Jiang Kai, Ye Lijia, Cao Chunling, Che Gen, Wang Yanxing, Hong Yu
College of Life Science and Technology, Inner Mongolia Normal University, Hohhot 010022, China.
Key Laboratory of Biodiversity Conservation and Sustainable Utilization in Mongolian Plateau for College and University of Inner Mongolia Autonomous Region, Hohhot 010022, China.
Microorganisms. 2025 Apr 24;13(5):972. doi: 10.3390/microorganisms13050972.
Groundwater harbors phylogenetically diverse Candidate Phyla Radiation (CPR) bacteria, representing an ideal ecosystem for studying this microbial dark matter. However, no CPR strains have been successfully isolated from groundwater, severely limiting further research. This study employed a multi-metagenome approach, integrating time-resolved sampling, antibiotic/nutrient interventions, and microbial correlation networks to unravel CPR ecological roles in groundwater and provide insights into their subsequent cultivation. Through 36 metagenomes from a groundwater system containing at least 68 CPR phyla, we revealed the time-sensitive collapse of CPR communities: total abundance plummeted from 7.9% to 0.15% within 48 h post-sampling, driven by competition with rapidly dividing non-CPR bacteria, such as members of . Ampicillin (100 mg/L) stabilized CPR communities by suppressing competitors, whereas low-nutrient conditions paradoxically reversed this effect. Long-term enrichment (14 months) recovered 63 CPR phyla (0.35% abundance), revealing their survival resilience despite nutrient deprivation. Correlation networks prioritized , a novel genus, , and as potential CPR partners, providing actionable targets for co-culture trials. Here, we propose actionable recommendations spanning groundwater sampling, activation status, identification of CPR symbiotic partners, and optimization of culture conditions, which bypass traditional blind cultivation and are critical for future efforts to cultivate CPR bacterial strains from groundwater. Cultivating CPR bacteria will contribute to clarifying their diversity, ecological roles, evolutionary mechanisms, metabolic pathways, and genetic potential.
地下水中含有系统发育多样的候选门类辐射菌(CPR菌),是研究这种微生物暗物质的理想生态系统。然而,尚未从地下水中成功分离出CPR菌株,这严重限制了进一步的研究。本研究采用多宏基因组方法,整合时间分辨采样、抗生素/营养干预和微生物关联网络,以揭示CPR菌在地下水中的生态作用,并为其后续培养提供见解。通过对一个包含至少68个CPR菌门的地下水系统进行36次宏基因组分析,我们揭示了CPR菌群落对时间敏感的崩溃:采样后48小时内,其总丰度从7.9%骤降至0.15%,这是由与快速分裂的非CPR菌(如某些成员)竞争所致。氨苄青霉素(100毫克/升)通过抑制竞争者稳定了CPR菌群落,而低营养条件却反常地逆转了这种效果。长期富集培养(14个月)恢复了63个CPR菌门(丰度为0.35%),揭示了它们在营养匮乏情况下的生存恢复力。关联网络将一个新的属、以及列为潜在的CPR菌伙伴,为共培养试验提供了可操作的目标。在此,我们提出了一系列可操作的建议,涵盖地下水采样、激活状态、CPR菌共生伙伴的鉴定以及培养条件的优化,这些建议绕过了传统的盲目培养方法,对于未来从地下水中培养CPR菌株的努力至关重要。培养CPR菌将有助于阐明它们的多样性、生态作用、进化机制、代谢途径和遗传潜力。