Evidence map›Paper›PMID 41941490›Full record

ArticlePLoS pathogens2026

Dynamics of the microbiota in patients with Clostridioides difficile: Recurrence, treatment, sex, and immunosuppression.

Maria Paz Ventero, Rocio Herrero, Iryna Tyshkovska, Maria-Dolores Valverde-Fredet, Juan Carlos Rodríguez, Miguel Rodríguez-Fernández, Pilar González-De-La-Aleja, Marta Trigo, Monica Parra, Ana-Isabel Aller and 17 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Association betweenmedRxiv : the preprint server for health sciences · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Maria Paz VenteroMicrobiology Service, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.
Rocio HerreroClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Iryna TyshkovskaMicrobiology Service, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.
Maria-Dolores Valverde-FredetClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Juan Carlos RodríguezMicrobiology Service, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.ORCID 0000-0001-8007-5739
Miguel Rodríguez-FernándezClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Pilar González-De-La-AlejaUnit of Infectious Diseases, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.
Marta TrigoClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Monica ParraMicrobiology Service, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.
Ana-Isabel AllerClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Silvia OteroUnit of Infectious Diseases, Alicante General University Hospital - Alicante Institute of Health and Biomedical Research (ISABIAL), Alicante, Spain.
Reinaldo Espindola-GomezClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
José Manuel RamosClinical Medicine Department, Miguel Hernández University, Elche, Spain.
Eva M LeónClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Maria GarcíaUnit of Infectious Diseases, Vega Baja University Hospital - Orihuela, Spain-FISABIO, Foundation for the Promotion of Health and Biomedical Research of the Valencian Community, Valencia, Spain.
Miguel Nicolas Navarrete-LoriteUnit of Infectious Diseases, Virgen Macarena University Hospital, Sevilla, Spain.
Jara Llenas-GarcíaClinical Medicine Department, Miguel Hernández University, Elche, Spain.
Ines PortilloUnit of Infectious Diseases, Virgen Macarena University Hospital, Sevilla, Spain.
Francisco JoverUnit of Infectious Diseases, Sant Joan D'Alacant University Hospital, Sant Joan D'Alacant, Spain.
Maria TasiasInfectious Diseases Service, La Fe University and Polytechnic Hospital, Valencia, Spain.
Juan Jose CastonUnit of Infectious Diseases, Reina Sofía University Hospital, Córdoba, Spain.
Concepción GilUnit of Infectious Diseases, Marina Baixa Hospital, VillaJoiosa, Spain.
David Vinuesa-GarciaUnit of Infectious Diseases, San Cecilio University Hospital, Granada, Spain.
Cristina Gomez-AyerbeUnit of Infectious Diseases, Virgen de la Victoria University Hospital, Malaga, Spain.
Francisco J Martínez MarcosUnit of Infectious Diseases, Juan Ramón Jimenez University Hospital, Huelva, Spain.
Nicolas MerchanteClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.
Esperanza Merino De LucasClinical Unit of Infectious Diseases and Microbiology, Valme University Hospital, Institute of Biomedicine of Seville (IBiS), University of Seville, Sevilla, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlterations in the gut microbiome are central to the pathogenesis and recurrence of Clostridioides difficile infection (CDI).

objectiveTo evaluate intestinal microbiome changes during CDI and their association with recurrence, sex, age, and immunosuppression.

methodsPatients from the CDI-ANCRAID-SEICV cohort were consecutively enrolled. Stool samples were obtained at diagnosis (Dx), end of treatment (ET), and eight weeks post-treatment (8W) or upon recurrence. Microbiota composition was analyzed by 16S rRNA sequencing using QIIME2 and R. Outcomes were compared by demographics, immunosuppression, and treatment (vancomycin [VNC], vancomycin-bezlotuzumab [VNC-BZL], fidaxomicin [FDX]).

resultsAmong 143 patients, non-recurrent cases showed higher biodiversity at 8W versus diagnosis (H p = 0.002, ASVs p < 0.001), unlike recurrent cases. Diversity decreased with VNC (H p > 0.001, ASVs p < 0.001) but was preserved with FDX (H p = 0.15). Recovery of Shannon diversity was limited in women (p = 0.50) and immunocompromised patients (p = 0.31). At ET, Fusobacteria and Verrucomicrobiota were less abundant in recurrent than non-recurrent cases (0.77%, 0.53% vs 3.43%, 3.50%). FDX-treated samples showed higher Bacteroidetes (31.33%) compared to VNC (5.23%) or VNC-BZL (3.12%). Women exhibited increased Firmicutes abundance (p = 0.034).

conclusionsRestoration of microbial diversity correlates with CDI resolution. FDX preserves gut microbiota better than VNC or VNC-BZL. Women and immunocompromised patients demonstrate impaired microbiota recovery.

Indexed as

Clostridioides difficileClostridium InfectionsGastrointestinal MicrobiomeAdultAgedAnti-Bacterial AgentsFecesFemaleHumansImmunocompromised HostImmunosuppression TherapyMaleMiddle AgedRecurrenceRNA, Ribosomal, 16SSex FactorsAnti-Bacterial AgentsRNA, Ribosomal, 16SVancomycin

Identifiers

PMID41941490
PMCPMC13086424

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.