4.1 Article

Systems biology evaluation of refractory Clostridioides difficile infection including multiple failures of fecal microbiota transplantation

期刊

ANAEROBE
卷 70, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.anaerobe.2021.102387

关键词

Clostridium difficile; N-of-1 studies; Microbiome; Shotgun sequencing; Metabolic analysis

资金

  1. National Institutes of Health, National Institute of Allergy and Infectious Diseases (NIAID) [U01 AI124290-01, R01 AI139261]
  2. Society of Infectious Diseases Pharmacists/BioMerieux Microbial Diagnostics in Antimicrobial Stewardship Research Award

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This study evaluated a patient with four failed FMTs, finding differences in the microbiome after antibiotic therapy and FMT failures. A SNP variant related to metabolic shifts was identified in the final isolated strain, highlighting the impact of continued antibiotic use on transplanted microbiomes.
Background: Fecal microbiota transplantation (FMT) aims to cure Clostridioides difficile infection (CDI) through reestablishing a healthy microbiome and restoring colonization resistance. Although often effective after one infusion, patients with continued microbiome disruptions may require multiple FMTs. In this N-of-1 study, we use a systems biology approach to evaluate CDI in a patient receiving chronic suppressive antibiotics with four failed FMTs over two years. Methods: Seven stool samples were obtained between 2016-18 while the patient underwent five FMTs. Stool samples were cultured for C. difficile and underwent microbial characterization and functional gene analysis using shotgun metagenomics. C. difficile isolates were characterized through ribotyping, whole genome sequencing, metabolic pathway analysis, and minimum inhibitory concentration (MIC) determinations. Results: Growing ten strains from each sample, the index and first four recurrent cultures were single strain ribotype F078-126, the fifth was a mixed culture of ribotypes F002 and F054, and the final culture was ribotype F002. One single nucleotide polymorphism (SNP) variant was identified in the RNA polymerase (RNAP) b-subunit RpoB in the final isolated F078-126 strain when compared to previous F078-126 isolates. This SNV was associated with metabolic shifts but phenotypic differences in fidaxomicin MIC were not observed. Microbiome differences were observed over time during vancomycin therapy and after failed FMTs. Conclusion: This study highlights the importance of antimicrobial stewardship in patients receiving FMT. Continued antibiotics play a destructive role on a transplanted microbiome and applies selection pressure for resistance to the few antibiotics available to treat CDI. Crown Copyright (C) 2021 Published by Elsevier Ltd.

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