Seres Therapeutics, Cambridge, Massachusetts, USA.
Albany College of Pharmacy and Health Sciences, Albany, New York, USA.
Clin Infect Dis. 2024 Apr 10;78(4):833-841. doi: 10.1093/cid/ciad636.
The gastrointestinal microbiota is an important line of defense against colonization with antimicrobial resistant (AR) bacteria. In this post hoc analysis of the phase 3 ECOSPOR III trial, we assessed impact of a microbiota-based oral therapeutic (fecal microbiota spores, live; VOWST Oral Spores [VOS], formerly SER-109]; Seres Therapeutics) compared with placebo, on AR gene (ARG) abundance in patients with recurrent Clostridioides difficile infection (rCDI).
Adults with rCDI were randomized to receive VOS or placebo orally for 3 days following standard-of-care antibiotics. ARG and taxonomic profiles were generated using whole metagenomic sequencing of stool at baseline and weeks 1, 2, 8, and 24 posttreatment.
Baseline (n = 151) and serial posttreatment stool samples collected through 24 weeks (total N = 472) from 182 patients (59.9% female; mean age: 65.5 years) in ECOSPOR III as well as 68 stool samples obtained at a single time point from a healthy cohort were analyzed. Baseline ARG abundance was similar between arms and significantly elevated versus the healthy cohort. By week 1, there was a greater decline in ARG abundance in VOS versus placebo (P = .003) in association with marked decline of Proteobacteria and repletion of spore-forming Firmicutes, as compared with baseline. We observed abundance of Proteobacteria and non-spore-forming Firmicutes were associated with ARG abundance, while spore-forming Firmicutes abundance was negatively associated.
This proof-of-concept analysis suggests that microbiome remodeling with Firmicutes spores may be a potential novel approach to reduce ARG colonization in the gastrointestinal tract.
胃肠道微生物群是防止定植抗菌药物耐药(AR)细菌的重要防线。在 3 期 ECOSPOR III 试验的事后分析中,我们评估了一种基于微生物组的口服治疗(粪便微生物组孢子,活菌;VOWST 口服孢子[VOS],前身为 SER-109;Seres Therapeutics)与安慰剂相比,对复发性艰难梭菌感染(rCDI)患者 AR 基因(ARG)丰度的影响。
rCDI 成人在接受标准护理抗生素治疗后,随机接受 VOS 或安慰剂口服治疗 3 天。使用粪便的全宏基因组测序在基线和治疗后第 1、2、8 和 24 周生成 ARG 和分类群谱。
从 ECOSPOR III 中 182 例患者(59.9%为女性;平均年龄:65.5 岁)的基线(n = 151)和治疗后 24 周的连续粪便样本(总 N = 472)以及从健康队列中单次采集的 68 个粪便样本进行了分析。基线 ARG 丰度在两组之间相似,与健康队列相比显著升高。到第 1 周,与基线相比,VOS 组的 ARG 丰度下降更大(P =.003),同时 Proteobacteria 大量减少,产孢子的Firmicutes 得到补充。我们观察到 Proteobacteria 和非产孢子Firmicutes 的丰度与 ARG 丰度相关,而产孢子Firmicutes 的丰度与 ARG 丰度呈负相关。
这一概念验证分析表明,用Firmicutes 孢子重塑微生物组可能是减少胃肠道中 ARG 定植的一种潜在新方法。