Leo Stefano, Lazarevic Vladimir, Girard Myriam, Gaïa Nadia, Schrenzel Jacques, de Lastours Victoire, Fantin Bruno, Bonten Marc, Carmeli Yehuda, Rondinaud Emilie, Harbarth Stephan, Huttner Benedikt D
Genomic Research Laboratory, Division of Infectious Diseases, University Hospitals and University of Geneva, Rue Michel Servet 1, 1211 Geneva, Switzerland.
Division of Infectious Diseases, Geneva University Hospitals and Faculty of Medicine, Rue Gabrielle-Perret-Gentil 4, 1211 Geneva, Switzerland.
Microorganisms. 2020 Jun 23;8(6):941. doi: 10.3390/microorganisms8060941.
The R-GNOSIS (Resistance in Gram-Negative Organisms: Studying Intervention Strategies) WP3 study was the first multicenter randomized clinical trial systematically investigating fecal microbiota transplantation (FMT) for intestinal decolonization of extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-E) or carbapenemase-producing Enterobacteriaceae (CPE). Here, we characterized the temporal dynamics of fecal microbiota changes in a sub-cohort of the R-GNOSIS WP3 participants before and after antibiotics/FMT using whole metagenome shotgun sequencing. We sequenced fecal DNA obtained from 16 ESBL-E/CPE carriers having received oral colistin/neomycin followed by FMT and their corresponding seven donors. Ten treatment-naïve controls from the same trial were included. Fecal samples were collected at baseline (V0), after antibiotics but before FMT (V2) and three times after FMT (V3, V4 and V5). Antibiotic treatment transiently decreased species richness and diversity and increased the abundance of antibiotic resistance determinants (ARDs). species, together with butyrate- and propionate-producing species from Lachnospiraceae and Ruminococcaceae families were significantly enriched in post-FMT microbiota of treated carriers. After FMT, the proportion of Enterobacteriaceae was lower compared to baseline but without statistical significance. Combined antibiotic and FMT treatment resulted in enrichment of species that are likely to limit the gut colonization by ESBL-E/CPE.
R-GNOSIS(革兰氏阴性菌耐药性:研究干预策略)WP3研究是第一项系统性调查粪便微生物群移植(FMT)用于产超广谱β-内酰胺酶肠杆菌科细菌(ESBL-E)或产碳青霉烯酶肠杆菌科细菌(CPE)肠道去定植的多中心随机临床试验。在此,我们使用全基因组鸟枪法测序对R-GNOSIS WP3参与者亚组在使用抗生素/FMT前后粪便微生物群变化的时间动态进行了表征。我们对从16名接受口服黏菌素/新霉素随后进行FMT的ESBL-E/CPE携带者及其相应的7名供体获得的粪便DNA进行了测序。纳入了来自同一试验的10名未经治疗的对照。在基线(V0)、抗生素治疗后但FMT前(V2)以及FMT后三次(V3、V4和V5)采集粪便样本。抗生素治疗使物种丰富度和多样性暂时降低,并增加了抗生素抗性决定因素(ARDs)的丰度。在接受治疗的携带者FMT后的微生物群中,来自毛螺菌科和瘤胃球菌科的物种以及产生丁酸盐和丙酸盐的物种显著富集。FMT后,肠杆菌科的比例与基线相比有所降低,但无统计学意义。抗生素和FMT联合治疗导致可能限制ESBL-E/CPE在肠道定植的物种富集。