# Gut Microbiome Recovery in Clostridioides difficile Infection Patients Receiving Multi-Strain Probiotics During Convalescence: A Prospective Pilot Series of Longitudinal Dynamics

**Authors:** Dorin Novacescu, Talida Georgiana Cut, Adelina Baloi, Alexandra Herlo, Ioana-Melinda Luput-Andrica, Andra Elena Saizu, Amelia Uzum, Maria Daniela Mot, Flavia Zara, Dorel Sandesc, Voichita Elena Lazureanu, Adelina Marinescu

PMC · DOI: 10.3390/diseases14020077 · 2026-02-18

## TL;DR

This study explores how the gut microbiome recovers in patients with Clostridioides difficile infection after using multi-strain probiotics, showing variable and complex recovery patterns.

## Contribution

The study introduces a novel pilot approach to assess microbiome recovery dynamics and remodeling during probiotic supplementation after CDI.

## Key findings

- Probiotic supplementation was associated with increased microbial diversity and partial improvement in dysbiosis in four out of five patients.
- Microbiome recovery was heterogeneous and non-linear, with variable reductions in Proteobacteria and recovery of Actinobacteria.
- Enterotype shifts and ecological reorganization were observed, rather than full restoration of the microbiome.

## Abstract

Background/Objectives: Clostridioides difficile infection (CDI) is a major healthcare-associated infection associated with profound antibiotic-induced gut microbiome disruption that frequently persists after clinical resolution. This pilot study aimed to characterize early post-infectious gut microbiome recovery following an inaugural CDI episode and to descriptively assess microbiome remodeling during adjunctive multi-strain probiotic supplementation. Methods: Adult patients with mild-to-moderate CDI were prospectively enrolled after completing standard antimicrobial therapy and received a 30-day course of a high-potency, 10-strain probiotic formulation. Stool samples were collected before and after supplementation and analyzed using 16S rRNA gene sequencing with microbiome-inferred functional profiling, alongside targeted screening for enteric protozoa and yeasts. Results: Five patients completed paired analyses. At baseline, all patients exhibited severe dysbiosis characterized by markedly reduced microbial diversity, depletion of Actinobacteria and short-chain fatty acid-producing taxa, expansion of Proteobacteria, and unfavorable inferred metabolic signatures. After supplementation, four of five patients were observed to exhibit increased microbial diversity and partial improvement in global dysbiosis indices. Microbiome recovery was heterogeneous and non-linear, involving variable reductions in Proteobacteria, recovery of Actinobacteria, or both, with incomplete normalization of taxonomic balances and inferred functions. Enterotype shifts were observed in three patients, consistent with ecological reorganization rather than full restoration. Baseline protozoal colonization resolved in affected patients, while fungal dynamics showed clearance or species-level replacement. No early CDI recurrences were observed during follow-up. Conclusions: Interpretation is limited by the single-arm design without a control group, which precludes distinguishing supplementation-associated changes from natural post-antibiotic recovery. Even so, our findings highlight the complexity and inter-individual variability of early post-CDI microbiome recovery and support further investigation of integrative microbiome profiling to describe post-infectious dysbiosis dynamics.

## Linked entities

- **Species:** Clostridioides difficile (taxon 1496)

## Full-text entities

- **Genes:** GUSB (glucuronidase beta) [NCBI Gene 2990] {aka BG, MPS7}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}
- **Diseases:** colitis (MESH:D003092), diabetes mellitus (MESH:D003920), ischemic heart disease (MESH:D017202), Dysbiosis (MESH:D064806), IBS (MESH:D053560), bacteremia (MESH:D016470), infection (MESH:D007239), cardiovascular disease (MESH:D002318), uremic toxin (MESH:D006463), mucosal irritation (MESH:D001523), chronic kidney disease (MESH:D051436), microbiome abnormalities (MESH:D000014), metabolic syndrome (MESH:D024821), diarrheal (MESH:D004403), inflammation (MESH:D007249), Disease (MESH:D004194), injury to (MESH:D014947), C. difficile (MESH:D003015), gut disorders (MESH:C536735), Parkinson's disease (MESH:D010300), AAD (MESH:D004761), colonic perforation (MESH:D015179), hypertension (MESH:D006973), fungemia (MESH:D016469), fungal (MESH:D009181), bloating (MESH:C535647), Infectious Diseases (MESH:D003141), ulcerative colitis (MESH:D003093), obesity (MESH:D009765), renal impairment (MESH:D007674), inflammatory bowel (MESH:D015212), heart failure (MESH:D006333), Irritable Bowel Syndrome (MESH:D043183), enteric (MESH:D004751), type II diabetes mellitus (MESH:D003924), Constipation (MESH:D003248), acute kidney injury (MESH:D058186), diarrhea (MESH:D003967)
- **Chemicals:** methane (MESH:D008697), choline (MESH:D002794), Polyols (MESH:C024617), bilirubin (MESH:D001663), butyrate (MESH:D002087), carbohydrate (MESH:D002241), metronidazole (MESH:D008795), phenols (MESH:D010636), starch (MESH:D013213), Monosaccharides (MESH:D009005), propionate (MESH:D011422), bile acid (MESH:D001647), H2S (MESH:D006862), Histamine (MESH:D006632), glucuronides (MESH:D020719), FODMAP (-), betaine (MESH:D001622), aromatic amino acid (MESH:D024322), oxygen (MESH:D010100), Sulfate (MESH:D013431), carnitine (MESH:D002331), Indoxyl sulfate (MESH:D007200), ammonia (MESH:D000641), Oligosaccharides (MESH:D009844), TMAO (MESH:C005855), nitrate (MESH:D009566), sugar (MESH:D000073893), A (MESH:D001151), alcohol (MESH:D000438), tryptophan (MESH:D014364), trimethylamine (MESH:C023336), SCFA (MESH:D005232), Indole (MESH:C030374), Phenol (MESH:D019800), water (MESH:D014867), p-cresol (MESH:C032538), Disaccharides (MESH:D004187), indoles (MESH:D007211), vancomycin (MESH:D014640), TMA (MESH:C071868)
- **Species:** Bacteroides (genus) [taxon 816], Clavispora lusitaniae (species) [taxon 36911], Ligilactobacillus salivarius (species) [taxon 1624], Nakaseomyces glabratus (species) [taxon 5478], Prevotella (genus) [taxon 838], Faecalibacterium prausnitzii (species) [taxon 853], Homo sapiens (human, species) [taxon 9606], Clostridioides difficile (species) [taxon 1496], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], S. boulardii [taxon 252598], Cyclospora cayetanensis (species) [taxon 88456], Giardia duodenalis (species) [taxon 5741], Blastocystis hominis (species) [taxon 12968], Acinetobacter (genus) [taxon 469], Haemophilus (genus) [taxon 724], Clostridium (genus) [taxon 1485], Lacticaseibacillus rhamnosus (species) [taxon 47715], Candida albicans (species) [taxon 5476], Cryptosporidium (genus) [taxon 5806], Akkermansia muciniphila (species) [taxon 239935], Faecalibacterium (genus) [taxon 216851], Proteus (genus) [taxon 210425], Pichia kudriavzevii (species) [taxon 4909], Lodderomyces parapsilosis (species) [taxon 5480], Escherichia coli (E. coli, species) [taxon 562], Candida dubliniensis (species) [taxon 42374], Ammonia (genus) [taxon 29189], Klebsiella (genus) [taxon 570], Lacticaseibacillus paracasei (species) [taxon 1597], Agathobacter rectalis (species) [taxon 39491], Enterobacter (genus) [taxon 547], Enterococcus faecium (species) [taxon 1352], Lactiplantibacillus plantarum (species) [taxon 1590], Actinomycetota (actinobacteria, phylum) [taxon 201174], Citrobacter (genus) [taxon 544], Bacteroidia (class) [taxon 200643], Dientamoeba fragilis (species) [taxon 43352], Clostridia (class) [taxon 186801], gut metagenome (species) [taxon 749906], Ruminococcus (genus) [taxon 1263], Bifidobacterium animalis subsp. lactis (subspecies) [taxon 302911], Lactobacillus acidophilus (species) [taxon 1579], Entamoeba histolytica (species) [taxon 5759], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Enterobacteriaceae (enterobacteria, family) [taxon 543], Desulfovibrio (genus) [taxon 872], Morganella (genus) [taxon 108061], Bifidobacterium bifidum (species) [taxon 1681], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Pseudomonas (RNA similarity group I, genus) [taxon 286], Pseudomonadota (proteobacteria, phylum) [taxon 1224]
- **Mutations:** tyrosine/phenylalanine

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939515/full.md

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Source: https://tomesphere.com/paper/PMC12939515