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dc.contributor.authorGonzález Rico, Claudiaes_ES
dc.contributor.authorHernández, Martaes_ES
dc.contributor.authorRodríguez Grande, Jorgees_ES
dc.contributor.authorFernández Luis, Saraes_ES
dc.contributor.authorBermúdez Rodríguez, María Aranzazu es_ES
dc.contributor.authorGonzález Huerta, Ana Juliaes_ES
dc.contributor.authorLlaneza Velasco, Eugeniaes_ES
dc.contributor.authorVázquez López, Lourdeses_ES
dc.contributor.authorGarcía García, Inmaculadaes_ES
dc.contributor.authorArnaiz de las Revillas Almajano, Franciscoes_ES
dc.contributor.authorFariñas Álvarez, María Concepciónes_ES
dc.contributor.authorCalvo Montes, Jorgees_ES
dc.contributor.authorOcampo Sosa, Alaines_ES
dc.contributor.authorFernández Martínez, Martaes_ES
dc.contributor.authorFariñas Álvarez, María del Carmen es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-12-12T11:58:23Z
dc.date.available2025-12-12T11:58:23Z
dc.date.issued2025es_ES
dc.identifier.issn1201-9712es_ES
dc.identifier.issn1878-3511es_ES
dc.identifier.urihttps://hdl.handle.net/10902/38504
dc.description.abstractObjectives Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is associated with significant alterations in gut microbiota (GM) composition, affecting transplant success. This study aimed to correlate these GM changes with post-transplant (post-HSCT) outcomes. Methods A prospective multicentre cohort study was conducted between June 2017 and December 2021 in three Spanish hospitals. Stool samples from allo-HSCT recipients were collected before HSCT, and at 14-, 30-, 60-, and 100-days post-HSCT. Bacterial 16S rRNA gene sequences were characterized and microbial diversity assessed. Results Analysis of 409 samples from 95 patients revealed significant longitudinal GM shifts. Alpha diversity significantly decreased at days 14 ( P < 0.001), 30 ( P < 0.001), and 60 ( P = 0.002) compared to baseline. A distinct shift in dominant taxonomic profiles was observed, notably a significant decrease in Blautia abundance ( P < 0.001). Patients with acute gastrointestinal graft-versus-host disease (GI-GVHD) ( P = 0.009), bacteraemia ( P = 0.014), or death ( P < 0.001) exhibited significantly lower Blautia levels. LEfSe analysis identified 22 differential taxa between deceased and surviving patients; the former showed higher abundance of potential pathogens such as Enterococcus_H ( P = 0.026), Enterococcus_A ( P = 0.019), and Staphylococcus ( P = 0.009). Conclusions Significant variations in the GM?s taxonomic profiles and relative abundances post-HSCT, particularly the decrease in Blautia and the increase in certain pathogens, are associated with poorer clinical outcomes.es_ES
dc.description.sponsorshipThis work was supported by Instituto de Salud Carlos III through the project ‘PI16/01415’ (Co-funded by European Regional Development Fund ‘A way to make Europe’) under Grant number [PI16/01415 to MCF]; Instituto de Investigación Marqués de Valdecilla (IDIVAL) through the emerging researchers support program, ‘NEXT-VAL’ 2021 under Grant number [NVAL21/18 to CGR]; and CIBER -Consorcio Centro de Investigación Biomédica en Red-(CB21/13/00068), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea—NextGenerationEU.es_ES
dc.format.extent20 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2025 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceInternational Journal of Infectious Diseases, 2025, 161, 108117es_ES
dc.titleChanges in the bacterial profile and diversity of the gut microbiota in allogeneic hematopoietic stem cell transplant recipientses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.ijid.2025.108117es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.ijid.2025.108117es_ES
dc.type.versionpublishedVersiones_ES


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© 2025 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND
license (http://creativecommons.org/licenses/by-nc-nd/4.0/)Excepto si se señala otra cosa, la licencia del ítem se describe como © 2025 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)