Abstract

Simple SummaryChildhood cancer survivors suffer from many oral complications during and after primary therapy. Our study focuses on changes in the oral microbiome of cancer survivors. Using 16S rRNA sequencing, we observed global and distinct changes in oral microbiome associated with a patient’s age and therapy duration, but not antibiotic therapy or cancer type. Observed changes in the oral microbiome could differentiate patients at higher risk of long-term oral complications.A child’s mouth is the gateway to many species of bacteria. Changes in the oral microbiome may affect the health of the entire body. The aim of the study was to evaluate the changes in the oral microbiome of childhood cancer survivors. Saliva samples before and after anti-cancer treatment were collected from 20 patients aged 6–18 years, diagnosed de novo with cancer in 2018–2019 (7 girls and 13 boys, 7.5–19 years old at the second time point). Bacterial DNA was extracted, and the microbial community profiles were assessed by 16S rRNA sequencing. The relative abundances of Cellulosilyticum and Tannerella genera were found to significantly change throughout therapy (p = 0.043 and p = 0.036, respectively). However, no differences in the alpha-diversity were observed (p = 0.817). The unsupervised classification revealed two clusters of patients: the first with significant changes in Campylobacter and Fusobacterium abundance, and the other with change in Neisseria. These two groups of patients differed in median age (10.25 vs. 16.16 years; p = 0.004) and the length of anti-cancer therapy (19 vs. 4 months; p = 0.003), but not cancer type or antibiotic treatment.

Highlights

  • The emergence of new molecular biology techniques, such as high-throughput sequencing techniques, has completely changed the face of clinical microbiology

  • The present study examines whether the salivary microbiome of childhood patients is altered over the course of anti-cancer chemotherapy

  • A total of 71 children newly diagnosed with various types of cancer at the Department of Pediatrics, Oncology & Hematology, between March 2018 and February 2019, were approached to participate in the study

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Summary

Introduction

The emergence of new molecular biology techniques, such as high-throughput sequencing techniques, has completely changed the face of clinical microbiology. Their use in metagenomics research has increased the speed and accuracy of diagnosis [1]. One of the latest strategies involves the use of targeted sequencing for the bacterial 16S rRNA gene. This method has already gained many positive results in examining microbiota changes in such regions as the lungs, vagina, urinary tract, or gut [4,5,6,7].

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