Detection of pathogens in the gut microbiome prior to bloodstream infection in children with acute myeloid leukemia or mature B-cell non-Hodgkin lymphoma

Abstract 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.

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Journal
Journal of the Pediatric Infectious Diseases Society
Published
2026-07-27
DOI
https://doi.org/10.1093/jpids/piag066
Primary Topic
Gut microbiota and health
Type
article
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article

Detection of pathogens in the gut microbiome prior to bloodstream infection in children with acute myeloid leukemia or mature B-cell non-Hodgkin lymphoma

Juliëtte Schmidt, wim tissing, Sofia el Manouni el Hassani, Friederike Meyer- Wentrup et al.
Journal of the Pediatric Infectious Diseases Society
Gut microbiota and health
article

Detection of pathogens in the gut microbiome prior to bloodstream infection in children with acute myeloid leukemia or mature B-cell non-Hodgkin lymphoma

Juliëtte Schmidt, wim tissing, Sofia el Manouni el Hassani, Friederike Meyer- Wentrup, Hermie Harmsen, Tim G. J. de Meij, María Miguélez Sánchez, Jan‐Tom van der Bruggen, Tom Wolfs, Louis Bont, Andries Budding, Bianca Goemans, Jop Jans
article en

Abstract

Abstract 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.

Journal of the Pediatric Infectious Diseases Society
University Medical Center Groningen (NL), University Medical Center Utrecht (NL), Princess Máxima Center (NL), Proteome Sciences (United Kingdom) (GB), Amsterdam University Medical Centers (NL), Wilhelmina Children's Hospital (NL), University of Amsterdam (NL)
Good health and well-being
Openalex Percentile: Top 14%
Gut microbiota and health
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