Abstract
Abstract Background Children with cancer are at risk for healthcare associated infections (HAIs) given their immunosuppression as well as frequent hospitalizations and antibiotic and antiseptic exposure. The degree to which the healthcare environment impacts the flora of children with cancer and its subsequent role in infection is uncertain. We prospectively evaluated the nasal microbiome in children with malignancy relative to healthy children. Methods Subjects were enrolled into two cohorts. The high risk cohort included children with a new diagnosis of malignancy recruited from the Texas Children’s Hospital Cancer Center. Children in the low risk cohort were otherwise healthy and enrolled from two Houston area general pediatrics clinics. Subjects had anterior nares swab samples obtained at 3-month intervals for one year. Genomic material was extracted from samples and the 16S rRNA V4 region was amplified and sequenced. Microbiome analysis was performed using QIIME 2, and comparisons in both bacterial diversity (alpha diversity via Shannon index) and composition (genus-level) were made based on cohort and time point. We present early data from the time of subject enrollment and first follow-up. Results 272 subjects were enrolled. Cohorts were similar in terms of demographics. No subjects were neutropenic at time of sample collection. High-risk subjects were significantly more likely to have received antibiotics (96.4% vs. 17.5%, p< 0.01) and/or chlorhexidine gluconate containing products (91.6% vs. 0%, p< 0.01) in the 90 days prior to enrollment. Within the high-risk cohort, 98.8% had received antineoplastic chemotherapy. Alpha diversity (Shannon index) was lower in the high risk cohort compared to the low risk cohort. In the high-risk cohort, the genera Staphylococcus and Corynebacterium were disproportionately represented relative to the low-risk cohort in which Moraxella predominated (Figure 1). Nasal microbiota were similar across cancer diagnoses. Conclusion There are significant changes in the nasal microbiota of children with cancer relative to healthy children. These findings suggest a high impact of healthcare exposure and specifically antibiotics and antiseptics on colonizing flora. Further work is needed to understand how these microbiome perturbations modify risk for HAI. Disclosures Jonathon C. McNeil, MD, Allergan: Grant/Research Support|Nabriva Therapeutics: Grant/Research Support
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.