Infectious Complications Are Associated With Alterations in the Gut Microbiome in Pediatric Patients With Acute Lymphoblastic Leukemia

Jacob T. Nearing, Jessica Connors, Scott Whitehouse, Johan Van Limbergen, Tamara Macdonald, Ketan Kulkarni, Morgan G.I. Langille

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54 Citas (Scopus)

Resumen

Acute lymphoblastic leukemia is the most common pediatric cancer. Fortunately, survival rates exceed 90%, however, infectious complications remain a significant issue that can cause reductions in the quality of life and prognosis of patients. Recently, numerous studies have linked shifts in the gut microbiome composition to infection events in various hematological malignances including acute lymphoblastic leukemia (ALL). These studies have been limited to observing broad taxonomic changes using 16S rRNA gene profiling, while missing possible differences within microbial functions encoded by individual species. In this study we present the first combined 16S rRNA gene and metagenomic shotgun sequencing study on the gut microbiome of an independent pediatric ALL cohort during treatment. In this study we found distinctive differences in alpha diversity and beta diversity in samples from patients with infectious complications in the first 6 months of therapy. We were also able to find specific species and functional pathways that were significantly different in relative abundance between samples that came from patients with infectious complications. Finally, machine learning models based on patient metadata and bacterial species were able to classify samples with high accuracy (84.09%), with bacterial species being the most important classifying features. This study strengthens our understanding of the association between infection and pediatric acute lymphoblastic leukemia treatment and warrants further investigation in the future.

Idioma originalEnglish
Número de artículo28
PublicaciónFrontiers in cellular and infection microbiology
Volumen9
DOI
EstadoPublished - feb. 19 2019

Nota bibliográfica

Funding Information:
We would like to acknowledge all of the patients and nurses at the IWK Health Center that made this study possible. We would also like to acknowledge the Langille lab for consistently providing constructive criticism. Funding. This study is funded through the Nova Scotia Health Research Foundation (NSHRF) establishment grant for KK and ML's NSERC Discovery Grant. JN is a trainee in the Cancer Research Training Program of the Beatrice Hunter Cancer Research Institute, with funds provided by the Terry Fox Research Institute (TFRI). JV was supported by a Canadian Institutes of Health Research (CIHR)-CAG-CCC New Investigator Award (2015–2018), a Canada Research Chair Tier 2 in Translational Microbiomics (2018–2023) and a Canadian Foundation of Innovation John R. Evans Leadership fund (awards #35235 and #36764), a Nova Scotia Health Research Foundation (NSHRF) establishment award (2015–2017), an IWK Health Centre Research Associateship, a donation from the MacLeod family and by a CIHR-SPOR-Chronic Diseases grant (Inflammation, Microbiome, and Alimentation: Gastro-Intestinal and Neuropsychiatric Effects: the IMAGINE-SPOR chronic disease network).

Publisher Copyright:
© Copyright © 2019 Nearing, Connors, Whitehouse, Van Limbergen, Macdonald, Kulkarni and Langille.

ASJC Scopus Subject Areas

  • Microbiology
  • Immunology
  • Microbiology (medical)
  • Infectious Diseases

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