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Impact of a Purified Microbiome Therapeutic on Abundance of Antimicrobial Resistance Genes in Patients With Recurrent Clostridioides difficile Infection.
Straub, Timothy J; Lombardo, Mary-Jane; Bryant, Jessica A; Diao, Liyang; Lodise, Thomas P; Freedberg, Daniel E; Wortman, Jennifer R; Litcofsky, Kevin D; Hasson, Brooke R; McGovern, Barbara H; Ford, Christopher B; Henn, Matthew R.
  • Straub TJ; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Lombardo MJ; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Bryant JA; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Diao L; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Lodise TP; Albany College of Pharmacy and Health Sciences, Albany, New York, USA.
  • Freedberg DE; Division of Digestive and Liver Diseases, Columbia University Irving Medical Center-New York Presbyterian Hospital, New York, New York, USA.
  • Wortman JR; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Litcofsky KD; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Hasson BR; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • McGovern BH; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Ford CB; Seres Therapeutics, Cambridge, Massachusetts, USA.
  • Henn MR; Seres Therapeutics, Cambridge, Massachusetts, USA.
Clin Infect Dis ; 78(4): 833-841, 2024 Apr 10.
Article en En | MEDLINE | ID: mdl-37823484
BACKGROUND: 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). METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Clostridioides difficile / Infecciones por Clostridium / Microbiota Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Clostridioides difficile / Infecciones por Clostridium / Microbiota Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male Idioma: En Año: 2024 Tipo del documento: Article