Patterns of salivary microbiota injury and oral mucositis in recipients of allogeneic hematopoietic stem cell transplantation

Author:

Shouval Roni123ORCID,Eshel Adi4ORCID,Dubovski Bar5,Kuperman Amir A.46ORCID,Danylesko Ivetta1ORCID,Fein Joshua A.17ORCID,Fried Shalev1ORCID,Geva Mika1,Kouniavski Elizaveta1,Neuman Hadar8,Armon-Omer Ayelet8,Shahien Radi48,Muller Efrat9ORCID,Noecker Cecilia10ORCID,Borenstein Elhanan91112,Louzoun Yoram5ORCID,Nagler Arnon1,Koren Omry4ORCID

Affiliation:

1. Hematology and Bone Marrow Transplantation Division, Chaim Sheba Medical Center, Tel Hashomer, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel;

2. Dr Pinchas Bornstein Talpiot Medical Leadership Program, Chaim Sheba Medical Center, Tel Hashomer, Israel;

3. Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, NY;

4. Azrieli Faculty of Medicine, Bar Ilan University, Safed, Israel;

5. Department of Mathematics, Bar Ilan University, Ramat Gan, Israel;

6. Blood Coagulation Service and Pediatric Hematology Clinic, Galilee Medical Center, Nahariya, Israel;

7. University of Connecticut Medical Center, Farmington, CT;

8. Ziv Medical Center, Zefat, Israel;

9. The Blavatnik School of Computer Science, Tel Aviv University, Tel Aviv, Israel;

10. Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA;

11. Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; and

12. Santa Fe Institute, Santa Fe, NM

Abstract

Abstract 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- and post-HSCT. Transplantation was associated with a decrease in oral α diversity in all patients. In contrast to the gut microbiome, an association with overall survival was not detected. Among 135 patients given methotrexate for graft-versus-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.

Publisher

American Society of Hematology

Subject

Hematology

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