Dekeukeleire Max, Vandenheuvel Dieter, Khondee Tippapron, Delanghe Lize, Van Rillaer Tim, Thys Sofie, Timmermans Jean-Pierre, Lebeer Sarah, Spacova Irina
Laboratory of Applied Microbiology and Biotechnology (LAMB), Department of Bioscience Engineering, University of Antwerp, Antwerp, Belgium.
Research group EnVOC (Environmental Organic Chemistry and Technology), Department of Green Chemistry and Technology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Sci Rep. 2025 Aug 20;15(1):30604. doi: 10.1038/s41598-025-12833-7.
The spore-forming capacity of Bacillus spp. enables environmental persistence and stable product formulations, yet the interactions of environmental Bacillus spores and vegetative cells with the human immune system are not fully understood. We investigated the immunostimulatory potential of seven environmental Bacillus isolates (B. subtilis, B. velezensis, B. licheniformis, B. pumilus) and optimized their inactivation methods to preserve surface integrity and immunostimulatory activity. Inactivation was evaluated using heat/UV-C and 10-100% formalin, followed by scanning electron microscopy and human reporter cell assays (THP1-Dual monocytes, HEK-Blue hTLR2/6 and hTLR4). Heat/UV-C treatment retained Bacillus morphology and enhanced immune activation compared to 10-100% formalin treatment. Spores and vegetative cells activated key immune transcription factors (nuclear factor kappa B and interferon regulatory factors) in human monocytes, with spores inducing 1.5- to 8-fold lower responses compared to vegetative cells, and strain- and species-dependent effects observed. All tested Bacillus isolates significantly activated Toll-like receptor TLR2/6, but not TLR4. Genome analysis identified Bacillus spore envelope components (SpsAEIK, CotBCGQ) that may influence differences in immune responses. Our findings improve understanding of Bacillus-human immune interactions, revealing strain- and species-specific immunostimulatory activity. These results support further exploration of Bacillus isolates for immune-related and environmental applications.
芽孢杆菌属的芽孢形成能力使其能够在环境中持久存在并形成稳定的产品配方,但环境中的芽孢杆菌孢子和营养细胞与人类免疫系统之间的相互作用尚未完全了解。我们研究了七种环境芽孢杆菌分离株(枯草芽孢杆菌、贝莱斯芽孢杆菌、地衣芽孢杆菌、短小芽孢杆菌)的免疫刺激潜力,并优化了它们的灭活方法,以保持表面完整性和免疫刺激活性。使用热/紫外线-C和10-100%福尔马林进行灭活评估,随后进行扫描电子显微镜和人类报告细胞检测(THP1-Dual单核细胞、HEK-Blue hTLR2/6和hTLR4)。与10-100%福尔马林处理相比,热/紫外线-C处理保留了芽孢杆菌的形态并增强了免疫激活。孢子和营养细胞激活了人类单核细胞中的关键免疫转录因子(核因子κB和干扰素调节因子),与营养细胞相比,孢子诱导的反应低1.5至8倍,并且观察到菌株和物种依赖性效应。所有测试的芽孢杆菌分离株均显著激活了Toll样受体TLR2/6,但未激活TLR4。基因组分析确定了可能影响免疫反应差异的芽孢杆菌孢子包膜成分(SpsAEIK、CotBCGQ)。我们的研究结果增进了对芽孢杆菌与人类免疫相互作用的理解,揭示了菌株和物种特异性的免疫刺激活性。这些结果支持进一步探索芽孢杆菌分离株在免疫相关和环境应用中的潜力。