Institute of Immunology and Microbiology, Charles University in Prague, Prague, Czech Republic.
Folia Microbiol (Praha). 2013 Mar;58(2):111-21. doi: 10.1007/s12223-012-0181-y. Epub 2012 Aug 9.
Mucosal immunization with non-living antigens usually requires the use of an adjuvant. The adjuvant activity of Bacillus firmus in the mucosal immunization of mice was described by our laboratory previously. In the present study, subcellular localization of B. firmus activities was followed. After mechanical disintegration, subcellular components of bacterium were fractionated by differential centrifugation and salting out. Bacterial cell walls, cytoplasmic membrane fraction, soluble cytoplasmic proteins, and ribosomal fractions were isolated. Their effect on the mouse immune system was studied. Lymphocyte proliferation and immunoglobulin formation in vitro were stimulated by bacterial cell wall (BCW), cytoplasmic membrane (CMF), and ribosomal fractions. BCW and CMF increased antibody formation after intratracheal immunization of mice with influenza A and B viruses, and increased protection against subsequent infection with influenza virus. The BCW fraction even induced intersubtypic cross-protection: Mice immunized with A/California/7/04 (H3N2) + BCW were resistant to the infection by the highly pathogenic A/PR/8/34 (H1N1) virus.
黏膜免疫用非活体抗原通常需要佐剂。本实验室之前曾描述过 Firmus 芽孢杆菌在黏膜免疫中的佐剂活性。在本研究中,我们对 Firmus 芽孢杆菌活性的亚细胞定位进行了跟踪。通过机械破碎后,采用差速离心和盐析对细菌的亚细胞成分进行了分级分离。分离出细胞壁、细胞质膜部分、可溶性细胞质蛋白和核糖体部分。研究了它们对小鼠免疫系统的影响。细菌细胞壁(BCW)、细胞质膜(CMF)和核糖体部分可刺激体外淋巴细胞增殖和免疫球蛋白形成。BCW 和 CMF 增加了流感 A 和 B 病毒经气管内免疫接种后抗体的形成,并增加了对随后流感病毒感染的保护。BCW 部分甚至诱导了亚型间交叉保护:用 A/California/7/04(H3N2)+BCW 免疫的小鼠对高致病性 A/PR/8/34(H1N1)病毒感染具有抗性。