TY - JOUR
T1 - Detection of Pathogens in the Gut Microbiome Prior to Bloodstream Infection in Children with Acute Myeloid Leukemia or Mature B-Cell Non-Hodgkin Lymphoma
AU - Schmidt, Juliëtte
AU - Miguélez Sánchez, Maria
AU - Wolfs, Tom
AU - Jans, Jop
AU - van der Bruggen, Jan Tom
AU - Budding, Andries
AU - el Manouni el Hassani, Sofia
AU - de Meij, Tim
AU - Harmsen, Hermie
AU - Goemans, Bianca
AU - Meyer-Wentrup, Friederike
AU - Bont, Louis
AU - Tissing, Wim
N1 - Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press on behalf of the Pediatric Infectious Diseases Society. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2026/8
Y1 - 2026/8
N2 - Background: Bloodstream infections (BSIs) cause significant morbidity and mortality in children with hematological malignancies. The gut may serve as a potential reservoir for BSI-causing bacteria. Therefore, this longitudinal study aimed to assess the abundance of BSI-causing bacterial strains in the gut microbiota prior to BSI. Methods: This prospective longitudinal cohort study included children (1-18 years) diagnosed with acute myeloid leukemia or mature B-cell non-Hodgkin lymphoma. Fecal samples were collected twice weekly, and additionally whenever a BSI was suspected. Gut microbiota were profiled at species level using the PCR-based assay Molecular Culture. Results: We recruited 26 children, of whom 16 experienced a total of 31 BSI episodes. In total, 18 out of 38 BSI pathogens (47.4%) could be detected in fecal samples prior to BSI. In the BSI episodes caused by enteric bacteria, 75% of all causative enteric bacteria could be found prior to BSI. Also, bacteria not typically associated with the gut could be detected prior to BSI in feces (Streptococcus mitis in 100% of cases, Staphylococcus epidermidis in 29% of cases). Furthermore, in fecal samples collected after BSI onset and start of antibiotic treatment, 58% of the BSI pathogens could be detected. Conclusions: BSI pathogens, both gram-negative and gram-positive, can be detected in the gut microbiome prior to BSI, and an increase in relative abundance is related to BSI. Secondly, BSI pathogens may persist despite BSI-directed intravenous antibiotic therapy, potentially preceding future BSIs.
AB - Background: Bloodstream infections (BSIs) cause significant morbidity and mortality in children with hematological malignancies. The gut may serve as a potential reservoir for BSI-causing bacteria. Therefore, this longitudinal study aimed to assess the abundance of BSI-causing bacterial strains in the gut microbiota prior to BSI. Methods: This prospective longitudinal cohort study included children (1-18 years) diagnosed with acute myeloid leukemia or mature B-cell non-Hodgkin lymphoma. Fecal samples were collected twice weekly, and additionally whenever a BSI was suspected. Gut microbiota were profiled at species level using the PCR-based assay Molecular Culture. Results: We recruited 26 children, of whom 16 experienced a total of 31 BSI episodes. In total, 18 out of 38 BSI pathogens (47.4%) could be detected in fecal samples prior to BSI. In the BSI episodes caused by enteric bacteria, 75% of all causative enteric bacteria could be found prior to BSI. Also, bacteria not typically associated with the gut could be detected prior to BSI in feces (Streptococcus mitis in 100% of cases, Staphylococcus epidermidis in 29% of cases). Furthermore, in fecal samples collected after BSI onset and start of antibiotic treatment, 58% of the BSI pathogens could be detected. Conclusions: BSI pathogens, both gram-negative and gram-positive, can be detected in the gut microbiome prior to BSI, and an increase in relative abundance is related to BSI. Secondly, BSI pathogens may persist despite BSI-directed intravenous antibiotic therapy, potentially preceding future BSIs.
KW - children
KW - infections
KW - leukemia
KW - lymphoma
KW - microbiome
UR - https://www.scopus.com/pages/publications/105047012433
U2 - 10.1093/jpids/piag066
DO - 10.1093/jpids/piag066
M3 - Article
C2 - 42520215
AN - SCOPUS:105047012433
SN - 2048-7193
VL - 15
JO - Journal of the Pediatric Infectious Diseases Society
JF - Journal of the Pediatric Infectious Diseases Society
IS - 8
M1 - piag066
ER -