Evidence map›Paper›PMID 41733389›Full record

ArticleThe Journal of infectious diseases2026

Gut Microbiota and Intestinal Monodomination as a Predictor for Bacteremia in Allogeneic Hematopoietic Cell Transplant Recipients.

M M DeMeules, S C Proll, X Hua, S Srinivasan, T Loeffelholz, C Liu, M C Wu, T L Fiedler, N G Hoffman, L A Bourassa and 2 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

M M DeMeulesVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0001-8393-587X
S C ProllVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
X HuaPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
S SrinivasanVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-7267-3859
T LoeffelholzVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
C LiuVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
M C WuPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
T L FiedlerVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-5661-1199
N G HoffmanDepartment of Laboratory Medicine, University of Washington, Seattle, Washington, USA.
L A BourassaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
S A PergamVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-6333-5196
D N FredricksVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0003-2735-6800

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
The Gut Microbiota and Graft versus Host Disease (GVHD)R01AI134808 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI FREDRICKS, DAVID NEAL · 2018 to 2022
$4.0M
Fred Hutch Cancer Center P30CA015704National Institute of Allergy and Infectious DiseasesNCI NIH HHS P30 CA015704NIAID NIH HHS R01 AI134808NIH HHS R01 AI134808
6 · The paper itself

Abstract

backgroundBacteremia is a frequent complication in patients undergoing allogeneic hematopoietic cell transplantation (HCT). Alterations to the gut microbiota after HCT have been associated with adverse outcomes including bacteremia and reduced overall survival. Previous studies suggest that loss of gut bacterial diversity and domination by a single species may predict bloodstream infections, but the degree of domination leading to the optimal positive predictive value (PPV) has not been defined.

methodsStool samples were collected weekly from allogeneic HCT recipients and were analyzed by 16S rRNA gene PCR with sequencing to determine gut microbiota composition and document domination events. Bacteremia events were captured by review of medical records. The PPV for bacteremia of any detection of that species in stool and for domination events at 10%, 30%, and 50% abundance were calculated.

resultsOf 277 HCT recipients, 95 experienced bacteremia, with 130 bacteremia events. Intestinal domination was associated with but not highly predictive for bacteremia, reflected by low PPV. Presence of coagulase-negative Staphylococcus in the gut at >30% relative abundance was associated with increased risk of coagulase-negative Staphylococcus bloodstream infections with PPV of 38%.

conclusionsHematopoietic cell transplantation is associated with significant disruption to the gut microbiota, particularly in patients who subsequently develop bacteremia. Intestinal domination may not be as useful as previously thought given its low PPV for most species implicated in bloodstream infections. The association between gut colonization with Staphylococcus and bacteremia events suggests that the gut may be an under-recognized portal of entry for these organisms in patients after HCT.

Indexed as

BacteremiaGastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationAdolescentAdultAgedFecesFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16STransplantation, HomologousYoung AdultRNA, Ribosomal, 16Sbacteremiahematopoietic cell transplantmicrobiota

Identifiers

PMID41733389
PMCPMC13431778

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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.