Oh Ji Hoon, Hild Benedikt, Yoshida Tomoaki, Badger Jonathan H, Seishima Jun, McCulloch John A, Jung Min Kyung, Azar Shahar, Trinchieri Giorgio, Rehermann Barbara
Immunology Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, DHHS, Bethesda, MD 20892, USA.
Laboratory of Integrative Cancer Immunology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD 20892, USA.
Immunity. 2025 Jul 22. doi: 10.1016/j.immuni.2025.07.004.
Free-living mammals carry complex microbiota that co-evolved with their hosts over eons of years. The transfer of such microbiota from wild mice to genetically tractable laboratory mice has been shown to enhance modeling of human immune responses in preclinical studies. Here, we assessed the long-term stability of microbiota and immune phenotype of the first C57BL/6 mouse colony with natural microbiota (wildling mice). The bacterial gut microbiota of wildling mice maintained its increased α-diversity and richness over 5 years, with significantly greater stability than the gut microbiota of laboratory mice. Wildling mice had increased myeloid cell numbers across organs and increased activation and function of natural killer, B, and T cells, which was transferable to laboratory mice via co-housing. Immunological readouts in two preclinical models remained stable throughout the follow-up. These results demonstrate the feasibility of maintaining mouse colonies with natural, wild-derived microbiota as a sharable resource for basic and preclinical research.
自由生活的哺乳动物携带复杂的微生物群,这些微生物群与它们的宿主经过数十亿年的共同进化。在临床前研究中,已证明将此类微生物群从野生小鼠转移到基因易处理的实验室小鼠中可增强对人类免疫反应的建模。在此,我们评估了首个具有天然微生物群的C57BL/6小鼠群体(野生小鼠)的微生物群长期稳定性和免疫表型。野生小鼠的肠道细菌微生物群在5年中保持了其增加的α多样性和丰富度,其稳定性明显高于实验室小鼠的肠道微生物群。野生小鼠各器官中的髓样细胞数量增加,自然杀伤细胞、B细胞和T细胞的激活及功能增强,通过同笼饲养可将这些特性转移到实验室小鼠身上。在两个临床前模型中的免疫检测结果在整个随访过程中保持稳定。这些结果证明了维持具有天然野生来源微生物群的小鼠群体作为基础和临床前研究的可共享资源的可行性。