Journal of Clinical Medicine · 2020 · 30 citations · 20 references
DentistryImmunologyInfectious DiseasesDiagnostic MicrobiologyMedical MicrobiologyOral MicrobiologyOral CandidiasisOral InfectionsOral Microbial DysbiosisOral Microbial PathogenesisOral MucosaOral Mucosal Diseases16S Rrna Gene PhylogenyChemotherapy-induced Oral MucositisMucositis Severity AssessmentOral Microbial Diversity AnalysisOral Microbiome DiversityOral Mucosal HealthOral Mucosal MicrobiomeOral Viral Diversity
Oral mucositis (OM) is a common complication of chemotherapy and remains a significant unmet need. The aim of this study was to investigate the role of oral bacteriota and HSV-1 in OM. Forty-six patients admitted for autologous hematopoietic stem cell transplantation were longitudinally evaluated for OM, Candida, HSV-1, and leukocyte count, and buccal mucosal bacterial samples were obtained during their admission period. The bacterial communities collected at the baseline and post-chemotherapy, chosen from the time with the highest severity, were analyzed by sequencing the 16S rRNA gene. Twenty (43.5%) patients developed OM, the severity of which ranged from 1 to 5 according to the Oral Mucositis Assessment Scale (OMAS). Chemotherapy significantly increased the prevalence of HSV-1 detection but not that of Candida. The bacterial communities of patients after conditioning chemotherapy were characterized by aberrant enrichment of minor species and decreased evenness and Shannon diversity. After adjustment for age, gender, and neutropenia, the presence of HSV-1 was associated with the incidence of OM (odds ratio = 3.668, p = 0.004), while the decrease in Shannon diversity was associated with the severity of OM (β = 0.533 ± 0.220, p = 0.015). The control of HSV-1 and restoration of oral bacterial diversity may be a novel option to treat or prevent OM.
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Chemotherapy-induced oral mucositis is associated with detrimental bacterial dysbiosis
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Dentistry, Microbiology, Oncology +17