TY - JOUR
T1 - Patterns of salivary microbiota injury and oral mucositis in recipients of allogeneic hematopoietic stem cell transplantation
AU - Shouval, Roni
AU - Eshel, Adi
AU - Dubovski, Bar
AU - Danylesko, Ivetta
AU - Fein, Joshua A.
AU - Fried, Shalev
AU - Geva, Mika
AU - Kouniavski, Elizaveta
AU - Neuman, Hadar
AU - Armon-Omer, Ayelet
AU - Muller, Efrat
AU - Noecker, Cecilia
AU - Borenstein, Elhanan
AU - Louzoun, Yoram
AU - Nagler, Arnon
AU - Koren, Omry
N1 - Publisher Copyright: © 2020 American Society of Hematology. All rights reserved.
PY - 2020/7/14
Y1 - 2020/7/14
N2 - Oral mucositis (OM) is a common debilitating dose-limiting toxicity of cancer treatment, including hematopoietic stem cell transplantation (HSCT). We hypothesized that the oral microbiome is disturbed during allogeneic HSCT, partially accounting for the variability in OM severity. Using 16S ribosomal RNA gene sequence analysis, metabolomic profiling, and computational methods, we characterized the behavior of the salivary microbiome and metabolome of 184 patients pre- A nd post-HSCT. Transplantation was associated with a decrease in oral a diversity in all patients. In contrast to the gut microbiome, an association with overall survival was not detected. Among 135 patients given methotrexate for graftversus-host disease prophylaxis pre-HSCT, Kingella and Atopobium abundance correlated with future development of severe OM. Posttransplant, Methylobacterium species were significantly enriched in patients with severe OM. Moreover, the oral microbiome and metabolome of severe OM patients underwent distinct changes post-HSCT, compared with patients with no or mild OM. Changes in specific metabolites were well explained by microbial composition, and the common metabolic pathway was the polyamines pathway, which is essential for epithelial homeostasis. Together, our findings suggest that salivary microbial composition and metabolites are associated with the development of OM, offering new insights on pathophysiology and potential avenues of intervention.
AB - Oral mucositis (OM) is a common debilitating dose-limiting toxicity of cancer treatment, including hematopoietic stem cell transplantation (HSCT). We hypothesized that the oral microbiome is disturbed during allogeneic HSCT, partially accounting for the variability in OM severity. Using 16S ribosomal RNA gene sequence analysis, metabolomic profiling, and computational methods, we characterized the behavior of the salivary microbiome and metabolome of 184 patients pre- A nd post-HSCT. Transplantation was associated with a decrease in oral a diversity in all patients. In contrast to the gut microbiome, an association with overall survival was not detected. Among 135 patients given methotrexate for graftversus-host disease prophylaxis pre-HSCT, Kingella and Atopobium abundance correlated with future development of severe OM. Posttransplant, Methylobacterium species were significantly enriched in patients with severe OM. Moreover, the oral microbiome and metabolome of severe OM patients underwent distinct changes post-HSCT, compared with patients with no or mild OM. Changes in specific metabolites were well explained by microbial composition, and the common metabolic pathway was the polyamines pathway, which is essential for epithelial homeostasis. Together, our findings suggest that salivary microbial composition and metabolites are associated with the development of OM, offering new insights on pathophysiology and potential avenues of intervention.
KW - Are associated with mucositis development
KW - Dysbiosis of the oral microbiome with flourishment of pathobionts are accentuated in patients undergoing hsct with oral mucositis.
KW - Key points
KW - Salivary microbial composition and associated metabolites
KW - Specifically the polyamine pathway
UR - http://www.scopus.com/inward/record.url?scp=85088287756&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2020001827
DO - 10.1182/bloodadvances.2020001827
M3 - مقالة
C2 - 32598476
SN - 2473-9529
VL - 4
SP - 2912
EP - 2917
JO - Blood Advances
JF - Blood Advances
IS - 13
ER -