菌/ BCG芽孢杆菌在没有磷酸盐的情况下培养时的效率更高。我们分离细菌膜以寻找可参与这些过程的分枝杆菌分子;通过免疫印迹,发现磷酸盐脱贫的血浆膜表达粘附素PSTS-1,LPQ,LPRG和APA抗原。这些蛋白质未以常用量的磷酸盐生长的杆菌膜中检测到。我们观察的兴趣是表明,在磷酸盐剥夺中隐含的代谢应力下,分枝杆菌响应越高的粘附物,可以提高其感染巨噬细胞的能力。这些观察结果与了解Bovis / BCG如何诱导保护性免疫力。

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