Siguenza Nicole, Bailey Sharyl, Sadegi Mohammad, Gootin Hanna, Tiu Maria, Price Jeffrey D, Ramer-Tait Amanda, Zarrinpar Amir
Division of Gastroenterology, University of California, San Diego, La Jolla, CA, USA.
Biomedical Sciences Graduate Program, University of California, San Diego, La Jolla, CA, USA.
bioRxiv. 2025 Jan 21:2025.01.21.634159. doi: 10.1101/2025.01.21.634159.
Competitive exclusion is conventionally believed to prevent the establishment of a secondary strain of the same bacterial species in the gut microbiome, raising concerns for the deployment of live bacterial therapeutics (LBTs), especially if the bacterial chassis is a strain native to the gut. In this study, we investigated factors influencing competition dynamics in the murine gut using isogenic native strains. We found that competition outcomes are context-dependent, modulated by microbiome complexity, LBT transgene expression, intestinal inflammation, and host diet. Furthermore, we demonstrated that native LBTs can establish long-term engraftment in the gut alongside a parental strain, with transgene-associated fitness effects influencing competition. We identified various interventions, including strategic dosing and dietary modulation, that significantly enhanced LBT colonization levels by 2 to 3 orders of magnitude. These insights provide a framework for optimizing LBT engraftment and efficacy, supporting their potential translation for human therapeutic applications.
传统观点认为,竞争排斥会阻止同一细菌物种的次生菌株在肠道微生物群中定植,这引发了人们对活体细菌疗法(LBTs)应用的担忧,尤其是当细菌底盘是肠道原生菌株时。在本研究中,我们使用同基因原生菌株研究了影响小鼠肠道内竞争动态的因素。我们发现,竞争结果取决于具体情况,受到微生物群复杂性、LBT转基因表达、肠道炎症和宿主饮食的调节。此外,我们证明原生LBTs可以与亲本菌株一起在肠道中长期定植,转基因相关的适应性效应会影响竞争。我们确定了各种干预措施,包括策略性给药和饮食调节,这些措施可将LBT定植水平显著提高2至3个数量级。这些见解为优化LBT定植和疗效提供了一个框架,支持其在人类治疗应用中的潜在转化。